Hiratsuka A, Yamane H, Yamazaki S, Ozawa N, Watabe T
Department of Drug Metabolism and Molecular Toxicology, School of Pharmacy, Tokyo University of Pharmacy and Life Science, Hachioji-shi, Tokyo 192-03, Japan.
J Biol Chem. 1997 Feb 21;272(8):4763-9. doi: 10.1074/jbc.272.8.4763.
Dermal 7alpha- and 7beta-hydroperoxycholest-5-en-3beta-ols (cholesterol 7alpha- and 7beta-hydroperoxides), regarded as good aging markers in the rat (Ozawa, N., Yamazaki, S., Chiba, K., Aoyama, H., Tomisawa, H., Tateishi, M., and Watabe, T. (1991) Biochem. Biophys. Res. Commun. 178, 242-247), were reduced in the presence of glutathione (GSH) with concomitant formation of GSSG by cytosol from rat liver in which no detectable level of the hydroperoxides had been demonstrated to occur. The GSH peroxidase (GSH Px) activity toward the toxic steroid hydroperoxides was exerted to almost the same extent by both Alpha-class GSH S-transferases (GSTs), Ya-Ya and Ya-Yc, and by selenium-containing GSH Px (Se-GSH Px) in rat liver cytosol. None of three Mu-class GSTs, Yb1-Yb1, Yb1-Yb2, and Yb2-Yb2, and a Theta-class GST, Yrs-Yrs, from rat liver and a Pi-class GST, Yp-Yp, from rat kidney showed any appreciable GSH Px activity toward the hydroperoxides. The subunit Ya-bearing GSTs and Se-GSH Px purified from rat liver cytosol showed marked differences in apparent specific activity toward the cholesterol hydroperoxides (GSTs Ya-Ya > Ya-Yc >> Se-GSH Px). However, a kinetic study indicated that Se-GSH Px had a higher affinity for steroid hydroperoxides than did the GSTs, so that Se-GSH Px could catalyze the reduction of lower concentrations of cholesterol 7-hydroperoxides with approximately equal Vmax/Km values to those by the GSTs. Rat skin had no GST bearing the subunit Ya but contained only a very low concentration of Se-GSH Px, possibly resulting in the accumulation of cholesterol 7-hydroperoxides in the skin but not in the liver. From rat skin cytosol, GSTs Yc-Yc, Yb1-Yb1, Yb1-Yb2, Yb2-Yb2, and Yp-Yp were isolated, purified to homogeneity, and identified with the corresponding GSTs from liver and kidney. The GSTs accounted for 0.23% of total skin cytosolic protein, and the most abundant isoform of skin GSTs was Yb2-Yb2, followed by Yc-Yc, Yp-Yp, Yb1-Yb1, and Yb1-Yb2 in decreasing order.
皮肤中的7α-和7β-氢过氧化胆甾-5-烯-3β-醇(胆固醇7α-和7β-氢过氧化物)在大鼠中被视为良好的衰老标志物(小泽直、山崎秀、千叶健、青山宏、富泽秀、立石正、渡边彻(1991年)《生物化学与生物物理研究通讯》178卷,242 - 247页),在谷胱甘肽(GSH)存在的情况下,大鼠肝脏胞质溶胶能将其还原,同时伴随生成GSSG,而在该胞质溶胶中未检测到可察觉水平的氢过氧化物。大鼠肝脏胞质溶胶中的α类谷胱甘肽S-转移酶(GSTs)Ya - Ya和Ya - Yc以及含硒谷胱甘肽过氧化物酶(Se - GSH Px)对有毒类固醇氢过氧化物的谷胱甘肽过氧化物酶(GSH Px)活性发挥程度几乎相同。大鼠肝脏中的三种μ类GSTs(Yb1 - Yb1、Yb1 - Yb2和Yb2 - Yb2)、一种θ类GST(Yrs - Yrs)以及大鼠肾脏中的一种π类GST(Yp - Yp)对氢过氧化物均未表现出任何明显的GSH Px活性。从大鼠肝脏胞质溶胶中纯化的含亚基Ya的GSTs和Se - GSH Px对胆固醇氢过氧化物的表观比活性存在显著差异(GSTs Ya - Ya > Ya - Yc >> Se - GSH Px)。然而,动力学研究表明,Se - GSH Px对类固醇氢过氧化物的亲和力高于GSTs,因此Se - GSH Px能够催化还原较低浓度的胆固醇7 - 氢过氧化物,其Vmax/Km值与GSTs催化时大致相等。大鼠皮肤不含含亚基Ya的GST,但仅含有极低浓度的Se - GSH Px,这可能导致皮肤中胆固醇7 - 氢过氧化物的积累,而肝脏中则不会。从大鼠皮肤胞质溶胶中分离、纯化得到了均一的GSTs Yc - Yc、Yb1 - Yb1、Yb1 - Yb2、Yb2 - Yb2和Yp - Yp,并与肝脏和肾脏中的相应GSTs进行了鉴定。这些GSTs占皮肤总胞质蛋白的0.23%,皮肤GSTs中最丰富的同工型是Yb2 - Yb2,其次依次为Yc - Yc、Yp - Yp、Yb1 - Yb1和Yb1 - Yb2。