The cognition-enhancing drug tenilsetam is an inhibitor of protein crosslinking by advanced glycosylation.

G Münch, Y Taneli, E Schraven, U Schindler, R Schinzel, D Palm, P Riederer
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引用次数: 66

Abstract

Non-enzymatic glycosylation of proteins, also called Maillard reaction, which occurs at an accelerated rate in diabetes, can lead to the formation of advanced glycosylation endproducts (AGEs). Tenilsetam (CAS 997: (+/-)-3-(2-thienyl)-2-piperazinone), a cognition-enhancing drug successfully used for treatment of patients suffering from Alzheimer's disease, when included in the Maillard reaction apparently inhibits protein crosslinking by AGEs in vitro. According to the mechanism proposed, Tenilsetam acts via covalent attachment to glycated proteins, thus blocking the reactive sites for further polymerisation reactions. A beneficial effect of Tenilsetam in Alzheimer's disease could come from the interference with AGE-derived crosslinking of amyloid plaques and a decreased inflammatory response by diminished activation of phagocytosing microglia.

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认知增强药物替尼西坦是一种通过糖基化晚期蛋白交联的抑制剂。
蛋白质的非酶糖基化,也称为美拉德反应,在糖尿病中以加速的速度发生,可导致晚期糖基化终产物(AGEs)的形成。Tenilsetam (CAS 997:(+/-)-3-(2-噻吩基)-2-哌嗪酮)是一种成功用于治疗阿尔茨海默病患者的认知增强药物,当参与美拉德反应时,在体外明显抑制AGEs的蛋白质交联。根据提出的机制,Tenilsetam通过与糖化蛋白的共价附着起作用,从而阻断进一步聚合反应的反应位点。替尼西坦对阿尔茨海默病的有益作用可能来自于对age衍生的淀粉样斑块交联的干扰,以及通过减少吞噬小胶质细胞的激活来减少炎症反应。
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