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Master List of Kava Research Articles

Master List of Kava Research Articles

Best Fiji Kava on Sep 13th 2023

Here it is, kava lovers, the main list of all research on kava and kava related topics. This information is where all of the "Facts of the Day" originate. If you've found any other articles, please post them here and I will keep our list updated.

Kuchta, K., Hladikova, M., Thomsen, M., Nahrstedt, A. & Schmidt, M. Kava (Piper methysticum) Extract for the Treatment of Nervous Anxiety, Tension and Restlessness. Drug Res (Stuttg)71, 83-93 (2021).

(https://pubmed.ncbi.nlm.nih.gov/33207379/)

Connor, K., Davidson, J., & Connor, K. M. (2002). A placebo-controlled study of Kava kava in generalized anxiety disorder.

(https://doi.org/10.1097/00004850-200207000-00005)

Tabudravu, J. N., & Jaspars, M. (2005). Anticancer activities of constituents of kava (Piper methysticum).

(https://www.publish.csiro.au/sp/SP05005)

Schmidt, N., & Ferger, B. (2001). Neuroprotective Effects of ()-Kavain in the MPTP Mouse Model of Parkinson’s Disease.

(https://doi.org/10.1002/1098-2396(200104)40:1<47::aid-syn1025>3.0.co;2-s)

Food Standards Australia New Zealand. (2004). KAVA A Human Health Risk Assessment.

(https://www.foodstandards.gov.au/publications/documents/30_Kava1.pdf)

Cairney, S., Maruff, P. & Clough, A. R. The neurobehavioural effects of kava. , (2002).

(https://pubmed.ncbi.nlm.nih.gov/12225450)

Sarris J. Herbal medicines in the treatment of psychiatric disorders: 10-year updated review. Phytother Res. 2018 Jul;32(7):1147-1162. doi: 10.1002/ptr.6055. Epub 2018 Mar 25. PMID: 29575228.

(https://doi.org/10.1002/ptr.6055)

Kuchta K, Schmidt M, Nahrstedt A. German Kava Ban Lifted by Court: The Alleged Hepatotoxicity of Kava (Piper methysticum) as a Case of Ill-Defined Herbal Drug Identity, Lacking Quality Control, and Misguided Regulatory Politics. Planta Med. 2015 Dec;81(18):1647-53. doi: 10.1055/s-0035-1558295. Epub 2015 Dec 22. PMID: 26695707.

(https://doi.org/10.1055/s-0035-1558295)

Ernst E. A re-evaluation of kava (Piper methysticum). Br J Clin Pharmacol. 2007 Oct;64(4):415-7. doi: 10.1111/j.1365-2125.2007.02932.x. Epub 2007 Jun 6. PMID: 17555466; PMCID: PMC2048557.

(https://doi.org/10.1111/j.1365-2125.2007.02932.x)

Volgin A, Yang L, Amstislavskaya T, Demin K, Wang D, Yan D, Wang J, Wang M, Alpyshov E, Hu G, Serikuly N, Shevyrin V, Wappler-Guzzetta E, de Abreu M, Kalueff A. DARK Classics in Chemical Neuroscience: Kava. ACS Chem Neurosci. 2020 Jan 21. doi: 10.1021/acschemneuro.9b00587. Epub ahead of print. PMID: 31904216.

(https://doi.org/10.1021/acschemneuro.9b00587)

Sarris J, Teschke R, Stough C, Scholey A, Schweitzer I. Re-introduction of kava (Piper methysticum) to the EU: is there a way forward? Planta Med. 2011 Jan;77(2):107-10. doi: 10.1055/s-0030-1250290. Epub 2010 Sep 2. PMID: 20814850.

(https://doi.org/10.1055/s-0030-1250290)

PHAMA. (2018). FIJI KAVA VALUE CHAIN ANALYSIS.

(https://phama.com.au/wp-content/uploads/2018/06/Fiji-Kava-Value-Chain-Analysis-Report-FINAL.pdf)

Foo H, Lemon J. Acute effects of kava, alone or in combination with alcohol, on subjective measures of impairment and intoxication and on cognitive performance. Drug Alcohol Rev. 1997 Jun;16(2):147-55. doi: 10.1080/09595239700186441. PMID: 16203421.

(https://doi.org/10.1080/09595239700186441)

Singh YN. Potential for interaction of kava and St. John's wort with drugs. J Ethnopharmacol. 2005 Aug 22;100(1-2):108-13. doi: 10.1016/j.jep.2005.05.014. PMID: 16005588.

(https://doi.org/10.1016/j.jep.2005.05.014)

Republic of Vanuatu, Kava Act No 7 of 2002

(https://biosecurity.gov.vu/images/Export/kava-act-2002.pdf)

Waldeni, J., VON WEGERERl, J., Winterz, U., BERGERl, M., & Grunze, H. (1997). Effects of kawain and dihydromethysticin on field potential changes in the hippocampus. In Elsevler Science Inc. Neuro-Psychopharmacol. & Biol. Psychiat (Vol. 21).

(https://doi.org/10.1016/s0278-5846(97)00042-0)

Aporosa, S. G. (2006). Yaqona and Education in Fiji: A Clash of Cultures?

(https://www.academia.edu/1134788/Yaqona_kava_Education_and_Development_in_Fiji)

Kubatova, A., Miller, D. J., & Hawthorne, S. B. (2001). Comparison of subcritical water and organic solvents for extracting kava lactones from kava root. In Journal of Chromatography A.

(https://doi.org/10.1016/s0021-9673(01)00979-7)


De Leo, V., La Marca, A., Morgante, G., Lanzetta, D., Florio, P., & Petraglia, F. (2001). Evaluation of combining kava extract with hormone replacement therapy in the treatment of postmenopausal anxiety. In Maturitas (Vol. 39). 

(www.elsevier.com/locate/maturitas)


Lopez-Avila, V., & Benedicto, J. (1997). Supercritical Fluid Extraction of Kava Lactones from Piper methysticum (Kava) Herb.

(https://doi.org/10.1002/jhrc.1240201007)

Balick, M. J., & Lee, R. A. (2009). The Sacred Root. In Ethnobotany of Pohnpei.

(https://doi.org/10.1515/9780824837495-008)

Anke, J., & Ramzan, I. (2004). Pharmacokinetic and pharmacodynamic drug interactions with Kava (Piper methysticum Forst. f.). In Journal of Ethnopharmacology (Vol. 93, Issues 2–3, pp. 153–160).

(https://doi.org/10.1016/j.jep.2004.04.009)


Tanaka, A., Hamada, N., Fujita, Y., Itoh, T., Nozawa, Y., Iinuma, M. & Ito, M. A novel kavalactone derivative protects against H2O2-induced PC12 cell death via Nrf2/ARE activation. Bioorganic and Medicinal Chemistry 18, 3133-3139 (2010).
(https://pubmed.ncbi.nlm.nih.gov/20371185/)

Boerner, J. R. & Klement, S. Attenuation of neuroleptic-induced extrapyramidal side effects. Wiener medizinische Wochenschrift 154, 508-510 (2004).
(https://pubmed.ncbi.nlm.nih.gov/15638068/)


Lindstrom, L., Kava Pirates in Vanuatu?. International Journal of Cultural Property 16, 291-308 (2009).
(https://doi.org/10.1017/S0940739109990208)

Jayararnan, T. K., BUILDING ECONOMIC RESILIENCE : THE CASE OF VANUATU. Economic Vulnerability and Resilience of Small States. , 135-148 (2004).
(https://www.semanticscholar.org/pap...aman/3b67e7bdff8f68b4a1582f0758d9550465ddc029)

Ben Dhaou, S. I. & Rohman, I. K. Everything and its opposite. 80, 631-639 (2018).
(https://www.jstor.org/stable/30052773)

Yuan CS, Dey L, Wang A, Mehendale S, Xie JT, Aung HH, Ang-Lee MK. Kavalactones and dihydrokavain modulate GABAergic activity in a rat gastric-brainstem preparation. Planta Med. 2002 Dec;68(12):1092-6. doi: 10.1055/s-2002-36338. PMID: 12494336.
(https://pubmed.ncbi.nlm.nih.gov/12494336/)

Cox, P. A. & O'Rourke, L. Kava (Piper methysticum, Piperaceae). Economic Botany 41, 452-454 (1987).
(https://www.jstor.org/stable/4254999)

Long, D. D., Urs, S., Karin Berger Bueter, Bernd Bueter, Kenneth Lundstrom, & Willi Schaffner. (2001). Interaction of Various Piper methysticum Cultivars with CNS Receptors in vitro. Planta Med, 67(4), 306–311.
https://doi.org/10.1055/s-2001-14334

Kawa-pyrone, A. W., I + 13,8. , (1965).

