| Autor: |
Vanover, K. E., Suruki, Michael, Robledo, Silvia, Huber, Matthew, Wieland, Scott, Lan, Nancy C., Gee, Kelvin W., Wood, Paul L., Carter, Richard B. |
| Předmět: |
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| Zdroj: |
Psychopharmacology; 1999, Vol. 141 Issue 1, p77, 6p |
| Abstrakt: |
Abstract Endogenous pregnane steroids, such as allopregnanolone (3 proportional to-hydroxy-5 proportional to-pregnan-20-one; 3 proportional to, 5 proportional to-P) and pregnanolone (3 proportional to-hydroxy-5 beta-pregnan-20-one; 3 proportional to, 5 beta-P), allosterically modulate GABA[sub A] receptor function and exhibit behavioral effects similar to benzodiazepines, though acting at a distinct recognition site. Inasmuch as some positive allosteric modulators of GABA[sub A] receptor function exhibit profound interactions with ethanol, the effects of 3 proportional to, 5 proportional to-P and 3 proportional to, 5 beta-P were compared to those of two benzodiazepines, triazolam diazepam, on the motor function of mice and rats when administered either alone or in combination with ethanol. All four test compounds exhibited dose-related impairment of motor function in the horizontal wire task in mice and the rotorod task in rats. Ethanol caused a marked enhancement of triazolam- and diazepam-induced motor impairment. In contrast, ethanol enhanced to a lesser extent the motor impairment induced by both neurosteroids in mice and not at all in rats. All four compounds increased ethanol-induced behavioral sleep time in mice, although the benzodiazepines did so at a much smaller fraction of their ataxic doses as compared to the neurosteroids. As one of the undesired side-effects of therapeutic use of benzodiazepines is their interaction with ethanol, development of neuroactive steroids as drugs may offer therapeutic advantages. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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