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Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model

OBJECTIVE: Guiera senegalensis is distributed in the Sudano-Sahelian zone and used traditionally for the treatment of diabetes. This study was designed to assess the hypoglycemic effects of G. senegalensis in Wistar diabetic rats. MATERIALS AND METHODS: Phytochemical analysis was carried out on aque...

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Autores principales: Miaffo, David, Ntchapda, Fidèle, Kamgue, Oulianovie Guessom, Mahamad, Abba Talba, Kamanyi, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711294/
https://www.ncbi.nlm.nih.gov/pubmed/33299821
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author Miaffo, David
Ntchapda, Fidèle
Kamgue, Oulianovie Guessom
Mahamad, Abba Talba
Kamanyi, Albert
author_facet Miaffo, David
Ntchapda, Fidèle
Kamgue, Oulianovie Guessom
Mahamad, Abba Talba
Kamanyi, Albert
author_sort Miaffo, David
collection PubMed
description OBJECTIVE: Guiera senegalensis is distributed in the Sudano-Sahelian zone and used traditionally for the treatment of diabetes. This study was designed to assess the hypoglycemic effects of G. senegalensis in Wistar diabetic rats. MATERIALS AND METHODS: Phytochemical analysis was carried out on aqueous and methanolic extracts of G. senegalensis. Type 2 diabetes was induced in male rats using nicotinamide/streptozotocin (65 mg/kg/110 mg/kg, i.p.). After diabetes induction, normal and negative control groups received distilled water, positive control group received glibenclamide (0.25 mg/kg) and the others group received aqueous and methanolic extracts (200 and 400 mg/kg, each) orally for 4 weeks. Glycaemia, body weight, insulin level, total cholesterol (TC), high density lipoprotein cholesterol (HDL-c), low density lipoprotein cholesterol (LDL-c), triglycerides (TG), aspartate amino transferase (AST) and alanine amino transferase (ALT) activities, urea and creatinine (Cr) were evaluated. RESULTS: The content of phenols, flavonoids and tannins were 34.54 mg gallic acid equivalent (GAE)/gE, 4.86 mg quercetin equivalent (QE)/gE and 16.81 mg catechin equivalent (EC)/gE in the aqueous extract, respectively. Phenol (26.01 mg GAE/gE), flavonoid (4.47 mg QE/gE) and tannin (7.67 mg EC/gE) contents were also obtained for the methanolic extract. G. senegalensis and glibenclamide resulted in a significant increase (p<0.001) in body weight and HDL-c in diabetic group rats receiving glibenclamide and different doses of extracts. . The level of insulin, glycaemia, TG, TC, LDL-c, urea and creatinine significantly decreased (p<0.05 to 0.001) in diabetic animals treated with G. senegalensis extracts. CONCLUSION: These results confirm the potential of G. senegalensis for the treatment of diabetes and its complications.
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spelling pubmed-77112942020-12-08 Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model Miaffo, David Ntchapda, Fidèle Kamgue, Oulianovie Guessom Mahamad, Abba Talba Kamanyi, Albert Avicenna J Phytomed Original Research Article OBJECTIVE: Guiera senegalensis is distributed in the Sudano-Sahelian zone and used traditionally for the treatment of diabetes. This study was designed to assess the hypoglycemic effects of G. senegalensis in Wistar diabetic rats. MATERIALS AND METHODS: Phytochemical analysis was carried out on aqueous and methanolic extracts of G. senegalensis. Type 2 diabetes was induced in male rats using nicotinamide/streptozotocin (65 mg/kg/110 mg/kg, i.p.). After diabetes induction, normal and negative control groups received distilled water, positive control group received glibenclamide (0.25 mg/kg) and the others group received aqueous and methanolic extracts (200 and 400 mg/kg, each) orally for 4 weeks. Glycaemia, body weight, insulin level, total cholesterol (TC), high density lipoprotein cholesterol (HDL-c), low density lipoprotein cholesterol (LDL-c), triglycerides (TG), aspartate amino transferase (AST) and alanine amino transferase (ALT) activities, urea and creatinine (Cr) were evaluated. RESULTS: The content of phenols, flavonoids and tannins were 34.54 mg gallic acid equivalent (GAE)/gE, 4.86 mg quercetin equivalent (QE)/gE and 16.81 mg catechin equivalent (EC)/gE in the aqueous extract, respectively. Phenol (26.01 mg GAE/gE), flavonoid (4.47 mg QE/gE) and tannin (7.67 mg EC/gE) contents were also obtained for the methanolic extract. G. senegalensis and glibenclamide resulted in a significant increase (p<0.001) in body weight and HDL-c in diabetic group rats receiving glibenclamide and different doses of extracts. . The level of insulin, glycaemia, TG, TC, LDL-c, urea and creatinine significantly decreased (p<0.05 to 0.001) in diabetic animals treated with G. senegalensis extracts. CONCLUSION: These results confirm the potential of G. senegalensis for the treatment of diabetes and its complications. Mashhad University of Medical Sciences 2020 /pmc/articles/PMC7711294/ /pubmed/33299821 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Miaffo, David
Ntchapda, Fidèle
Kamgue, Oulianovie Guessom
Mahamad, Abba Talba
Kamanyi, Albert
Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title_full Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title_fullStr Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title_full_unstemmed Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title_short Glucose-lowering potential of Guiera senegalensis roots in a diabetic rat model
title_sort glucose-lowering potential of guiera senegalensis roots in a diabetic rat model
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711294/
https://www.ncbi.nlm.nih.gov/pubmed/33299821
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