Martin, H., McCallum, M., Stofer, D. W. & Eichinger, M. R. Kavain attenuates vascular contractility through inhibition of calcium channels. Planta Med 68, 784-789 (2002).
(https://pubmed.ncbi.nlm.nih.gov/12357387/)

Guiart, J., JOHN FRUM MOVEMENT IN TANNA. Oceania 22, 165-177 (1952).
(https://www.jstor.org/stable/40328340)

Klohs, W., Keller, F., Williar, R. E., Toekes, M. I. & Cronheim, G. E. A Chemical and Pharmacological Investigation of Piper Methysticum Forst. J. Med. Chem. 1, 95-103 (1959).
(https://pubs.acs.org/doi/abs/10.1021/jm50002a007/)

Norton, S. A., Kava dermopathy. Journal of the American Academy of Dermatology 31, 89-97 (1994).
(https://pubmed.ncbi.nlm.nih.gov/8021378/)

Schmitz, D., Zhang, C., Chatterjee, S., Heinemaun, U., {Chatterjee Abteilung Pharmakologie Fa Schwabe}, S. W. & Heinemann, U. Effects of methysticin on three different models of seizure like events studied in rat hippocampal and entorhinal cortex slices. Naunyn-Schmiedeberg's Arch Pharmacol 351, 348-355 (1995).
(https://pubmed.ncbi.nlm.nih.gov/7630425/)

Aporosa, S. A., Yaqona ( Kava ) As a Symbol of Cultural Identity. , 79-101 (2012).
(https://www.semanticscholar.org/pap...rosa/70058a9269f3a52aa8d09b9f4dca400fe4267f7e)

Whitton, A. P., Response to Schmidt "Are Kavalactones the Hepatotoxic Principle of Kava Extracts? The Pitfalls of the Glutathione Theory. The Journal of Alternative and Complementary Medicine 9, 187-188 (2003).
(https://doi.org/10.1089/10755530360623293 )

Munte, T., Heinze, H., Matzke, M. & Steiz, J. Effects of oxazepam and an extract of kava roots (Piper methysticum) on event-related potentials in a word recognition task. Neuropsychobiology 27, 46-53 (1993).
(https://www.karger.com/Article/Abstract/118952)

Apo' Aporosa}, S. '., The new kava user: Diasporic identity formation in reverse. New Zealand Sociology 30, 58-77 (2015).
(https://researchcommons.waikato.ac.nz/handle/10289/12796)

Aporosa, S. A., Kava and Ethno-cultural Identity in Oceania. The Palgrave Handbook of Ethnicity , 1-15 (2019).
(https://researchcommons.waikato.ac.nz/handle/10289/12377)

Aporosa, S. A., Atkins, M. & Leov, J. N. Decolonising quantitative methods within a Pacific research space to explore cognitive effects following kava use. Pacific Dynamics 5, 2021 (2021).
(https://researchcommons.waikato.ac.nz/handle/10289/14153)

'Apo', A. S., Is Kava Alcohol?: The Myths and the Facts. Pacific Health Dialog 17, 157-164 (2011).
(https://pubmed.ncbi.nlm.nih.gov/23008981/)

Aporosa, S. & Tomlinson, M. Kava hangover and gold-standard science. Anthropologica 56, 163-175 (2014).
(https://www.jstor.org/stable/24469648)

Mathews, J. M., Etheridge, A. S., Valentine, J. L., Black, S. R., Coleman, D. P., Patel, P., So, J. & Burka, L. T. Pharmacokinetics and disposition of the kavalactone kawain: Interaction with kava extract and kavalactones in vivo and in vitro. Drug Metabolism and Disposition 33, 1555-1563 (2005).
(https://doi.org/10.1124/dmd.105.004317)

Lebot, V., Aradhya, M. & Manshardt, R. Geographic Survey of Genetic Variation in Kava (Piper methysticum Forst. f.and P. wichmannii C. DC.). Pacific Science 45, 169-185 (1991).
(https://scholarspace.manoa.hawaii.edu/bitstream/10125/518/1/v45n2-169-185.pdf)

Boerner, R. J., Kava kava in the treatment of generalized anxiety disorder, simple phobia and specific social phobia. Phytotherapy Research 15, 646-647 (2001).
(https://doi.org/10.1002/ptr.1006)

McDonald, D. & Jowitt, A. Kava in the Pacific Islands: A contemporary drug of abuse?. Drug and Alcohol Review 19, 217-227 (2000).
(https://onlinelibrary.wiley.com/doi/abs/10.1080/713659319)

Vandenbroucke, H., Mournet, P., Malapa, R., Glaszmann, J. C., Chair, H. & Lebot, V. Comparative analysis of genetic variation in kava (Piper methysticum) assessed by SSR and DArT reveals zygotic foundation and clonal diversification. Genome 58, 1-11 (2015).
(https://pubmed.ncbi.nlm.nih.gov/25973616/)

Krum, B. N., Molz de Freitas, C., Chiapinotto Ceretta, A. P., Barbosa, C. P., de Moraes Reis, E., Scussel, R., da Silva Córneo, E., Machado-de-Ávila, R. A., Boligon, A. A., & Fachinetto, R. (2020). Kava decreases the stereotyped behavior induced by amphetamine in mice. Journal of Ethnopharmacology, 265(July 2020).
(https://doi.org/10.1016/j.jep.2020.113293)

Luxminarayan, L., Neha, S., Amit, V. & Khinchi, M. A Research Article on Antistress Activity of Herbal Extract Oil of Piper Methysticum on Wistar Albino. Asian Journal of Pharmaceutical Research and Development. Asian Journal of Pharmaceutical Research and Development 5, 1-8 (2017).
(https://ajprd.com/index.php/journal/article/view/892)

Boonen1, G., Ferger2, B., Kuschinsky2, K., & Häberleinl, H. (1998). In vivo Effects of the Kavapyrones (+)- dihydromethysticin and (±)-Kavain on Dopamine, 3,4-Dihydroxyphenylacetic Acid, Serotonin and 5-Hydroxyindoleacetic Acid Levels in Striatal and Cortical Brain Regions. 4.Watkins, L. L., Connor, K. M. & Davidson, J. R. Effect of kava extract on vagal cardiac control in generalized anxiety disorder: Preliminary findings. Journal of Psychopharmacology 15, 283-286 (2001).
(https://pubmed.ncbi.nlm.nih.gov/9741294/)

Narayanapillai, S. C., Leitzman, P., O'Sullivan, M. G. & Xing, C. Flavokawains A and B in kava, not dihydromethysticin, potentiate acetaminophen-induced hepatotoxicity in C57BL/6 mice. Chem. Res. Toxicol. 27, 1871-1876 (2014).
(https://pubmed.ncbi.nlm.nih.gov/25185080/)

Food,, Nations, A. O. o. t. U. & Organization, W. H. Kava: a review of the safety of traditional and recreational beverage consumption. World Health Organization , 1-47 (2016).
(http://www.fao.org/publications/card/en/c/1b72914b-8ac8-428f-8fc9-40f1fb4e6f3a/)

Lehrl, S., Clinical efficacy of kava extract WS1490 in sleep disturbances associated with anxiety disorders: Results of a multicenter, randomized, placebo-controlled, double-blind clinical trial. Journal of Affective Disorders 78, 101-110 (2004).
(https://pubmed.ncbi.nlm.nih.gov/14706720/)

Chaurasiya, N. D., León, F., Ding, Y., Gómez-Betancur, I., Benjumea, D., Walker, L. A., Cutler, S. J., & Tekwani, B. L. (2017). Interactions of Desmethoxyyangonin, a Secondary Metabolite from Renealmia alpinia, with Human Monoamine Oxidase-A and Oxidase-B. Evidence-Based Complementary and Alternative Medicine, 2017.
(https://doi.org/10.1155/2017/4018724)

Whitton, P. A., Lau, A., Salisbury, A., Whitehouse, J. & Evans, C. S. Kava lactones and the kava-kava controversy. Phytochemistry 64, 673-679 (2003).
(https://pubmed.ncbi.nlm.nih.gov/13679089/)

Abu, N., Mohamed, N. E., Yeap, S. K., Lim, K. L., Akhtar, M. N., Zulfadli, A. J., Kee, B. B., Abdullah, M. P., Omar, A. R. & Alitheen, N. B. In vivo antitumor and antimetastatic effects of flavokawain B in 4T1 breast cancer cell-challenged mice. Drug Design, Development and Therapy 9, 1401-1417 (2015).
(https://pubmed.ncbi.nlm.nih.gov/25834398/)

Martin, A. C., Johnston, E., Xing, C. & Hegeman, A. D. Measuring the chemical and cytotoxic variability of commercially available kava (Piper methysticum G. Forster). PLoS One 9, (2014).
(https://pubmed.ncbi.nlm.nih.gov/25365244/)

Jaiswal, Y. S., Yerke, A. M., Bagley, M. C., Ekelöf, M., Weber, D., Haddad, D., Fodor, A., Muddiman, D. C., & Williams, L. L. (2020). 3D Imaging and metabolomic profiling reveal higher neuroactive kavalactone contents in lateral roots and crown root peels of Piper methysticum (kava). GigaScience, 9(9), 1–13. https://doi.org/10.1093/gigascience/giaa096 Clouatre, D. L., Kava kava: Examining new reports of toxicity. Toxicol. Lett. 150, 85-96 (2004).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507772/)

Lebot, V., Do, T. K. & Legendre, L. Detection of flavokavins (A, B, C) in cultivars of kava (Piper methysticum) using high performance thin layer chromatography (HPTLC). Food Chem. 151, 554-560 (2014).
(https://pubmed.ncbi.nlm.nih.gov/24423570/)

