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Design and synthesis of new DHEA and pregnenolone derivatives with anti-apoptotic, neuroprotective activity

机译:具有抗凋亡,神经保护活性的新DHEA和妊娠衍生物的设计与合成

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Neuronal cell death by apoptosis is the 'end-point' of many human neurological disorders, including Alzheimer's, Parkinson's and Huntington's diseases, stroke/trauma, multiple and amyotrophic lateral sclerosis. A fundamental approach for reducing the burden of neurodegenerative diseases is to slow or halt progression, and ultimately, to prevent the onset of the disease process. Thus, strategies for neuroprotection, preventing apoptotic neuronal cell loss may offer new therapeutic interventions. Natural neurosteroids such as DHEA and allopregnanolone possess important neuroprotective and neurogenic properties in vitro and in vivo, in experimental animals.
机译:细胞凋亡的神经细胞死亡是许多人类神经障碍的“终点”,包括阿尔茨海默,帕金森和亨廷顿的疾病,中风/创伤,多发性和肌萎缩的外壳。降低神经退行性疾病负担的基本方法是缓慢或停止进展,最终,以防止疾病过程的发作。因此,神经保护的策略,预防凋亡神经元细胞损失可以提供新的治疗干预措施。在实验动物中,DHEA和allopregheanolone等天然神经激素具有重要的神经保护和神经原性特性,在实验动物中。

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