Bioprocessing shrimp shells to rat intestinal α- glucosidase inhibitor and its effect on reducing blood glucose in a mouse model

doi:10.1007/s11164-019-03869-2

淡江大學機構典藏 > 理學院 > 化學學系暨研究所 > 期刊論文 > Item 987654321/117141

請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/117141

題名:	Bioprocessing shrimp shells to rat intestinal α- glucosidase inhibitor and its effect on reducing blood glucose in a mouse model
作者:	VB, Nguyen;TH, Nguyen;AD, Nguyen;Le, T;YH, Kuo;SL, Wang
關鍵詞:	Shrimp shells;α-Glucosidase inhibitors;Anti-cancer;Diabetes;Process biochemistry
日期:	2019
上傳時間:	2019-09-26 12:10:59 (UTC+8)
出版者:	Springers
摘要:	The α-Glucosidase inhibitors (aGIs) from natural resources have been recognized as a safe and efficacious way to manage type 2 diabetes—an ongoing global health problem. The objective of this study was to synthesize aGIs from demineralized shrimp shell powder (deSSP), a low-cost fishery processing by-product, via microbial fermentation. Its effect on reducing plasma glucose in an ICR mouse model was then evaluated, and its other beneficial bioactivities investigated. Among the various marine chitinous materials, fermented deSSP (fdeSSP) via Paenibacillus conversion demonstrated potent inhibition against rat intestinal α-glucosidase that was comparable to acarbose, a commercial anti-diabetic drug, with max inhibition and IC50 values 87% and 120 μg/mL, and 89% and 110 μg/mL, respectively. After optimization of the fermentation process, activity increased 1.52-fold (2500–3800 U/ mL). By comparing the HPLC fingerprints and bioactivity of fermented and unfermented deSSP, it was confirmed that aGIs were produced as they were not present in the deSSP medium prior to fermentation. In animal tests, at a dose of 100 mg/kg bw, fdeSSP significantly reduced plasma glucose in ICR mice with no signs of diarrhea. The fdeSSP also demonstrated acceptable antioxidant activity ( IC50 = 250 μg/ mL) and potential anti-NO activity (70.08 μg/mL). Though not toxic to normal cells, fdeSSP reduced the viability of some cancer cells, including A549, Hep G2, MCF-7 and WIDR with inhibition values of 78%, 71%, 45% and 35%, respectively. The results above suggest that fdeSSP may be a good candidate for development as a health food or drug, due to its potential hypoglycemic and added value bioactivities.
關聯:	Research on Chemical Intermediates 45(10), p.4829-4846
DOI:	10.1007/s11164-019-03869-2
顯示於類別:	[化學學系暨研究所] 期刊論文

文件中的檔案:

檔案	描述	大小	格式	瀏覽次數
index.html		0Kb	HTML	162	檢視/開啟

在機構典藏中所有的資料項目都受到原著作權保護.

TAIR相關文章

資料載入中.....