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©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Diabetes. Apr 15, 2024; 15(4): 724-734
Published online Apr 15, 2024. doi: 10.4239/wjd.v15.i4.724
Published online Apr 15, 2024. doi: 10.4239/wjd.v15.i4.724
Teneligliptin mitigates diabetic cardiomyopathy by inhibiting activation of the NLRP3 inflammasome
Gu-Lao Zhang, Yuan Liu, Yan-Feng Liu, Xian-Tao Huang, Yu Tao, Zhen-Huan Chen, Heng-Li Lai, Department of Cardiology, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Nanchang 330000, Jiangxi Province, China
Co-corresponding authors: Zhen-Huan Chen and Heng-Li Lai.
Author contributions: Zhang GL, Chen ZH, Lai HL designed the research study; Liu Y, Liu YF, Huang XT performed the research; Zhang GL, Chen ZH, Tao Y, and Lai HL analyzed the data and wrote the manuscript; all authors have read and approve the final manuscript. Lai HL and Chen ZH contributed equally to this work as co-corresponding authors. They made equally important contributions in the process of design, submission and revision, and interpreted all the research data.
Supported by National Natural Science Foundation of China , No. 82000276 ; and the Science and Technology Project of Jiangxi Provincial Health Commission , No. 202310005 .
Institutional animal care and use committee statement: The study was reviewed and approved by the Jiangxi Provincial People's Hospital Institutional Review Board (Approval No. KT089).
Conflict-of-interest statement: All the Authors declare that they have no conflicts of interest related to this manuscript.
Data sharing statement: The data are available on reasonable request.
ARRIVE guidelines statement: The authors have read the ARRIVE Guidelines, and the manuscript was prepared and revised according to the ARRIVE Guidelines.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Heng-Li Lai, MD, Chief Physician, Department of Cardiology, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Aiguo Road, Donghu District, Nanchang 330000, Jiangxi Province, China. laihengli@163.com
Received: October 8, 2023
Peer-review started: October 8, 2023
First decision: December 6, 2023
Revised: December 20, 2023
Accepted: February 27, 2024
Article in press: February 27, 2024
Published online: April 15, 2024
Processing time: 186 Days and 14.5 Hours
Peer-review started: October 8, 2023
First decision: December 6, 2023
Revised: December 20, 2023
Accepted: February 27, 2024
Article in press: February 27, 2024
Published online: April 15, 2024
Processing time: 186 Days and 14.5 Hours
Core Tip
Core Tip: Teneligliptin mitigated diabetic cardiomyopathy by mitigating the activation of NLRP3 (NOD-like receptor protein 3) inflammasome. Teneligliptin reversal markedly increased cardiomyocyte area and heart weight/tibia length, reduced fractional shortening, ejection fraction, and heart rate, increased creatine kinase-MB (CK-MB), aspartate transaminase (AST), and lactate dehydrogenase (LDH) levels, and upregulated NADPH oxidase 4 in streptozotocin-induced diabetic mice. Teneligliptin repressed activated NLRP3 inflammasome and increased CK-MB, AST, and LDH levels in glucose-stimulated cardiomyocytes, accompanied by an upregulation of phosphorylated-adenosine 5‘-monophosphate and activated protein kinase.