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小鼠体内的多巴胺D2受体与脊髓兴奋

Dopamine D2 receptors and spinal cord excitation in mice.

作者信息

Hasegawa Y, Kurachi M, Otomo S

机构信息

Department of Pharmacology, Research Center, Taisho Pharmaceutical Co., Ltd., Saitama, Japan.

出版信息

Eur J Pharmacol. 1990 Aug 10;184(2-3):207-12. doi: 10.1016/0014-2999(90)90611-9.

Abstract

Spinal cord excitation was induced in mice by morphine and the effects of dopamine D1 and D2 receptor antagonists on the Straub tail reaction were investigated. The dopamine D2 receptor antagonist, sulpiride (25-100 mg/kg i.p.), or haloperidol (0.25-1.0 mg/kg dose dependently inhibited the Straub tail reaction induced by subcutaneously injected morphine. A low dose of apomorphine (50 micrograms/kg s.c.) also reduced the Straub tail reaction. The dopamine D1 receptor antagonist, SCH-23390 (25-100 micrograms/kg i.p.), had no significant effect. Sulpiride (50 mg/kg i.p.) significantly inhibited the Straub tail reaction induced by intrathecally injected morphine (6 microgram/mouse). Intrathecal injection of apomorphine (12.5-25 micrograms/mouse) induced the Straub tail reaction dose dependently. The Straub tail reaction induced by intrathecally injected apomorphine was significantly inhibited by sulpiride. SCH-23390 had no significant effect on the Straub tail reaction induced by intrathecally injected morphine or apomorphine. These results support the proposal that the dopamine response involved in the Straub tail reaction is mediated by postsynaptic dopamine D2 receptors in the spinal cord of mice.

摘要

通过吗啡诱导小鼠脊髓兴奋,并研究多巴胺D1和D2受体拮抗剂对斯特劳布尾反应的影响。多巴胺D2受体拮抗剂舒必利(25 - 100毫克/千克腹腔注射)或氟哌啶醇(0.25 - 1.0毫克/千克)剂量依赖性地抑制皮下注射吗啡诱导的斯特劳布尾反应。低剂量阿扑吗啡(50微克/千克皮下注射)也可减轻斯特劳布尾反应。多巴胺D1受体拮抗剂SCH - 23390(25 - 100微克/千克腹腔注射)无显著作用。舒必利(50毫克/千克腹腔注射)显著抑制鞘内注射吗啡(6微克/小鼠)诱导的斯特劳布尾反应。鞘内注射阿扑吗啡(12.5 - 25微克/小鼠)剂量依赖性地诱导斯特劳布尾反应。鞘内注射阿扑吗啡诱导的斯特劳布尾反应被舒必利显著抑制。SCH - 23390对鞘内注射吗啡或阿扑吗啡诱导的斯特劳布尾反应无显著作用。这些结果支持这样的观点,即参与斯特劳布尾反应的多巴胺反应是由小鼠脊髓中的突触后多巴胺D2受体介导的。

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