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慢性右旋苯丙胺治疗后A10多巴胺自身受体敏感性降低的电生理证据。

Electrophysiological evidence for A10 dopamine autoreceptor subsensitivity following chronic D-amphetamine treatment.

作者信息

White F J, Wang R Y

出版信息

Brain Res. 1984 Sep 10;309(2):283-92. doi: 10.1016/0006-8993(84)90594-8.

Abstract

Extracellular single unit recording techniques were used to determine whether chronic treatment with D-amphetamine (AMP) causes a subsensitivity of dopamine (DA) autoreceptors on A10 DA neurons in the rat ventral tegmental area. Either once daily or twice daily intraperitoneal (i.p.) administration of 5.0 mg/kg AMP for 1 week significantly reduced the ability of intravenous (i.v.) AMP and apomorphine (APO) to suppress the firing of A10 DA neurons when tested 24-32 h after the final administration of i.p. AMP. For both of these treatment regimens, the dose-response curves for AMP and APO induced suppression were shifted approximately 4-fold to the right of control. Following an 8 day abstinence period, only the rats that received twice daily AMP injections exhibited subsensitivity to i.v. AMP and APO; the degree of subsensitivity was reduced by 50% as compared to that observed 24-32 h post-treatment. These results were not due to acute tolerance phenomena since a single i.p. injection of AMP 24-32 h before testing failed to alter sensitivity to i.v. AMP and APO. Rather, the results indicate that chronic AMP treatment reduces the sensitivity of A10 DA neurons to DA agonists. DA autoreceptor subsensitivity was demonstrated further by the finding that the ability of microiontophoretically applied DA to suppress A10 DA neuronal activity was markedly reduced (5.8-fold shift of the dose-response curve) by chronic AMP treatment (2 X 5 mg/kg/day). In contrast, there was no alteration in the ability of iontophoretic gamma-amino butyric acid (GABA) to suppress A10 DA activity in chronic AMP rats. Chronic AMP-treatment also increased the number of spontaneously active A10 DA neurons as well as their basal firing rate. It is suggested that the ability of chronic AMP treatment to decrease the auto-regulatory ability of A10 DA neurons may be related to the phenomena of behavioral sensitization and AMP psychosis.

摘要

采用细胞外单单位记录技术来确定长期给予D-苯丙胺(AMP)是否会导致大鼠腹侧被盖区A10多巴胺(DA)神经元上的DA自身受体出现敏感性降低。在腹腔注射(i.p.)AMP(5.0mg/kg),每日1次或每日2次,持续1周后,于末次腹腔注射AMP后24 - 32小时进行测试时,静脉注射(i.v.)AMP和阿扑吗啡(APO)抑制A10 DA神经元放电的能力显著降低。对于这两种给药方案,AMP和APO诱导抑制的剂量反应曲线均向右移动约4倍至对照曲线。在8天的戒断期后,只有每日接受2次AMP注射的大鼠对静脉注射的AMP和APO表现出敏感性降低;与治疗后24 - 32小时观察到的情况相比,敏感性降低程度减少了50%。这些结果并非由于急性耐受现象,因为在测试前24 - 32小时单次腹腔注射AMP未能改变对静脉注射AMP和APO的敏感性。相反,结果表明长期AMP治疗会降低A10 DA神经元对DA激动剂的敏感性。通过以下发现进一步证明了DA自身受体敏感性降低:长期AMP治疗(2×5mg/kg/天)使微量离子导入的DA抑制A10 DA神经元活动的能力显著降低(剂量反应曲线右移5.8倍)。相比之下,慢性AMP处理的大鼠中,离子导入γ-氨基丁酸(GABA)抑制A10 DA活动的能力没有改变。长期AMP治疗还增加了自发活动的A10 DA神经元数量及其基础放电频率。有人提出,长期AMP治疗降低A10 DA神经元自身调节能力的作用可能与行为敏化和AMP精神病现象有关。

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