# Superior thermotolerance in young versus adult rats undergoing heat stroke is associated with age-related differences in intestinal barrier integrity and heat shock protein responses

**Authors:** Yuanhao Cai, Lei Lei, Jikuai Chen, Xi Zhao, Juelin Chen, Jiawei Zhou, Yankun Pei, Yawei Wang, Yitong Gong, Jianyao You, Yangyang Cao, Muge Song, Jun Ma, Weiyi Ma, Meng Wang, Wenjun Chang, Qing Song, Lin Zhou, Lei Li, Shuogui Xu

PMC · DOI: 10.3389/fcell.2026.1642359 · Frontiers in Cell and Developmental Biology · 2026-02-13

## TL;DR

Young rats are more resistant to heat stroke than adults due to better intestinal protection and stronger heat shock protein responses.

## Contribution

This study reveals age-related differences in thermotolerance mechanisms, focusing on intestinal barrier integrity and heat shock proteins in young versus adult rats.

## Key findings

- Young rats showed prolonged core body temperature plateau and delayed heat stroke onset compared to adults.
- Young rats had reduced intestinal damage and higher levels of tight junction proteins like ZO-1 and Occludin.
- Enhanced expression of HSP40 and HSP70 in young rats likely contributes to better thermotolerance and cellular protection.

## Abstract

Heat stroke (HS) is a life-threatening condition exacerbated by rising global temperatures, with children identified as a particularly vulnerable population. Despite this, basic research on age-related differences in thermotolerance remains limited. In this study, we established a high-temperature and high-humidity exposure model with real-time core body temperature (CBT) monitoring to investigate thermotolerance in young versus adult rats. The results showed that young rats exhibited prolonged CBT plateau phases and delayed HS onset, indicating enhanced thermotolerance compared to adult rats. This was accompanied by significantly milder multi-organ injury and reduced intestinal barrier damage. Young rats displayed lower serum levels of D-lactate and intestinal fatty acid-binding protein, better-preserved intestinal epithelial ultrastructure, and higher expression of tight junction proteins such as ZO-1, Occludin, and E-cadherin. Moreover, young rats showed elevated expression of heat shock proteins (HSP40 and HSP70) in intestinal tissues, which likely contributed to improved barrier integrity and cellular protection. These findings suggest that enhanced intestinal barrier stability and robust HSP responses underlie the superior thermotolerance observed in young rats. However, despite their physiological advantages, infants and young children often suffer poor HS outcomes due to behavioral limitations and caregiver negligence, especially in enclosed environments such as parked vehicles. This highlights the critical need for enhanced caregiver awareness, improved pediatric emergency response training, and preventive strategies to mitigate pediatric HS risk.

## Linked entities

- **Proteins:** TJP1 (tight junction protein 1), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), shg (shotgun), DNAJB1 (DnaJ heat shock protein family (Hsp40) member B1), HSPA1A (heat shock protein family A (Hsp70) member 1A)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}, Hspd1 (heat shock protein family D (Hsp60) member 1) [NCBI Gene 63868] {aka Hsp60, Hspd1-30p}, Ocln (occludin) [NCBI Gene 83497], Hsph1 (heat shock protein family H (Hsp110) member 1) [NCBI Gene 288444] {aka Hsp105}, Hspa1b (heat shock protein family A (Hsp70) member 1B) [NCBI Gene 108348108] {aka HSP70, HSP70-1, HSP70.1, HSP70.2, Hsp70-2, Hsp72}, Tjp1 (tight junction protein 1) [NCBI Gene 292994] {aka ZO-1}, Fabp2 (fatty acid binding protein 2) [NCBI Gene 25598] {aka FABP}, Cdh1 (cadherin 1) [NCBI Gene 83502], Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Hsp90aa1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 299331] {aka Hsp86, Hsp90, Hspca}
- **Diseases:** inflammatory (MESH:D007249), emphysema (MESH:D004646), edema (MESH:D004487), acute lung injury (MESH:D055371), hemorrhage (MESH:D006470), multi-organ injury (MESH:D009102), hypoxia (MESH:D000860), EHS (MESH:D018882), hyperthermia (MESH:D005334), deaths (MESH:D003643), acute tubular injury (MESH:D001930), atelectasis (MESH:D001261), systemic injury (MESH:D057772), dehydration (MESH:D003681), acute hepatic injury (MESH:D056486), mucosal damage (MESH:D052016), multi-organ damage (MESH:D000092124), necrosis (MESH:D009336), intestinal damage (MESH:D007410), AHS (MESH:D018883), hepatocellular degeneration (MESH:D006528)
- **Chemicals:** osmium tetroxide (MESH:D009993), paraffin (MESH:D010232), ORS (MESH:C034130), nitrogen (MESH:D009584), isoflurane (MESH:D007530), glycogen (MESH:D006003), water (MESH:D014867), TSA (MESH:C481298), hematoxylin (MESH:D006416), HE (-), uranyl acetate (MESH:C005460), urea (MESH:D014508), DAPI (MESH:C007293), CREA (MESH:D003404), PVDF (MESH:C024865), PBS (MESH:D007854), eosin (MESH:D004801)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** C +- 1  C, L00686C

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946125/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946125/full.md

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Source: https://tomesphere.com/paper/PMC12946125