Articolo in rivista, 2000, ENG, 10.1016/S0091-3057(00)00237-9
Concas A.; Porcu P.; Sogliano C.; Serra M.; Purdy R.H.; Biggio G.
Universita degli Studi di Cagliari; University of California, San Diego
The effects of caffeine, a naturally occurring stimulant, on the brain and plasma concentrations of neuroactive steroids were examined in the rat. A single intraperitoneal injection of caffeine induced dose- and time-dependent increases in the concentrations of pregnenolone, progesterone, and 3alpha- hydroxy-5alpha-pregnan-20-one (allopregnanolone) in the cerebral cortex. The increases were significant at a caffeine dose of 25 mg/kg and greatest (+188, +388, and +71%, respectively) at a dose of 100 mg/kg in rats killed 30 min after caffeine administration. Caffeine also increased the plasma concentrations of pregnenolone and progesterone with a dose-response relation similar to that observed in the brain, whereas the caffeine-induced increase in the plasma concentration of allopregnanolone was maximal at a dose of 50 mg/kg. Caffeine increased the plasma concentration of corticosterone, but it had no effect on the brain or plasma concentrations of 3alpha,21-dihydroxy-5alpha- pregnan-20-one and dehydroepiandrosterone. Moreover, the brain and plasma concentrations of pregnenolone, progesterone, and allopregnanolone were not affected by caffeine in adrenalectomized-orchiectomized rats. These results suggest that neuroactive steroids may modulate the stimulant and anxiogenic effects of caffeine. (C) 2000 Elsevier Science Inc.
Pharmacology, biochemistry and behavior 66 (1), pp. 39–45
Allopregnanolone, Brain, Caffeine, Corticosterone, HPA axis, Neuroactive steroids, Plasma, Rat
ID: 319154
Year: 2000
Type: Articolo in rivista
Creation: 2015-02-25 15:23:29.000
Last update: 2021-04-15 10:53:10.000
CNR authors
External links
OAI-PMH: Dublin Core
OAI-PMH: Mods
OAI-PMH: RDF
DOI: 10.1016/S0091-3057(00)00237-9
URL: http://www.scopus.com/record/display.url?eid=2-s2.0-0034105173&origin=inward
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:319154
DOI: 10.1016/S0091-3057(00)00237-9
Scopus: 2-s2.0-0034105173
PubMed: 10837842
ISI Web of Science (WOS): 000087322500006