Department of Pharmacology, M. M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, Haryana, 133206, India.
Department of Pharmacology, Chitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, 140401, India.
Endocr Metab Immune Disord Drug Targets. 2024;24(3):348-362. doi: 10.2174/1871530323666230822095932.
Cellular senescence is associated with the formation and progression of a range of illnesses, including ageing and metabolic disorders such as diabetes mellitus and pancreatic beta cell dysfunction. Ageing and reduced glucose tolerance are interconnected. Often, Diabetes is becoming more common, which is concerning since it raises the risk of a variety of age-dependent disorders such as cardiovascular disease, cancer, Parkinson's disease, stroke, and Alzheimer's disease.
The objectives of this study are to find out the most recent research on how ageing affects the functions of pancreatic beta cells, beta cell mass, beta cell senescence, mitochondrial dysfunction, and hormonal imbalance.
Various research and review manuscripts are gathered from various records such as Google Scholar, PubMed, Mendeley, Scopus, Science Open, the Directory of Open Access Journals, and the Education Resources Information Centre, using different terms like "Diabetes, cellular senescence, beta cells, ageing, insulin, glucose".
In this review, we research novel targets in order to discover new strategies to treat diabetes. Abnormal glucose homeostasis and type 2 diabetes mellitus in the elderly may aid in the development of novel medicines to delay or prevent diabetes onset, improve quality of life, and, finally, increase life duration.
Aging accelerates beta cell senescence by generating premature cell senescence, which is mostly mediated by high glucose levels. Despite higher plasma glucose levels, hepatic gluconeogenesis accelerates and adipose tissue lipolysis rises, resulting in an increase in free fatty acid levels in the blood and worsening insulin resistance throughout the body.
细胞衰老与一系列疾病的形成和发展有关,包括衰老和代谢紊乱,如糖尿病和胰腺β细胞功能障碍。衰老和葡萄糖耐量降低是相互关联的。通常,糖尿病变得越来越普遍,这令人担忧,因为它会增加各种与年龄相关的疾病的风险,如心血管疾病、癌症、帕金森病、中风和阿尔茨海默病。
本研究的目的是了解最新的研究,了解衰老如何影响胰腺β细胞的功能、β细胞质量、β细胞衰老、线粒体功能障碍和激素失衡。
使用“糖尿病、细胞衰老、β细胞、衰老、胰岛素、葡萄糖”等不同术语,从 Google Scholar、PubMed、Mendeley、Scopus、Science Open、开放获取期刊目录和教育资源信息中心等各种记录中收集各种研究和综述手稿。
在这项综述中,我们研究了新的靶点,以寻找治疗糖尿病的新策略。老年人异常的葡萄糖稳态和 2 型糖尿病可能有助于开发新的药物来延迟或预防糖尿病的发生,提高生活质量,并最终延长寿命。
衰老通过产生过早的细胞衰老加速β细胞衰老,这主要是由高血糖水平介导的。尽管血糖水平较高,但肝糖异生加速,脂肪组织脂解增加,导致血液中游离脂肪酸水平升高,全身胰岛素抵抗恶化。