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没食子酸对阿卡波糖抑制α-淀粉酶和α-葡萄糖苷酶活性的影响。

Influence of gallic acid on α-amylase and α-glucosidase inhibitory properties of acarbose.

机构信息

Department of Biochemistry, Federal University of Technology Akure, Akure, Nigeria.

Department of Biochemistry, Federal University Oye, Oye-Ekiti, Nigeria.

出版信息

J Food Drug Anal. 2016 Jul;24(3):627-634. doi: 10.1016/j.jfda.2016.03.003. Epub 2016 Apr 11.

DOI:10.1016/j.jfda.2016.03.003
PMID:28911570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9336674/
Abstract

Acarbose is an antidiabetic drug which acts by inhibiting α-amylase and α-glucosidase activities but with deleterious side effects. Gallic acid (GA) is a phenolic acid that is widespread in plant foods. We therefore investigated the influence of GA on α-amylase and α-glucosidase inhibitory properties of acarbose (in vitro). Aqueous solutions of acarbose and GA were prepared to a final concentration of 25μM each. Thereafter, mixtures of the samples (50% acarbose + 50% GA; 75% acarbose+25% GA; and 25% acarbose+75% GA) were prepared. The results revealed that the combination of 50% acarbose and 50% GA showed the highest α-glucosidase inhibitory effect, while 75% acarbose+25% GA showed the highest α-amylase inhibitory effect. Furthermore, all the samples caused the inhibition of Fe-induced lipid peroxidation (in vitro) in rat pancreatic tissue homogenate, with the combination of 50% acarbose and 50% GA causing the highest inhibition. All the samples also showed antioxidant properties (reducing property, 2,2'-azino-bis (-3-ethylbenzthiazoline-6-sulphonate [ABTS*] and 1,1-diphenyl-2-picrylhydrazyl [DPPH] free radicals scavenging abilities, and Fe chelating ability). Therefore, combinations of GA with acarbose could be employed as antidiabetic therapy, with a possible reduction of side effects of acarbose; nevertheless, the combination of 50% acarbose and 50% GA seems the best.

摘要

阿卡波糖是一种抗糖尿病药物,通过抑制α-淀粉酶和α-葡萄糖苷酶的活性起作用,但具有有害的副作用。没食子酸(GA)是一种广泛存在于植物性食物中的酚酸。因此,我们研究了 GA 对阿卡波糖(体外)抑制α-淀粉酶和α-葡萄糖苷酶活性的影响。将阿卡波糖和 GA 的水溶液制备至终浓度为 25μM。然后,制备样品的混合物(50%阿卡波糖+50%GA;75%阿卡波糖+25%GA;和 25%阿卡波糖+75%GA)。结果表明,50%阿卡波糖和 50%GA 的组合显示出最高的α-葡萄糖苷酶抑制作用,而 75%阿卡波糖+25%GA 显示出最高的α-淀粉酶抑制作用。此外,所有样品均导致大鼠胰腺组织匀浆中 Fe 诱导的脂质过氧化(体外)抑制,其中 50%阿卡波糖和 50%GA 的组合抑制作用最强。所有样品还显示出抗氧化特性(还原能力、2,2'-联氮双(-3-乙基苯并噻唑啉-6-磺酸)[ABTS*]和 1,1-二苯基-2-苦基肼[DPPH]自由基清除能力和 Fe 螯合能力)。因此,GA 与阿卡波糖的组合可用于抗糖尿病治疗,可能减少阿卡波糖的副作用;然而,50%阿卡波糖和 50%GA 的组合似乎是最好的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/2ab3b75c3cce/jfda-24-03-627f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/f82fc54d8ac9/jfda-24-03-627f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/a7f1f9ca2c4a/jfda-24-03-627f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/c553c7e4a606/jfda-24-03-627f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/52f397780236/jfda-24-03-627f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/2ab3b75c3cce/jfda-24-03-627f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/f82fc54d8ac9/jfda-24-03-627f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/57ff5b73f867/jfda-24-03-627f2.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/99933b2be26c/jfda-24-03-627f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/a7f1f9ca2c4a/jfda-24-03-627f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/c553c7e4a606/jfda-24-03-627f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/52f397780236/jfda-24-03-627f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91e/9336674/2ab3b75c3cce/jfda-24-03-627f8.jpg

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