A review: Pancreatic enzymes in the treatment of chronic pancreatic insufficiency in companion animals

Author:

Szkopek Dominika1ORCID,Pierzynowski Stefan G.234,Pierzynowska Kateryna45,Zaworski Kamil5,Kondej Agata1,Wychowański Piotr6,Konieczka Paweł78,Seklecka Blanka9,Donaldson Janine10,Jank Michał11ORCID,Woliński Jarosław15

Affiliation:

1. Laboratory of Large Animal Models, The Kielanowski Institute of Animal Physiology and Nutrition Polish Academy of Sciences, Instytucka 3 Jabłonna Poland

2. Anara AB Trelleborg Sweden

3. Department of Medical Biology Witold Chodźka Institute of Rural Medicine Lublin Poland

4. Department of Biology Lund University Lund Sweden

5. Department of Animal Physiology, The Kielanowski Institute of Animal Physiology and Nutrition Polish Academy of Sciences, Instytucka 3 Jabłonna Poland

6. Oral Surgery and Implantology Unit, Division of Oral Surgery and Implantology, Department of Head and Neck, Institute of Clinical Dentistry Fondazione Policlinico Universitario A. Gemelli IRCCS, Universita Cattolica del Sacro Coure Rome Italy

7. Department of Animal Nutrition, The Kielanowski Institute of Animal Physiology and Nutrition Polish Academy of Sciences, Instytucka 3 Jabłonna Poland

8. Department of Poultry Science and Apiculture University of Warmia and Mazury, Oczapowskiego 5 Olsztyn Poland

9. Phase Research Team, Adamed Pharma S.A. Pieńków Poland

10. School of Physiology, Faculty of Health Sciences University of the Witwatersrand Parktown, Johannesburg 2193 South Africa

11. Department of Pre‐Clinical Sciences and Infectious Diseases, Faculty of Veterinary Medicine and Animal Science Poznan University of Life Sciences Poznań Poland

Abstract

AbstractThe purpose of this review was to analyze the scientific literature on exocrine pancreatic insufficiency (EPI) in dogs and cats and our own research on porcine model to compare animal‐ and microbial‐derived enzymes in the treatment of animals with this disease. Clinical signs of EPI occur when more than 85% of the pancreatic parenchyma is non‐functional. EPI can be a consequence of various diseases. The insufficient activity or deficiency of pancreatic enzymes leads to impaired digestion and absorption, and consequently, to malnutrition. The primary treatment for enzyme insufficiency is pancreatic enzyme replacement therapy (PERT). PERT in animals with EPI is a lifetime therapy. Most commercially available products are of animal origin (processed pancreata obtained from a slaughter house) and contain lipases, alpha‐amylase, and proteases. Enzymes of microbial and plant origin seem to be a promising alternative to animal‐derived enzymes, but to date there are no registered preparations containing all enzymes simultaneously for use in clinical practice to treat EPI. Results from some previous studies have highlighted the “extra‐digestive” functions of pancreatic enzymes, as well as the actions of pancreatic‐like microbial enzymes. For example, trypsin activates protease‐activated receptor and provokes maturation of enterocytes and enterostatin inhibits fat absorption. It has been postulated that intrapancreatic amylase is the main component of the acini‐islet‐acinar axis—the reflex which down regulates insulin release, while gut and blood amylase exhibit anti‐incretin actions “per se.” Additionally, high but still physiological blood amylase activity coincide with physiological glucose homeostasis and a lack of obesity.

Publisher

Wiley

Reference63 articles.

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