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首页> 外文期刊>Japanese Journal of Pharmacology >Effect of Isofloxythepin, a Novel Neuroleptic, on Hippocampal Stimulation-Induced Wet-Dog Shaking in the Rat
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Effect of Isofloxythepin, a Novel Neuroleptic, on Hippocampal Stimulation-Induced Wet-Dog Shaking in the Rat

机译:新型抗精神病药异佛洛西平对海马刺激诱导的湿狗震动的影响

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References(20) Cited-By(2) (±)isofloxythepin (0.32-3.2 mg/kg, i.p.) significantly inhibited in a dose-dependent manner wet-dog shaking (WDS) induced by electrical stimulation of the rat hippocampus. In addition, both optical isomers of isofloxythepin inhibited WDS, with the (-)-isomer being almost 3 times more potent than the (+)-isomer. Other neuroleptics such as haloperidol, chlorpromazine, zotepine and sulpiride also reduced significantly the number of WDS. The inhibitory potency of haloperidol was comparable to that of (±)isofloxythepin, which was approximately 3 times more potent than that of chlorpromazine or zotepine. Sulpiride suppressed significantly WDS only at the high dose of 100 mg/kg. None of the drugs affected hippocampal afterdischarge. Inhibition of WDS produced by (±)isofloxythepin or haloperidol was antagonized by pretreatment with a dopamine receptor agonist, lisuride. The present results indicate that isofloxythepin shares with other neuroleptics an inhibitory effect on WDS; dopaminergic blocking action appears to be important in the inhibition of WDS induced by hippocampal stimulation.
机译:参考文献(20)被引用的By(2)(±)异氟西平(0.32-3.2 mg / kg,i.p.)以剂量依赖性方式显着抑制大鼠海马电刺激引起的湿狗摇动(WDS)。此外,两种异氟醚灵的光学异构体均能抑制WDS,(-)异构体的效力几乎是(+)异构体的3倍。其他抗精神病药,如氟哌啶醇,氯丙嗪,唑替平和舒必利,也明显减少了WDS的数量。氟哌啶醇的抑制效力与(±)异氟西平相同,约比氯丙嗪或唑替平的抑制效力高3倍。舒必利仅在100 mg / kg的高剂量下才能显着抑制WDS。出院后没有一种药物影响海马。用多巴胺受体激动剂利苏利德预处理可拮抗由(±)异氟西平或氟哌啶醇产生的WDS的抑制作用。目前的结果表明异氟西平与其他抗精神病药共有对WDS的抑制作用。多巴胺能阻断作用似乎在抑制海马刺激诱导的WDS中很重要。

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