Antidiabetic properties of dietary phenolic compounds: Inhibition effects on α-amylase, aldose reductase, and α-glycosidase

被引:100
作者
Demir, Yeliz [1 ]
Durmaz, Lokman [2 ]
Taslimi, Parham [3 ]
Gulcin, Ilhami [4 ]
机构
[1] Ardahan Univ, Nihat Delibalta Gole Vocat High Sch, Dept Pharm Serv, Ardahan, Turkey
[2] Erzincan Binali Yildirim Univ, Cayirli Vocat Sch, Dept Med Serv & Technol, Erzincan, Turkey
[3] Bartin Univ, Dept Biotechnol, Fac Sci, Bartin, Turkey
[4] Ataturk Univ, Dept Chem, Fac Sci, Erzurum, Turkey
关键词
aldose reductase; phenolic compounds; alpha-glycosidase; alpha-amylase; GLUCOSIDASE ACTIVITY; IDENTIFICATION; EXTRACT; CANCER; LEAVES;
D O I
10.1002/bab.1781
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
Aldose reductase (AR), alpha-amylase, and alpha-glycosidase are vital enzymes to prevent diabetic complications. Here, AR was purified from sheep kidney using elementary methods with 111.11-purification fold and with 0.85% purification yield. The interactions between some phenolic compounds and the AR, alpha-glycosidase, and alpha-amylase enzyme were determined. It was found that phenolic compounds exhibit potential inhibitor properties for these enzymes. For alpha-amylase, studied phenolic compounds showed IC50 values in the range of 601.56-2,067.78 nM. For alpha-glycosidase, K-i values were found in the range of 169.25 +/- 27.22-572.88 +/- 106.76 nM. For AR, K-i values in the range of 8.48 +/- 0.56-43.26 +/- 7.63 mu M. However, genistein showed the best inhibition effect toward AR and alpha-glycosidase, but delphinidin chloride exhibited the best inhibition effect against alpha-amylase enzyme. We determined that all compounds showed noncompetitive inhibition effect against AR and alpha-glycosidase. Also, studied phenolic compounds may be useful in the prevention or treatment of diabetic complications.
引用
收藏
页码:781 / 786
页数:6
相关论文
共 47 条
[1]   Phenolic compounds: The inhibition effect on polyol pathway enzymes [J].
Aslan, Hatice Esra ;
Beydemir, Sukru .
CHEMICO-BIOLOGICAL INTERACTIONS, 2017, 266 :47-55
[2]   Antiepileptic drugs: Impacts on human serum paraoxonase-1 [J].
Beydemir, Sukru ;
Demir, Yeliz .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2017, 31 (06)
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Microsimulation Modeling in Oncology [J].
Caglayan, Caglar ;
Terawaki, Hiromi ;
Chen, Qiushi ;
Rai, Ashish ;
Ayer, Turgay ;
Flowers, Christopher R. .
JCO CLINICAL CANCER INFORMATICS, 2018, 2 :1-11
[5]   ANTIINFLAMMATORY AND ALDOSE REDUCTASE INHIBITORY ACTIVITY OF SOME TRICYCLIC ARYLACETIC ACIDS [J].
CERELLI, MJ ;
CURTIS, DL ;
DUNN, JP ;
NELSON, PH ;
PEAK, TM ;
WATERBURY, LD .
JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (11) :2347-2351
[6]   Inhibitory Effects of Usnic and Carnosic Acid on Some Metabolic Enzymes: An in vitro Study [J].
Ceylan, Hamid ;
Demir, Yeliz ;
Beydemir, Sukru .
PROTEIN AND PEPTIDE LETTERS, 2019, 26 (05) :364-370
[7]   Inhibition of aldose reductase from cataracted eye lenses by finger millet (Eleusine coracana) polyphenols [J].
Chethan, S. ;
Dharmesh, Shylaja M. ;
Malleshi, Nagappa G. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (23) :10085-10090
[8]   Inhibition effects of quinones on aldose reductase: Antidiabetic properties [J].
Demir, Yeliz ;
Ozaslan, Muhammet Serhat ;
Duran, Hatice Esra ;
Kufrevioglu, Omer Irfan ;
Beydemir, Sukru .
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2019, 70
[9]   The inhibition effects of some sulfonamides on human serum paraoxonase-1 (hPON1) [J].
Demir, Yeliz ;
Koksal, Zeynep .
PHARMACOLOGICAL REPORTS, 2019, 71 (03) :545-549
[10]   Antidiabetic potential: In vitro inhibition effects of bromophenol and diarylmethanones derivatives on metabolic enzymes [J].
Demir, Yeliz ;
Taslimi, Parham ;
Ozaslan, Muhammet Serhat ;
Oztaskin, Necla ;
Cetinkaya, Yasin ;
Gulcin, Ilhami ;
Beydemir, Sukru ;
Goksu, Suleyman .
ARCHIV DER PHARMAZIE, 2018, 351 (12)