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通过液相色谱-串联质谱法和气相色谱-质谱法对[提取物名称]甲醇提取物进行代谢物谱分析及其抗糖尿病和抗氧化活性研究。 (注:原文中“of Methanolic Extract of ”后面缺少具体提取物名称)

Metabolite Profiling of Methanolic Extract of by LC-MS/MS and GC-MS and Its Anti-Diabetic, and Anti-Oxidant Activities.

作者信息

Saravanakumar Kandasamy, Park SeonJu, Sathiyaseelan Anbazhagan, Kim Kil-Nam, Cho Su-Hyeon, Mariadoss Arokia Vijaya Anand, Wang Myeong-Hyeon

机构信息

Department of Bio-Health Convergence, Kangwon National University, Chuncheon 24341, Korea.

Chuncheon Center, Korea Basic Science Institute (KBSI), Chuncheon 24341, Korea.

出版信息

Pharmaceuticals (Basel). 2021 Jan 28;14(2):102. doi: 10.3390/ph14020102.

DOI:10.3390/ph14020102
PMID:33525758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7912419/
Abstract

In this study, the methanolic extract from seeds of exhibited strong antioxidant and enzyme inhibition activities with less toxicity to NIH3T3 and HepG2 cells at the concentration of 100 µg/mL. The antioxidant activities (DPPH and ABTS), α-amylase, and α-glucosidase inhibition activities were found higher in methanolic extract (MeOH-E) than HO extract. Besides, 9.82 ± 0.62 µg and 6.42 ± 0.26 µg of MeOH-E were equivalent to 1 µg ascorbic acid for ABTS and DPPH scavenging, respectively while 9.02 ± 0.25 µg and 6.52 ± 0.15 µg of MeOH-E were equivalent to 1 µg of acarbose for inhibition of α-amylase and α-glucosidase respectively. Moreover, the cell assay revealed that the addition of MeOH-E (12.5 µg/mL) increased about 37% of glucose uptake in insulin resistant (IR) HepG2 as compared to untreated IR HepG2 cells. The LC- MS/MS and GC-MS analysis of MeOH-E revealed a total of 54 compounds including terpenoids, glycosides, fatty acid, phenolic acid derivatives. Among the identified compounds, chlorogenic acid and jasminoside A were found promising for anti-diabetic activity revealed by molecular docking study and these molecules are deserving further purification and molecular analysis.

摘要

在本研究中,[植物名称]种子的甲醇提取物在100 µg/mL浓度下表现出较强的抗氧化和酶抑制活性,对NIH3T3和HepG2细胞的毒性较小。发现甲醇提取物(MeOH-E)的抗氧化活性(DPPH和ABTS)、α-淀粉酶和α-葡萄糖苷酶抑制活性高于水提取物(HO提取物)。此外,对于ABTS和DPPH清除,9.82±0.62 µg和6.42±0.26 µg的MeOH-E分别相当于1 µg抗坏血酸,而对于α-淀粉酶和α-葡萄糖苷酶的抑制,9.02±0.25 µg和6.52±0.15 µg的MeOH-E分别相当于1 µg阿卡波糖。此外,细胞试验表明,与未处理的胰岛素抵抗(IR)HepG2细胞相比,添加MeOH-E(12.5 µg/mL)可使IR HepG2细胞的葡萄糖摄取增加约37%。MeOH-E的LC-MS/MS和GC-MS分析共鉴定出54种化合物,包括萜类、糖苷、脂肪酸、酚酸衍生物。在鉴定出的化合物中,通过分子对接研究发现绿原酸和茉莉糖苷A具有抗糖尿病活性,这些分子值得进一步纯化和分子分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/ff9fb6b5480d/pharmaceuticals-14-00102-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/2ac89fd77aa4/pharmaceuticals-14-00102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/993f229bbbb0/pharmaceuticals-14-00102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/ccd43548d8b3/pharmaceuticals-14-00102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/4c10cc8d4353/pharmaceuticals-14-00102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/0e3541466a8d/pharmaceuticals-14-00102-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/ff9fb6b5480d/pharmaceuticals-14-00102-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/2ac89fd77aa4/pharmaceuticals-14-00102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/993f229bbbb0/pharmaceuticals-14-00102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/ccd43548d8b3/pharmaceuticals-14-00102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/4c10cc8d4353/pharmaceuticals-14-00102-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/0e3541466a8d/pharmaceuticals-14-00102-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4943/7912419/ff9fb6b5480d/pharmaceuticals-14-00102-g006.jpg

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