Ouwerkerk-Mahadevan S, van Boom J H, Dreef-Tromp M C, Ploemen J H, Meyer D J, Mulder G J
Division of Toxicology, Leiden/Amsterdam Center for Drug Research, Leiden University, The Netherlands.
Biochem J. 1995 May 15;308 ( Pt 1)(Pt 1):283-90. doi: 10.1042/bj3080283.
Inhibitors of rat and human Alpha- and Mu-class glutathione S-transferases that effectively inhibit the glutathione (GSH) conjugation of bromosulphophthalein in the rat liver cytosolic fraction, isolated rat hepatocytes and in the rat liver in vivo have been developed. The GSH analogue (R)-5-carboxy-2-gamma-(S)-glutamylamino-N-hexylpentamide [Adang, Brussee, van der Gen and Mulder (1991) J. Biol. Chem. 266, 830-836] was used as the lead compound. To obtain more potent inhibitors, it was modified by replacement of the N-hexyl moiety by N-2-heptyl and by esterification of the 5-carboxy group with ethyl and dodecyl groups. In isolated hepatocytes, the branched N-2-heptyl derivatives were stronger inhibitors of GSH conjugation of bromosulphophthalein than the N-hexyl derivatives. The ethyl ester compounds were more efficient than the corresponding unesterified derivatives. The dodecyl ester of the N-2-heptyl analogue was the most effective inhibitor in isolated hepatocytes, but was relatively toxic in vivo. However, the corresponding ethyl ester was a potent in vivo inhibitor: GSH conjugation of bromosulphophthalein (as assessed by biliary excretion of the conjugate) was decreased by 70% after administration of a dose of 200 mumol/kg. The isoenzyme specificity of the inhibitors towards purified rat and human glutathione S-transferases was also examined. The unesterified compounds were more potent than the esterified analogues, and inhibited Alpha- and Mu-class isoenzymes of both rat and human glutathione S-transferase (Ki range 1-40 microM). Other GSH-dependent enzymes, i.e. GSH peroxidase, GSH reductase and gamma-glutamyltranspeptide, were not inhibited. Thus (R)-5-ethyloxycarbonyl-2-gamma-(S)-glutamylamino-N-2-hept ylpentamide, the in vivo inhibitor of GSH conjugation, may be useful in helping to assess the role of the Alpha and Mu classes of glutathione S-transferases in cellular biochemistry, physiology and pathology.
已开发出大鼠和人α-及μ-类谷胱甘肽S-转移酶的抑制剂,这些抑制剂能有效抑制大鼠肝脏胞质部分、分离的大鼠肝细胞以及大鼠肝脏体内溴磺酞钠的谷胱甘肽(GSH)结合反应。谷胱甘肽类似物(R)-5-羧基-2-γ-(S)-谷氨酰胺基-N-己基戊酰胺[阿当、布鲁斯、范德根和穆德(1991年)《生物化学杂志》266卷,830 - 836页]被用作先导化合物。为获得更有效的抑制剂,通过用N-2-庚基取代N-己基部分以及用乙基和十二烷基对5-羧基进行酯化对其进行了修饰。在分离的肝细胞中,支链N-2-庚基衍生物比N-己基衍生物对溴磺酞钠的谷胱甘肽结合反应具有更强的抑制作用。乙酯化合物比相应的未酯化衍生物更有效。N-2-庚基类似物的十二烷基酯是分离肝细胞中最有效的抑制剂,但在体内具有相对毒性。然而,相应的乙酯是一种有效的体内抑制剂:给予200 μmol/kg剂量后,溴磺酞钠的谷胱甘肽结合反应(通过结合物的胆汁排泄评估)降低了70%。还研究了这些抑制剂对纯化的大鼠和人谷胱甘肽S-转移酶的同工酶特异性。未酯化的化合物比酯化类似物更有效,并且抑制大鼠和人谷胱甘肽S-转移酶的α-和μ-类同工酶(Ki范围为1 - 40 μM)。其他依赖谷胱甘肽的酶,即谷胱甘肽过氧化物酶、谷胱甘肽还原酶和γ-谷氨酰转肽酶未被抑制。因此,谷胱甘肽结合反应的体内抑制剂(R)-5-乙氧羰基-2-γ-(S)-谷氨酰胺基-N-2-庚基戊酰胺可能有助于评估α和μ类谷胱甘肽S-转移酶在细胞生物化学、生理学和病理学中的作用。