Evidence map›Paper›PMID 39604666›Full record

ArticleDigestive diseases and sciences2025

Comparative Study of Non-invasive Mouse Models of Pancreatitis.

Kamatam Swetha, Mylanayakanahosahalli Chandrashekar Indumathi, Shiva Siddappa, Chu-Huang Chen, Gopal K Marathe

Abstract readComparative Study
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In one paragraph

Article in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kamatam SwethaDepartment of Studies in Biochemistry, University of Mysore, Manasagangotri, Mysore-06, India.
Mylanayakanahosahalli Chandrashekar IndumathiDepartment of Studies in Biochemistry, University of Mysore, Manasagangotri, Mysore-06, India.
Shiva SiddappaDivision of Biochemistry, School of Life Sciences, JSS Academy of Higher Education and Research, Mysore-15, India.
Chu-Huang ChenVascular and Medicinal Research, The Texas Heart Institute, Houston, TX, 77030, USA.
Gopal K MaratheDepartment of Studies in Biochemistry, University of Mysore, Manasagangotri, Mysore-06, India. marathe1962@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsAlthough 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.

methodsIn 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).

resultsOur 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.

conclusionsThe 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.

Indexed as

Disease Models, AnimalPancreatitisAmylasesAnimalsArginineCeruletideInjections, IntraperitonealLipaseLipopolysaccharidesMaleMicePancreasReproducibility of ResultsAmylasesArginineCeruletideLipaseLipopolysaccharidesCaerulein-induced modelCaerulein + LPS-induced modelL-Arginine-induced modelMouse pancreatitis modelsPancreatitis

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.