The Salvia divinorum Research and Information Center - Shroomery

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Salvia divinorum and Salvinorin A: new pharmacologic findings Regulatory sites: Benzodiazepine(centrl), glycine (stry insens.), PCP, MK-801. Brain/gut peptides: angiotensin Ty2, arg-vasopressin Vl, bombesin, CCK central, CCK peripheral, substance P, substance K, NPY, neurotensin, somatostatin, VIP. Growth factors and peptides: ANF I, EGF, NGF. Ion channels: Calcium (type N), calcium (type T and L), chloride, potassium (low conduct). Second messengers: Forskolin, phorbol ester, inositol triphosphate. Monoamine oxidase inhibition: Monoamine oxidase A, monoamine oxidase B. 3. Discussion and conclusions When S. divinorum leaves are consumed, either by chewing the fresh leaves or by retaining the leaf juices in the mouth, enough of the highly active compound salvinorin A is absorbed through the oral mucosa and into the blood stream to produce a psychoactive effect. Swallowing of the herb is unnecessary and its effects are increased by lengthening the amount of time that the herb remains in the mouth. When the leaf juices are quickly swallowed, minimizing contact with the oral mucosa, the only route of absorption is through the gastrointestinal system where salvinorin A is deactivated before entering the blood stream. When pure salvinorin A is encapsulated and swallowed it is inactive even at relatively large doses, but when absorbed through the oral mucosa or vaporized and inhaled is extremely active. It is likely that if salvinorin A were administered by injection, it would prove to be active at even lower doses than those described in this paper. Salvinorin A is the first entheogenic diterpene reported and is active in humans at extraordinarily low doses. It does not appear to affect any of the receptor sites affected by other hallucinogens. Further research into the methods of action and possible medicinal values of this and similar compounds may prove to be quite rewarding. Acknowledgments I am grateful to Dr Leander Valdes III for supplying a reference sample of salvinorin A, and Dr David Nichols for his role in the receptor site screening of salvinorin A through his NIMH-funded research program. References Ortega, A., Blount, J.F. and Manchand, P.S. (1982) Salvinorin. a new lrans-neoclerodane diterpene from Salvia divinorum (Labiatae). Journal of the Chemical Society. Perkin Trans-actions 1: Organic and Bio-Organic Chemistry 2505-2508. Valdes, L.J. III., Diaz J.L. and Ara G. Paul. (1983) Ethnopharmacology of Ska Maria Pastora (Salvia divinorum Epling and Jativa-M.). Journal of Ethnopharmacology 7, 287-312. Valdes, L. J.III., Butler, W.M., Hatfield, G.M., Paul. A.G. and Koreeda, M. (1984) Divinorin A, a psychotropic terpenoid, and divinorin B from the hallucinogenic mint Salvia divinorum. Journal of Organic Chemistry 49, 4716- 4720. Valdes, L.J. III., Hatfield, G.M., Paul, A.G.and Koreeda M. (1987) Studies of Salvia divinorum (Lamiaceae), an hallucinogenic mint from the Sierra Mazateca in Oaxaca. Central Mexico. Economic Botany 41(2), 283-291. Wasson, R.G. (1962) A new Mexican psychotropic drug from the mint family. Botanical Museum Leaflets Harvard University 20 77-84. Wasson, R.G. (1963) Notes on the present status of ololuiqui and the other hallucinogens of Mexico. Botanical Museum Leaflets Harvard University 20, 161 - 193. http://www.sagewisdom.org/jep.html (4 of 5) [04.09.01 10:20:43]
Salvia divinorum and Salvinorin A: new pharmacologic findings http://www.sagewisdom.org/jep.html (5 of 5) [04.09.01 10:20:43]
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loliolide LITERATURE CITED 1. L.J.
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