# Calcitriol Administration Attenuates Acute Lung Injury by Improving Angiopoietin/Tie2 Dysregulation and Alveolar-Capillary Barrier Integrity in a Mouse Model of Ovariectomy Complicated With Sepsis

**Authors:** Chiu-Li Yeh, Shang-Ming Tseng, Mei-Pei Huang, Wei-Hsin Lin, Ting-Chun Kuo, Jin-Ming Wu, Kuen-Yuan Chen, Ming-Hsun Wu, Po-Jen Yang, Po-Chu Lee, Chien-Chia Chen, Chih-Yuan Lee, Sung-Ling Yeh, Ming-Tsan Lin

PMC · DOI: 10.1155/mi/4374164 · Mediators of Inflammation · 2025-10-07

## TL;DR

Calcitriol treatment reduces lung injury in ovariectomized mice with sepsis by improving blood vessel stability and reducing harmful metal overload.

## Contribution

This study demonstrates calcitriol's novel protective effects against sepsis-induced lung injury in a menopause-like mouse model.

## Key findings

- Calcitriol improved the Ang1/Ang2 ratio and tight junction proteins in lung tissue.
- Treatment reduced oxidative stress, iron/copper overload, and ferroptosis/cuproptosis in septic mice.
- Higher survival rates and lower lung injury scores were observed in calcitriol-treated mice.

## Abstract

Menopause is associated with excessive weight, increased systemic inflammation, and oxidative stress. Menopause with obesity may aggravate the severity of organ damage when complicated with sepsis. This study investigated the impacts of calcitriol on acute lung injury (ALI)-associated angiopoietin (Ang)/tyrosine kinase with immunoglobulin-like and epidermal growth factor-like domain 2 (Tie2) dysregulation, impairment of the barrier integrity, and ion disturbance in ovariectomized mice with sepsis. 6-month-old female C57BL/6 mice were divided into three groups: the OB group, which contained mice with a sham ovariectomy and high-fat diet (HFD); the OVSS group, which contained mice with an ovariectomy, an HFD, cecal ligation and puncture (CLP), and an intravenous saline injection after CLP; and the OVSD group, which contained mice with an ovariectomy, an HFD, CLP, and a calcitriol injection. The HFD was fed for 12 weeks. Mice in the respective groups were sacrificed on 24 or 72 h after CLP. Results showed that compared to the OB group, the OVSS group had higher oxidative stress, iron and copper overload, whereas the Ang1/Ang2 ratio and tight junction (TJ) protein levels were lower in the lungs. Calcitriol treatment in mice with ovariectomy and CLP enhanced Tie2 levels and the Ang1/Ang2 ratio, increased zona occludens (ZOs)-1, occludin, and claudin-5 levels. Elevated reduced glutathione (GSH) levels and glutathione peroxidase 4 (GPX4) activities, reduced iron and copper contents, and suppressed ferroptosis- and cuproptosis-associated components were found in the lungs. Also, higher survival rates and lower lung injury scores were noted in the OVSD groups. These findings suggest that calcitriol treatment mitigated the dysregulated Ang/Tie2 pathway, improved the integrity of the alveolar-capillary barrier, elicited a more balanced redox status, alleviated ferroptosis and cuproptosis in the lungs in an ovariectomy model complicated with sepsis.

## Linked entities

- **Genes:** TEK (TEK receptor tyrosine kinase) [NCBI Gene 7010], ANGPT1 (angiopoietin 1) [NCBI Gene 284], ANGPT2 (angiopoietin 2) [NCBI Gene 285], si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3) [NCBI Gene 103182021], cldn5.L (claudin 5 (transmembrane protein deleted in velocardiofacial syndrome) L homeolog) [NCBI Gene 398929], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879]
- **Proteins:** TEK (TEK receptor tyrosine kinase), ANGPT1 (angiopoietin 1), ANGPT2 (angiopoietin 2), si:ch73-61d6.3 (uncharacterized si:ch73-61d6.3), cldn5.L (claudin 5 (transmembrane protein deleted in velocardiofacial syndrome) L homeolog), GPX4 (glutathione peroxidase 4)
- **Chemicals:** calcitriol (PubChem CID 5280453), glutathione (PubChem CID 124886), iron (PubChem CID 23925), copper (PubChem CID 23978), doxorubicin (PubChem CID 31703)
- **Diseases:** acute lung injury (MONDO:0006502)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tek (TEK receptor tyrosine kinase) [NCBI Gene 21687] {aka Cd202b, Hyk, STK1, Tie-2, Tie2}, Ang2 (angiogenin, ribonuclease A family, member 2) [NCBI Gene 11731] {aka Angrp, Raa3, Rnase5b}, Ang (angiogenin, ribonuclease, RNase A family, 5) [NCBI Gene 11727] {aka Ang1, Rnase5, Rnase5a}, Cldn5 (claudin 5) [NCBI Gene 12741] {aka MBEC1, Tmvcf}, Gpx4 (glutathione peroxidase 4) [NCBI Gene 625249] {aka GPx-4, GSHPx-4, PHGPx, mtPHGPx, snGPx}, Ocln (occludin) [NCBI Gene 18260] {aka Ocl}
- **Diseases:** lung injury (MESH:D055370), Menopause (MESH:D008594), inflammation (MESH:D007249), organ damage (MESH:D000092124), obesity (MESH:D009765), Sepsis (MESH:D018805), ALI (MESH:D055371)
- **Chemicals:** GSH (MESH:D005978), fat (MESH:D005223), Calcitriol (MESH:D002117), iron (MESH:D007501), copper (MESH:D003300)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12520812/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12520812/full.md

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Source: https://tomesphere.com/paper/PMC12520812