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Effect of cyclic dipeptides containing histidine on pentobarbital narcosis.

作者信息

Suzuki T, Sakurada T, Tadano T, Kisara K, Sasaki Y, Suzuki K

出版信息

J Pharmacobiodyn. 1981 May;4(5):377-9. doi: 10.1248/bpb1978.4.377.

DOI:10.1248/bpb1978.4.377
PMID:6793707
Abstract

We examined the effect of cyclo (His-Pro) and its analogs on pentobarbital narcosis in mice. Cyclo (His-Pro), 500 nmol/mouse, administered via intracerebroventricular (i.c.v.) route significantly prolonged the sleeping time. Methylation of histidine in the structure of cyclo (His-Pro) did not increase the activity of cyclo (His-Pro). Some of other cyclo (His-Pro) analogs, of which proline was replaced with other amino acids, cyclo (His-Phe), cyclo (His-Tyr), cyclo (His-His) and cyclo (D-His-Leu) produced significant prolongation of the sleeping time as compared with cyclo (His-Pro). These results suggest that cyclo (His-Pro) has opposing effect to that of thyrotropin releasing hormone (TRH) and the prolongation of pentobarbital narcosis by cyclic dipeptides might be caused by their central action.

摘要

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