Sarris, J., Laporte, E. & Schweitzer, I. Kava: A comprehensive review of efficacy, safety, and psychopharmacology. Australian and New Zealand Journal of Psychiatry 45, 27-35 (2011).
(https://doi.org/10.3109/00048674.2010.522554)

Vandenbroucke, H., Mournet, P., Malapa, R., Glaszmann, J. C., Chair, H. & Lebot, V. Colorimetric assessment of kava (Piper methysticum Forst) quality. Genome 58, 1-11 (2015).
(https://doi.org/10.1016/j.jfca.2017.02.005)

Lebot, V. & Levesque, J. Genetic control of kavalactone chemotypes in Piper methysticum cultivars. Phytochemistry 43, 397-403 (1996).
(https://doi.org/10.1016/0031-9422(96)00209-9)

Connor, K. M., Davidson, J. R. & Churchill, L. E. Adverse-effect profile of kava. CNS Spectrums 6, 848-853 (2001).
(https://doi.org/10.1017/s109285290000167x)

Christl, S. U., Seifert, A. & Seeler, D. Toxic hepatitis after consumption of traditional kava preparation. Journal of Travel Medicine 16, 55-56 (2009).
(https://doi.org/10.1111/j.1708-8305.2008.00259.x)
(https://academic.oup.com/jtm/article/16/1/55/1803384)

Puppala, M., Narayanapillai, S. C., Leitzman, P., Sun, H., Upadhyaya, P., O'Sullivan, M. G., Hecht, S. S. & Xing, C. Pilot in Vivo Structure-Activity Relationship of Dihydromethysticin in Blocking 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone-Induced O6-Methylguanine and Lung Tumor in A/J Mice. J. Med. Chem. 60, 7935-7940 (2017).
(https://doi.org/10.1021/acs.jmedchem.7b00921)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/28806079/)

Teschke, R., Schwarzenboeck, A. & Hennermann, K. H. Kava hepatotoxicity: A clinical survey and critical analysis of 26 suspected cases. European Journal of Gastroenterology and Hepatology 20, 1182-1193 (2008).
(https://doi.org/10.1097/meg.0b013e3283036768)

Sharma, A., Anchariya, R. & Dubey, C. Asian Journal of Pharmaceutical Research and Development A Review on Anti-Stress Activity of Piper Methysticum. A Review on Anti-Stress Activity of Piper Methysticum, Asian Journal of Pharmaceutical Research and Development 8, 130-136 (2020).
(https://doi.org/10.22270/ajprd.v8i4.688)

H.-P. Volz, M. K., Kava-kava Extract WS 1490 versus Placebo in Anxiety Disorders-A Randomized Placebo-controlled 25-week Outpatient Trial. Pharmacopsychiatry 30, 1-5 (1997).
(https://doi.org/10.1055/s-2007-979474)

Jaiswal, Y., Shaikh, M. F., Wang, I., Yong, Y., Lee, V. L. L. & Williams, L. Evaluation of anti-convulsive properties of aqueous kava extract on zebrafish using the ptz-induced seizure model. Brain Sciences 10, 1-11 (2020).
(https://doi.org/10.3390/brainsci10080541)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/32796575/)

Lebot, V. & Legendre, L. Comparison of kava (Piper methysticum Forst.) varieties by UV absorbance of acetonic extracts and high-performance thin-layer chromatography. Journal of Food Composition and Analysis 48, 25-33 (2016).
(https://doi.org/10.1016/j.jfca.2016.01.009)

Stickel, F., Baumüller, H. M., Seitz, K., Vasilakis, D., Seitz, G., Seitz, H. K., & Schuppan, D. (2003). Hepatitis induced by Kava (Piper methysticum rhizoma). Journal of Hepatology, 39(1), 62–67.
(https://doi.org/10.1016/S0168-8278(03)00175-2)

Tang, Y., Li, X., Liu, Z., Simoneau, A. R., Xie, J. & Zi, X. Flavokawain B, a kava chalcone, induces apoptosis via up-regulation of death-receptor 5 and Bim expression in androgen receptor negative, hormonal refractory prostate cancer cell lines and reduces tumor growth. Int. J. Cancer 127, 1758-1768 (2010).
(https://doi.org/10.1002/ijc.25210)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20112340/)

Davies, L. P., Drew, C. A., Duftield, P., {R Johnston}, G. A. & Jamieson, D. D. Kava Pyrones and Resin: Studies on GABAA, GABAB and Benzodiazepine Binding Sites in Rodent Brain. Pharmacology & Toxicology 71, 120-126 (1992).
(https://doi.org/10.1111/j.1600-0773.1992.tb00530.x)

Lüde, S., Török, M., Dieterle, S., Jäggi, R., Büter, K. B., & Krähenbühl, S. (2008). Hepatocellular toxicity of kava leaf and root extracts. Phytomedicine, 15(1–2), 120–131.
(https://doi.org/10.1016/j.phymed.2007.11.003)

Zi, X. & Simoneau, A. R. Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and tumor growth in mice. Cancer Res. 65, 3479-3486 (2005).
(https://doi.org/10.1158/0008-5472.can-04-3803)
(https://cancerres.aacrjournals.org/content/65/8/3479.long)

Mohanty, M., Fiji Kava: production, trade, role and challenges. The Journal of Pacific Studies 37, 5-30 (2017).
(http://repository.usp.ac.fj/11179/1/Fiji_Kava.pdf)

Lhuissier, T., Mercier, P. E., Michalet, S., Lebot, V. & Legendre, L. Colorimetric assessment of kava (Piper methysticum Forst.) quality. Journal of Food Composition and Analysis 59, 27-34 (2017).
(https://doi.org/10.1016/j.jfca.2017.02.005)

Teschke, R., Sarris, J., Glass, X. & Schulze, J. Kava, the anxiolytic herb: Back to basics to prevent liver injury?. British Journal of Clinical Pharmacology 71, 445-448 (2011).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045554/)

Musselmann, B., & Cappellaro, C. (2015). Kava Kava. Zeitschrift Für Komplementärmedizin, 07(03), 44–45. (https://doi.org/10.1055/s-0035-1554957)

Wang, Y., Narayanapillai, S. C., Tessier, K. M., Strayer, L. G., Upadhyaya, P., Hu, Q., Kingston, R., Salloum, R. G., Lu, J., Hecht, S. S., Hatsukami, D. K., Fujioka, N. & Xing, C. The Impact of One-week Dietary Supplementation with Kava on Biomarkers of Tobacco Use and Nitrosamine-based Carcinogenesis Risk among Active Smokers. Cancer prevention research (Philadelphia, Pa.) 13, 483-492 (2020).
(https://doi.org/10.1158/1940-6207.capr-19-0501)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/32102948/)

Lebot, V., & Levesque, J. (1989). THE ORIGIN AND DISTRIBUTION OF KAVA (PIPER METHYSTICUM FORST. F., PIPERACEAE): A PHYTOCHEMICAL APPROACH. Allertonia, 5(2), 223–281.
(https://www.jstor.org/stable/23187398)

Côté, C. S., Kor, C., Cohen, J., & Auclair, K. (2004). Composition and biological activity of traditional and commercial kava extracts. Biochemical and Biophysical Research Communications, 322(1), 147–152. (https://doi.org/10.1016/j.bbrc.2004.07.093)

Yuan Chun-Su, Dey, L., Wang, A., Mehendale, S., Xie Jing, Aung Han, & Ang-Lee Michael. (2002). Kavalactones and Dihdrokavain Modulate GABAergic Activity in Rat Gastric-Brainstem Preparation. Planta Medica, 1092–1096.
(https://pubmed.ncbi.nlm.nih.gov/12494336/)

Singh, Y. N. & Singh, N. N. Therapeutic potential of kava in the treatment of anxiety disorders. CNS Drugs 16, 731-743 (2002).
(https://pubmed.ncbi.nlm.nih.gov/12383029/)

Kuchta, K., de Nicola, P. & Schmidt, M. Randomized, dose-controlled double-blind trial: Efficacy of an ethanolic kava ( Piper methysticum rhizome) extract for the treatment of anxiety in elderly patients. Traditional & Kampo Medicine 5, 3-10 (2018).
(https://doi.org/10.1002/tkm2.1079)

Smith, T. E., Djang, M., Velander, A. J., Downey, C. W., Carroll, K. A. & Van Alphen, S. Versatile asymmetric synthesis of the kavalactones: First synthesis of (+)-kavain. Org. Lett. 6, 2317-2320 (2004).
(https://doi.org/10.1021/ol0493960)

Triolet, J., Shaik, A. A., Gallaher, D. D., Osullivan, M. G. & Xing, C. Reduction in colon cancer risk by consumption of kava or kava fractions in carcinogen-treated rats. Nutrition and Cancer 64, 838-846 (2012).
(https://doi.org/10.1080/01635581.2012.689917)

Singh, Y. N., Kava: An old drug in a new world. Cultural Critique 71, 107-128 (2009).
(https://www.jstor.org/stable/25475503)

Berry, J., Gilbert, A. & Grodnitzky, J. Cases of Kava Impairment in Iowa Drivers. Journal of Forensic Sciences 64, 1943-1949 (2019).
(https://doi.org/10.1111/1556-4029.14130)

Sällström Baum, S., Hill, R., & Rommelspacher, H. (1998). Effect of kava extract and individual kavapyrones on neurotransmitter levels in the nucleus accumbens of rats. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 22(7), 1105–1120.
(https://doi.org/10.1016/S0278-5846(98)00062-1)

