2019
DOI: 10.1080/10408398.2018.1548428
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The inhibitory effects of flavonoids on α-amylase and α-glucosidase

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Cited by 107 publications
(67 citation statements)
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“…The probable participation of catechin and several anthocyanins in the inhibition of α-amylases has already been discussed above. Considering the type of molecules found in the extract, the results obtained in this study partially diverge with the general concept that phenolic compounds, such as flavonoids and polyphenols, have the ability of inhibiting the αglucosidase activity (Ishikawa et al, 2007;Hargrove, Greenspan, Hartle, & Dowd, 2011;Kumar, Narwal, Kumar, & Prakash, 2011;Yin, Zhang, Feng, Zhang, & Kang, 2014;Kadouh, Sun, Zhu, & Zhou, 2016;Martinez-Gonzalez et al, 2017;Zhu et al, 2020). It should be stressed, however, that there are reports showing that the intestinal enzyme and the yeast enzyme generally present different sensitivities to flavonoids and polyphenols (Babu et al, 2004;Tadera, Minami, Takamatsu, & Matsuoka, 2006).…”
Section: In Vivo Inhibition Of the Activities Of Carbohydrate Digesticontrasting
confidence: 87%
See 1 more Smart Citation
“…The probable participation of catechin and several anthocyanins in the inhibition of α-amylases has already been discussed above. Considering the type of molecules found in the extract, the results obtained in this study partially diverge with the general concept that phenolic compounds, such as flavonoids and polyphenols, have the ability of inhibiting the αglucosidase activity (Ishikawa et al, 2007;Hargrove, Greenspan, Hartle, & Dowd, 2011;Kumar, Narwal, Kumar, & Prakash, 2011;Yin, Zhang, Feng, Zhang, & Kang, 2014;Kadouh, Sun, Zhu, & Zhou, 2016;Martinez-Gonzalez et al, 2017;Zhu et al, 2020). It should be stressed, however, that there are reports showing that the intestinal enzyme and the yeast enzyme generally present different sensitivities to flavonoids and polyphenols (Babu et al, 2004;Tadera, Minami, Takamatsu, & Matsuoka, 2006).…”
Section: In Vivo Inhibition Of the Activities Of Carbohydrate Digesticontrasting
confidence: 87%
“…This, in turn, would reduce the risk of excessive bacterial fermentation. Polyphenolics, including tannins of various types, flavonoids, catechins and gallic acid among others, have been denoted as antioxidants and inhibitors of hydrolytic enzymes, especially of α-amylases and α-glucosidase (Silva et al, 2014;Martinez-Gonzalez et al, 2017;Kato et al, 2017;Kato-Schwartz et al, 2018;Shanmugam et al, 2018;Gutiérrez-Grijalva, Antunes-Ricardo, Acosta-Estrada, Gutiérrez-Uribe, & Heredia, 2019;Cardullo et al, 2020;Zhu, Chen, Zhang, & Huang, 2020).…”
Section: Introductionmentioning
confidence: 99%
“…DSOR 21 and DSOR 24 exhibited a slightly lower lipase inhibition with IC 50 values of 6.70 ± 0.12 and 6.51 ± 0.17 µg/mL, respectively, compared to Orlistat and other tested decorticated sorghum grain extracts ( Figure 2 C). Evidence from several in vitro, in vivo and some human studies have revealed that flavonoids enhance ROS scavenging activities, interaction and inhibition of carbohydrate and fat catabolism enzymes, thus decreasing fat accumulation and, therefore, preventing obesity [ 34 , 35 , 36 ].…”
Section: Resultsmentioning
confidence: 99%
“…Many biofunctionalities and potential health benefits of cocoa polyphenols have been reviewed by Rojo-Poveda et al [3], such as antidiabetic activity; anticariogenic, anticarcinogenic, and anti-inflammatory effects; and actions on cardiovascular health. In particular, flavonoids have been suggested as natural inhibitors of the α-amylase and α-glucosidase enzymes directly involved in the degradation of complex carbohydrates; in other words, they are able to lower the amount of glucose intake directly binding to amino acid residues in the enzyme active sites and exclude substrate binding [10]. The inhibition capacity of flavonoids depends on their molecular structure and is higher when planar structure of the rings, double bonds in the 2 and 3 positions in the C 3 part of the flavonoid skeleton (C 6 -C 3 -C 6 ), and hydroxylation in the rings occur [11].…”
Section: Introductionmentioning
confidence: 99%
“…The inhibition capacity of flavonoids depends on their molecular structure and is higher when planar structure of the rings, double bonds in the 2 and 3 positions in the C 3 part of the flavonoid skeleton (C 6 -C 3 -C 6 ), and hydroxylation in the rings occur [11]. By reducing the post-prandial level of glucose in the bloodstream, flavonoids can therefore be used in diabetes treatment as substitutes for some drugs (e.g., acarbose) that cause side effects, such as abdominal distension, flatulence, meteorism, and diarrhoea [10].…”
Section: Introductionmentioning
confidence: 99%