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Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals

BACKGROUND: Arjunarishta (AA), a formulation used as cardiotonic is a hydroalcoholic formulation of Terminalia arjuna (Roxb.) Wight and Arn. (TA) belonging to family Combretaceae. OBJECTIVE: To evaluate the anti-hyperglycemic and anti-hyperlipidemic effect of Arjunarishta on high-fat diet fed animal...

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Autores principales: Shengule, Sushant A., Mishra, Sanjay, Joshi, Kalpana, Apte, Kishori, Patil, Dada, Kale, Prathmesh, Shah, Tejas, Deshpande, Mandavi, Puranik, Amrutesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884182/
https://www.ncbi.nlm.nih.gov/pubmed/29249636
http://dx.doi.org/10.1016/j.jaim.2017.07.004
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author Shengule, Sushant A.
Mishra, Sanjay
Joshi, Kalpana
Apte, Kishori
Patil, Dada
Kale, Prathmesh
Shah, Tejas
Deshpande, Mandavi
Puranik, Amrutesh
author_facet Shengule, Sushant A.
Mishra, Sanjay
Joshi, Kalpana
Apte, Kishori
Patil, Dada
Kale, Prathmesh
Shah, Tejas
Deshpande, Mandavi
Puranik, Amrutesh
author_sort Shengule, Sushant A.
collection PubMed
description BACKGROUND: Arjunarishta (AA), a formulation used as cardiotonic is a hydroalcoholic formulation of Terminalia arjuna (Roxb.) Wight and Arn. (TA) belonging to family Combretaceae. OBJECTIVE: To evaluate the anti-hyperglycemic and anti-hyperlipidemic effect of Arjunarishta on high-fat diet fed animals. MATERIALS AND METHODS: High-fat diet fed (HFD) Wistar rats were randomly divided into three groups and treated with phytochemically standardized Arjunarishta (1.8 ml/kg), and hydroalcoholic extract of T. arjuna (TAHA) (250 mg/kg) and rosuvastatin (10 mg/kg), for 3 months. Intraperitoneal glucose tolerance test, blood biochemistry, liver triglyceride and systolic blood pressure were performed in all the groups. Effect of these drugs on the expression of tumor necrosis factor-α (TNF-α) and insulin receptor substrate-1 (IRS-1) and peroxisome proliferators activated receptor γ coactivator 1-α (PGC-1α) were studied in liver tissue using Quantitative Real-time PCR. RESULTS: HFD increased fasting blood glucose, liver triglyceride, systolic blood pressure and gene expression of TNF-α, IRS-1 and PGC-1α. Treatment of AA and TAHA significantly reduced fasting blood glucose, systolic blood pressure, total cholesterol and triglyceride levels. These treatments significantly decreased gene expression of TNF-α (2.4, 2.2 and 2.6 fold change); increased IRS-1 (2.8, 2.9 and 2.8 fold change) and PGC-1α (2.9, 3.7 and 3.3 fold change) as compared to untreated HFD. CONCLUSION: Anti-hyperglycemic, anti-hyperlipidemic effect of Arjunarishta may be mediated by decreased TNF-α and increased PGC-1α and IRS-1.
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spelling pubmed-58841822018-04-06 Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals Shengule, Sushant A. Mishra, Sanjay Joshi, Kalpana Apte, Kishori Patil, Dada Kale, Prathmesh Shah, Tejas Deshpande, Mandavi Puranik, Amrutesh J Ayurveda Integr Med Original Research Article- Experimental BACKGROUND: Arjunarishta (AA), a formulation used as cardiotonic is a hydroalcoholic formulation of Terminalia arjuna (Roxb.) Wight and Arn. (TA) belonging to family Combretaceae. OBJECTIVE: To evaluate the anti-hyperglycemic and anti-hyperlipidemic effect of Arjunarishta on high-fat diet fed animals. MATERIALS AND METHODS: High-fat diet fed (HFD) Wistar rats were randomly divided into three groups and treated with phytochemically standardized Arjunarishta (1.8 ml/kg), and hydroalcoholic extract of T. arjuna (TAHA) (250 mg/kg) and rosuvastatin (10 mg/kg), for 3 months. Intraperitoneal glucose tolerance test, blood biochemistry, liver triglyceride and systolic blood pressure were performed in all the groups. Effect of these drugs on the expression of tumor necrosis factor-α (TNF-α) and insulin receptor substrate-1 (IRS-1) and peroxisome proliferators activated receptor γ coactivator 1-α (PGC-1α) were studied in liver tissue using Quantitative Real-time PCR. RESULTS: HFD increased fasting blood glucose, liver triglyceride, systolic blood pressure and gene expression of TNF-α, IRS-1 and PGC-1α. Treatment of AA and TAHA significantly reduced fasting blood glucose, systolic blood pressure, total cholesterol and triglyceride levels. These treatments significantly decreased gene expression of TNF-α (2.4, 2.2 and 2.6 fold change); increased IRS-1 (2.8, 2.9 and 2.8 fold change) and PGC-1α (2.9, 3.7 and 3.3 fold change) as compared to untreated HFD. CONCLUSION: Anti-hyperglycemic, anti-hyperlipidemic effect of Arjunarishta may be mediated by decreased TNF-α and increased PGC-1α and IRS-1. Elsevier 2018 2017-12-15 /pmc/articles/PMC5884182/ /pubmed/29249636 http://dx.doi.org/10.1016/j.jaim.2017.07.004 Text en © 2017 Transdisciplinary University, Bangalore and World Ayurveda Foundation. Publishing Services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article- Experimental
Shengule, Sushant A.
Mishra, Sanjay
Joshi, Kalpana
Apte, Kishori
Patil, Dada
Kale, Prathmesh
Shah, Tejas
Deshpande, Mandavi
Puranik, Amrutesh
Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title_full Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title_fullStr Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title_full_unstemmed Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title_short Anti-hyperglycemic and anti-hyperlipidaemic effect of Arjunarishta in high-fat fed animals
title_sort anti-hyperglycemic and anti-hyperlipidaemic effect of arjunarishta in high-fat fed animals
topic Original Research Article- Experimental
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5884182/
https://www.ncbi.nlm.nih.gov/pubmed/29249636
http://dx.doi.org/10.1016/j.jaim.2017.07.004
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