Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells

Diabetes has been one of the top ten causes of death in Malaysia. Recently, the oil palm Elaeis guineensis has been explored in several antidiabetic studies. Nevertheless, the oil palm fruit has never been investigated for its antidiabetic effect. Therefore, this study was conducted to evaluate the...

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Main Authors: Sharif, Faez, Hamid, Muhajir, Ismail, Amin, Adam, Zainah
Format: Article
Language:English
Published: Nutrition Society of Malaysia 2015
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Online Access:http://irep.iium.edu.my/43309/1/P75-82_MohdFaez.pdf
http://irep.iium.edu.my/43309/
http://www.nutriweb.org.my/publications/mjn0021_1/P75-82%20MohdFaez.php
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spelling my.iium.irep.433092017-08-08T04:02:27Z http://irep.iium.edu.my/43309/ Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells Sharif, Faez Hamid, Muhajir Ismail, Amin Adam, Zainah Q Science (General) Diabetes has been one of the top ten causes of death in Malaysia. Recently, the oil palm Elaeis guineensis has been explored in several antidiabetic studies. Nevertheless, the oil palm fruit has never been investigated for its antidiabetic effect. Therefore, this study was conducted to evaluate the antidiabetic properties of oil palm fruit which specifically focusing on its effects in stimulating insulin secretion from pancreatic ß cell. The insulinotropic activity of oil palm fruit aqueous extract (OPF) on clonal pancreatic ß cell line was investigated using BRIN BD11 cell line. The cell lines were incubated with different concentrations of OPF to evaluate the stimulatory effect of OPF toward insulin secretion from BRIN BD11 cells using the Rat Insulin ELISA Assay Kits. OPF (100-1000µg/ml) were shown to significantly induce insulin secretion by a multiple of 1.97-2.58 in the BRIN BD11 cells. The highest insulin secretion increase (2.58-fold, p<0.001) was induced by 500 µg/ml in the OPF treated group. Evaluation of the possible mechanisms involved suggested that the mechanisms of insulin secreting activity of the 500 µg/ml OPF extract may involve the K+ATP channel-dependent pathway which exerts an insulin secretion effect through depolarizing the membrane of pancreatic-ß cells. The present study has revealed the presence of insulinotropic activity in Elaeis guineensis fruit. Future work assessing its use as a source of active components may provide new opportunities for the treatment of diabetes which are safe, efficient and exert a lesser amount of side effects. Nutrition Society of Malaysia 2015-04 Article REM application/pdf en http://irep.iium.edu.my/43309/1/P75-82_MohdFaez.pdf Sharif, Faez and Hamid, Muhajir and Ismail, Amin and Adam, Zainah (2015) Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells. Malaysian Journal of Nutrition, 21 (1). pp. 75-82. ISSN 1394-035X http://www.nutriweb.org.my/publications/mjn0021_1/P75-82%20MohdFaez.php
institution Universiti Islam Antarabangsa Malaysia
building IIUM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider International Islamic University Malaysia
content_source IIUM Repository (IREP)
url_provider http://irep.iium.edu.my/
language English
topic Q Science (General)
spellingShingle Q Science (General)
Sharif, Faez
Hamid, Muhajir
Ismail, Amin
Adam, Zainah
Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
description Diabetes has been one of the top ten causes of death in Malaysia. Recently, the oil palm Elaeis guineensis has been explored in several antidiabetic studies. Nevertheless, the oil palm fruit has never been investigated for its antidiabetic effect. Therefore, this study was conducted to evaluate the antidiabetic properties of oil palm fruit which specifically focusing on its effects in stimulating insulin secretion from pancreatic ß cell. The insulinotropic activity of oil palm fruit aqueous extract (OPF) on clonal pancreatic ß cell line was investigated using BRIN BD11 cell line. The cell lines were incubated with different concentrations of OPF to evaluate the stimulatory effect of OPF toward insulin secretion from BRIN BD11 cells using the Rat Insulin ELISA Assay Kits. OPF (100-1000µg/ml) were shown to significantly induce insulin secretion by a multiple of 1.97-2.58 in the BRIN BD11 cells. The highest insulin secretion increase (2.58-fold, p<0.001) was induced by 500 µg/ml in the OPF treated group. Evaluation of the possible mechanisms involved suggested that the mechanisms of insulin secreting activity of the 500 µg/ml OPF extract may involve the K+ATP channel-dependent pathway which exerts an insulin secretion effect through depolarizing the membrane of pancreatic-ß cells. The present study has revealed the presence of insulinotropic activity in Elaeis guineensis fruit. Future work assessing its use as a source of active components may provide new opportunities for the treatment of diabetes which are safe, efficient and exert a lesser amount of side effects.
format Article
author Sharif, Faez
Hamid, Muhajir
Ismail, Amin
Adam, Zainah
author_facet Sharif, Faez
Hamid, Muhajir
Ismail, Amin
Adam, Zainah
author_sort Sharif, Faez
title Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
title_short Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
title_full Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
title_fullStr Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
title_full_unstemmed Effects of oil palm (Elaeis guineensis) fruit extracts on insulin secretion from BRIN BD11 cells
title_sort effects of oil palm (elaeis guineensis) fruit extracts on insulin secretion from brin bd11 cells
publisher Nutrition Society of Malaysia
publishDate 2015
url http://irep.iium.edu.my/43309/1/P75-82_MohdFaez.pdf
http://irep.iium.edu.my/43309/
http://www.nutriweb.org.my/publications/mjn0021_1/P75-82%20MohdFaez.php
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score 13.160551