Xi Meiyang, Sun Tianyu, Chai Shejie, Xie Mengjiao, Chen Siqi, Deng Liping, Du Kui, Shen Runpu, Sun Haopeng
College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing, 312000, China; Zhejiang Engineering Research Center of Fat-soluble Vitamin, Shaoxing University, Shaoxing, 312000, China.
Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing, 210009, China.
Eur J Med Chem. 2022 Mar 15;232:114170. doi: 10.1016/j.ejmech.2022.114170. Epub 2022 Feb 3.
Alzheimer's disease (AD), one of the greatest threats to human health, is characterized by declined cognition and changed behavior. Cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) that play an important role in learning and memory are hydrolyzed by phosphodiesterases (PDEs). Most PDE isoforms are highly expressed in the brain, and the inhibition of PDEs is beneficial to counteract AD. Thus, targeting PDEs represents a therapeutic potential for this disease. So far, a variety of PDE inhibitors have been discovered with significant cognitive enhancement effects in animal models and more than ten agents have entered into clinical trials. In this review, we summarize PDE mediated cyclic nucleotide signaling pathways, PDE family members involved in AD and recent advance of PDE inhibitors in preclinical and clinical studies, trying to provide an outlook of PDE inhibitors for the treatment of AD in future.
阿尔茨海默病(AD)是对人类健康最大的威胁之一,其特征是认知能力下降和行为改变。在学习和记忆中起重要作用的环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)会被磷酸二酯酶(PDEs)水解。大多数PDE亚型在大脑中高度表达,抑制PDEs有助于对抗AD。因此,靶向PDEs代表了这种疾病的一种治疗潜力。到目前为止,已经发现了多种PDE抑制剂,它们在动物模型中具有显著的认知增强作用,并且有十多种药物已进入临床试验。在这篇综述中,我们总结了PDE介导的环核苷酸信号通路、参与AD的PDE家族成员以及PDE抑制剂在临床前和临床研究中的最新进展,试图为未来治疗AD的PDE抑制剂提供一个展望。