Sofer, M., Yaqona and the Fijian periphery revisited. Asia Pacific Viewpoint 48, 234-249 (2007).
(https://doi.org/10.1111/j.1467-8373.2007.00342.x)

Lebot, V. & Cabalion, P. KAVAS OF VANUATU: Cultivars of Piper Methysticum Forst. South Pacific Commission , 3-191 (1998).
(https://core.ac.uk/download/pdf/39867287.pdf)

Clough, A., Enough! or too much. What is 'excessive' kava use in Arnhem Land?. Drug and Alcohol Review 22, 43-51 (2003).
(https://doi.org/10.1080/0959523021000059820)

Scherer, J., Kava-kava extract in anxiety disorders: An outpatient observational study. Advances in Therapy 15, 261-269 (1998).
(https://pubmed.ncbi.nlm.nih.gov/10186945/)

Clough, A. R., Rowley, K. & O'Dea, K. Kava use, dyslipidaemia and biomarkers of dietary quality in Aboriginal people in Arnhem Land in the Northern Territory (NT), Australia. European Journal of Clinical Nutrition 58, 1090-1093 (2004).
(https://www.nature.com/articles/1601921)

Groth-Marnat, G., Leslie, S. & Renneker, M. TOBACCO CONTROL IN A TRADITIONAL FIJIAN VILLAGE: INDIGENOUS METHODS OF SMOKING CESSATION AND RELAPSE PREVENTION. Soc. Sci. Med 43, 473-477 (1996).
(https://doi.org/10.1016/0277-9536(95)00425-4)

Tang, X. & Amar, S. Kavain Involvement in LPS-Induced Signaling Pathways. J. Cell. Biochem. , 2272-2280 (2016).
(https://doi.org/10.1002/jcb.25525)

Jhoo, J. W., Freeman, J. P., Heinze, T. M., Moody, J. D., Schnackenberg, L. K., Beger, R. D., Dragull, K., Tang, C. S. & Ang, C. Y. In vitro cytotoxicity of nonpolar constituents from different parts of kava plant (Piper methysticum). J. Agric. Food Chem. 54, 3157-3162 (2006).
(https://doi.org/10.1021/jf051853j)

Clayton, N. P., Yoshizawa, K., Kissling, G. E., Burka, L. T., Chan, P. C. & Nyska, A. Immunohistochemical analysis of expressions of hepatic cytochrome P450 in F344 rats following oral treatment with kava extract. Experimental and Toxicologic Pathology 58, 223-236 (2007).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1839869/)

Botello, J. F., Corral, P., Bian, T. & Xing, C. Kava and its kavalactones inhibit norepinephrine-induced intracellular calcium influx in lung cancer cells. Planta Med. 86, 26-31 (2020).
(https://doi.org/10.1055/a-1035-5183)

Li, X., Xu, X., Ji, T., Liu, Z., Gu, M., Hoang, B. H. & Zi, X. Dietary feeding of flavokawain A, a Kava chalcone, exhibits a satisfactory safety profile and its association with enhancement of phase II enzymes in mice. Toxicology Reports 1, 2-11 (2014).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219529/)

Wang, J., Qu, W., Bittenbender, H. C. & Li, Q. X. Kavalactone content and chemotype of kava beverages prepared from roots and rhizomes of Isa and Mahakea varieties and extraction efficiency of kavalactones using different solvents. Journal of Food Science and Technology 52, 1164-1169 (2013).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4325077/)

Sarris, J., Stough, C., Bousman, C. A., Wahid, Z. T., Murray, G., Teschke, R., Savage, K. M., Dowell, A., Ng, C. & Schweitzer, I. Kava in the treatment of generalized anxiety disorder: A double-blind, randomized, placebo-controlled study. Journal of Clinical Psychopharmacology 33, 643-648 (2013).
(https://doi.org/10.1097/jcp.0b013e318291be67)

Uebelhock, R., Fronke, L. & Schewe, H.-1. Inhibition of Platelet MAO-6 by Kava Pyrone-Enriched Extract from Piper Methysticum Forster (Kava-Kava). Pharmacopsychiatry 31, 187-192 (1998).
(https://doi.org/10.1055/s-2007-979325)

O'hara, M. J., Kinnard, W. J. & Buckley, J. P. Preliminary Characterization of Aqueous Extracts of P+er methysticzm (Kava, Kawa Kawa). J. Pharm. Sci. 54, 1021-1025 (1965).
(https://doi.org/10.1002/jps.2600540715)

Singh, Y. N., Kava: an overview. Journal of Ethnophurmacology 37, 13-45 (1992).
(https://doi.org/10.1016/0378-8741(92)90003-a)

Gurley, B. J., Swain, A., Hubbard, M. A., Williams, D. K., Barone, G., Hartsfield, F., Tong, Y., Carrier, D. J., Cheboyina, S. & Battu, S. K. Clinical assessment of CYP2D6-mediated herb-drug interactions in humans: Effects of milk thistle, black cohosh, goldenseal, kava kava, St. John's wort, and Echinacea. Molecular Nutrition and Food Research 52, 755-763 (2008).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2562884/)

Hegazy, N. H., Breitinger, H. G. & Breitinger, U. Kavalactones from Kava (Piper methysticum) root extract as modulators of recombinant human glycine receptors. Biol. Chem. 400, 1205-1215 (2019).
(https://doi.org/10.1515/hsz-2019-0112)

Celentano, A., Tran, A., Testa, C., Thayanantha, K., Tan-Orders, W., Tan, S., Syamal, M., McCullough, M. J. & Yap, T. The protective effects of Kava (Piper Methysticum) constituents in cancers: A systematic review. Journal of Oral Pathology and Medicine 48, 510-529 (2019).
(https://doi.org/10.1111/jop.12900)

Moulds, R. F. & Malani, J. Kava: Herbal panacea or liver poison?. Medical Journal of Australia 178, 451-453 (2003).
(https://doi.org/10.5694/j.1326-5377.2003.tb05289.x)

Connor, K. M., Payne, V. & Davidson, J. R. Kava in generalized anxiety disorder: Three placebo-controlled trials. International Clinical Psychopharmacology 21, 249-253 (2006).
(https://doi.org/10.1097/00004850-200609000-00001)

Boerner, R. J., Sommer, H., Berger, W., Kuhn, U., Schmidt, U. & Mannel, M. Kava-Kava extract LI 150 is as effective as Opipramoland Buspirone in Generalised Anxiety Disorder –An 8-week randomized, double-blind multi-centre clinicaltrial in 129 out-patients. , (2003).
(https://doi.org/10.1078/1433-187x-00309)

Wang, D., Yang, L. E., Wang, J., Hu, G., Liu, Z. Y., Yan, D., Serikuly, N., Alpyshov, E. T., Demin, K. A., Galstyan, D. S., Strekalova, T., de Abreu, M. S., Amstislavskaya, T. G. & Kalueff, A. V. Behavioral and physiological effects of acute and chronic kava exposure in adult zebrafish. Neurotoxicol. Teratol. 79, 106881 (2020).
(https://doi.org/10.1016/j.ntt.2020.106881)

Prinsloo, D., Van Dyk, S., Petzer, A. & Petzer, J. P. Monoamine Oxidase Inhibition by Kavalactones from Kava (Piper Methysticum). Planta Med. 85, 1136-1142 (2019).
(https://doi.org/10.1055/a-1008-9491)

Murray, M., Toxicological actions of plant-derived and anthropogenic methylenedioxyphenyl-substituted chemicals in mammals and insects. Journal of Toxicology and Environmental Health - Part B: Critical Reviews 15, 365-395 (2012).
(https://doi.org/10.1080/10937404.2012.705105)

Lin, C. T., Kumar, K. J. S., Tseng, Y. H., Wang, Z. J., Pan, M. Y., Xiao, J. H., Chien, S. C. & Wang, S. Y. Anti-inflammatory activity of flavokawain B from Alpinia pricei hayata. J. Agric. Food Chem. 57, 6060-6065 (2009).
(https://doi.org/10.1021/jf900517d)

Witte, S., Loew, D. & Gaus, W. Meta-analysis of the efficacy of the acetonic kava-kava extract WS 1490 in patients with non-psychotic anxiety disorders. Phytotherapy Research 19, 183-188 (2005).
(https://doi.org/10.1002/ptr.1609)

Aporosa, S. A., De-mythologizing and re-branding of kava as the new ‘world drug' of choice. Drug Science, Policy and Law 5, 205032451987613 (2019).
(https://doi.org/10.1177/2050324519876131)

Shaik, A. A., Hermanson, D. L., & Xing, C. (2009). Identification of methysticin as a potent and non-toxic NF-κB inhibitor from kava, potentially responsible for kava’s chemopreventive activity. Bioorganic and Medicinal Chemistry Letters, 19, 5732–5736.
(https://doi.org/10.1016/j.bmcl.2009.08.003)

Zou, L., Harkey, M. R. & Henderson, G. L. Effects of herbal components on cDNA-expressed cytochrome P450 enzyme catalytic activity. Life Sci. 71, 1579-1589 (2002).
(https://doi.org/10.1016/s0024-3205(02)01913-6)

