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环孢素A的抗寄生虫作用:可能的药物靶点及临床应用

The antiparasite effects of cyclosporin A: possible drug targets and clinical applications.

作者信息

Bell A, Roberts H C, Chappell L H

机构信息

Dept of Microbiology, Moyne Institute, Trinity College, Dublin 2, Ireland.

出版信息

Gen Pharmacol. 1996 Sep;27(6):963-71. doi: 10.1016/0306-3623(95)02148-5.

Abstract
  1. The immunosuppressive drug cyclosporin A, and some of its nonimmunosuppressive derivatives, are potent inhibitors of a range of parasites of humans. 2. Cyclosporin A and the structurally unrelated immunosuppressant FK506 are known to act on T-lymphocytes as complexes with their binding proteins, cyclophilins and FKBPs, respectively. 3. Cyclophilins and FKBPs have been structurally identified in a number of parasites and, in some instances, are believed to play roles in the antiparasitic actions of these drugs. 4. Nonimmunosuppressive cyclosporins and FK506 derivatives may have clinical potential in certain parasitic diseases, especially malaria and schistosomiasis, and identification of the targets of these drugs in parasites may lead to development of novel chemotherapeutic agents.
摘要
  1. 免疫抑制药物环孢素A及其一些非免疫抑制衍生物是多种人体寄生虫的有效抑制剂。2. 已知环孢素A和结构不相关的免疫抑制剂FK506分别作为与其结合蛋白亲环蛋白和FK结合蛋白的复合物作用于T淋巴细胞。3. 亲环蛋白和FK结合蛋白已在多种寄生虫中得到结构鉴定,在某些情况下,被认为在这些药物的抗寄生虫作用中发挥作用。4. 非免疫抑制性环孢素和FK506衍生物在某些寄生虫病,特别是疟疾和血吸虫病中可能具有临床潜力,确定这些药物在寄生虫中的作用靶点可能会导致新型化疗药物的开发。

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