PPARα activation attenuated heat-induced myocardial injury in mice

With climate change and global warming, extreme heatwaves occurred with more intense and higher frequency, significantly increasing the mortality rate associated with cardiovascular diseases. Using a mouse model of heat stress, the study aimed to clarify the adverse effects on heart, elucidate the underlying mechanism and explore the potential preventative strategies. Firstly, heat stress induced significant myocardial injury, which was further exacerbated even after termination of heat exposure. Next, PPARα (Peroxisome Proliferator-Activated Receptor Alpha) was screened and its downregulation in response to heat stress was confirmed at mRNA and protein levels. Then, pre-treatment with PPARα agonist fenofibrate significantly mitigated myocardial injury, accompanied with improved mitochondrial function in the myocardial tissues. In addition, PPARα activation may restore the mitochondrial homeostasis through enhancement of both antioxidation and mitophagy. These findings will highlight the pivotal role of PPARα in alleviating heat-induced myocardial injury and cardiovascular incidence, providing valuable target for drug development to prevent/treat heat stress-related diseases.

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Publication Details

Journal
Ecotoxicology and Environmental Safety
Published
2025-06-18
DOI
https://doi.org/10.1016/j.ecoenv.2025.118520
Citations
1
Primary Topic
Endoplasmic Reticulum Stress and Disease
Type
article
Field-Weighted Citation Impact
1.15

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article

PPARα activation attenuated heat-induced myocardial injury in mice

Cuiqing Liu, Tong Hou, Qin Li, Lu Zhang et al.
1 citations
Ecotoxicology and Environmental Safety
Endoplasmic Reticulum Stress and Disease
1.15
article

PPARα activation attenuated heat-induced myocardial injury in mice

Cuiqing Liu, Tong Hou, Qin Li, Lu Zhang, Guoqing Zhang, Ran Li, Lisha Zhao, Xiaowen Ma, Zhoufan Hu
article en
1 citations

Abstract

With climate change and global warming, extreme heatwaves occurred with more intense and higher frequency, significantly increasing the mortality rate associated with cardiovascular diseases. Using a mouse model of heat stress, the study aimed to clarify the adverse effects on heart, elucidate the underlying mechanism and explore the potential preventative strategies. Firstly, heat stress induced significant myocardial injury, which was further exacerbated even after termination of heat exposure. Next, PPARα (Peroxisome Proliferator-Activated Receptor Alpha) was screened and its downregulation in response to heat stress was confirmed at mRNA and protein levels. Then, pre-treatment with PPARα agonist fenofibrate significantly mitigated myocardial injury, accompanied with improved mitochondrial function in the myocardial tissues. In addition, PPARα activation may restore the mitochondrial homeostasis through enhancement of both antioxidation and mitophagy. These findings will highlight the pivotal role of PPARα in alleviating heat-induced myocardial injury and cardiovascular incidence, providing valuable target for drug development to prevent/treat heat stress-related diseases.

Ecotoxicology and Environmental SafetyVol. 302
Zhejiang Chinese Medical University (CN)
National Natural Science Foundation of China, Sichuan Province Science and Technology Support Program, West China Hospital, Sichuan University
Good health and well-being
Openalex Percentile: Top 23%
Endoplasmic Reticulum Stress and Disease
1.15
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PPARα activation attenuated heat-induced myocardial injury in mice — Cuiqing Liu, Tong Hou, et al. · Ecotoxicology and Environmental Safety (2025) | TGRS Research Map | TGRS