# Optimal surgical timing after high-altitude de-adaptation: day-30 post-descent marks physiologic recalibration and improved small bowel repair in rats

**Authors:** Yizhi Yue, Xiaohua Wang, Yaning Song, Yi Sun, Lin Xue, Guangyu Chen, Ze Feng, Guode Luo, Tao Wang

PMC · DOI: 10.3389/fphys.2026.1742306 · Frontiers in Physiology · 2026-02-09

## TL;DR

Rats that descend from high altitude need about 30 days to recover physiologically before surgery to ensure better intestinal repair outcomes.

## Contribution

The study identifies day-30 post-descent as an optimal surgical window due to physiological recalibration and improved tissue repair in rats.

## Key findings

- Chronic hypoxia adaptations resolve by day 30 post-relocation to normoxia.
- Day-30 post-descent is marked by reduced inflammation and improved intestinal tissue repair.
- Systemic inflammatory cytokines and oxidative stress peak at day 1 and normalize by day 30.

## Abstract

High-altitude de-adaptation following rapid transition from chronic hypoxia to normoxia has been associated with increased postoperative risk, yet its temporal physiological features and impact on intestinal repair remain poorly defined.

Male Sprague–Dawley rats (n = 84) were exposed to simulated high altitude (5,000 m) for 90 days and then relocated to normoxia. Standardized small bowel rupture repair was performed at 1, 10, 20, 30, 40, 50, or 60 days after relocation. Hypoxia adaptation and reversibility were assessed using arterial oxygen saturation, hematological indices, hypoxia-responsive molecular markers, respiratory rate, body weight, and behavior. Postoperative outcomes were evaluated 10 days after surgery, including inflammatory cytokines, oxidative stress markers, immune cell infiltration, and histopathology.

Chronic hypoxia induced a stable hypoxia-adapted state characterized by reduced oxygen saturation, enhanced erythropoiesis, increased respiratory rate, and upregulation of intestinal HIF-1α and vascular endothelial growth factor, all of which progressively normalized after return to normoxia and resolved by approximately 30 days. Perioperative survival did not differ among groups. In contrast, systemic inflammatory cytokines and lipid peroxidation peaked at day 1 post-relocation and declined to nadir levels by day 30. This period was marked by reduced macrophage infiltration, peak fibroblast density, and more organized granulation tissue and collagen deposition.

The duration of high-altitude de-adaptation is closely associated with intestinal repair quality. Approximately 30 days of normoxic re-acclimation correspond to coordinated resolution of hypoxia-related physiological perturbations and optimized tissue repair, identifying a critical post-relocation window relevant to surgical timing after descent from high altitude.

## Linked entities

- **Genes:** HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091]

## Full-text entities

- **Genes:** Hif1a (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 29560] {aka HIF1-alpha, MOP1}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, Il17a (interleukin 17A) [NCBI Gene 301289] {aka CTLA-8, IL-17, IL-17A, Il17}, MPO (myeloperoxidase) [NCBI Gene 4353], CAT (catalase) [NCBI Gene 847], Actb (actin, beta) [NCBI Gene 81822] {aka Actx}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, Crp (C-reactive protein) [NCBI Gene 25419] {aka Aa1249, Ab1-341, Ab2-196, Ac1-114, Ac1262, Ac2-069}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, VIM (vimentin) [NCBI Gene 7431]
- **Diseases:** mucosal injury (MESH:D052016), dysfunction (MESH:D006331), Heat stroke (MESH:D018883), intestinal injury (MESH:D007410), death (MESH:D003643), impaired mobility (MESH:D014086), infection (MESH:D007239), anastomotic leakage (MESH:D057868), weight loss (MESH:D015431), hypoxic (MESH:D002534), functional (MESH:D003291), ischemia (MESH:D007511), inflammatory dysregulation (MESH:D021081), Hypoxia (MESH:D000860), cervical dislocation (MESH:D002575), analgesia (MESH:D000699), trauma (MESH:D014947), Inflammatory (MESH:D007249), pain (MESH:D010146), SIRS (MESH:D018746), bowel rupture (MESH:D012421), edema (MESH:D004487), Small Bowel Injury (MESH:D007409)
- **Chemicals:** lipid (MESH:D008055), paraformaldehyde (MESH:C003043), Meloxicam (MESH:D000077239), polypropylene (MESH:D011126), eosin (MESH:D004801), DAB (MESH:C000469), ROS (MESH:D017382), FKE50217 (-), H&amp;E (MESH:D006371), hematoxylin (MESH:D006416), MDA (MESH:D008315), chloral hydrate (MESH:D002697), isoflurane (MESH:D007530), Paraffin (MESH:D010232), O2 (MESH:D010100), nitrogen (MESH:D009584)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C-40  C

## Full text

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## Figures

13 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926153/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926153/full.md

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Source: https://tomesphere.com/paper/PMC12926153