2022
DOI: 10.1016/j.jff.2022.105077
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Antioxidative mechanisms and anticolitic potential of Desmodium styracifolium (Osb.) Merr. in DSS-induced colitic mice

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Cited by 8 publications
(25 citation statements)
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“…Anthocyanins have been reported to scavenge free radicals via electron transfer reaction pathway, and the mechanism involves regulation of antioxidant enzyme such as SOD ( Khoo et al, 2017 ). Bioactive compounds containing catechol group have higher antioxidant activities ( Li et al, 2022 ). These phytochemicals found in litchi peels help to retard the fruit senescence besides the exogenous melatonin.…”
Section: Discussionmentioning
confidence: 99%
“…Anthocyanins have been reported to scavenge free radicals via electron transfer reaction pathway, and the mechanism involves regulation of antioxidant enzyme such as SOD ( Khoo et al, 2017 ). Bioactive compounds containing catechol group have higher antioxidant activities ( Li et al, 2022 ). These phytochemicals found in litchi peels help to retard the fruit senescence besides the exogenous melatonin.…”
Section: Discussionmentioning
confidence: 99%
“…Polyphenols and alkaloids are considered the primary components responsible for the majority of the pharmacological effects of plants in this genus [ 5 , 15 , [20] , [21] , [22] ]. Table 2 demonstrates a list of compounds isolated from plants of the D. styracifolium species, according to literature data [ 5 , 14 , [23] , [24] , [25] , [26] , [27] , [28] , [29] , [30] , [31] , [32] , [33] , [34] , [35] , [36] , [37] , [38] , [39] , [40] ]. The greatest importance in the phamacological action of D. styracifolium have following polyphenols: apigenin (IUPAC: 5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one), genistein (IUPAC: 5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one), kaemferol (IUPAC: 3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one), luteolin (IUPAC: 2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one), quercetin (IUPAC: 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one), and shaftoside (IUPAC: 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,6S, 7R)-3,4,6-trihydroxy-7-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S, 6S)-3,4,6-trihydroxyoxan-2-yl]chromen-4-one).…”
Section: Phytochemical Studiesmentioning
confidence: 99%
“… Ambonin Aerial parts [ 7 , 37 ] 11. Apigenin Whole plant/Aerial parts [ 7 , 26 , 28 , 29 ] 12. Astragalin Aerial parts [ 7 , 37 ] 13.…”
Section: Phytochemical Studiesmentioning
confidence: 99%
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“…Moreover, the comparison of double BDE with BDE indicated that in the gas phase, 3-OH can be activated by 4′-O⋅ to scavenge free radicals through the double HAT mechanism [39,40]. Furthermore, IPs were greatly affected by the solvent effect, and in the polar solvent (ethanol and water) systems, the IP values were significantly lower than BDEs and PAs, indicating that the SET-PT mechanism was more likely to occur [41]. By comparing PA and proton dissociation enthalpy, it can be found that the proton transfer ability of neutral molecules was worse than that of phenoxy cationic radicals.…”
Section: Theoretical Mechanismmentioning
confidence: 99%