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帕金森病患者脑脊液中哈尔满和去甲哈尔满水平升高。

Elevated levels of harman and norharman in cerebrospinal fluid of parkinsonian patients.

作者信息

Kuhn W, Müller T, Grosse H, Rommelspacher H

机构信息

Department of Neurology, Ruhr University, Bochum, Federal Republic of Germany.

出版信息

J Neural Transm (Vienna). 1996;103(12):1435-40. doi: 10.1007/BF01271257.

Abstract

Death of dopaminergic neurons in Parkinson's disease (PD) may partially be caused by synthesis and accumulation of endogenous and exogenous toxins. Because of structural similarity to MPTP, beta-carbolines, like norharman and harman, have been proposed as putative neurotoxins. In vivo they may easily be formed by cyclization of indoleamines with e.g. aldehydes. For further elucidation of the role of beta-carbolines in neurodegenerative disorders harman and norharman levels in cerebrospinal fluid (CSF) were measured in 14 patients with PD and compared to an age- and sex-matched control group (n = 14). CSF levels of norharman and harman in PD were significantly higher compared to controls. These results may suggest a possible role of harman and norharman or its N-methylated carbolinium ions in the pathophysiological processes initiating PD. However the origin of increased levels of these beta-carbolines remains unclear. On the one hand one may speculate, that unknown metabolic processes induce the increased synthesis of harman and norharman in PD. On the other hand a possible impact of exogenous sources may also be possible.

摘要

帕金森病(PD)中多巴胺能神经元的死亡可能部分是由内源性和外源性毒素的合成与积累所致。由于与1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)结构相似,β-咔啉,如去甲哈尔满和哈尔满,被认为是潜在的神经毒素。在体内,它们可能很容易由吲哚胺与醛等物质环化形成。为了进一步阐明β-咔啉在神经退行性疾病中的作用,对14例帕金森病患者脑脊液(CSF)中的哈尔满和去甲哈尔满水平进行了测量,并与年龄和性别匹配的对照组(n = 14)进行比较。与对照组相比,帕金森病患者脑脊液中去甲哈尔满和哈尔满的水平显著更高。这些结果可能表明哈尔满和去甲哈尔满或其N-甲基化咔啉离子在引发帕金森病的病理生理过程中可能发挥作用。然而,这些β-咔啉水平升高的来源仍不清楚。一方面,可以推测,未知的代谢过程导致帕金森病中哈尔满和去甲哈尔满的合成增加。另一方面,外源性来源也可能产生影响。

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