Evaluation of the antidiabetic potential of selected medicinal plant extracts from the Canadian boreal forest used to treat symptoms of diabetes: part II

Author:

Harbilas Despina12345,Martineau Louis C.12345,Harris Cory S.12345,Adeyiwola-Spoor Danielle C.A.12345,Saleem Ammar12345,Lambert Jennifer12345,Caves Dayna12345,Johns Timothy12345,Prentki Marc12345,Cuerrier Alain12345,Arnason John T.12345,Bennett Steffany A.L.12345,Haddad Pierre S.12345

Affiliation:

1. Department of Pharmacology, Université de Montréal, P.O. Box 6128, Centre-ville Station, Montréal, QC H3C 3J7, Canada.

2. Nutraceuticals and Functional Foods Institute, Université Laval, Québec, QC G1K 7P4, Canada.

3. Montreal Diabetes Research Center, Centre de recherche du Centre hospitalier de l’Université de Montréal, 2901 Rachel East, Montréal, QC H1W 4A4, Canada.

4. Department of Biology and Center for Research in Biopharmaceuticals and Biotechnology, University of Ottawa, Ottawa, ON K1N 6N5, Canada.

5. Neural Regeneration Laboratory, Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

Abstract

Among the Cree of northern Quebec, the disproportionately high rate of diabetic complications is largely due to the cultural inadequacy of modern therapies for type 2 diabetes. To establish culturally adapted antidiabetic treatments, our team identified several candidate plant species used by the Cree to treat symptoms of diabetes. An initial study focused on 8 species and revealed that most possess significant in vitro antidiabetic activity. The purpose of the present study was to assess a further 9 species identified through the ethnobotanical survey. Crude plant extracts were screened for (i) potentiation of basal and insulin-stimulated glucose uptake by skeletal muscle cells (C2C12) and adipocytes (3T3-L1); (ii) potentiation of glucose-stimulated insulin secretion by pancreatic β cells (βTC); (iii) potentiation of adipogenesis in 3T3-L1 cells; (iv) protection against glucose toxicity and glucose deprivation in PC12-AC neuronal precursor cells; and (v) diphenylpicrylhydrazyl (DPPH) oxygen free radical scavenging. Four species potentiated basal glucose uptake in muscle cells or adipocytes, one species being as potent as metformin. Adipogenesis was accelerated by 4 species with a potency roughly half that of rosiglitazone. Five species protected PC12-AC cells against glucose toxicity and 4 protected against glucose deprivation. Five species exhibited antioxidant activity comparable to ascorbic acid. However, no species increased insulin secretion. The present study revealed that Gaultheria hispidula , Rhododendron tomentosum , and Vaccinium vitis-idaea exhibit a promising profile of antidiabetic potential and are good candidates for more in-depth evaluation.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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