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Effect of PACAP on Heat Exposure
Keisuke Suzuki1,2, Hiroki Yamaga1,2, Hirokazu Ohtaki2,3
1Department of Emergency and Disaster Medicine, School of Medicine, Showa University, Tokyo 142-8555, Japan.
International Journal of Molecular Sciences
|February 25, 2023
Summary
Mice lacking pituitary adenylate cyclase-activating polypeptide (PACAP) showed increased survival and lower body temperatures during heat stress, indicating PACAP plays a role in heat sensitivity.
Area of Science:
- Physiology
- Neuroendocrinology
- Climate Change Biology
Background:
- Heat stroke is a severe illness exacerbated by rising global temperatures.
- Pituitary adenylate cyclase-activating polypeptide (PACAP) is involved in thermoregulation, but its specific role in heat stress is not fully understood.
Purpose of the Study:
- To investigate the role of PACAP in the physiological response to heat stress.
- To determine if PACAP knockout mice exhibit altered thermoregulation and survival under heat exposure.
Main Methods:
- PACAP knockout (KO) and wild-type ICR mice were exposed to high heat (36°C, 99% humidity).
- Survival rates, body temperatures, and c-Fos expression in the hypothalamus were measured.
- Differences in brown adipose tissue (heat production site) were analyzed.
Main Results:
- PACAP KO mice demonstrated significantly higher survival rates and maintained lower body temperatures compared to wild-type mice.
- Reduced c-Fos gene expression and immunoreaction were observed in the hypothalamus of PACAP KO mice.
- Distinct differences in brown adipose tissue activity were noted between PACAP KO and wild-type mice, suggesting altered heat production.
Conclusions:
- Mice lacking PACAP are more resistant to heat exposure, indicating PACAP contributes to heat sensitivity.
- PACAP influences thermoregulation and survival during heat stress, potentially via hypothalamic pathways and brown adipose tissue activity.
- These findings highlight a novel role for PACAP in the body's response to extreme heat, relevant to climate change adaptation.
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