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Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation
BACKGROUND: Chandraprabha vati is a classical Ayurvedic formulation, markedly used for mitigation of Prameha, which correlates in many ways with obesity, metabolic syndrome and diabetes mellitus. OBJECTIVE: The present study was aimed to investigate effect of Chandraprabha vati in experimentally-ind...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052381/ https://www.ncbi.nlm.nih.gov/pubmed/27665674 http://dx.doi.org/10.1016/j.jaim.2016.08.010 |
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author | Wanjari, Manish M. Mishra, Sujata Dey, Yadu Nandan Sharma, Deepti Gaidhani, Sudesh N. Jadhav, Ankush D. |
author_facet | Wanjari, Manish M. Mishra, Sujata Dey, Yadu Nandan Sharma, Deepti Gaidhani, Sudesh N. Jadhav, Ankush D. |
author_sort | Wanjari, Manish M. |
collection | PubMed |
description | BACKGROUND: Chandraprabha vati is a classical Ayurvedic formulation, markedly used for mitigation of Prameha, which correlates in many ways with obesity, metabolic syndrome and diabetes mellitus. OBJECTIVE: The present study was aimed to investigate effect of Chandraprabha vati in experimentally-induced hyperglycemia and lipid profile alterations. MATERIALS AND METHODS: Antidiabetic effect of Chandraprabha vati was studied in fifty five Wistar rats. Graded doses of Chandraprabha vati (50, 100 and 200 mg/kg) were administered orally for 7 days to normal and alloxan-hyperglycemic rats (65 mg/kg, intravenously), and to glucose loaded normal rats for oral glucose tolerance test (OGTT). Fasting plasma glucose levels were assessed on different time intervals along with plasma cholesterol and triglycerides. Metformin (500 mg/kg, orally) was used as standard drug. RESULTS: Chandraprabha vati did not cause any significant reduction in plasma glucose levels of normal rats (p > 0.05) but normalized the impaired glucose tolerance at 60 and 120 min (p < 0.05–p < 0.001) in OGTT when compared to vehicle control. In alloxan-hyperglycemic rats, administration of Chandraprabha vati (200 mg/kg) significantly reduced plasma glucose at 3 h, 12 h, 3rd day and 7th day (p < 0.01–p < 0.001) along with reduction in cholesterol and triglycerides levels (p < 0.01–p < 0.001) when compared to diabetic control group. The effects were comparable with metformin. CONCLUSIONS: Chandraprabha vati exhibited anti-hyperglycemic effect and attenuated alterations in lipid profile. The results support the use of Chandraprabha vati for correction of Prameha in clinical practice. |
format | Online Article Text |
id | pubmed-5052381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-50523812016-10-12 Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation Wanjari, Manish M. Mishra, Sujata Dey, Yadu Nandan Sharma, Deepti Gaidhani, Sudesh N. Jadhav, Ankush D. J Ayurveda Integr Med Original Research Article (Experimental) BACKGROUND: Chandraprabha vati is a classical Ayurvedic formulation, markedly used for mitigation of Prameha, which correlates in many ways with obesity, metabolic syndrome and diabetes mellitus. OBJECTIVE: The present study was aimed to investigate effect of Chandraprabha vati in experimentally-induced hyperglycemia and lipid profile alterations. MATERIALS AND METHODS: Antidiabetic effect of Chandraprabha vati was studied in fifty five Wistar rats. Graded doses of Chandraprabha vati (50, 100 and 200 mg/kg) were administered orally for 7 days to normal and alloxan-hyperglycemic rats (65 mg/kg, intravenously), and to glucose loaded normal rats for oral glucose tolerance test (OGTT). Fasting plasma glucose levels were assessed on different time intervals along with plasma cholesterol and triglycerides. Metformin (500 mg/kg, orally) was used as standard drug. RESULTS: Chandraprabha vati did not cause any significant reduction in plasma glucose levels of normal rats (p > 0.05) but normalized the impaired glucose tolerance at 60 and 120 min (p < 0.05–p < 0.001) in OGTT when compared to vehicle control. In alloxan-hyperglycemic rats, administration of Chandraprabha vati (200 mg/kg) significantly reduced plasma glucose at 3 h, 12 h, 3rd day and 7th day (p < 0.01–p < 0.001) along with reduction in cholesterol and triglycerides levels (p < 0.01–p < 0.001) when compared to diabetic control group. The effects were comparable with metformin. CONCLUSIONS: Chandraprabha vati exhibited anti-hyperglycemic effect and attenuated alterations in lipid profile. The results support the use of Chandraprabha vati for correction of Prameha in clinical practice. Elsevier 2016 2016-09-22 /pmc/articles/PMC5052381/ /pubmed/27665674 http://dx.doi.org/10.1016/j.jaim.2016.08.010 Text en © 2016 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) Wanjari, Manish M. Mishra, Sujata Dey, Yadu Nandan Sharma, Deepti Gaidhani, Sudesh N. Jadhav, Ankush D. Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title | Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title_full | Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title_fullStr | Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title_full_unstemmed | Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title_short | Antidiabetic activity of Chandraprabha vati – A classical Ayurvedic formulation |
title_sort | antidiabetic activity of chandraprabha vati – a classical ayurvedic formulation |
topic | Original Research Article (Experimental) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052381/ https://www.ncbi.nlm.nih.gov/pubmed/27665674 http://dx.doi.org/10.1016/j.jaim.2016.08.010 |
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