Cargando…

Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis

OBJECTIVE(S): This study aims to evaluate the activity of mangosteen peels extract (MPE) as protection agent on induced-glucose mesangial cells (SV40 MES 13 cell line (Glomerular Mesangial Kidney, Mus Musculus)). MATERIALS AND METHODS: MPE was performed based on maceration method. Cytotoxic assay wa...

Descripción completa

Detalles Bibliográficos
Autores principales: Widowati, Wahyu, Laksmitawati, Dian Ratih, Wargasetia, Teresa Liliana, Afifah, Ervi, Amalia, Annisa, Arinta, Yukko, Rizal, Rizal, Suciati, Tri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272065/
https://www.ncbi.nlm.nih.gov/pubmed/30524699
http://dx.doi.org/10.22038/IJBMS.2018.29349.7094
_version_ 1783377072795680768
author Widowati, Wahyu
Laksmitawati, Dian Ratih
Wargasetia, Teresa Liliana
Afifah, Ervi
Amalia, Annisa
Arinta, Yukko
Rizal, Rizal
Suciati, Tri
author_facet Widowati, Wahyu
Laksmitawati, Dian Ratih
Wargasetia, Teresa Liliana
Afifah, Ervi
Amalia, Annisa
Arinta, Yukko
Rizal, Rizal
Suciati, Tri
author_sort Widowati, Wahyu
collection PubMed
description OBJECTIVE(S): This study aims to evaluate the activity of mangosteen peels extract (MPE) as protection agent on induced-glucose mesangial cells (SV40 MES 13 cell line (Glomerular Mesangial Kidney, Mus Musculus)). MATERIALS AND METHODS: MPE was performed based on maceration method. Cytotoxic assay was performed based on MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) method, while the level of TGF-β1 (Transforming growth factor-β1) and fibronectin in glucose-induced mesangial cells were assayed and determined using ELISA KIT. RESULTS: In viability assay, MPE 5 and 20 µg/ml has the highest activity to increase cells proliferation in glucose-induced mesangial cells at 5, 10, and 15 days of incubation in glucose concentration (5 and 25 mM) (P<0.05). In inhibitory activity of TGF-β1 and fibronectin level, MPE 5 µg/ml (glucose-induced 5 mM) show the lowest level compared to positive control and other treatments (P<0.05). CONCLUSION: MPE can increase cell proliferation in glucose-induced mesangial cells and significantly reduce the level of TGF-β1 and fibronectin. MPE activity has correlates to inhibit the diabetic glomerulosclerosis condition and may increase mesangial cell proliferation.
format Online
Article
Text
id pubmed-6272065
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Mashhad University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-62720652018-12-06 Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis Widowati, Wahyu Laksmitawati, Dian Ratih Wargasetia, Teresa Liliana Afifah, Ervi Amalia, Annisa Arinta, Yukko Rizal, Rizal Suciati, Tri Iran J Basic Med Sci Short Communication OBJECTIVE(S): This study aims to evaluate the activity of mangosteen peels extract (MPE) as protection agent on induced-glucose mesangial cells (SV40 MES 13 cell line (Glomerular Mesangial Kidney, Mus Musculus)). MATERIALS AND METHODS: MPE was performed based on maceration method. Cytotoxic assay was performed based on MTS (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) method, while the level of TGF-β1 (Transforming growth factor-β1) and fibronectin in glucose-induced mesangial cells were assayed and determined using ELISA KIT. RESULTS: In viability assay, MPE 5 and 20 µg/ml has the highest activity to increase cells proliferation in glucose-induced mesangial cells at 5, 10, and 15 days of incubation in glucose concentration (5 and 25 mM) (P<0.05). In inhibitory activity of TGF-β1 and fibronectin level, MPE 5 µg/ml (glucose-induced 5 mM) show the lowest level compared to positive control and other treatments (P<0.05). CONCLUSION: MPE can increase cell proliferation in glucose-induced mesangial cells and significantly reduce the level of TGF-β1 and fibronectin. MPE activity has correlates to inhibit the diabetic glomerulosclerosis condition and may increase mesangial cell proliferation. Mashhad University of Medical Sciences 2018-09 /pmc/articles/PMC6272065/ /pubmed/30524699 http://dx.doi.org/10.22038/IJBMS.2018.29349.7094 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Widowati, Wahyu
Laksmitawati, Dian Ratih
Wargasetia, Teresa Liliana
Afifah, Ervi
Amalia, Annisa
Arinta, Yukko
Rizal, Rizal
Suciati, Tri
Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title_full Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title_fullStr Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title_full_unstemmed Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title_short Mangosteen peel extract (Garcinia mangostana L.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
title_sort mangosteen peel extract (garcinia mangostana l.) as protective agent in glucose-induced mesangial cell as in vitro model of diabetic glomerulosclerosis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272065/
https://www.ncbi.nlm.nih.gov/pubmed/30524699
http://dx.doi.org/10.22038/IJBMS.2018.29349.7094
work_keys_str_mv AT widowatiwahyu mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT laksmitawatidianratih mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT wargasetiateresaliliana mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT afifahervi mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT amaliaannisa mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT arintayukko mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT rizalrizal mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis
AT suciatitri mangosteenpeelextractgarciniamangostanalasprotectiveagentinglucoseinducedmesangialcellasinvitromodelofdiabeticglomerulosclerosis