Sex-specific cardiovascular responses in cerulein-induced acute pancreatitis models

Cardiovascular (CV) dysfunction is common in severe acute pancreatitis (AP) and contributes substantially to mortality. Although sex differences in CV diseases are well recognized, with males generally exhibiting higher risk and poorer outcomes, their influence on AP-associated CV responses remains poorly defined. Here, we examined sex-dependent alterations in vascular integrity and cardiac function using cerulein-induced mouse models of AP. Because obesity is associated with more severe forms of AP, cerulein was used to induce mild AP in lean wild-type C57BL/6J mice and a more severe phenotype in obese C57BL/6J mice. Across both models, pancreatic injury was comparable between sexes. A modest sex difference in vascular permeability was observed in the mild but not severe AP model. In mild AP, both males and females showed similar compensatory increases in cardiac systolic function; however, in severe AP, only female mice maintained this adaptive systolic augmentation. Circulating levels of free fatty acids, reflecting systemic tissue lipolysis, were lower in females. Impaired cardiac adaptation in males was accompanied by higher levels of seven different myocardial inflammatory cytokines, as well as elevated circulating levels of angiopoietin-2 (Angpt2). While Angpt2 levels correlated with the severity of cardiac dysfunction, Angpt2 neutralization did not improve, and indeed worsened cardiac function in males. Together, these findings delineate both sex-dependent and sex-independent CV responses in mild and severe AP and identify Angpt2 as a potential compensatory cardioprotective factor under obesity-associated severe AP.

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Publication Details

Journal
American Journal of Physiology-Heart and Circulatory Physiology
Published
2026-10-06
DOI
https://doi.org/10.1152/ajpheart.00065.2026
Primary Topic
Pancreatitis Pathology and Treatment
Type
article
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article

Sex-specific cardiovascular responses in cerulein-induced acute pancreatitis models

Baoan Ji, Margaret M. Redfield, Yan Bi, S. Jeson Sangaralingham et al.
American Journal of Physiology-Heart and Circulatory Physiology
Pancreatitis Pathology and Treatment
article

Sex-specific cardiovascular responses in cerulein-induced acute pancreatitis models

Baoan Ji, Margaret M. Redfield, Yan Bi, S. Jeson Sangaralingham, 赵佳辉, Aurelia Lugea, Richard T. Waldron, Ahmed U. Fayyaz, Ying Wang, Jiale Wang, Yu Henry Huo, Aolin Du, Bin Wang, Stephen J. Pandol, Debiao Zhao, Junmeng Zhang
article en

Abstract

Cardiovascular (CV) dysfunction is common in severe acute pancreatitis (AP) and contributes substantially to mortality. Although sex differences in CV diseases are well recognized, with males generally exhibiting higher risk and poorer outcomes, their influence on AP-associated CV responses remains poorly defined. Here, we examined sex-dependent alterations in vascular integrity and cardiac function using cerulein-induced mouse models of AP. Because obesity is associated with more severe forms of AP, cerulein was used to induce mild AP in lean wild-type C57BL/6J mice and a more severe phenotype in obese C57BL/6J mice. Across both models, pancreatic injury was comparable between sexes. A modest sex difference in vascular permeability was observed in the mild but not severe AP model. In mild AP, both males and females showed similar compensatory increases in cardiac systolic function; however, in severe AP, only female mice maintained this adaptive systolic augmentation. Circulating levels of free fatty acids, reflecting systemic tissue lipolysis, were lower in females. Impaired cardiac adaptation in males was accompanied by higher levels of seven different myocardial inflammatory cytokines, as well as elevated circulating levels of angiopoietin-2 (Angpt2). While Angpt2 levels correlated with the severity of cardiac dysfunction, Angpt2 neutralization did not improve, and indeed worsened cardiac function in males. Together, these findings delineate both sex-dependent and sex-independent CV responses in mild and severe AP and identify Angpt2 as a potential compensatory cardioprotective factor under obesity-associated severe AP.

American Journal of Physiology-Heart and Circulatory Physiology
Cedars-Sinai Medical Center (US), Mayo Clinic (US), China Medical University (CN)
Openalex Percentile: Top 9%
Pancreatitis Pathology and Treatment
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