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Bitter melon protects against ER stress in LS174T colonic epithelial cells
Kunde, DA and Chong, WC and Nerurkar, PV and Ahuja, KDK and Just, J and Smith, JA and Guven, N and Eri, RD, Bitter melon protects against ER stress in LS174T colonic epithelial cells, BMC Alternative Medicine, 17 Article 2. ISSN 1472-6882 (2017) [Refereed Article]
© The Author(s). 2017 Licensed under Creative Commons Attribution 4.0 International (CC BY 4.0) https://creativecommons.org/licenses/by/4.0/
Background: Bitter Melon (BM) has been used as a functional food in traditional Chinese and Indian medicine for many generations and has gained a great deal of attention due to its apparent benefits in moderating some of the pathogenic processes in a variety of inflammatory conditions. BM extract (BME) has been shown to possess strong anti-oxidant properties. In addition, it can ameliorate oxidative stress and potentially ER stress. There is increasing evidence that oxidative and ER stress are major contributors for intestinal secretory cell dysfunction which leads to local inflammation and disease pathogenesis that are hallmarks of inflammatory bowel diseases (IBD). Hence, the search for potential therapeutics against ER stress and oxidative stress in intestinal epithelial secretory cells may provide valuable resources for the management of IBD. The aim of the present study was to investigate the effects of BME in ameliorating ER stress in colonic epithelial cells.
Methods: Human colonic adenocarcinoma LS174T cells were used for the assessment of BME effects on colonic epithelial cells in vitro. Cell viability was assessed using trypan blue exclusion and the effect of BME in ameliorating tunicamycin (TM)-induced ER stress was determined by analysing the mRNA expression of the common ER stress markers; ATF6, XBP1, GRP78, CHOP and PERK by quantitative RT-PCR and GRP78 and CHOP by western blot.
Results: In the absence of ER stress, BME exhibited no cell toxicity up to 2.0% w/v and no significant effect on the basal mRNA expression of ER stress markers in LS174T cells. In contrast, pre-treatment of LS174T cells with BME followed by induction of ER stress resulted in a significant decrease in mRNA expression of ATF6, XBP1, GRP78, CHOP and PERK and protein expression of GRP78 and CHOP. Co-treatment during induction of ER stress and posttreatment following induction of ER Stress in LS174T cells resulted in a lower but still significant reduction in mRNA expression levels of most ER stress markers.
Conclusions: This is one of the first studies demonstrating the efficacy of BME in reducing expression of ER stress markers in colonic epithelial cells suggesting the potential of BME as a dietary intervention in ameliorating ER stress and oxidation in IBD. Interestingly, while the most significant effect was seen with pre-treatment of cells with BME there was a reduced but still significant effect when co-treated or even post-treated. This suggests that BME may even be effective in modulating ER stress in the face of an existing cell stress environment.
|Item Type:||Refereed Article|
|Keywords:||inflammatory bowel disease, intestinal secretory cells, endoplasmic reticulum stress, oxidative stress, unfolded protein responses, bitter melon|
|Research Division:||Health Sciences|
|Research Group:||Traditional, complementary and integrative medicine|
|Research Field:||Traditional, complementary and integrative medicine not elsewhere classified|
|Objective Group:||Public health (excl. specific population health)|
|Objective Field:||Preventive medicine|
|UTAS Author:||Kunde, DA (Dr Dale Kunde)|
|UTAS Author:||Chong, WC (Mr Wai Chong)|
|UTAS Author:||Ahuja, KDK (Dr Kiran Ahuja)|
|UTAS Author:||Just, J (Mr Jeremy Just)|
|UTAS Author:||Smith, JA (Professor Jason Smith)|
|UTAS Author:||Guven, N (Dr Nuri Guven)|
|UTAS Author:||Eri, RD (Associate Professor Raj Eri)|
|Web of Science® Times Cited:||11|
|Deposited By:||Health Sciences|
|Downloads:||133 View Download Statistics|
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