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Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats

BACKGROUND: Solanum torvum Swartz, a medicinal plant belonging to the family Solanaceae, is an important medicinal plant widely distributed throughout the world and used as medicine to treat diabetes, hypertension, tooth decay, and reproductive problems in traditional systems of medicine around the...

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Autores principales: Satyanarayana, Namani, Chinni, Suresh V., Gobinath, Ramachawolran, Sunitha, Paripelli, Uma Sankar, Akula, Muthuvenkatachalam, Bala Sundaram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650639/
https://www.ncbi.nlm.nih.gov/pubmed/36386935
http://dx.doi.org/10.3389/fnut.2022.987552
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author Satyanarayana, Namani
Chinni, Suresh V.
Gobinath, Ramachawolran
Sunitha, Paripelli
Uma Sankar, Akula
Muthuvenkatachalam, Bala Sundaram
author_facet Satyanarayana, Namani
Chinni, Suresh V.
Gobinath, Ramachawolran
Sunitha, Paripelli
Uma Sankar, Akula
Muthuvenkatachalam, Bala Sundaram
author_sort Satyanarayana, Namani
collection PubMed
description BACKGROUND: Solanum torvum Swartz, a medicinal plant belonging to the family Solanaceae, is an important medicinal plant widely distributed throughout the world and used as medicine to treat diabetes, hypertension, tooth decay, and reproductive problems in traditional systems of medicine around the world including Malaysia. The objective of this study was to investigate hypoglycemic, antilipidemic, and hepatoprotective activities, histopathology of the pancreas, and specific glucose regulating gene expression of the ethanolic extract of S. torvum fruit in streptozotocin-induced diabetic Sprague–Dawley rats. MATERIALS AND METHODS: Acute toxicity study was done according to OECD-423 guidelines. Diabetes was induced by intraperitoneal (i.p.) injection of streptozotocin (55 mg/kg) in male Sprague–Dawley rats. Experimental diabetic rats were divided into six different groups; normal, diabetic control, and glibenclamide at 6 mg/kg body weight, and the other three groups of animals were treated with oral administration of ethanolic extract of S. torvum fruit at 120, 160, and 200 mg/kg for 28 days. The effect of ethanolic extract of S. torvum fruit on body weight, blood glucose, lipid profile, liver enzymes, histopathology of pancreas, and gene expression of glucose transporter 2 (slc2a2), and phosphoenolpyruvate carboxykinase (PCK1) was determined by RT-PCR. RESULTS: Acute toxicity studies showed LD(50) of ethanolic extract of S. torvum fruit to be at the dose of 1600 mg/kg body weight. Blood glucose, total cholesterol, triglycerides, low-density lipoproteins, very low-density lipoproteins, serum alanine aminotransferase, and aspartate aminotransferase were significantly reduced, whereas high-density lipoproteins were significantly increased in S. torvum fruit (200 mg/kg)-treated rats. Histopathological study of the pancreas showed an increase in number, size, and regeneration of β-cell of islets of Langerhans. Gene expression studies revealed the lower expression of slc2a2 and PCK1 in treated animals when compared to diabetic control. CONCLUSION: Ethanolic extract of S. torvum fruits showed hypoglycemic, hypolipidemic, and hepatoprotective activity in streptozocin-induced diabetic rats. Histopathological studies revealed regeneration of β cells of islets of Langerhans. Gene expression studies indicated lower expression of slc2a2 and PCK1 in treated animals when compared to diabetic control, indicating that the treated animals prefer the gluconeogenesis pathway.
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spelling pubmed-96506392022-11-15 Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats Satyanarayana, Namani Chinni, Suresh V. Gobinath, Ramachawolran Sunitha, Paripelli Uma Sankar, Akula Muthuvenkatachalam, Bala Sundaram Front Nutr Nutrition BACKGROUND: Solanum torvum Swartz, a medicinal plant belonging to the family Solanaceae, is an important medicinal plant widely distributed throughout the world and used as medicine to treat diabetes, hypertension, tooth decay, and reproductive problems in traditional systems of medicine around the world including Malaysia. The objective of this study was to investigate hypoglycemic, antilipidemic, and hepatoprotective activities, histopathology of the pancreas, and specific glucose regulating gene expression of the ethanolic extract of S. torvum fruit in streptozotocin-induced diabetic Sprague–Dawley rats. MATERIALS AND METHODS: Acute toxicity study was done according to OECD-423 guidelines. Diabetes was induced by intraperitoneal (i.p.) injection of streptozotocin (55 mg/kg) in male Sprague–Dawley rats. Experimental diabetic rats were divided into six different groups; normal, diabetic control, and glibenclamide at 6 mg/kg body weight, and the other three groups of animals were treated with oral administration of ethanolic extract of S. torvum fruit at 120, 160, and 200 mg/kg for 28 days. The effect of ethanolic extract of S. torvum fruit on body weight, blood glucose, lipid profile, liver enzymes, histopathology of pancreas, and gene expression of glucose transporter 2 (slc2a2), and phosphoenolpyruvate carboxykinase (PCK1) was determined by RT-PCR. RESULTS: Acute toxicity studies showed LD(50) of ethanolic extract of S. torvum fruit to be at the dose of 1600 mg/kg body weight. Blood glucose, total cholesterol, triglycerides, low-density lipoproteins, very low-density lipoproteins, serum alanine aminotransferase, and aspartate aminotransferase were significantly reduced, whereas high-density lipoproteins were significantly increased in S. torvum fruit (200 mg/kg)-treated rats. Histopathological study of the pancreas showed an increase in number, size, and regeneration of β-cell of islets of Langerhans. Gene expression studies revealed the lower expression of slc2a2 and PCK1 in treated animals when compared to diabetic control. CONCLUSION: Ethanolic extract of S. torvum fruits showed hypoglycemic, hypolipidemic, and hepatoprotective activity in streptozocin-induced diabetic rats. Histopathological studies revealed regeneration of β cells of islets of Langerhans. Gene expression studies indicated lower expression of slc2a2 and PCK1 in treated animals when compared to diabetic control, indicating that the treated animals prefer the gluconeogenesis pathway. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9650639/ /pubmed/36386935 http://dx.doi.org/10.3389/fnut.2022.987552 Text en Copyright © 2022 Satyanarayana, Chinni, Gobinath, Sunitha, Uma Sankar and Muthuvenkatachalam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Satyanarayana, Namani
Chinni, Suresh V.
Gobinath, Ramachawolran
Sunitha, Paripelli
Uma Sankar, Akula
Muthuvenkatachalam, Bala Sundaram
Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title_full Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title_fullStr Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title_full_unstemmed Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title_short Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats
title_sort antidiabetic activity of solanum torvum fruit extract in streptozotocin-induced diabetic rats
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650639/
https://www.ncbi.nlm.nih.gov/pubmed/36386935
http://dx.doi.org/10.3389/fnut.2022.987552
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