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D1和D2多巴胺受体在腹外侧纹状体多巴胺能刺激诱导的口腔刻板行为中的作用。

The role of D1 and D2 dopamine receptors in oral stereotypy induced by dopaminergic stimulation of the ventrolateral striatum.

作者信息

Delfs J M, Kelley A E

机构信息

Department of Psychology, Harvard University, Cambridge, MA 02138.

出版信息

Neuroscience. 1990;39(1):59-67. doi: 10.1016/0306-4522(90)90221-o.

Abstract

Microinjection of amphetamine into the ventrolateral region of the striatum results in compulsive and intense oral stereotypies in the rat. Although these stereotyped behaviors are known to be a direct result of excessive stimulation of the striatal dopamine neurons, the relative roles of the D1 and D2 receptors in oral stereotypies are not clearly understood. It is reported here that microinjection of the selective D1 agonist, SKF 38393 (0, 0.3, 3.0, 30.0 micrograms in 0.5 microliters vehicle) into the ventrolateral striatum resulted in no observable changes in behavior during the 30-min test period. However, it was observed that intense self-biting emerged 3-4 h following injection. Examination of histology from these animals revealed extensive tissue damage and the delayed onset of biting was hypothesized to result from a neurotoxic effect of SKF 38393. Infusion of quinpirole (0, 0.3, 3.0, 30.0 micrograms in 0.5 microliter vehicle), a selective D2 agonist, resulted in a dose-dependent increase in orofacial behaviors such as licking, wood-chip eating, head-down sniffing and mouth movements. Intense oral stereotypies such as biting or gnawing were not observed following treatment with quinpirole. Infusion of the mixed agonist dopamine (0, 2.0, 10.0, 20.0 micrograms in 0.5 microliter vehicle) into the ventrolateral striatum was found to elicit intense oral stereotypy. This behavior consisted almost exclusively of self-biting similar to that observed following amphetamine microinjection into this region. Haloperidol, when given as either a systemic (0.2 mg/kg) or intra-ventrolateral striatum (2.5 micrograms/0.5 microliter) pretreatment, effectively blocked oral stereotypies induced by amphetamine microinjection into the ventrolateral striatum. Pretreatment with either the D1 antagonist SCH 23390 (0, 0.01, 0.1 mg/kg, i.p.) or the D2 antagonist raclopride (0, 0.05, 0.50, 1.0 mg/kg, i.p.) antagonized amphetamine-induced oral stereotypy in a dose-dependent manner. These findings demonstrate that within the striatal site specifically implicated in oral behavior, concurrent stimulation of both receptor subtypes is necessary for the expression of intense oral stereotypies.

摘要

向大鼠纹状体腹外侧区域微量注射苯丙胺会导致其出现强迫性且强烈的口部刻板行为。尽管已知这些刻板行为是纹状体多巴胺能神经元过度刺激的直接结果,但D1和D2受体在口部刻板行为中的相对作用尚不清楚。本文报道,向腹外侧纹状体微量注射选择性D1激动剂SKF 38393(0、0.3毫克、3.0毫克、30.0毫克溶于0.5微升溶媒),在30分钟测试期内未观察到行为有明显变化。然而,在注射后3 - 4小时观察到出现强烈的自咬行为。对这些动物的组织学检查显示有广泛的组织损伤,且推测咬行为延迟出现是由SKF 38393的神经毒性作用所致。注入选择性D2激动剂喹吡罗(0、0.3毫克、3.0毫克、30.0毫克溶于0.5微升溶媒)会导致口面部行为如舔舐、啃食木屑、低头嗅闻和嘴部动作呈剂量依赖性增加。用喹吡罗治疗后未观察到如咬或啃咬等强烈的口部刻板行为。向腹外侧纹状体注入混合激动剂多巴胺(0、2.0毫克、10.0毫克、20.0毫克溶于0.5微升溶媒)会引发强烈的口部刻板行为。这种行为几乎完全由自咬组成,类似于向该区域微量注射苯丙胺后观察到的行为。当给予氟哌啶醇进行全身预处理(0.2毫克/千克)或腹外侧纹状体内预处理(2.5微克/0.5微升)时,可有效阻断向腹外侧纹状体微量注射苯丙胺所诱导的口部刻板行为。用D1拮抗剂SCH 23390(0、0.01毫克/千克、0.1毫克/千克,腹腔注射)或D2拮抗剂雷氯必利(0、0.05毫克/千克、0.50毫克/千克、1.0毫克/千克,腹腔注射)进行预处理,会以剂量依赖性方式拮抗苯丙胺诱导的口部刻板行为。这些发现表明,在与口部行为特别相关的纹状体部位,两种受体亚型的同时刺激对于强烈口部刻板行为的表达是必要的。

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