Sarris, J., Byrne, G. J., Bousman, C. A., Cribb, L., Savage, K. M., Holmes, O., Murphy, J., Macdonald, P., Short, A., Nazareth, S., Jennings, E., Thomas, S. R., Ogden, E., Chamoli, S., Scholey, A. & Stough, C. Kava for generalised anxiety disorder: A 16-week double-blind, randomised, placebo-controlled study. Australian and New Zealand Journal of Psychiatry 54, 288-297 (2020).
(https://doi.org/10.1177/0004867419891246)

Johnson, T. E., Kassie, F., O'Sullivan, M. G., Negia, M., Hanson, T. E., Upadhyaya, P., Ruvolo, P. P., Hecht, S. S. & Xing, C. Chemopreventive effect of kava on 4-(methylnitrosamino)-1-(3-pyridyl)-1- butanone plus benzo[a]pyrene-induced lung tumorigenesis in A/J mice. Cancer Prevention Research 1, 430-438 (2008).
(https://doi.org/10.1158/1940-6207.capr-08-0027)

Sarris, J., Kavanagh, D. J., Byrne, G., Bone, K. M., Adams, J. & Deed, G. The Kava Anxiety Depression Spectrum Study (KADSS): A randomized, placebo-controlled crossover trial using an aqueous extract of Piper methysticum. Psychopharmacology 205, 399-407 (2009).
(https://doi.org/10.1007/s00213-009-1549-9)

Behl, M., Nyska, A., Chhabra, R. S., Travlos, G. S., Fomby, L. M., Sparrow, B. R., Hejtmancik, M. R. & Chan, P. C. Liver toxicity and carcinogenicity in F344/N rats and B6C3F1 mice exposed to Kava Kava. Food Chem. Toxicol. 49, 2820-2829 (2011).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190036/)

Thomsen, M. & Schmidt, M. Health policy versus kava (Piper methysticum): Anxiolytic efficacy may be instrumental in restoring the reputation of a major South Pacific crop. Journal of Ethnopharmacology , 113582 (2020).
(https://doi.org/10.1016/j.jep.2020.113582)

Teschke, R., Genthner, A. & Wolff, A. Kava hepatotoxicity: Comparison of aqueous, ethanolic, acetonic kava extracts and kava-herbs mixtures. Journal of Ethnopharmacology 123, 378-384 (2009).
(https://doi.org/10.1016/j.jep.2009.03.038)

Johnson, T. E., Hermanson, D., Wang, L., Kassie, F., Upadhyaya, P., O'Sullivan, M. G., Hecht, S. S., Lu, J. & Xing, C. Lung tumorigenesis suppressing effects of a commercial kava extract and its selected compounds in A/J mice. American Journal of Chinese Medicine 39, 727-742 (2011).
(https://doi.org/10.1142/s0192415x11009202)

Amdidouche-Hussain, D. & Levesque, J. Selection of kavalactones by complexation of kava extract with cyclodextrins. Drug Dev. Ind. Pharm. 23, 1223-1226 (1997).
(https://doi.org/10.3109/03639049709146161)

Magura, E. I., Kopanitsa, ‡. M. V., Gleitz, J., Peters, T. & Krishtal, O. A. Kava extract ingredients, (+)-methysticin and (±)-kavain inhibit voltage-operated Na+-channels in rat CA1 hippocampal neurons. Neuroscience 81, 345-351 (1997).
(https://doi.org/10.1016/s0306-4522(97)00177-2)

Cairney, S., Clough, A. R., Maruff, P., Collie, A., Currie, B. J. & Currie, J. Saccade and cognitive function in chronic kava users. Neuropsychopharmacology 28, 389-396 (2003).
(https://doi.org/10.1038/sj.npp.1300052)

Gastpar M, Klimm HD. Treatment of anxiety, tension and restlessness states with Kava special extract WS 1490 in general practice: a randomized placebo-controlled double-blind multicenter trial. Phytomedicine. 2003 Nov;10(8):631-9. doi: 10.1078/0944-7113-00369. PMID: 14692723.
(https://doi.org/10.1078/0944-7113-00369)

Tugcu, G., Kırmızıbekmez, H. & Aydın, A. The integrated use of in silico methods for the hepatotoxicity potential of Piper methysticum. Food Chem. Toxicol. 145, (2020).
(https://doi.org/10.1016/j.fct.2020.111663)

Gow, P. J., Connelly, N. J., Hill, R. L., Crowley, P. & Angus, P. W. Fatal fulminant hepatic failure induced by a natural therapy containing kava. Medical Journal of Australia 178, 442-443 (2003).
(https://www.mja.com.au/journal/2003...ilure-induced-natural-therapy-containing-kava)

Kava (Piper methysticum) Extract for the Treatment of Nervous Anxiety, Tension and Restlessness. Drug Res , (2020).
(https://doi.org/10.1055/a-1268-7135)

Wruck, C. J., Götz, M. E., Herdegen, T., Varoga, D., Brandenburg, L. O., & Pufe, T. (2008). Kavalactones protect neural cells against amyloid β peptide-induced neurotoxicity via extracellular signal-regulated kinase 1/2-dependent nuclear factor erythroid 2-related factor 2 activation. Molecular Pharmacology, 73(6), 1785–1795. (https://doi.org/10.1124/mol.107.042499)

Coulter, D., Tamayo, C., Sotheeswaran, S. & Ulbricht, C. Assessment of the risk of hepatotoxicity with kava products. WHO Library Cataloguing-in-Publication Data , 1-82 (2007).
(https://apps.who.int/iris/handle/10665/43630)

Rivers, Z., Kava as a Pharmacotherapy of Anxiety Disorders: Promises and Concerns. Medicinal Chemistry 6, 81-87 (2016).
(https://www.researchgate.net/deref/http://dx.doi.org/10.4172/2161-0444.1000329)

Atezaz Saeed}, S., Bloch, R. M. & Antonacci, D. J. Herbal and Dietary Supplements for Treatment of Anxiety Disorders. Complementary and Alternative Medicine , (2007).
(https://www.aafp.org/afp/2007/0815/p549.html)

Pluskal, T., Torrens-Spence, M. P., Fallon, T. R., De Abreu, A., Shi, C. H. & Weng, J. K. The biosynthetic origin of psychoactive kavalactones in kava. Nature Plants 5, 867-878 (2019).
(https://www.biorxiv.org/content/10.1101/294439v1.full)

Barnes, J., Anderson, L. A. & Phillipson, D. J. Kava - Herbal Medicine - Overview. Herbal Medicines - Third Edition , 389-402 (2007).
(https://naturalingredient.org/wp/wp...nneBarnesJ.DavidPhillipsonLindaA.Anderson.pdf)

Gleitz1', J., Beiie1, A., Wiikens1, P., Amen1, A. & Peterst, T. Antithrombotic Action of the Kava Pyrone (+)-Kavain Prepared from Piper methysticum on Human Platelets. , (1997).
(https://doi.org/10.1055/s-2006-957597)

Aporosa, A. S., Atkins, M. & Brunton, R. Kava drinking in traditional settings: Towards understanding effects on cognitive function. Human Psychopharmacology 35, 1-11 (2020).
(https://doi.org/10.1002/hup.2725)

Ketola, R. A., Viinam{\"{a}}ki, J., Rasanen, I., Pelander, A. & Goebeler, S. Fatal kavalactone intoxication by suicidal intravenous injection. Forensic Science International 249, e7-e11 (2015).
(https://doi.org/10.1016/j.forsciint.2015.01.032)

Li, Y., Mei, H., Wu, Q., Zhang, S., Fang, J. L., Shi, L. & Guo, L. Methysticin and 7,8-dihydromethysticin are two major kavalactones in kava extract to induce CYP1A1. Toxicol. Sci. 124, 388-399 (2011).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736320/)

Teschke, R., Sarris, J. & Lebot, V. Contaminant hepatotoxins as culprits for kava hepatotoxicity - Fact or fiction?. Phytotherapy Research 27, 472-474 (2013).
(https://doi.org/10.1002/ptr.4729)

Teschke, R., Sarris, J. & Lebot, V. Kava hepatotoxicity solution: A six-point plan for new kava standardization. Phytomedicine 18, 96-103 (2011).
(https://doi.org/10.1016/j.phymed.2010.10.002)

Weiss, J., Sauer, A., Frank, A. & Unger, M. Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro. Drug Metabolism and Disposition 33, 1580-1583 (2005).
(https://doi.org/10.1124/dmd.105.005892)

Tarbah, F., Mahler, H., Kardel, B., Weinmann, W., Hafner, D. & Daldrup, T. Kinetics of kavain and its metabolites after oral application. J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. 789, 115-130 (2003).
(https://doi.org/10.1016/s1570-0232(03)00046-1)

Fu, P. P., Xia, Q., Guo, L., Yu, H. & Chan, P. C. Toxicity of kava kava. Journal of Environmental Science and Health - Part C Environmental Carcinogenesis and Ecotoxicology Reviews 26, 89-112 (2008).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868963)

Huynh, J. C., Asgari, M. M. & Moore, M. M. Sebotropic eruption associated with use of oral kava kava supplement. Clinical and Experimental Dermatology 39, 816-818 (2014).
(https://doi.org/10.1111/ced.12439)

