The impact of some natural phenolic compounds on carbonic anhydrase, acetylcholinesterase, butyrylcholinesterase, and -glycosidase enzymes: An antidiabetic, anticholinergic, and antiepileptic study

被引:131
作者
Taslimi, Parham [1 ]
Caglayan, Cuneyt [2 ]
Gulcin, Ilhami [1 ]
机构
[1] Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey
[2] Bingol Univ, Dept Biochem, Fac Vet Med, TR-12000 Bingol, Turkey
关键词
acetylcholinesterase; butyrylcholinesterase; carbonic anhydrase; Phenolic compounds; -glycosidase; GLUCOSIDASE INHIBITORY-ACTIVITIES; ALPHA-GLUCOSIDASE; IN-VITRO; ANTIOXIDANT ACTIVITY; ESTERASE-ACTIVITIES; POLYPHENOL CONTENTS; MANNICH-BASES; ISOENZYMES I; DERIVATIVES; PROFILES;
D O I
10.1002/jbt.21995
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural products from food and plant sources have been used for medicinal usage for ages. Also, natural products with therapeutic significance are compounds derived from animals, plants, or any microorganism. In this study, chrysin, carvacrol, hesperidin, zingerone, and naringin as natural phenols showed excellent inhibitory effects against human (h) carbonic anhydrase (CA) isoforms I and II (hCA I and II), -glucosidase (-Gly), acetylcholinesterase (AChE), and butyrylcholinesterase (BChE). These phenolic compounds were tested for the inhibition of -glycosidase, hCA I, hCA II, AChE, and BChE enzymes and demonstrated efficient inhibition profiles with K-i values in the range of 3.70 +/- 0.92-79.66 +/- 20.81nM against hCA I, 2.98 +/- 0.33-84.88 +/- 40.32nM against hCA II, 4.93 +/- 2.01-593.60 +/- 134.74nM against -Gly, 0.52 +/- 0.18-46.80 +/- 17.15nM against AChE, and 1.25 +/- 0.22-32.08 +/- 2.68 against BChE.
引用
收藏
页数:7
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