Acute pancreatitis (AP) is a life-threatening condition, with a higher mortality rate in men than women and in which estrogens might play a protective role. This study aimed to investigate sex-dependent differences in a mouse model of caerulein-induced AP. Thirty-six C57BL/6J mice (19 females and 17 males) were treated intraperitoneally with phosphate-buffered saline or caerulein, and sacrificed 12 hours, 2 days, or 7 days after the last injection. Blood was collected for amylase, lipase, and glucose determination. Severity and extent of inflammation, apoptosis, and acinar to ductal metaplasia (ADM) in pancreatic tissue were scored histologically and total macrophages, major histocompatibility complex (MHC)-II+ cells, M2 macrophages, T and B cells, neutrophils, apoptosis, and ADM were marked immunohistochemically and quantified by digital image analysis. Serum amylase had a peak at 12 hours, without differences between the sexes. In females, pancreatitis reached a peak at 12 hours with a fast recovery while, in males, the peak was delayed to day 2 with residual apoptosis still present. Macrophages were the main inflammatory cell population, followed by T cells, B cells and neutrophils, without differences between sexes. In males, CD206+ cells and apoptosis were higher at both days 2 and 7, and cytokeratin-19+ (CK19+) ADM was higher at day 7 compared with females. The results of this study revealed a faster onset and resolution of caerulein-induced AP in female mice compared with male mice, supporting a sex-dependent modulation of acute pancreatitis.

Sex-dependent modulation of caerulein-induced acute pancreatitis in C57BL/6J mice / L. Bertola, G. Pepe, A. Dolce, C. Lecchi, E.M. Borroni, B. Savino, S. Canesi, L. Sala, P. Moretti, A. Giordano, L. Ressel, E. Scanziani, E. Vegeto, C. Recordati. - In: VETERINARY PATHOLOGY. - ISSN 1544-2217. - 62:3(2025 May), pp. 382-396. [10.1177/03009858241312606]

Sex-dependent modulation of caerulein-induced acute pancreatitis in C57BL/6J mice

L. Bertola
Primo
;
G. Pepe
Secondo
;
A. Dolce;C. Lecchi;E.M. Borroni;B. Savino;S. Canesi;L. Sala;P. Moretti;A. Giordano;E. Scanziani;E. Vegeto
Penultimo
;
C. Recordati
Ultimo
2025

Abstract

Acute pancreatitis (AP) is a life-threatening condition, with a higher mortality rate in men than women and in which estrogens might play a protective role. This study aimed to investigate sex-dependent differences in a mouse model of caerulein-induced AP. Thirty-six C57BL/6J mice (19 females and 17 males) were treated intraperitoneally with phosphate-buffered saline or caerulein, and sacrificed 12 hours, 2 days, or 7 days after the last injection. Blood was collected for amylase, lipase, and glucose determination. Severity and extent of inflammation, apoptosis, and acinar to ductal metaplasia (ADM) in pancreatic tissue were scored histologically and total macrophages, major histocompatibility complex (MHC)-II+ cells, M2 macrophages, T and B cells, neutrophils, apoptosis, and ADM were marked immunohistochemically and quantified by digital image analysis. Serum amylase had a peak at 12 hours, without differences between the sexes. In females, pancreatitis reached a peak at 12 hours with a fast recovery while, in males, the peak was delayed to day 2 with residual apoptosis still present. Macrophages were the main inflammatory cell population, followed by T cells, B cells and neutrophils, without differences between sexes. In males, CD206+ cells and apoptosis were higher at both days 2 and 7, and cytokeratin-19+ (CK19+) ADM was higher at day 7 compared with females. The results of this study revealed a faster onset and resolution of caerulein-induced AP in female mice compared with male mice, supporting a sex-dependent modulation of acute pancreatitis.
C57BL/6 mice; caerulein; immunohistochemistry; macrophages; pancreatitis; polarization; sex;
Settore MVET-02/A - Patologia generale e anatomia patologica veterinaria
Settore BIOS-11/A - Farmacologia
   Piano Sviluppo Unimi - Linea 3 - Bando SEED 2019 - Progetto MACROGENDE
   MACROGENDE
   UNIVERSITA' DEGLI STUDI DI MILANO
mag-2025
29-gen-2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1162816
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