Ritanserin, a 5HT2/1C receptor antagonist, does not block cocaine-induced behavioral alterations and zif268 mRNA expression in the striatum of the rats.
- Author:
Eun Sang CHOE
1
;
Jong Yeon KIM
Author Information
1. Department of Physiology, Yeungnam University College of Medicine, Taegu, South Korea. jykim@medical.yeungnam.ac.kr
- Publication Type:Original Article
- MeSH:
Animals;
Basal Ganglia;
Cocaine;
Dopamine;
Gene Expression;
In Situ Hybridization;
Neurons;
Rats*;
Ritanserin*;
RNA, Messenger*;
Serotonin;
Zinc Fingers
- From:The Korean Journal of Physiology and Pharmacology
2000;4(5):355-359
- CountryRepublic of Korea
- Language:English
-
Abstract:
Cocaine induces immediate early gene expression and behavioral changes by blocking dopamine transporters in the terminals of nigrostriatal neurons in the striatum. The pharmacological role of serotonin 2/1C (5HT2/1C) receptors in cocaine-induced expression of zif268 (NGFI-A, egr1 and Krox-24) mRNA, a member of the zinc finger, was investigated using quantitative in situ hybridization histochemistry in vivo. Behavioral alterations induced by cocaine were also monitored in relation with blockade of the receptors. Systemic injection of ritanserin (1 mg/kg, s.c.), a 5HT2/1C receptor antagonist, did not reverse behavioral alterations and zif268 mRNA gene expression induced by 15 mg/kg cocaine, i.p., in the dorsal and ventral striatum. These data indicate that ritanserin-sensitive 5HT2/1C receptors are not necessary for cocaine-induced behavioral alterations and zif268 mRNA gene expression in the striatum.
