The role of histamine H-1-receptors in the anticonvulsive effect of morphine against maximal electroconvulsive shock in mice

Küçük Resim Yok

Tarih

1996

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Japanese Pharmacological Soc

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Morphine is known to release histamine from mast cells. It is also known that histamine receptors mediate some of morphine's effects on the central nervous system. The contribution of H-1- and H-2-receptors to the effect of morphine on maximal electroconvulsive shock in mice was investigated in the present experiments. Morphine showed a dose-dependent anticonvulsive effect, but produced spontaneous clonic convulsions at higher doses (100 mg/kg, i.p.). The anticonvulsive effect of morphine (1 mg/kg, i.p.) was antagonized by histamine Hi-receptor antagonists, dimethindene (0.1 mg/kg, i.p.), promethazine (0.4 mg/kg, i.p.) and pheniramine (30 mg/kg, i.p.), and naloxone (10 mg/kg, i.p.), but not by the H-2-receptor antagonist ranitidine (10-50 mu g, i.c.v.). These results show that morphine has an anticonvulsive effect via histamine H-1-receptors against maximal electroconvulsive shock in mice.

Açıklama

Anahtar Kelimeler

Morphine, Anticonvulsive Effect, Histamine, Histamine H-1-Receptor, Maximal Electroconvulsive Shock, Central Nervous-System, Mast-Cells, Brain Histamine, Mouse-Brain, Rat, Transmitter, Involvement, Receptors, Turnover, Release

Kaynak

Japanese Journal Of Pharmacology

WoS Q Değeri

N/A

Scopus Q Değeri

N/A

Cilt

71

Sayı

2

Künye