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α-二氢麦角隐亭在动物模型中的神经保护活性。

Neuroprotective activity of alpha-dihydroergocryptine in animal models.

作者信息

Coppi G

机构信息

Research Centre, Poli Indutria Chimica, Rozzano, Milan, Italy.

出版信息

J Neural Transm Suppl. 1995;45:307-18.

PMID:8748639
Abstract

alpha-Dihydroergocryptine (alpha-DHEC) is a well known dopaminergic agent successfully employed in the treatment of Parkinson's disease. alpha-DHEC showed a neuroprotective activity against total cerebral ischemia induced by MgCl2 in mice and histocytic anoxia by NaCN in mice and rats. Moreover the drug promoted the recovery of locomotor activity in rats after cerebral ischemic damage and protected mice against convulsions induced by intracerebroventricular injections of NMDA and glutamate. alpha-DHEC showed a protective activity on neuronal degeneration induced by MPTP in monkeys, as evaluated through animal's behaviour and morphological-cytochemical changes in the substantia nigra, suggesting a preservative effect on neuronal morphology and brain architecture. In the MPTP-treated monkeys, the alpha-DHEC administration induced a restoration of the unstimulated MDA values to control levels. The neuroprotective activity of alpha-DHEC is related to its peculiar activity on antioxidative enzymes of GSH system and to reduction of lipid-peroxide-induced cellular degeneration.

摘要

α-二氢麦角隐亭(α-DHEC)是一种著名的多巴胺能药物,已成功用于治疗帕金森病。α-DHEC对小鼠因MgCl₂诱导的全脑缺血以及小鼠和大鼠因NaCN诱导的组织细胞缺氧具有神经保护活性。此外,该药物可促进脑缺血损伤后大鼠运动活动的恢复,并保护小鼠免受脑室内注射NMDA和谷氨酸诱导的惊厥。通过动物行为以及黑质的形态 - 细胞化学变化评估,α-DHEC对MPTP诱导的猴子神经元变性具有保护活性,表明对神经元形态和脑结构具有保护作用。在MPTP处理的猴子中,给予α-DHEC可使未受刺激的丙二醛值恢复到对照水平。α-DHEC的神经保护活性与其对谷胱甘肽系统抗氧化酶的特殊作用以及减少脂质过氧化物诱导的细胞变性有关。

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