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α2-肾上腺素能受体介导对注意力缺陷多动障碍大鼠模型伏隔核切片中[3H]多巴胺释放及单胺水平的抑制作用。

Alpha 2-adrenoceptor mediated inhibition of [3H]dopamine release from nucleus accumbens slices and monoamine levels in a rat model for attention-deficit hyperactivity disorder.

作者信息

de Villiers A S, Russell V A, Sagvolden T, Searson A, Jaffer A, Taljaard J J

机构信息

Department of Chemical Pathology, University of Stellenbosch, Tygerberg Hospital, Republic of South Africa.

出版信息

Neurochem Res. 1995 Apr;20(4):427-33. doi: 10.1007/BF00973098.

Abstract

The spontaneously hypertensive rat (SHR) has been proposed as an animal model for attention-deficit hyperactivity disorder (ADHD). The behavioural problems have been suggested to be secondary to altered reinforcement mechanisms in which nucleus accumbens dopaminergic activity plays an important role. Interaction between the noradrenergic and dopaminergic system in the nucleus accumbens has been implicated in the locomotor hyperactivity and impaired discriminative performance of SHR. The present study therefore investigated whether there was any change in the alpha 2-adrenoceptor mediated inhibition of dopamine release from nucleus accumbens slices of SHR in comparison with their normotensive Wistar-Kyoto (WKY) controls. The electrically stimulated release of [3H]dopamine (DA) from nucleus accumbens slices was decreased to a similar extent by UK14,304, an alpha 2-adrenoceptor agonist, in SHR and WKY. Basal norepinephrine (NE) levels were increased in locus coeruleus (LC) and A2 noradrenergic nuclei, but not in the A1 nucleus of SHR, while basal serotonin (5-HT) levels were increased in all these pons-medulla nuclei. These results suggest that a primarily dysfunctional LC and A2 nucleus does not have a secondary effect on dopaminergic transmission in the nucleus accumbens via alpha 2-adrenoceptor mediated inhibition of DA release. Basal monoamine levels in several brain areas of SHR were significantly different from that of WKY. DA, and 5-HT turnover were decreased in SHR versus WKY suggesting hypofunctional dopaminergic and serotonergic systems in some brain areas of SHR.

摘要

自发性高血压大鼠(SHR)已被提议作为注意力缺陷多动障碍(ADHD)的动物模型。有人认为其行为问题是强化机制改变的继发结果,其中伏隔核多巴胺能活动起着重要作用。伏隔核中去甲肾上腺素能和多巴胺能系统之间的相互作用与SHR的运动性多动及辨别能力受损有关。因此,本研究调查了与正常血压的Wistar-Kyoto(WKY)对照相比,SHR伏隔核切片中α2-肾上腺素能受体介导的多巴胺释放抑制是否存在任何变化。α2-肾上腺素能受体激动剂UK14,304使SHR和WKY伏隔核切片中[3H]多巴胺(DA)的电刺激释放减少到相似程度。SHR蓝斑(LC)和A2去甲肾上腺素能核中的基础去甲肾上腺素(NE)水平升高,但A1核中未升高,而所有这些脑桥-延髓核中的基础5-羟色胺(5-HT)水平均升高。这些结果表明,主要功能失调的LC和A2核不会通过α₂-肾上腺素能受体介导的DA释放抑制而对伏隔核中的多巴胺能传递产生继发影响。SHR几个脑区的基础单胺水平与WKY有显著差异。与WKY相比,SHR中的DA和5-HT周转率降低,表明SHR某些脑区的多巴胺能和5-羟色胺能系统功能减退。

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