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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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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 |
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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 |
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