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Do Animal Models of Acute Pancreatitis Reproduce Human Disease?

Journal

Publisher

ELSEVIER INC
DOI: 10.1016/j.jcmgh.2017.05.007

Keywords

Acute Pancreatitis; Animal Models; Caerulein; Alcohol

Funding

  1. NIK [R01 DK54021]
  2. NIH P01 [DK098108]
  3. Veterans Administration Merit and Career development awards
  4. Deutsche Krebshilfe/Dr. Mildred-Scheel-Stiftung [109102]
  5. Deutsche Forschungsgemeinschaft (DFG) [GRK1947, A3]
  6. Federal Ministry of Education and Research (BMBF) [GANI-MED 03IS2061A]
  7. BMBF [0314107, 01ZZ9603, 01ZZ0103, 01ZZ0403, 03ZIK012]
  8. European Union (EU) [FP-7, EU-FP7-REGPOT-2010-1, EPC-TM]

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Acute pancreatitis is currently the most common cause of hospital admission among all nonmalignant gastrointestinal diseases. To understand the pathophysiology of the disease and as a potential step toward developing targeted therapies, attempts to induce the disease experimentally began more than 100 years ago. Recent decades have seen progress in developing new experimental pancreatitis models as well as elucidating many underlying cell biological and pathophysiological disease mechanisms. Some models have been developed to reflect specific causes of acute pancreatitis in human beings. However, the paucity of data relating to the molecular mechanisms of human disease, the likelihood that multiple genetic and environmental factors affect the risk of disease development and its severity, and the limited information regarding the natural history of disease in human beings make it difficult to evaluate the value of disease models. Here, we provide an overview of key models and discuss our views on their strengths for characterizing cell biological disease mechanisms or for identifying potential therapeutic targets. We also acknowledge their limitations.

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