Swetha Kamatam, Indumathi Mylanayakanahosahalli Chandrashekar, Siddappa Shiva, Chen Chu-Huang, Marathe Gopal K
Department of Studies in Biochemistry, University of Mysore, Manasagangotri, Mysore-06, India.
Division of Biochemistry, School of Life Sciences, JSS Academy of Higher Education and Research, Mysore-15, India.
Dig Dis Sci. 2025 Jan;70(1):233-244. doi: 10.1007/s10620-024-08771-5. Epub 2024 Nov 27.
Although a relevant animal model is essential for studying human diseases, one has yet to be established for mouse pancreatitis. Early non-invasive models of mouse pancreatitis have serious limitations.
In this study, we compared the efficiency, consistency, and reproducibility of inducing pancreatitis in 3 non-invasive mouse models of pancreatitis in Wistar albino mice: (1) L-arginine-induced model (2 intraperitoneal injections of 4 g/kg body weight of L-arginine spaced 1 h apart), (2) caerulein-induced model (6 intraperitoneal injections of 50 µg/kg body weight of caerulein at hourly intervals), and (3) caerulein + LPS (lipopolysaccharide)-induced model (6 intraperitoneal doses of 50 µg/kg body weight of caerulein at hourly intervals, along with an LPS [10 mg/kg body weight] injection immediately after the last caerulein injection).
Our findings showed that the L-arginine-induced model was inconsistent. The levels of the pancreatic enzymes, amylase and lipase, were higher in the caerulein and caerulein + LPS groups. Histological examination showed tissue destruction in the induced groups, with varying degrees of fibrosis in the caerulein + LPS group.
The caerulein + LPS model was the most reliable model in Wistar albino mice. Our findings may be useful in helping investigators choose the most appropriate animal model for pancreatitis research.
尽管相关动物模型对于研究人类疾病至关重要,但小鼠胰腺炎的动物模型尚未建立。早期的小鼠胰腺炎非侵入性模型存在严重局限性。
在本研究中,我们比较了在Wistar白化小鼠中3种胰腺炎非侵入性小鼠模型诱导胰腺炎的效率、一致性和可重复性:(1)L-精氨酸诱导模型(间隔1小时腹腔注射2次4 g/kg体重的L-精氨酸),(2)雨蛙素诱导模型(每小时腹腔注射6次50 μg/kg体重的雨蛙素),以及(3)雨蛙素+脂多糖(LPS)诱导模型(每小时腹腔注射6次50 μg/kg体重的雨蛙素,在最后一次雨蛙素注射后立即注射LPS[10 mg/kg体重])。
我们的研究结果表明,L-精氨酸诱导模型不一致。雨蛙素组和雨蛙素+LPS组的胰腺酶、淀粉酶和脂肪酶水平较高。组织学检查显示诱导组有组织破坏,雨蛙素+LPS组有不同程度的纤维化。
雨蛙素+LPS模型是Wistar白化小鼠中最可靠的模型。我们的研究结果可能有助于研究人员为胰腺炎研究选择最合适的动物模型。