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遗传性肌张力障碍仓鼠大脑中单胺能神经递质代谢的明显区域紊乱。

Marked regional disturbances in brain metabolism of monoaminergic neurotransmitters in the genetically dystonic hamster.

作者信息

Löscher W, Annies R, Richter A

机构信息

Department of Pharmacology, Toxicology, and Pharmacy, School of Veterinary Medicine, Hannover, Germany.

出版信息

Brain Res. 1994 Sep 26;658(1-2):199-208. doi: 10.1016/s0006-8993(09)90027-0.

Abstract

The genetically dystonic hamster is an animal model of idiopathic (torsion) dystonia that displays sustained abnormal movements and postures either spontaneously or in response to mild environmental stimuli. Since dystonic attacks occur in the absence of any lesion which can be defined by standard histopathological techniques in the central nervous system, the presumption is that dystonia in mutant hamsters is due to some biochemical disturbance activity in brain regions involved in motor functions. In the present study we determined the monoamine neurotransmitters dopamine, noradrenaline, adrenaline and serotonin (5-HT) as well as the dopamine metabolites homovanillic acid (HVA) and dihydroxyphenylacetic acid (DOPAC) and the 5-HT metabolite 5-hydroxyindoleacetic acid (5-HIAA) in 14 brain regions of male and female dystonic hamsters and age-matched non-dystonic controls. All determinations were done at age of maximum susceptibility for induction of dystonic attacks. Since both genders of dystonic hamsters exhibit the same characteristic age-dependent time-course of dystonia, it was assumed that only those biochemical alterations are critically involved in dystonia that occur in both female and male animals. The neurochemical data show that except for a significant decrease of dopamine and HVA in the olfactory bulb, no consistent changes in dopamine metabolism are present across brain regions, including the basal ganglia, of dystonic hamsters. In contrast, marked increases in noradrenaline and 5-HT or 5-HIAA were found in several brain areas of both genders, indicating an enhanced activity of central noradrenergic and serotonergic nuclei in the brainstem. The present results suggest the involvement of noradrenergic and serotonergic neural systems in the pathophysiology of dystonia. Based on these data and recent theoretical suggestions from clinical findings, drugs which reduce noradrenergic and serotonergic neurotransmission may be a useful therapeutic approach to dystonia.

摘要

遗传性肌张力障碍仓鼠是特发性(扭转性)肌张力障碍的动物模型,该模型会自发地或在受到轻度环境刺激时出现持续的异常运动和姿势。由于肌张力障碍发作时,中枢神经系统中不存在任何可通过标准组织病理学技术界定的病变,因此推测突变仓鼠的肌张力障碍是由于参与运动功能的脑区发生了某种生化紊乱活动所致。在本研究中,我们测定了雄性和雌性肌张力障碍仓鼠以及年龄匹配的非肌张力障碍对照仓鼠14个脑区中的单胺类神经递质多巴胺、去甲肾上腺素、肾上腺素和5-羟色胺(5-HT),以及多巴胺代谢产物高香草酸(HVA)和二羟基苯乙酸(DOPAC),还有5-HT代谢产物5-羟吲哚乙酸(5-HIAA)。所有测定均在诱发肌张力障碍发作的最大易感性年龄时进行。由于肌张力障碍仓鼠的雌雄两性都表现出相同的与年龄相关的肌张力障碍特征性时间进程,因此假定只有那些在雌性和雄性动物中都出现的生化改变才与肌张力障碍密切相关。神经化学数据表明,除嗅球中多巴胺和HVA显著降低外,肌张力障碍仓鼠包括基底神经节在内的各个脑区的多巴胺代谢均无一致变化。相反,在两性的几个脑区中均发现去甲肾上腺素和5-HT或5-HIAA显著增加,表明脑干中中枢去甲肾上腺素能和5-羟色胺能核的活性增强。目前的结果提示去甲肾上腺素能和5-羟色胺能神经系统参与了肌张力障碍的病理生理过程。基于这些数据以及临床研究结果最近提出的理论建议,降低去甲肾上腺素能和5-羟色胺能神经传递的药物可能是治疗肌张力障碍的一种有效方法。

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