Ma, Y., Sachdeva, K., Liu, J., Ford, M., Yang, D., Khan, I. A., Chichester, C. O. & Yan, B. Desmethoxyyangonin and dihydromethysticin are two major pharmacologigal kavalactones with marked activity on the induction of CYP3A23. Drug Metabolism and Disposition 32, 1317-1324 (2004).
(https://doi.org/10.1124/dmd.104.000786)

Russmann, S., Barguil, Y., Cabalion, P., Kritsanida, M., Duhet, D. & Lauterburg, B. H. Hepatic injury due to traditional aqueous extracts of kava root in New Caledonia. European Journal of Gastroenterology & Hepatology , 1033-1036 (2003).
(https://doi.org/10.1097/00042737-200309000-00015)

Martin HB, McCallum M, Stofer WD, Eichinger MR. Kavain attenuates vascular contractility through inhibition of calcium channels. Planta Med. 2002 Sep;68(9):784-9. doi: 10.1055/s-2002-34443. PMID: 12357387.
(https://doi.org/10.1055/s-2002-34443)

Upadhyay, A., Tuenter, E., Ahmad, R., Amin, A., Exarchou, V., Apers, S., Hermans, N. & Pieters, L. Kavalactones, A novel class of protein glycation and lipid peroxidation inhibitors. Planta Med. 80, 1001-1008 (2014).
(https://doi.org/10.1055/s-0034-1382949)

Geier, F. P. & Konstantinowicz, T. Kava Treatment in Patients with Anxiety. Phytotherapy Research 18, 297-300 (2004).
(https://doi.org/10.1002/ptr.1422)

Tawfiq, R. A., Nassar, N. N., El-Eraky, W. I. & El-Denshary, E. S. Enhanced efficacy and reduced side effects of diazepam by kava combination. Journal of Advanced Research 5, 587-594 (2014).
(https://doi.org/10.1016/j.jare.2013.08.002)

Tang, S. N., Zhang, J., Jiang, P., Datta, P., Leitzman, P., O’Sullivan, M. G., Jiang, C., Xing, C., & Lü, J. (2016). Gene expression signatures associated with suppression of TRAMP prostate carcinogenesis by a kavalactone-rich Kava fraction. Molecular Carcinogenesis, 55(12), 2291–2303.
(https://doi.org/10.1002/mc.22469)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/26840761/)

Becker, M. W., Lourençone, E. M. S., De Mello, A. F., Branco, A., Filho, E. M. R., Blatt, C. R., Mallmann, C. A., Schneider, M., Caregnato, R. C. A., & Blatt, C. R. (2019). Liver transplantation and the use of KAVA: Case report. Phytomedicine, 56, 21–26. (https://doi.org/10.1016/j.phymed.2018.08.011)

Olsen, L. R., Grillo, M. P. & Skonberg, C. Constituents in Kava extracts potentially involved in hepatotoxicity: A review. Chem. Res. Toxicol. 24, 992-1002 (2011).
(https://doi.org/10.1021/tx100412m)

Jaleel, G. A. A., Saleh, D. O. & El-Awdan, S. A. Antihyperglycaemic effect of kava kava (piper methysticum) in streptozotocin-induced diabetic rats. Scholars Research Library , (2013).
(https://www.scholarsresearchlibrary...cum-in-streptozotocininduceddiabetic-rats.pdf)

Showman, A. F., Baker, J. D., Linares, C., Naeole, C. K., Borris, R., Johnston, E., Konanui, J. & Turner, H. Contemporary Pacific and Western perspectives on 'awa (Piper methysticum) toxicology. Fitoterapia 100, 56-67 (2015).
(https://doi.org/10.1016/j.fitote.2014.11.012)

Yang, X. & Salminen, W. F. Kava extract, an herbal alternative for anxiety relief, potentiates acetaminophen-induced cytotoxicity in rat hepatic cells. Phytomedicine 18, 592-600 (2011).
(https://doi.org/10.1016/j.phymed.2011.02.006)

Steiner, G. G., The Correlation between Cancer Incidence and Kava Consumption. Hawaii Med J 59, 420-422 (2000).
(https://core.ac.uk/download/pdf/77123272.pdf)

Sorrentino, L., Capasso, A. & Schmidt, M. Safety of ethanolic kava extract: Results of a study of chronic toxicity in rats. Phytomedicine 13, 542-549 (2006).
(https://doi.org/10.1016/j.phymed.2006.01.006)

Li, X., Liu, Z., Xu, X., Blair, C. A., Sun, Z., Xie, J., Lilly, M. B. & Zi, X. Kava components down-regulate expression of AR and AR splice variants and reduce growth in patient-derived prostate cancer xenografts in mice. PLoS One 7, (2012).
(https://doi.org/10.1371/journal.pone.0031213)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22347450/)

Ulbricht, C., Basch, E., Boon, H., Ernst, E., Hammerness, P., Sollars, D., Tsourounis, C., Woods, J. & Bent, S. Safety review of kava (Piper methysticum) by the Natural Standard Research Collaboration. Expert Opinion on Drug Safety 4, 779-794 (2005).
(https://doi.org/10.1517/14740338.4.4.779)

Pittler, M. H. & Ernst, E. Kava extract versus placebo for treating anxiety. Cochrane Database of Systematic Reviews , (2003).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6999799/)

Li, X., Yokoyama, N. N., Zhang, S., Ding, L., min Liu, H., Lilly, M. B., Mercola, D. & Zi, X. Flavokawain A induces deNEDDylation and Skp2 degradation leading to inhibition of tumorigenesis and cancer progression in the TRAMP transgenic mouse model. Oncotarget 6, 41809-41824 (2015).
(https://doi.org/10.18632/oncotarget.6166)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/26497688/)

Xuan, T. D., Elzaawely, A. A., Fukuta, M. & Tawata, S. Herbicidal and fungicidal activities of lactones in Kava (Piper methysticum). J. Agric. Food Chem. 54, 720-725 (2006).
(https://doi.org/10.1021/jf0519461)

Fragoulis, A., Siegl, S., Fendt, M., Jansen, S., Soppa, U., Brandenburg, L. O., Pufe, T., Weis, J. & Wruck, C. J. Oral administration of methysticin improves cognitive deficits in a mouse model of Alzheimer's disease. Redox Biol. 12, 843-853 (2017).
(https://doi.org/10.1016/j.redox.2017.04.024)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/28448946/)

Liu, Z., Xu, X., Li, X., Liu, S., Simoneau, A. R., He, F., Wu, X. R. & Zi, X. KAVA chalcone, flavokawain A, inhibits urothelial tumorigenesis in the UPII-SV40T transgenic mouse model. Cancer Prevention Research 6, 1365-1375 (2013).
(https://doi.org/10.1158/1940-6207.capr-13-0219)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24121102/)

Backleh, M., Ekici, P., Leupold, G. & Parlar, H. Quantitative elimination of flavokavines A and B from Kava Kava (Piper methysticum G. Forst) by isoelectric focused adsorptive bubble separation. Naturwissenschaften 90, 366-369 (2003).
(https://doi.org/10.1007/s00114-003-0440-5)

Kong, Y., Gao, X., Wang, C., Ning, C., Liu, K., Liu, Z., Sun, H., Ma, X., Sun, P. & Meng, Q. Protective effects of yangonin from an edible botanical Kava against lithocholic acid-induced cholestasis and hepatotoxicity. Eur. J. Pharmacol. 824, 64-71 (2018).
(https://doi.org/10.1016/j.ejphar.2018.02.002)

Lebot, V., Kaoh, J. & Legendre, L. High-Throughput Analysis of Flavokawains in Kava (Piper methysticum Forst. f.) Roots, Chips and Powders and Correlations with Their Acetonic Extracts Absorbance. Food Analytical Methods 13, 1583-1593 (2020).
(https://link.springer.com/article/10.1007/s12161-020-01781-9)

Davis, R. I. & Brown, J. F. Kava (Piper methysticum) in the South Pacific. Canberra: ACIAR Technical Reports , (1999).
(http://dx.doi.org/10.22004/ag.econ.113917)

Tang, Y., Simoneau, A. R., Xie, J., Shahandeh, B. & Zi, X. Effects of the kava chalcone flavokawain A differ in bladder cancer cells with wild-type versus mutant p53. Cancer Prevention Research 1, 439-451 (2008).
(https://doi.org/10.1158/1940-6207.capr-08-0165)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19138991/)

Zhou, P., Gross, S., Liu, J.-H., Yu, B.-Y., Feng, L.-L., Nolta, J., Sharma, V., Piwnica-Worms, D., & Qiu, S. X. (2010). Flavokawain B, the hepatotoxic constituent from kava root, induces GSH-sensitive oxidative stress through modulation of IKK/NF-κB and MAPK signaling pathways. The FASEB Journal, 24(12), 4722–4732.
(https://doi.org/10.1096/fj.10-163311)

Bian, T., Corral, P., Wang, Y., Botello, J., Kingston, R., Daniels, T., Salloum, R. G., Johnston, E., Huo, Z., Lu, J. & Liu, A. C. Kava as a Clinical Nutrient : Promises and Challenges. Nutrients 12, 3044-undefined (2020).
(https://doi.org/10.3390/nu12103044)

