Cargando…

Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression

BACKGROUND: DLBS3233 is a standardized extract combination containing Lagerstroemia speciosa and Cinnamomum burmannii. The effect of DLBS3233 on glucose uptake, adiponectin secretion, and insulin signaling was examined in this study. METHODS: 3T3 Swiss albino preadipocytes and adipocytes were used t...

Descripción completa

Detalles Bibliográficos
Autores principales: Tandrasasmita, Olivia Mayasari, Wulan, Deasy Diah, Nailufar, Florensia, Sinambela, James, Tjandrawinata, Raymond Rubianto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108202/
https://www.ncbi.nlm.nih.gov/pubmed/21674027
http://dx.doi.org/10.2147/IJGM.S16517
_version_ 1782205284910891008
author Tandrasasmita, Olivia Mayasari
Wulan, Deasy Diah
Nailufar, Florensia
Sinambela, James
Tjandrawinata, Raymond Rubianto
author_facet Tandrasasmita, Olivia Mayasari
Wulan, Deasy Diah
Nailufar, Florensia
Sinambela, James
Tjandrawinata, Raymond Rubianto
author_sort Tandrasasmita, Olivia Mayasari
collection PubMed
description BACKGROUND: DLBS3233 is a standardized extract combination containing Lagerstroemia speciosa and Cinnamomum burmannii. The effect of DLBS3233 on glucose uptake, adiponectin secretion, and insulin signaling was examined in this study. METHODS: 3T3 Swiss albino preadipocytes and adipocytes were used to investigate gene expression detected using the reverse transcription polymerase chain reaction method. Immunoblotting assay and in vitro glucose uptake assay were also carried out in the experiment. RESULTS: DLBS3233 was seen to increase phosphorylation at the tyrosine residue of the insulin receptor substrate. DLBS3233 was also found to enhance the expression of genes associated with increased insulin signaling and sensitivity, such as peroxisome proliferator-activated receptor gamma, phosphatidylinositol-3 kinase, Akt, and glucose transporter 4. In addition, glucose transporter 4 protein levels were seen to increase as a result of DLBS3233 administration. The combination of extracts also increased glucose uptake and adiponectin secretion, and decreased resistin secretion significantly relative to control cells. Moreover, DLBS3233 administered to insulin-resistant Wistar rats showed an ability to control blood sugar, insulin levels, and other lipoproteins, including high-density lipoprotein, low-density lipoprotein, triglycerides, and total cholesterol. CONCLUSION: DLBS3233, as a combination of herbal extracts, holds promise in the treatment of type 2 diabetes, and possibly also in prevention of the disease.
format Online
Article
Text
id pubmed-3108202
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-31082022011-06-13 Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression Tandrasasmita, Olivia Mayasari Wulan, Deasy Diah Nailufar, Florensia Sinambela, James Tjandrawinata, Raymond Rubianto Int J Gen Med Original Research BACKGROUND: DLBS3233 is a standardized extract combination containing Lagerstroemia speciosa and Cinnamomum burmannii. The effect of DLBS3233 on glucose uptake, adiponectin secretion, and insulin signaling was examined in this study. METHODS: 3T3 Swiss albino preadipocytes and adipocytes were used to investigate gene expression detected using the reverse transcription polymerase chain reaction method. Immunoblotting assay and in vitro glucose uptake assay were also carried out in the experiment. RESULTS: DLBS3233 was seen to increase phosphorylation at the tyrosine residue of the insulin receptor substrate. DLBS3233 was also found to enhance the expression of genes associated with increased insulin signaling and sensitivity, such as peroxisome proliferator-activated receptor gamma, phosphatidylinositol-3 kinase, Akt, and glucose transporter 4. In addition, glucose transporter 4 protein levels were seen to increase as a result of DLBS3233 administration. The combination of extracts also increased glucose uptake and adiponectin secretion, and decreased resistin secretion significantly relative to control cells. Moreover, DLBS3233 administered to insulin-resistant Wistar rats showed an ability to control blood sugar, insulin levels, and other lipoproteins, including high-density lipoprotein, low-density lipoprotein, triglycerides, and total cholesterol. CONCLUSION: DLBS3233, as a combination of herbal extracts, holds promise in the treatment of type 2 diabetes, and possibly also in prevention of the disease. Dove Medical Press 2011-05-03 /pmc/articles/PMC3108202/ /pubmed/21674027 http://dx.doi.org/10.2147/IJGM.S16517 Text en © 2011 Tandrasasmita et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Tandrasasmita, Olivia Mayasari
Wulan, Deasy Diah
Nailufar, Florensia
Sinambela, James
Tjandrawinata, Raymond Rubianto
Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title_full Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title_fullStr Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title_full_unstemmed Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title_short Glucose-lowering effect of DLBS3233 is mediated through phosphorylation of tyrosine and upregulation of PPARγ and GLUT4 expression
title_sort glucose-lowering effect of dlbs3233 is mediated through phosphorylation of tyrosine and upregulation of pparγ and glut4 expression
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108202/
https://www.ncbi.nlm.nih.gov/pubmed/21674027
http://dx.doi.org/10.2147/IJGM.S16517
work_keys_str_mv AT tandrasasmitaoliviamayasari glucoseloweringeffectofdlbs3233ismediatedthroughphosphorylationoftyrosineandupregulationofppargandglut4expression
AT wulandeasydiah glucoseloweringeffectofdlbs3233ismediatedthroughphosphorylationoftyrosineandupregulationofppargandglut4expression
AT nailufarflorensia glucoseloweringeffectofdlbs3233ismediatedthroughphosphorylationoftyrosineandupregulationofppargandglut4expression
AT sinambelajames glucoseloweringeffectofdlbs3233ismediatedthroughphosphorylationoftyrosineandupregulationofppargandglut4expression
AT tjandrawinataraymondrubianto glucoseloweringeffectofdlbs3233ismediatedthroughphosphorylationoftyrosineandupregulationofppargandglut4expression