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多巴胺D1和D2系统在可卡因对大鼠行为影响中的作用。

Involvement of D1 and D2 dopamine systems in the behavioral effects of cocaine in rats.

作者信息

Ushijima I, Carino M A, Horita A

机构信息

Department of Pharmacology, School of Medicine, University of Washington, Seattle 98195, USA.

出版信息

Pharmacol Biochem Behav. 1995 Dec;52(4):737-41. doi: 10.1016/0091-3057(95)00167-u.

Abstract

Cocaine (5-40 mg/kg, intraperitoneally) enhanced locomotion and rearing accompanied with head circling and body shaking. Although at 40 mg/kg typical stereotypy licking occasionally appeared, 40% of the rats died. At doses that did not affect physiologic locomotion and rearing, the D1-receptor antagonist SCH23390 but not D2 antagonist raclopride inhibited locomotion and rearing stimulated by cocaine (20 mg/kg). All behavioral responses of cocaine were abolished with increasing doses of raclopride and SCH23390. Sulpiride, a D2 antagonist, exerted a biphasic effect on locomotor activity (i.e., a low dose of sulpiride increased and a high dose decreased cocaine-induced locomotor activity). Sulpiride enhanced head circling, body shaking, and increases of rearing induced by cocaine. D2-receptor agonists quinpirole and bromocriptine inhibited these responses, presumably by activating the typical stereotyped behaviors such as sniffing at low doses, and licking and gnawing at high doses. The lowest dose of bromocriptine inhibited all behaviors induced by cocaine without producing typical stereotyped behaviors in itself. SK+F38393, a D1-receptor agonist, in combination with cocaine did not induce typical stereotype, which results in a synergistic effect of D1 and D2-receptor activities. The increases of locomotion and rearing, head circling, and body shaking induced by cocaine may involve the indirect activation of postsynaptic D1 and D2 receptors, presumably via dopamine release, resulting from inhibition of the presynaptic D2 receptors. These results also provide evidence that the indirect stimulation of postsynaptic D2 receptors by cocaine (20 mg/kg) is insufficient to induce stereotyped behaviors, and that the role of dopamine D1 receptors in mediating the behavioral actions of acute cocaine appears to be more important than that of D2 receptors. Our results also suggest that bromocriptine may be useful for the treatment of acute cocaine poisoning.

摘要

可卡因(5 - 40毫克/千克,腹腔注射)可增强运动和竖毛行为,并伴有头部旋转和身体颤抖。虽然在40毫克/千克时偶尔会出现典型的刻板性舔舐行为,但40%的大鼠死亡。在不影响生理性运动和竖毛行为的剂量下,D1受体拮抗剂SCH23390可抑制可卡因(20毫克/千克)刺激引起的运动和竖毛行为,而D2拮抗剂雷氯必利则无此作用。随着雷氯必利和SCH23390剂量的增加,可卡因的所有行为反应均被消除。D2拮抗剂舒必利对运动活动产生双相作用(即低剂量舒必利增加可卡因诱导的运动活动,高剂量则降低)。舒必利增强了可卡因诱导的头部旋转、身体颤抖和竖毛行为的增加。D2受体激动剂喹吡罗和溴隐亭抑制了这些反应,推测是通过激活典型的刻板行为,如低剂量时的嗅探,高剂量时的舔舐和啃咬。溴隐亭的最低剂量抑制了可卡因诱导的所有行为,且自身未产生典型的刻板行为。D1受体激动剂SK + F38393与可卡因联合使用未诱导出典型的刻板行为,这导致D1和D2受体活性产生协同效应。可卡因诱导的运动、竖毛、头部旋转和身体颤抖的增加可能涉及突触后D1和D2受体的间接激活,推测是通过多巴胺释放,这是由于突触前D2受体受到抑制所致。这些结果还提供了证据,表明可卡因(20毫克/千克)对突触后D2受体的间接刺激不足以诱导刻板行为,并且多巴胺D1受体在介导急性可卡因行为作用方面的作用似乎比D2受体更重要。我们的结果还表明,溴隐亭可能对治疗急性可卡因中毒有用。

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