Cargando…

Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line

BACKGROUND: Triphala, an Ayurvedic polyherbal formulation, is used for the treatment of various diseases including obesity. OBJECTIVE: The present study was planned to evaluate the anti-adipogenic potential of aqueous extract of Triphala (TP(aq)) using 3T3-L1 adipocyte cell line model. METHODS: The...

Descripción completa

Detalles Bibliográficos
Autores principales: Banjare, Jyotibala, Raina, Prerna, Mansara, Prakash, Ghanekar, Ruchika Kaul, Bhalerao, Supriya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822508/
https://www.ncbi.nlm.nih.gov/pubmed/29491641
http://dx.doi.org/10.4103/pm.pm_153_17
_version_ 1783301699419504640
author Banjare, Jyotibala
Raina, Prerna
Mansara, Prakash
Ghanekar, Ruchika Kaul
Bhalerao, Supriya
author_facet Banjare, Jyotibala
Raina, Prerna
Mansara, Prakash
Ghanekar, Ruchika Kaul
Bhalerao, Supriya
author_sort Banjare, Jyotibala
collection PubMed
description BACKGROUND: Triphala, an Ayurvedic polyherbal formulation, is used for the treatment of various diseases including obesity. OBJECTIVE: The present study was planned to evaluate the anti-adipogenic potential of aqueous extract of Triphala (TP(aq)) using 3T3-L1 adipocyte cell line model. METHODS: The effect of aqueous extract of Triphala (TP(aq)) was tested on the viability of 3T3- L1 cells by MTT assay. The cells were treated with a cocktail of dexamethasone (DEX), isobutylmethylxanthine (IBMX) and insulin to induce adipogenesis. The cells were treated either with the induction cocktail or with the cocktail containing different concentrations (1, 10 and100 μg/ml) of TP(aq). Intracellular lipid content was analyzed using Oil O Red stain and was quantified after extracting with isopropanol at 500 nm wavelength. The expression of early (PPAR-γ and C/EBP-α) and late (GLUT4 and FAS) phase adipogenic genes was studied by real time PCR. RESULTS: TP(aq) did not affect the viability of 3T3-L1 cell line. Interestingly, TP(aq) induced a concentration dependant decrease in the intracellular lipid content and expression of both early and late phase adipogenic genes. This decrease was statistically significant compared to cells treated with only induction cocktail. CONCLUSION: These results suggested that Triphala regulated lipid accumulation by down regulating expression of adipogenic genes, resulting into prevention of adipogenesis. SUMMARY: The purpose of this study was to evaluate the effect of an ayurvedic polyherbal drug Triphala on adipogenesis using 3T3-L1 cell line. The results suggested that Triphala regulated lipid accumulation by downregulating expression of adipogenic genes, resulting into the prevention of adipogenesis. Abbreviations used: TP(aq): Aqueous extract of Triphala; DMEM: Dulbecco's Modified Eagle's medium; FBS: Fetal Bovine Serum; IBMX: Isobutyl methylxanthine; DMX: Dexamethasone; MTT: [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide] assay; PPARγ: Peroxisome proliferator-activated receptor; C/EBP:Enhancer binding protein α, FAS:Fatty acid synthase; Glut-4: Glucose phosphate transporter 4.
format Online
Article
Text
id pubmed-5822508
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-58225082018-02-28 Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line Banjare, Jyotibala Raina, Prerna Mansara, Prakash Ghanekar, Ruchika Kaul Bhalerao, Supriya Pharmacogn Mag Original Article BACKGROUND: Triphala, an Ayurvedic polyherbal formulation, is used for the treatment of various diseases including obesity. OBJECTIVE: The present study was planned to evaluate the anti-adipogenic potential of aqueous extract of Triphala (TP(aq)) using 3T3-L1 adipocyte cell line model. METHODS: The effect of aqueous extract of Triphala (TP(aq)) was tested on the viability of 3T3- L1 cells by MTT assay. The cells were treated with a cocktail of dexamethasone (DEX), isobutylmethylxanthine (IBMX) and insulin to induce adipogenesis. The cells were treated either with the induction cocktail or with the cocktail containing different concentrations (1, 10 and100 μg/ml) of TP(aq). Intracellular lipid content was analyzed using Oil O Red stain and was quantified after extracting with isopropanol at 500 nm wavelength. The expression of early (PPAR-γ and C/EBP-α) and late (GLUT4 and FAS) phase adipogenic genes was studied by real time PCR. RESULTS: TP(aq) did not affect the viability of 3T3-L1 cell line. Interestingly, TP(aq) induced a concentration dependant decrease in the intracellular lipid content and expression of both early and late phase adipogenic genes. This decrease was statistically significant compared to cells treated with only induction cocktail. CONCLUSION: These results suggested that Triphala regulated lipid accumulation by down regulating expression of adipogenic genes, resulting into prevention of adipogenesis. SUMMARY: The purpose of this study was to evaluate the effect of an ayurvedic polyherbal drug Triphala on adipogenesis using 3T3-L1 cell line. The results suggested that Triphala regulated lipid accumulation by downregulating expression of adipogenic genes, resulting into the prevention of adipogenesis. Abbreviations used: TP(aq): Aqueous extract of Triphala; DMEM: Dulbecco's Modified Eagle's medium; FBS: Fetal Bovine Serum; IBMX: Isobutyl methylxanthine; DMX: Dexamethasone; MTT: [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide] assay; PPARγ: Peroxisome proliferator-activated receptor; C/EBP:Enhancer binding protein α, FAS:Fatty acid synthase; Glut-4: Glucose phosphate transporter 4. Medknow Publications & Media Pvt Ltd 2017 2018-01-31 /pmc/articles/PMC5822508/ /pubmed/29491641 http://dx.doi.org/10.4103/pm.pm_153_17 Text en Copyright: © 2018 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
Banjare, Jyotibala
Raina, Prerna
Mansara, Prakash
Ghanekar, Ruchika Kaul
Bhalerao, Supriya
Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title_full Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title_fullStr Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title_full_unstemmed Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title_short Triphala, Regulates Adipogenesis through Modulation of Expression of Adipogenic Genes in 3T3-L1 Cell Line
title_sort triphala, regulates adipogenesis through modulation of expression of adipogenic genes in 3t3-l1 cell line
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5822508/
https://www.ncbi.nlm.nih.gov/pubmed/29491641
http://dx.doi.org/10.4103/pm.pm_153_17
work_keys_str_mv AT banjarejyotibala triphalaregulatesadipogenesisthroughmodulationofexpressionofadipogenicgenesin3t3l1cellline
AT rainaprerna triphalaregulatesadipogenesisthroughmodulationofexpressionofadipogenicgenesin3t3l1cellline
AT mansaraprakash triphalaregulatesadipogenesisthroughmodulationofexpressionofadipogenicgenesin3t3l1cellline
AT ghanekarruchikakaul triphalaregulatesadipogenesisthroughmodulationofexpressionofadipogenicgenesin3t3l1cellline
AT bhaleraosupriya triphalaregulatesadipogenesisthroughmodulationofexpressionofadipogenicgenesin3t3l1cellline