Backhauß, C., & Krieglstein, J. (1992). Extract of kava (Piper methysticum) and its methysticin constituents protect brain tissue against ischemic damage in rodents. European Journal of Pharmacology, 215(2–3), 265–269. (https://doi.org/10.1016/0014-2999(92)90037-5)

Pollastri, M. P., Whitty, A., Merrill, J. C., Tang, X., Ashton, T. D., & Amar, S. (2009). Identification and characterization of kava-derived compounds mediating TNF-α suppression. Chemical Biology and Drug Design, 74(2), 121–128. (https://doi.org/10.1111/j.1747-0285.2009.00838.x)

Malsch, U. & Kieser, M. Efficacy of kava-kava in the treatment of non-psychotic anxiety, following pretreatment with benzodiazepines. Psychopharmacology 157, 277-283 (2001).
(https://doi.org/10.1007/s002130100792)

Cairney, S., Maruff, P., Clough, A. R., Collie, A., Currie, J. & Currie, B. J. Saccade and cognitive impairment associated with kava intoxication. Human Psychopharmacology 18, 525-533 (2003).
(https://doi.org/10.1002/hup.532)

Chou, T. W., Feng, J. H., Huang, C. C., Cheng, Y. W., Chien, S. C., Wang, S. Y. & Shyur, L. F. A Plant Kavalactone Desmethoxyyangonin Prevents Inflammation and Fulminant Hepatitis in Mice. PLoS One 8, (2013).
(https://doi.org/10.1371/journal.pone.0077626)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24143247/)

D. Wu, L. Yu, M. G. Nair, D. L. DeWitt, & R. S. Ramsewak. (2002). Cyclooxygenase enzyme inhibitory compounds with antioxidant activities from Piper methysticum (kava kava) roots. Phytomedicine, 9, 41–47.
(https://doi.org/10.1078/0944-7113-00068)

Garner, L. F. & Klinger, J. D. SOME VISUAL EFFECTS CAUSED BY THE BEVERAGE KAVA. Journal of Ethnopharmacology 13, 307-311 (1985).
(https://doi.org/10.1016/0378-8741(85)90076-5)

Abu, N., Mohamed, N. E., Tangarajoo, N., Yeap, S. K., Nadeem Akhtar, M., Abdullah, M. P., Omar, A. R. & Alitheen, N. B. In vitro toxicity and in vivo immunomodulatory effects of flavokawain a and flavokawain B in balb/C mice. Natural Product Communications 10, 1199-1202 (2015).
(https://journals.sagepub.com/doi/pdf/10.1177/1934578X1501000716)

Smith, K. & Leiras, C. The effectiveness and safety of Kava Kava for treating anxiety symptoms: A systematic review and analysis of randomized clinical trials. Complementary Therapies in Clinical Practice 33, 107-117 (2018).
(https://doi.org/10.1016/j.ctcp.2018.09.003)

Wainiqolo, I., Kool, B., Nosa, V. & Ameratunga, S. Is driving under the influence of kava associated with motor vehicle crashes? A systematic review of the epidemiological literature. Australian and New Zealand Journal of Public Health 39, 495-499 (2015).
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616936/)

JK, T., Flavokawains A and B from kava (Piper methysticum) activate heat shock and antioxidant responses and protect against hydrogen peroxide-induced cell death in HepG2 hepatocytes. Physiol. Behav. 176, 139-148 (2017).
(https://doi.org/10.3109/13880209.2015.1107104)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/26789234/)

Dragull, K., Yoshida, W. Y. & Tang, C. S. Piperidine alkaloids from piper methysticum. Phytochemistry 63, 193-198 (2003).
(https://doi.org/10.1016/s0031-9422(03)00111-0)

Barguil, Y., Choblet, E., Warter, S. & Nour, M. Kava ichthyosis: A nitric oxide synthase inhibition?. Annales de Toxicologie Analytique 25, 165-168 (2013).
(https://www.researchgate.net/deref/http://dx.doi.org/10.1051/ata/2014001)

Teschke, R., Qiu, S. X., Xuan, T. D. & Lebot, V. Kava and Kava hepatotoxicity: Requirements for novel experimental, ethnobotanical and clinical studies based on a review of the evidence. Phytotherapy Research 25, 1263-1274 (2011).
(https://doi.org/10.1002/ptr.3464)

Ashraf-Khorassani, M., Taylor, /. L. T. & Martin, M. /. Supercritical Fluid Extraction of Kava Lactones from Kava Root and Their Separation Via Supercritical Fluid Chromatography. Chromatographia 50, 287-292 (1999).
(https://doi.org/10.1002/jhrc.1240201007)

Li, J., Zheng, L., Yan, M., Wu, J., Liu, Y., Tian, X., Jiang, W., Zhang, L. & Wang, R. Activity and mechanism of flavokawain A in inhibiting P-glycoprotein expression in paclitaxel resistance of lung cancer. Oncology Letters 19, 379-387 (2020).
(https://dx.doi.org/10.3892/ol.2019.11069)
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923923/)

Robinson, D., Raven, M., Makin, E., Kalfatak, D., Hickey, F. & Tari, T. Legal geographies of kava, kastom and indigenous knowledge: Next steps under the Nagoya Protocol. Geoforum , (2020).
(https://doi.org/10.1016/j.geoforum.2020.11.001)

Einbond, L. S., Negrin, A., Kulakowski, D. M., Wu, H. A., Antonetti, V., Jalees, F., Law, W., Roller, M., Redenti, S., Kennelly, E. J. & Balick, M. J. Traditional preparations of kava (Piper methysticum) inhibit the growth of human colon cancer cells in vitro. Phytomedicine 24, 1-13 (2017).
(https://doi.org/10.1016/j.phymed.2016.11.002)

Petersen, G. E., Tang, Y. & Fields, C. Chemical and in vitro toxicity analysis of a supercritical fluid extract of Kava kava (Piper methysticum). Journal of Ethnopharmacology 235, 301-308 (2019).
(https://doi.org/10.1016/j.jep.2019.01.032)
(https://linkinghub.elsevier.com/retrieve/pii/S0378-8741(18)34053-4)

Balick, M. J. & Lee, R. Traditional Uses of Sakau (Kava) in Pohnpei - Lessons For Integrative Medicine (Balick, Lee). Alternative Therapies In Health & Medicine 8, 96-98 (2002).
(https://sciweb.nybg.org/science2/pdfs/mb/Kava.pdf)

Shimoda, L. M., Park, C., Stokes, A. J., Gomes, H. H. & Turner, H. Pacific Island 'Awa (Kava) extracts, but not isolated kavalactones, promote proinflammatory responses in model mast cells. Phytotherapy Research 26, 1934-1941 (2012).
(https://doi.org/10.1002/ptr.4652)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22473598/)

Pittler, M. H. & Ernst, E. Kava extract versus placebo for treating anxiety. Cochrane Database of Systematic Reviews , (2003).
(https://dx.doi.org/10.1002/14651858.CD003383)
(https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6999799/)

Liu, Y., Lund, J. A., Murch, S. J. & Brown, P. N. Single-Lab Validation for Determination of Kavalactones and Flavokavains in Piper methysticum (Kava). Planta Med. 84, 1213-1218 (2018).
(https://doi.org/10.1055/a-0637-2400)

Lebot, V. & Levesque, J. Evidence for conspecificity of Piper methysticum Forst. f. and Piper wichmannii C. DC. Biochem. Syst. Ecol. 24, 775-782 (1996).
(https://doi.org/10.1016/S0305-1978(96)00048-8)

Sarris, J., Stough, C., Teschke, R., Wahid, Z. T., Bousman, C. A., Murray, G., Savage, K. M., Mouatt, P., Ng, C. & Schweitzer, I. Kava for the treatment of generalized anxiety disorder RCT: Analysis of adverse reactions, liver function, addiction, and sexual effects. Phytotherapy Research 27, 1723-1728 (2013).
(https://doi.org/10.1002/ptr.4916)

Hannam, S., Murray, M., Pharm, B., Romani, L., Tuicakau, M., Whitfeld, M. J. & {Sarah Hannam}, C. Kava dermopathy in Fiji: an acquired ichthyosis?. Tropical Medicine Rounds , (2014).
(https://doi.org/10.1111/ijd.12546)

Ferreira, J. V., Pierotte, I. C., Pianetti, G. A., & César, I. C. (2020). Simultaneous quantitation of kavalactones in kava dry extracts: comparison of multi-standards and single standard validation approaches. Phytochemical Analysis. (https://doi.org/10.1002/pca.3019)

Boonen G, Häberlein H. Influence of genuine kavapyrone enantiomers on the GABA-A binding site. Planta Med. 1998 Aug;64(6):504-6. doi: 10.1055/s-2006-957502. PMID: 9776662.
(https://doi.org/10.1055/s-2006-957502)

Noor, N. A.. “Anxiolytic action and safety of Kava: Effect on rat brain acetylcholinesterase activity and some serum biochemical parameters.” African Journal of Pharmacy and Pharmacology 4 (2010): 823-828.
(https://www.researchgate.net/publication/228678736)

Baker, J. D., Tradition and toxicity: Evidential cultures in the kava safety debate. Social Studies of Science 41, 361-384 (2011).
(https://doi.org/10.1177/0306312710395341)

Tecun, A., Reeves, R. & Wolfgramm, M. The past before US: A brief history of tongan kava. Journal of the Polynesian Society 129, 171-192 (2020).
(https://orcid.org/0000-0001-5269-3978)

