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.的水提取物的抗炎和抗胰岛素抵抗活性

Anti-inflammatory and anti-insulin resistance activities of aqueous extract from .

作者信息

Budluang Phatcharaporn, Pitchakarn Pornsiri, Ting Pisamai, Temviriyanukul Piya, Wongnoppawich Ariyaphong, Imsumran Arisa

机构信息

Department of Biochemistry Faculty of Medicine Chiang Mai University Meung Chiang Mai Thailand.

Food and Nutritional Toxicology Unit Institute of Nutrition Mahidol University Salaya Nakhon Pathom Thailand.

出版信息

Food Sci Nutr. 2016 Aug 26;5(3):486-496. doi: 10.1002/fsn3.416. eCollection 2017 May.

DOI:10.1002/fsn3.416
PMID:28572933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5449198/
Abstract

This study investigated biological activities including antioxidative stress, anti-inflammation, and anti-insulin resistance of aqueous extract (ABE). The results showed abilities of ABE to scavenging DPPH and ABTS free radicals in a dose-dependent manner. Besides, ABE significantly reduced nitric oxide (NO) production in the lipopolysaccharide (LPS)-treated RAW 264.7 via inhibition of mRNA and protein expressions of nitric oxide synthase (iNOS). The LPS-induced mRNA expressions of cyclooxygenase-2 (COX-2) and interleukin 1β (IL-1β) were suppressed by ABE. Moreover, ABE exerted anti-insulin resistance activity as it significantly improved the glucose uptake in tumor necrosis factor (TNF)-α treated 3T3-L1 adipocytes. In addition, ABE at the concentration of up to 200 μg/mL was not toxic to human peripheral blood mononuclear cells (PBMCs) and did not induce mutations. Finally, the results of our study suggest the potential use of as anti-inflammatory, anti-insulin resistance agents, or food supplement for prevention of chronic diseases.

摘要

本研究调查了水提取物(ABE)的生物活性,包括抗氧化应激、抗炎和抗胰岛素抵抗。结果表明,ABE具有以剂量依赖性方式清除DPPH和ABTS自由基的能力。此外,ABE通过抑制一氧化氮合酶(iNOS)的mRNA和蛋白质表达,显著降低了脂多糖(LPS)处理的RAW 264.7细胞中一氧化氮(NO)的产生。LPS诱导的环氧化酶-2(COX-2)和白细胞介素1β(IL-1β)的mRNA表达受到ABE的抑制。此外,ABE具有抗胰岛素抵抗活性,因为它显著改善了肿瘤坏死因子(TNF)-α处理的3T3-L1脂肪细胞中的葡萄糖摄取。此外,浓度高达200μg/mL的ABE对人外周血单个核细胞(PBMCs)无毒,也不诱导突变。最后,我们的研究结果表明,ABE有潜力用作抗炎、抗胰岛素抵抗药物或预防慢性病的食品补充剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/9d2be86cf064/FSN3-5-486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/cfb14881b20a/FSN3-5-486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/202a97aefe32/FSN3-5-486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/efed487ff113/FSN3-5-486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/9d2be86cf064/FSN3-5-486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/cfb14881b20a/FSN3-5-486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/202a97aefe32/FSN3-5-486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/efed487ff113/FSN3-5-486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3e/5449198/9d2be86cf064/FSN3-5-486-g004.jpg

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