Qu Caiyan, Tan Xiyue, Hu Qichao, Tang Jiao, Wang Yangyang, He Caiying, He ZiJia, Li Bin, Fu Xiaoxu, Du Quanyu
Hospital of Chengdu University of Traditional Chinese Medicine, School of Clinical Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China.
Nanjiang County Hospital of Chinese Medicine, Bazhong, 635600, China.
Heliyon. 2024 Feb 22;10(5):e26863. doi: 10.1016/j.heliyon.2024.e26863. eCollection 2024 Mar 15.
Diabetes mellitus (DM) is one of the fastest-growing diseases worldwide; however, its pathogenesis remains unclear. Complications seriously affect the quality of life of patients in the later stages of diabetes, ultimately leading to suffering. Natural small molecules are an important source of antidiabetic agents.
Astragaloside IV (AS-IV) is an active ingredient of Astragalus mongholicus (Fisch.) Bunge. We reviewed the efficacy and mechanism of action of AS-IV in animal and cellular models of diabetes and the mechanism of action of AS-IV on diabetic complications in animal and cellular models. We also summarized the safety of AS-IV and provided ideas and rationales for its future clinical application.
Articles on the intervention in DM and its complications using AS-IV, such as those published in SCIENCE, PubMed, Springer, ACS, SCOPUS, and CNKI from the establishment of the database to February 2022, were reviewed. The following points were systematically summarized: dose/concentration, route of administration, potential mechanisms, and efficacy of AS-IV in animal models of DM and its complications.
AS-IV has shown therapeutic effects in animal models of DM, such as alleviating gestational diabetes, delaying diabetic nephropathy, preventing myocardial cell apoptosis, and inhibiting vascular endothelial dysfunction; however, the potential effects of AS-IV on DM should be investigated.
AS-IV is a potential drug for the treatment of diabetes and its complications, including diabetic vascular disease, cardiomyopathy, retinopathy, peripheral neuropathy, and nephropathy. In addition, preclinical toxicity studies indicate that it appears to be safe, but the safe human dose limit is yet to be determined, and formal assessments of adverse drug reactions among humans need to be further investigated. However, additional formulations or structural modifications are required to improve the pharmacokinetic parameters and facilitate the clinical use of AS-IV.
糖尿病(DM)是全球增长最快的疾病之一;然而,其发病机制仍不清楚。并发症严重影响糖尿病后期患者的生活质量,最终导致痛苦。天然小分子是抗糖尿病药物的重要来源。
黄芪甲苷IV(AS-IV)是蒙古黄芪的一种活性成分。我们综述了AS-IV在糖尿病动物和细胞模型中的疗效及作用机制,以及AS-IV在糖尿病动物和细胞模型中对糖尿病并发症的作用机制。我们还总结了AS-IV的安全性,并为其未来临床应用提供思路和理论依据。
回顾了从数据库建立到2022年2月发表在《科学》《PubMed》《施普林格》《美国化学会》《Scopus》和《中国知网》等上的关于使用AS-IV干预糖尿病及其并发症的文章。系统总结了以下几点:AS-IV在糖尿病及其并发症动物模型中的剂量/浓度、给药途径、潜在机制和疗效。
AS-IV在糖尿病动物模型中已显示出治疗效果,如缓解妊娠期糖尿病、延缓糖尿病肾病、预防心肌细胞凋亡和抑制血管内皮功能障碍;然而,AS-IV对糖尿病的潜在影响仍有待研究。
AS-IV是一种治疗糖尿病及其并发症的潜在药物,这些并发症包括糖尿病血管疾病、心肌病、视网膜病变、周围神经病变和肾病。此外,临床前毒性研究表明它似乎是安全的,但人体安全剂量限制尚未确定,需要进一步研究对人类药物不良反应的正式评估。然而,需要额外的制剂或结构修饰来改善药代动力学参数并促进AS-IV的临床应用。