Chemistry:Kavain
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| Preferred IUPAC name
4-Methoxy-6-[(E)-2-phenylethenyl]-5,6-dihydro-2H-pyran-2-one | |
| Other names
(E)-4-Methoxy-6-styryl-5,6-dihydro-2H-pyran-2-one
Kawain | |
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3D model (JSmol)
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| Properties | |
| C14H14O3 | |
| Molar mass | 230.263 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Kavain is the main kavalactone found mostly in the roots of the kava plant.
Pharmacology
Kavain has anticonvulsive properties, attenuating vascular smooth muscle contraction through interactions with voltage-dependent Na+
and Ca2+ channels.[1] How this effect is mediated, and to what extent this mechanism is involved in the anxiolytic and analgesic effects of kavalactones on the central nervous system, is unknown. The recent finding that kavain can reversibly inhibit both monoamine oxidase A and monoamine oxidase B suggests that kavain may exert some of its effects by modulating serotonin, norepinephrine, and dopamine signaling.[2]
However, the precise mechanisms underlying the psychotropic, sedative, and anxiolytic actions of kavain and related kavalactones are still debated. Direct binding to the benzodiazepine/flumazenil binding site of the GABA-A receptor does not occur with kavain enantiomers.[3] Many studies involved kava extracts from different plant parts and are, therefore, not applicable to kavain itself. In 2016, kavain was shown to bind at the extrasynaptic α4β2δ GABAA receptor and potentiate GABA efficacy, similarly to barbiturates.[4]
A comparative review of in-vivo studies with kavain (and related kavapyrones) to commonly used antiepileptic drugs and mood stabilizers affecting ion fluxes indicates that the kavapyrones are weakly Na+ antagonistic and therefore antiepileptic. They also have pronounced L- type Ca2+ channel antagonistic properties and act as a positive modulator of the early K+ outward current, which contribute to mood stabilizing properties similar to lamotrigine.[5]
Kavain and analogs remain interesting for drug discovery against a variety of cellular targets, including P-glycoprotein (Pgp), cytochrome P450, and cyclo-oxygenase (COX) enzymes among others.[6]
See also
References
- ↑ Bradić, I; Pasini, M (1975). "Hirschsprung's disease - therapy and results". Acta Chirurgica Iugoslavica 22 (2): 183–95. PMID 1235738.
- ↑ Prinsloo, Denise; van Dyk, Sandra; Petzer, Anél; Petzer, Jacobus P. (2019-09-20). "Monoamine Oxidase Inhibition by Kavalactones from Kava (Piper Methysticum)". Planta Medica 85 (14/15): 1136–1142. doi:10.1055/a-1008-9491. ISSN 0032-0943. PMID 31539917.
- ↑ Boonen, Georg; Häberlein, Hans (2007). "Influence of Genuine Kavapyrone Enantiomers on the GABAABinding Site". Planta Medica 64 (6): 504–6. doi:10.1055/s-2006-957502. PMID 9776662.
- ↑ "Kavain, the Major Constituent of the Anxiolytic Kava Extract, Potentiates GABAA Receptors: Functional Characteristics and Molecular Mechanism". PLOS ONE 11 (6): e0157700. 2016. doi:10.1371/journal.pone.0157700. PMID 27332705. Bibcode: 2016PLoSO..1157700C.
- ↑ Grunze, Heinz; Langosch, Jens; Schirrmacher, Karin; Bingmann, Dieter; Von Wegerer, Jörg; Walden, Jörg (2001). "Kava pyrones exert effects on neuronal transmission and transmembraneous cation currents similar to established mood stabilizers - a review". Progress in Neuro-Psychopharmacology and Biological Psychiatry 25 (8): 1555–70. doi:10.1016/S0278-5846(01)00208-1. PMID 11642654.
- ↑ Rowe, A.; Narlawar, R.; w. Groundwater, P.; Ramzan, I. (2011). "Kavalactone Pharmacophores for Major Cellular Drug Targets". Mini Reviews in Medicinal Chemistry 11 (1): 79–83. doi:10.2174/138955711793564088. PMID 21034404.
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