Kadoma Yoshinori, Fujisawa Seiichiro
Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Kanda-surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.
Molecules. 2008 Oct 15;13(10):2488-99. doi: 10.3390/molecules13102488.
Phenolcarboxylic acid antioxidants do not act in vivo as radical-scavengers in isolation, but rather together with GSH (glutathione), a coantioxidant, they constitute an intricate antioxidant network. Caffeic acid, p-coumaric acid, ferulic acid and chlorogenic acid with or without 2-mercaptoethanol (ME), as a substitute for GSH, was investigated by the induction period (IP) method for polymerization of methyl methacrylate (MMA) initiated by thermal decomposition of 2,2'-azobisisobutyronitrile (AIBN, a source of alkyl radicals, R(.)) and benzoyl peroxide (BPO, a source of peroxy radicals, PhCOO(.)) using differential scanning calorimetry (DSC). Upon PhCOO(. )radical scavenging, the stoichiometric factors (n, number of free radical trapped by one mole of antioxidant) for caffeic acid, ferulic acid, p-coumaric acid and chlorogenic acid were 2.4, 1.8, 1.7 and 0.9, whereas upon R(.) radical scavenging, the corresponding values were 1.3, 1.2, 1.0 and 0.8, respectively. Antioxidants with n values close to 2 suggest the stepwise formation of semiquinone radicals and quinones. By contrast, those with n values close to 1 suggest the formation of dimers after single-electron oxidation, possibly due to recombination of corresponding aryloxy radicals. The ratio of the rate constant of inhibition to that of propagation (k(inh)/k(p)) declined in the order chlorogenic acid > p-coumaric acid > ferulic acid > caffeic acid. The ratio of the observed IP for the phenolcarboxylic acid/2-mercapto-ethanol (ME) mixture (1:1 molar ratio) (A) to the calculated IP (the simple sum of phenol acid antioxidant and ME) (B) was investigated. Upon R(.) scavenging, the caffeic acid or p-coumaric acid/ME mixture was A/B > 1, particularly the former was 1.2, suggesting a synergic effect. By contrast, upon PhCOO(.) scavenging, the corresponding mixture was A/B < 1, particularly the latter was 0.7, suggesting an antagonistic effect. Upon both radicals scavenging, the A/B for the ferulic acid or chlorogenic acid/ME mixture was approximately 1. The reported beneficial antioxidant, anti-inflammatory and anticancer effects of caffeic acid and p-coumaric acid may be related to their prooxidant-antioxidant balance in the presence of GSH.
酚羧酸抗氧化剂在体内并非单独作为自由基清除剂起作用,而是与作为共抗氧化剂的谷胱甘肽(GSH)一起,构成一个复杂的抗氧化网络。采用差示扫描量热法(DSC),通过2,2'-偶氮二异丁腈(AIBN,烷基自由基R(.)的来源)和过氧化苯甲酰(BPO,过氧自由基PhCOO(.)的来源)热分解引发的甲基丙烯酸甲酯(MMA)聚合的诱导期(IP)方法,研究了咖啡酸、对香豆酸、阿魏酸和绿原酸,以及有或没有作为GSH替代物的2-巯基乙醇(ME)的情况。在清除PhCOO(.)自由基时,咖啡酸、阿魏酸、对香豆酸和绿原酸的化学计量系数(n,一摩尔抗氧化剂捕获的自由基数量)分别为2.4、1.8、1.7和0.9,而在清除R(.)自由基时,相应的值分别为1.3、1.2、1.0和0.8。n值接近2的抗氧化剂表明半醌自由基和醌逐步形成。相比之下,n值接近1的抗氧化剂表明单电子氧化后形成二聚体,这可能是由于相应的芳氧基自由基的重组。抑制速率常数与传播速率常数之比(k(inh)/k(p))按绿原酸>对香豆酸>阿魏酸>咖啡酸的顺序下降。研究了酚羧酸/2-巯基乙醇(ME)混合物(1:1摩尔比)的观察到的IP(A)与计算得到的IP(酚酸抗氧化剂和ME的简单总和)(B)的比值。在清除R(.)时,咖啡酸或对香豆酸/ME混合物的A/B>1,特别是前者为1.2,表明有协同效应。相比之下,在清除PhCOO(.)时,相应的混合物A/B<1,特别是后者为0.7,表明有拮抗效应。在清除两种自由基时,阿魏酸或绿原酸/ME混合物的A/B约为1。报道的咖啡酸和对香豆酸有益的抗氧化、抗炎和抗癌作用可能与其在GSH存在下的促氧化-抗氧化平衡有关。