Guo, L., Shi, Q., Dial, S., Xia, Q., Mei, N., zhen Li, Q., Chan, P. C. & Fu, P. Gene expression profiling in male B6C3F1 mouse livers exposed to kava identifies - Changes in drug metabolizing genes and potential mechanisms linked to kava toxicity. Food Chem. Toxicol. 48, 686-696 (2010).
(https://doi.org/10.1016/j.fct.2009.11.050)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19948201/)

Narayanapillai, S. C., Balbo, S., Leitzman, P., Grill, A. E., Upadhyaya, P., Shaik, A. A., Zhou, B., {Gerard O'Sullivan}, M., Peterson, L. A., Lu, J., Hecht, S. S. & Xing, C. Dihydromethysticin from kava blocks tobacco carcinogen 4-(methylnitrosamino)-1- (3-pyridyl)-1-butanone-induced lung tumorigenesis and differentially reduces DNA damage in A/J mice. Carcinogenesis 35, 2365-2372 (2014).
(https://doi.org/10.1093/carcin/bgu149)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25053626/)

L. Zou, G. L. Henderson, M. R. Harkey, Y. Sakai, & A. Li2. (2004). Effects of Kava (Kava-kava, ‘Awa, Yaqona, Piper methysticum) on c-DNA-expressed cytochrome P450 enzymes and human cryopreserved hepatocytes. Phytomedicine, 11(4), 285–294.
(https://doi.org/10.1078/0944711041495263)

Teschke R, Gaus W, Loew D. Kava extracts: safety and risks including rare hepatotoxicity. Phytomedicine. 2003;10(5):440-6. doi: 10.1078/0944-7113-00314. PMID: 12834011. .
(https://doi.org/10.1078/0944-7113-00314)

Lim, S. T., Dragull, K., Tang, C. S., Bittenbender, H. C., Efird, J. T. & Nerurkar, P. V. Effects of kava alkaloid, pipermethystine, and kavalactones on oxidative stress and cytochrome P450 in F-344 rats. Toxicol. Sci. 97, 214-221 (2007).
(https://doi.org/10.1093/toxsci/kfm035)

Xuan, T. D., Fukuta, M., Wei, A. C., Elzaawely, A. A., Khanh, T. D. & Tawata, S. Efficacy of extracting solvents to chemical components of kava (Piper methysticum) roots. Journal of Natural Medicines 62, 188-194 (2008).
(https://doi.org/10.1007/s11418-007-0203-2)

Loew, D. & Franz, G. Quality aspects of traditional and industrial Kava-extracts. Phytomedicine 10, 610-612 (2003).
(https://doi.org/10.1078/094471103322331638)

Teschke, R., Fuchs, J., Bahre, R., Genthner, A. & Wolff, A. Kava hepatotoxicity: Comparative study of two structured quantitative methods for causality assessment. Journal of Clinical Pharmacy and Therapeutics 35, 545-563 (2010).
(https://doi.org/10.1111/j.1365-2710.2009.01131.x)

DiSilvestro, R. A., Zhang, W. & DiSilvestro, D. J. Kava feeding in rats does not cause liver injury nor enhance galactosamine-induced hepatitis. Food Chem. Toxicol. 45, 1293-1300 (2007).
(https://doi.org/10.1016/j.fct.2007.01.015)

Pescitelli, G., Bilia, A. R., Bergonzi, M. C., Vincieri, F. F., & Di Bari, L. (2010). Cyclodextrins as carriers for kavalactones in aqueous media: Spectroscopic characterization of (S)-7,8-dihydrokavain and β-cyclodextrin inclusion complex. Journal of Pharmaceutical and Biomedical Analysis, 52(4), 479–483.
(https://doi.org/10.1016/j.jpba.2010.01.037)

Baker, J. D., Pills, potions, products: Kava's transformations in new and nontraditional contexts. Contemporary Pacific 24, 233-265 (2012).
(https://www.researchgate.net/deref/http://dx.doi.org/10.1353/cp.2012.0026)

Bilia, A. R., Gallori, S. & Vincieri, F. F. Kava-kava and anxiety: Growing knowledge about the efficacy and safety. Life Sci. 70, 2581-2597 (2002).
(https://doi.org/10.1016/s0024-3205(02)01555-2)

Chua, H. C., Christensen, E. T., Hoestgaard-Jensen, K., Hartiadi, L. Y., Ramzan, I., Jensen, A. A., Absalom, N. L. & Chebib, M. Kavain, the major constituent of the anxiolytic kava extract, potentiates gabaa receptors: Functional characteristics and molecular mechanism. PLoS One 11, 1-17 (2016).
(https://doi.org/10.1371/journal.pone.0157700)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/27332705/)

Teschke, R. & Lebot, V. Proposal for a Kava Quality Standardization Code. Food Chem. Toxicol. 49, 2503-2516 (2011).
(https://doi.org/10.1016/j.fct.2011.06.075)

Anke, J., Fu, S. & Ramzan, I. Kavalactones fail to inhibit alcohol dehydrogenase in vitro. Phytomedicine 13, 192-195 (2006).
(https://doi.org/10.1016/j.phymed.2004.07.005)

Feltenstein, M. W., Lambdin, L. C., Ganzera, M., Dharmaratne, H. R. W., Nanayakkara, N. P., Khan, I. A. & Sufka, K. J. Anxiolytic properties of Piper methysticum extract samples and fractions in the chick social-separation-stress procedure. Phytotherapy Research 17, 210-216 (2003).
(https://doi.org/10.1002/ptr.1107)

Lebot, V., Michalet, S. & Legendre, L. Kavalactones and Flavokavins Profiles Contribute to Quality Assessment of Kava (Piper methysticum G. Forst.), the Traditional Beverage of the Pacific. Beverages 5, 34 (2019).
(https://doi.org/10.3390/beverages5020034)
(https://agritrop.cirad.fr/592382/)

Ooi, S. L., Henderson, P. & Pak, S. C. Kava for generalized anxiety disorder: A review of current evidence. Journal of Alternative and Complementary Medicine 24, 770-780 (2018).
(https://doi.org/10.1089/acm.2018.0001)

Ligresti, A., Villano, R., Allarà, M., Ujváry, I., & Di Marzo, V. (2012). Kavalactones and the endocannabinoid system: The plant-derived yangonin is a novel CB 1 receptor ligand. Pharmacological Research, 66(2), 163–169. (https://doi.org/10.1016/j.phrs.2012.04.003)

Zhang, Y., Zvi, Y. S., Batko, B., Zaphiros, N., O'Donnell, E. F., Wang, J., Sato, K., Yang, R., Geller, D. S., Koirala, P., Zhang, W., Du, X., Piperdi, S., Liu, Y., Zheng, D., Roth, M., Gill, J., Zhang, J., Ren, T., Gorlick, R., Zi, X. & Hoang, B. H. Down-regulation of Skp2 expression inhibits invasion and lung metastasis in osteosarcoma. Sci. Rep. 8, 1-13 (2018).
(https://doi.org/10.1038/s41598-018-32428-9)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/30250282/)

Abu, N., Akhtar, M. N., Yeap, S. K., Lim, K. L., Ho, W. Y., Zulfadli, A. J., Omar, A. R., Sulaiman, M. R., Abdullah, M. P. & Alitheen, N. B. Flavokawain a induces apoptosis in MCF-7 and MDA-MB231 and inhibits the metastatic process in vitro. PLoS One 9, 1-12 (2014).
(https://doi.org/10.1371/journal.pone.0105244)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25286005/)

Anke, J. & Ramzan, I. Kava hepatotoxicity: Are we any closer to the truth?. Planta Med. 70, 193-196 (2004).
(https://doi.org/10.1055/s-2004-815533)

Van, T. M., Xuan, T. D., Minh, T. N. & Quan, N. V. Isolation and purification of potent growth inhibitors from piper methysticum root. Molecules 23, (2018).
(https://doi.org/10.3390/molecules23081907)
(https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/30065174/)

Heinze HJ, Münthe TF, Steitz J, Matzke M. Pharmacopsychological effects of oxazepam and kava-extract in a visual search paradigm assessed with event-related potentials. Pharmacopsychiatry. 1994 Nov;27(6):224-30. doi: 10.1055/s-2007-1014309. PMID: 7870743.
(https://doi.org/10.1055/s-2007-1014309)

Madhavaram, H., Patel, T. & Kyle, C. Kavain Interference with Amphetamine Immunoassay. J. Anal. Toxicol. , (2020).
(https://doi.org/10.1093/jat/bkaa178)

Keledjian, J., Duffield~, P. H., Jamieson, D. D., Lidcards, R. 0, & Duffields, A. M. (1988). Uptake into Mouse Brain of Four Compounds Present in the Psychoactive Beverage Kava. Journal of Pharmaceutical Sciences, 77(12), 1003–1006. (https://doi.org/10.1002/jps.2600771203).

Clough, A. R., Cairney, S., Maruff, P., Burns, C. B., & Currie, B. J. (2001). Possible toxicity and withdrawal seizures in Aboriginal kava drinkers in Arnhem Land, (Australia). South Pacific Journal of Psychology, 13, 26–33. (https://doi.org/10.1017/s025754340000033x)