Kamei C, Akahori H, Tasaka K
J Pharmacobiodyn. 1986 Jan;9(1):112-6. doi: 10.1248/bpb1978.9.112.
Intraventricular injection of histamine (Hi) significantly prolonged thiopental sleeping time at doses of 0.5 microgram or larger. Both 1-methylHi and imidazole-4-acetic acid, however, did not affect thiopental narcosis. Pretreatment with alpha-fluoromethylhistidine diminished the effect of Hi, while histidine, metoprine and quinacrine prolonged thiopental narcosis. Injection with 2-methylHi did not affect thiopental sleeping time, while as in the case of Hi, 4-methylHi augmented the thiopental effect. In addition, H2-receptor blocking agents such as cimetidine, ranitidine and famotidine clearly antagonized Hi-induced prolongation of thiopental narcosis, while pyrilamine and chlorpheniramine had no effect. These results indicate that Hi-induced prolongation of thiopental narcosis appears to be exerted via H2-receptors and is, in some way, related to the Hi content in the brain.
脑室内注射组胺(Hi)在剂量为0.5微克或更大时可显著延长硫喷妥钠的睡眠时间。然而,1-甲基组胺和咪唑-4-乙酸均不影响硫喷妥钠麻醉。用α-氟甲基组氨酸预处理可减弱Hi的作用,而组氨酸、甲氧苄氨嘧啶和奎纳克林可延长硫喷妥钠麻醉时间。注射2-甲基组胺不影响硫喷妥钠睡眠时间,而与Hi的情况一样,4-甲基组胺增强了硫喷妥钠的作用。此外,西咪替丁、雷尼替丁和法莫替丁等H2受体阻断剂明显拮抗Hi诱导的硫喷妥钠麻醉时间延长,而吡苄明和氯苯那敏则无作用。这些结果表明,Hi诱导的硫喷妥钠麻醉时间延长似乎是通过H2受体发挥作用的,并且在某种程度上与脑中的Hi含量有关。