Germacrone protects renal tubular cells against ferroptotic death and ROS release by re-activating mitophagy in diabetic nephropathy-Reference-Cited by-同舟云学术

Germacrone protects renal tubular cells against ferroptotic death and ROS release by re-activating mitophagy in diabetic nephropathy

Published:2023-10-28 Issue: Volume: Page:1-17
ISSN:1071-5762
Container-title:Free Radical Research
language:en
Short-container-title:Free Radical Research

Author:

Wang Yunguang¹,He Xinxin²,Xue Mengjiao²,Sun Wenbo³,He Qiang¹,Jin Juan¹

Affiliation:

1. Department of Nephrology, the First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, Zhejiang, P.R. China

2. School of Clinical Medicine, Hangzhou Medical College, Hangzhou, Zhejiang, P.R. China

3. Graduate School, Bengbu Medical College, Bengbu, Anhui, P.R. China

Funder

Zhejiang Provincial Traditional Chinese Medicine Science and Technology Project

Cultivation Program for Excellent Young Talents of Hangzhou First People’s Hospital

Zhejiang Province Chinese Medicine Modernization Program

The Key Project of Scientific Research Foundation of Chinese Medicine

"Pioneer" and "Leading Goose" R&D Program of Zhejiang

Huadong Medicine Joint Funds of the Zhejiang Provincial Natural Science Foundation of China

The Key project of Basic Scientific Research Operating Funds of Hangzhou Medical College

Publisher

Informa UK Limited

Subject

General Medicine,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10715762.2023.2277143

Reference38 articles.

1. End-stage renal disease and survival in people with diabetes: a national database linkage study

2. Diabetic nephropathy: diagnosis and treatment

3. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition

4. The role of tubular injury in diabetic nephropathy

5. NLRP3 deficiency ameliorates renal inflammation and fibrosis in diabetic mice

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