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Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes

BACKGROUND: Cucumis melo ssp. agrestis var. agrestis (CMA) is a wild variety of C. melo. This study aimed to explore anti-dyslipidemic and anti-adipogenic potential of CMA. MATERIALS AND METHODS: For initial anti-dyslipidemic and antihyperglycemic potential of CMA fruit extract (CMFE), male Syrian g...

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Autores principales: Shankar, Kripa, Singh, Sumit K., Kumar, Durgesh, Varshney, Salil, Gupta, Abhishek, Rajan, Sujith, Srivastava, Ankita, Beg, Muheeb, Srivastava, Anurag Kumar, Kanojiya, Sanjeev, Mishra, Dipak K., Gaikwad, Anil N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787080/
https://www.ncbi.nlm.nih.gov/pubmed/27013786
http://dx.doi.org/10.4103/0973-1296.172945
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author Shankar, Kripa
Singh, Sumit K.
Kumar, Durgesh
Varshney, Salil
Gupta, Abhishek
Rajan, Sujith
Srivastava, Ankita
Beg, Muheeb
Srivastava, Anurag Kumar
Kanojiya, Sanjeev
Mishra, Dipak K.
Gaikwad, Anil N.
author_facet Shankar, Kripa
Singh, Sumit K.
Kumar, Durgesh
Varshney, Salil
Gupta, Abhishek
Rajan, Sujith
Srivastava, Ankita
Beg, Muheeb
Srivastava, Anurag Kumar
Kanojiya, Sanjeev
Mishra, Dipak K.
Gaikwad, Anil N.
author_sort Shankar, Kripa
collection PubMed
description BACKGROUND: Cucumis melo ssp. agrestis var. agrestis (CMA) is a wild variety of C. melo. This study aimed to explore anti-dyslipidemic and anti-adipogenic potential of CMA. MATERIALS AND METHODS: For initial anti-dyslipidemic and antihyperglycemic potential of CMA fruit extract (CMFE), male Syrian golden hamsters were fed a chow or high-fat diet with or without CMFE (100 mg/kg). Further, we did fractionation of this CMFE into two fractions namely; CMA water fraction (CMWF) and CMA hexane fraction (CMHF). Phytochemical screening was done with liquid chromatography-mass spectrometry LC- (MS)/MS and direct analysis in real time-MS to detect active compounds in the fractions. Further, high-fat diet fed dyslipidemic hamsters were treated with CMWF and CMHF at 50 mg/kg for 7 days. RESULTS: Oral administration of CMFE and both fractions (CMWF and CMHF) reduced the total cholesterol, triglycerides, low‐density lipoprotein cholesterol, and very low‐density lipoprotein-cholesterol levels in high fat diet-fed dyslipidemic hamsters. CMHF also modulated expression of genes involved in lipogenesis, lipid metabolism, and reverse cholesterol transport. Standard biochemical diagnostic tests suggested that neither of fractions causes any toxicity to hamster liver or kidneys. CMFE and CMHF also decreased oil-red-O accumulation in 3T3-L1 adipocytes. CONCLUSION: Based on these results, it is concluded that CMA possesses anti-dyslipidemic and anti-hyperglycemic activity along with the anti-adipogenic activity. SUMMARY: The oral administration of Cucumis melo agrestis fruit extract (CMFE) and its fractions (CMWF and CMHF) improved serum lipid profile in HFD fed dyslipidemic hamsters. CMFE, CMWF and CMHF significantly attenuated body weight gain and eWAT hypertrophy. The CMHF decreased lipogenesis in both liver and adipose tissue. CMFE and CMHF also inhibited adipogenesis in 3T3-L1 adipocytes. [Image: see text] Abbreviation used: CMA: Cucumis melo ssp. agrestis var. agrestis, CMFE: CMA fruit extract, CMWF: CMA water fraction, CMHF: CMA hexane fraction, FAS: Fatty acid synthase, SREBP1c: Sterol regulatory element binding protein 1c, ACC: Acetyl CoA carboxylase, LXR α: Liver X receptor α.
