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肥胖导致的肾脏损伤及其可行的治疗药物。

Kidney Damage Caused by Obesity and Its Feasible Treatment Drugs.

机构信息

Neurobiology Laboratory, Department of Basic Veterinary Medicine, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.

Key Laboratory of Precision Nutrition and Food Quality, Ministry of Education, Department of Nutrition and Health, China Agricultural University, Beijing 100193, China.

出版信息

Int J Mol Sci. 2022 Jan 11;23(2):747. doi: 10.3390/ijms23020747.

Abstract

The rapid growth of obesity worldwide has made it a major health problem, while the dramatic increase in the prevalence of obesity has had a significant impact on the magnitude of chronic kidney disease (CKD), especially in developing countries. A vast amount of researchers have reported a strong relationship between obesity and chronic kidney disease, and obesity can serve as an independent risk factor for kidney disease. The histological changes of kidneys in obesity-induced renal injury include glomerular or tubular hypertrophy, focal segmental glomerulosclerosis or bulbous sclerosis. Furthermore, inflammation, renal hemodynamic changes, insulin resistance and lipid metabolism disorders are all involved in the development and progression of obesity-induced nephropathy. However, there is no targeted treatment for obesity-related kidney disease. In this review, RAS inhibitors, SGLT2 inhibitors and melatonin would be presented to treat obesity-induced kidney injury. Furthermore, we concluded that melatonin can protect the kidney damage caused by obesity by inhibiting inflammation and oxidative stress, revealing its therapeutic potential.

摘要

全球肥胖症的迅速增长使其成为一个主要的健康问题,而肥胖症患病率的急剧上升对慢性肾脏病(CKD)的严重程度产生了重大影响,特别是在发展中国家。大量研究人员报告了肥胖症与慢性肾脏病之间的强烈关系,并且肥胖症可以作为肾脏病的一个独立风险因素。肥胖症引起的肾损伤的肾脏组织学变化包括肾小球或肾小管肥大、局灶节段性肾小球硬化或球性硬化。此外,炎症、肾脏血流动力学变化、胰岛素抵抗和脂代谢紊乱均参与肥胖相关性肾病的发生和进展。然而,目前尚没有针对肥胖相关性肾脏疾病的靶向治疗方法。在这篇综述中,我们将介绍 RAS 抑制剂、SGLT2 抑制剂和褪黑素治疗肥胖诱导的肾损伤。此外,我们的结论表明,褪黑素通过抑制炎症和氧化应激来保护肥胖引起的肾脏损伤,显示出其治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc63/8775419/3eae8ff1596e/ijms-23-00747-g001.jpg

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