Center for Integrated Human Brain Science, Brain Research Institute, University of Niigata, 1 Asahi Machi-dori, Chuo-ku, Niigata 951-8585, Japan.
Mol Aspects Med. 2012 Oct-Dec;33(5-6):691-703. doi: 10.1016/j.mam.2012.01.002. Epub 2012 Jan 24.
Identification of the aquaporin (AQP) protein family more than twenty years ago has ushered in an era where water and neutral solute trafficking is considered a prime target for pharmacological intervention. Using AQP modulation as a basis for the treatment of human disorders has been suggested by phenotype analysis involving specific AQP-null animals, as well as by pathohistological studies. Based on those reports, a wide variety of disorders, such as cerebral edema, cancer and malaria, are considered indications for AQP modulators. Recent studies have also identified several small molecule AQP modulators that can be used to test those hypotheses in disease models. We believe these studies and compounds form the basis from which future treatments and diagnostic protocols of aquaporin-based disorders will be developed.
二十多年前,水通道蛋白(AQP)家族的鉴定开创了一个新纪元,人们开始认为水和中性溶质的转运是药物干预的主要靶点。通过对特定 AQP 基因敲除动物的表型分析以及病理组织学研究,提出了利用 AQP 调节作为治疗人类疾病的基础。基于这些报道,许多疾病,如脑水肿、癌症和疟疾,被认为是 AQP 调节剂的适应症。最近的研究还鉴定了几种小分子 AQP 调节剂,可用于在疾病模型中验证这些假说。我们相信,这些研究和化合物构成了未来基于水通道蛋白的疾病治疗和诊断方案发展的基础。