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Protective action on human LDL against oxidation and glycation by four organosulfur compounds derived from garlic
Author(s) -
Ou Chuchyn,
Tsao Shyhming,
Lin Mingcheng,
Yin Meichin
Publication year - 2003
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-003-1054-4
Subject(s) - organosulfur compounds , chemistry , glycation , antioxidant , xanthine oxidase , diallyl disulfide , deferasirox , biochemistry , pharmacology , enzyme , organic chemistry , sulfur , medicine , apoptosis , receptor , thalassemia
Human LDL were used to study the protective action of four organosulfur compounds (diallyl sulfide, DAS; diallyl disulfide, DADS; S ‐ethylcysteine, SEC; N ‐acetylcysteine, NAC) derived from garlic against oxidation and glycation. The four organosulfur compounds significantly inhibited superoxide production by xanthine‐xanthine oxidase ( P <0.05) and showed marked copper‐chelating capability. DAS and DADS exhibited greater antioxidant activities against copper‐ and amphotericin B‐induced LDL oxidation ( P <0.05) than SEC and NAC. However, SEC and NAC were more effective in sparing LDL α‐tocopherol ( P <0.05). When oxidation was minimized, SEC was the most powerful agent against LDL glycation ( P <0.05); however, DADS was superior to other agents in suppressing both oxidation and glycation when LDL oxidation occurred simultaneously with glycation. These results suggest that the four organosulfur compounds derived from garlic are potent agents for protecting LDL against oxidation and glycation, and that they may benefit patients with diabetes mellitus or cardiovascular diseases by preventing complications.