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D-cycloserine inhibits the development and the expression of locomotor sensitization to amphetamine in rats.

作者信息

Gaiardi Margherita, Colantoni Alessia, De Luca Valentina, Bartoletti Maria

机构信息

Department of Pharmacology, University of Bologna, Bologna, Italy.

出版信息

Behav Pharmacol. 2010 May;21(3):165-70. doi: 10.1097/FBP.0b013e32833a5bcb.

Abstract

Amphetamine use is now an epidemic of global proportions; however, no approved medications are available to treat amphetamine abusers. Since glutamate plays a crucial role in regulating the development and expression of addictive behaviors, such as sensitization, in the present study we examined the possible effect of D-cycloserine, a partial agonist at the glycine site of N-methyl-D-aspartate receptors, on the development and expression of locomotor sensitization to amphetamine. Rats were intraperitoneally injected with saline or D-cycloserine (6 mg/kg), before saline or amphetamine (1.5 mg/kg), on days 1-10. Three days after ceasing the chronic treatment, a challenge test was run. The animals received saline or 6 mg/kg D-cycloserine and, 1 h later, they received 0.75 or 1.5 mg/kg amphetamine; motility was recorded for 2 h. The chronic treatment with D-cycloserine alone had no influence on the acute behavioral response to amphetamine. However, D-cycloserine prevented the development and inhibited the expression of amphetamine sensitization; in both cases the D-cycloserine effect was not significantly different as a function of amphetamine challenge dose. As behavioral sensitization is proposed to model the enhanced 'drug wanting' observed in psychostimulant abusers, the present data suggest that D-cycloserine might be a useful therapeutic approach to its treatment.

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