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spelling pubmed-47870802016-03-24 Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes Shankar, Kripa Singh, Sumit K. Kumar, Durgesh Varshney, Salil Gupta, Abhishek Rajan, Sujith Srivastava, Ankita Beg, Muheeb Srivastava, Anurag Kumar Kanojiya, Sanjeev Mishra, Dipak K. Gaikwad, Anil N. Pharmacogn Mag Original Article BACKGROUND: Cucumis melo ssp. agrestis var. agrestis (CMA) is a wild variety of C. melo. This study aimed to explore anti-dyslipidemic and anti-adipogenic potential of CMA. MATERIALS AND METHODS: For initial anti-dyslipidemic and antihyperglycemic potential of CMA fruit extract (CMFE), male Syrian golden hamsters were fed a chow or high-fat diet with or without CMFE (100 mg/kg). Further, we did fractionation of this CMFE into two fractions namely; CMA water fraction (CMWF) and CMA hexane fraction (CMHF). Phytochemical screening was done with liquid chromatography-mass spectrometry LC- (MS)/MS and direct analysis in real time-MS to detect active compounds in the fractions. Further, high-fat diet fed dyslipidemic hamsters were treated with CMWF and CMHF at 50 mg/kg for 7 days. RESULTS: Oral administration of CMFE and both fractions (CMWF and CMHF) reduced the total cholesterol, triglycerides, low‐density lipoprotein cholesterol, and very low‐density lipoprotein-cholesterol levels in high fat diet-fed dyslipidemic hamsters. CMHF also modulated expression of genes involved in lipogenesis, lipid metabolism, and reverse cholesterol transport. Standard biochemical diagnostic tests suggested that neither of fractions causes any toxicity to hamster liver or kidneys. CMFE and CMHF also decreased oil-red-O accumulation in 3T3-L1 adipocytes. CONCLUSION: Based on these results, it is concluded that CMA possesses anti-dyslipidemic and anti-hyperglycemic activity along with the anti-adipogenic activity. SUMMARY: The oral administration of Cucumis melo agrestis fruit extract (CMFE) and its fractions (CMWF and CMHF) improved serum lipid profile in HFD fed dyslipidemic hamsters. CMFE, CMWF and CMHF significantly attenuated body weight gain and eWAT hypertrophy. The CMHF decreased lipogenesis in both liver and adipose tissue. CMFE and CMHF also inhibited adipogenesis in 3T3-L1 adipocytes. [Image: see text] Abbreviation used: CMA: Cucumis melo ssp. agrestis var. agrestis, CMFE: CMA fruit extract, CMWF: CMA water fraction, CMHF: CMA hexane fraction, FAS: Fatty acid synthase, SREBP1c: Sterol regulatory element binding protein 1c, ACC: Acetyl CoA carboxylase, LXR α: Liver X receptor α. Medknow Publications & Media Pvt Ltd 2015-10 /pmc/articles/PMC4787080/ /pubmed/27013786 http://dx.doi.org/10.4103/0973-1296.172945 Text en Copyright: © 2015 Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Shankar, Kripa
Singh, Sumit K.
Kumar, Durgesh
Varshney, Salil
Gupta, Abhishek
Rajan, Sujith
Srivastava, Ankita
Beg, Muheeb
Srivastava, Anurag Kumar
Kanojiya, Sanjeev
Mishra, Dipak K.
Gaikwad, Anil N.
Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title_full Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title_fullStr Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title_full_unstemmed Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title_short Cucumis melo ssp. Agrestis var. Agrestis Ameliorates High Fat Diet Induced Dyslipidemia in Syrian Golden Hamsters and Inhibits Adipogenesis in 3T3-L1 Adipocytes
title_sort cucumis melo ssp. agrestis var. agrestis ameliorates high fat diet induced dyslipidemia in syrian golden hamsters and inhibits adipogenesis in 3t3-l1 adipocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787080/
https://www.ncbi.nlm.nih.gov/pubmed/27013786
http://dx.doi.org/10.4103/0973-1296.172945
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