2006
DOI: 10.1016/j.foodchem.2005.05.057
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Protective effects of an aqueous extract of Welsh onion green leaves on oxidative damage of reactive oxygen and nitrogen species

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Cited by 40 publications
(25 citation statements)
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“…Inhibition of protein carbonyl formation The eff ect of milk thistle seed extract on protein oxidation was determined using a modifi ed method of Wang et al (22). Bovine serum albumin (BSA; 4 mg/mL) was treated with iron(III) chloride (50 μM), hydrogen peroxide (1 mM) and ascorbic acid (100 μM) in potassium phosphate buff er (20 mM, pH=7.4) in the presence of seed extract (10-1000 μg/mL) at 37 °C for 30 min and then the absorbance was measured at λ=370 nm.…”
Section: Protein Damage Protectionmentioning
confidence: 99%
“…Inhibition of protein carbonyl formation The eff ect of milk thistle seed extract on protein oxidation was determined using a modifi ed method of Wang et al (22). Bovine serum albumin (BSA; 4 mg/mL) was treated with iron(III) chloride (50 μM), hydrogen peroxide (1 mM) and ascorbic acid (100 μM) in potassium phosphate buff er (20 mM, pH=7.4) in the presence of seed extract (10-1000 μg/mL) at 37 °C for 30 min and then the absorbance was measured at λ=370 nm.…”
Section: Protein Damage Protectionmentioning
confidence: 99%
“…Indeed, Welsh onion possesses antioxidant compounds such as quercetin and kaempferol as main phenol compounds (Wang et al, 2006), ascorbic acid (Kähkönen and Heinonen, 2003), and volatile sulfur compounds (Wu et al, 2001). Thus, it is possible that the content of other antioxidant compounds besides phenol compounds may be increased in the…”
Section: Resultsmentioning
confidence: 99%
“…Welsh onion (Allium fistulosum L.), a member of the Allium family, is a popular vegetable in Asian countries and a reputed good source of phenol compounds with antioxidant activity, leading to beneficial medicinal effects (Helen et al, 2000;Wang et al, 2006).…”
Section: Introductionmentioning
confidence: 99%
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“…20 The reaction mixture (1.2 mL) containing extract, potassium phosphate buffer (20 mM, pH 7.4), BSA (4 mg), FeCl 3 (50 µM), H 2 O 2 (1 mM) and ascorbic acid (100 µM) were incubated for 60 min at 37 ºC. For determination of PCO content in samples, 1 mL of 10 mM DNPH (2, 4-Dinitrophenylhydrazine) in 2 N HCl was added to the reaction mixture.…”
Section: Inhibitory Activity Of Are On Protein Carbonyl (Pco) Formationmentioning
confidence: 99%