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作为洋葱次生代谢产物的绣线菊苷的潜在抗氧化、抗胆碱能、抗糖尿病和抗青光眼活性及分子对接

Potential antioxidant, anticholinergic, antidiabetic and antiglaucoma activities and molecular docking of spiraeoside as a secondary metabolite of onion ().

作者信息

Durmaz Lokman, Kiziltas Hatice, Karagecili Hasan, Alwasel Saleh, Gulcin İlhami

机构信息

Department of Medical Services and Technology, Cayirli Vocational School, Erzincan Binali Yildirim University, 24500, Cayirli, Erzincan, Turkey.

Department of Pharmacy Services, Vocational School of Health Services, Van Yuzuncu Yil University, 65080, Van, Turkey.

出版信息

Saudi Pharm J. 2023 Oct;31(10):101760. doi: 10.1016/j.jsps.2023.101760. Epub 2023 Aug 23.

Abstract

Onion contains many dietary and bioactive components including phenolics and flavonoids. Spiraeoside (quercetin-4-O-β-D-glucoside) is one of the most putative flavonoids in onion. Several antioxidant techniques were used in this investigation to assess the antioxidant capabilities of spiraeoside, including 1,1-diphenyl-2-picrylhydrazyl radical (DPPH·) scavenging, N,N-dimethyl-p-phenylenediamine radical (DMPD) scavenging, 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radical (ABTS) scavenging activities, cupric ions (Cu) reducing and potassium ferric cyanide reduction abilities. In contrast, the water-soluble α-tocopherol analogue trolox and the conventional antioxidants butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), and α-tocopherol were utilized as the standards for evaluation. Spiraeoside scavenged the DPPH radicals an IC of 28.51 μg/mL (r: 0.9705) meanwhile BHA, BHT, trolox, and α-tocopherol displayed IC of 10.10 μg/mL (r: 0.9015), 25.95 μg/mL (r: 0.9221), 7.059 μg/mL (r: 0.9614) and 11.31 μg/mL (r: 0.9642), accordingly. The results exhibited that spiraeoside had effects similar to BHT, but less potent than α-tocopherol, trolox and BHA. Also, inhibitory effects of spiraeoside were evaluated toward some metabolic enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), carbonic anhydrase II (CA II) and α-glycosidase, which are related to a number of illnesses, such as Alzheimer's disease (AD), diabetes mellitus and glaucoma disorder. Spiraeoside exhibited IC values of 4.44 nM (r: 0.9610), 7.88 nM (r: 0.9784), 19.42 nM (r: 0.9673) and 29.17 mM (r: 0.9209), respectively against these enzymes. Enzyme inhibition abilities were compared to clinical used inhibitors including acetazolamide (for CA II), tacrine (for AChE and BChE) and acarbose (for α-glycosidase). Spiraeoside demonstrated effective antioxidant, anticholinergic, antidiabetic and antiglaucoma activities. With these properties, it has shown that Spiraeoside has the potential to be a medicine for some metabolic diseases.

摘要

洋葱含有许多膳食和生物活性成分,包括酚类和黄酮类化合物。绣线菊苷(槲皮素 - 4 - O - β - D - 葡萄糖苷)是洋葱中最具代表性的黄酮类化合物之一。本研究采用了几种抗氧化技术来评估绣线菊苷的抗氧化能力,包括1,1 - 二苯基 - 2 - 苦基肼自由基(DPPH·)清除能力、N,N - 二甲基 - p - 苯二胺自由基(DMPD)清除能力、2,2'- 偶氮二(3 - 乙基苯并噻唑啉 - 6 - 磺酸盐)自由基(ABTS)清除活性、铜离子(Cu)还原能力和铁氰化钾还原能力。相比之下,水溶性α - 生育酚类似物曲克芦丁以及传统抗氧化剂丁基羟基甲苯(BHT)、丁基羟基茴香醚(BHA)和α - 生育酚被用作评估标准。绣线菊苷清除DPPH自由基的半数抑制浓度(IC)为28.51μg/mL(r:0.9705),同时BHA、BHT、曲克芦丁和α - 生育酚的IC分别为10.10μg/mL(r:0.9015)、25.95μg/mL(r:0.9221)、7.059μg/mL(r:0.9614)和11.31μg/mL(r:0.9642)。结果表明,绣线菊苷具有与BHT相似的效果,但效力低于α - 生育酚、曲克芦丁和BHA。此外,还评估了绣线菊苷对一些代谢酶的抑制作用,包括乙酰胆碱酯酶(AChE)、丁酰胆碱酯酶(BChE)、碳酸酐酶II(CA II)和α - 糖苷酶,这些酶与许多疾病有关,如阿尔茨海默病(AD)、糖尿病和青光眼。绣线菊苷对这些酶的IC值分别为4.44 nM(r:0.9610)、7.88 nM(r:0.9784)、19.42 nM(r:0.9673)和29.17 mM(r:0.9209)。将酶抑制能力与临床使用的抑制剂进行了比较,包括乙酰唑胺(用于CA II)、他克林(用于AChE和BChE)和阿卡波糖(用于α - 糖苷酶)。绣线菊苷表现出有效的抗氧化、抗胆碱能、抗糖尿病和抗青光眼活性。基于这些特性,表明绣线菊苷有潜力成为治疗某些代谢疾病的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19c2/10485163/1e5d316cc901/gr1.jpg

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