Mericle Kelly A, Kaphalia Bhupendra S, Ansari G A
Department of Pathology, University of Texas Medical Branch, Galveston, Texas, USA.
J Toxicol Environ Health A. 2004 Apr 9;67(7):583-93. doi: 10.1080/15287390490425551.
Formation and toxicity of fatty acid methyl esters (FAMEs) have been reported both in vitro and in vivo. In previous studies, it was shown that fatty acid ethyl ester synthase (FAEES), which catalyzes the formation of FAMEs, also expresses esterase activity. Therefore, it was hypothesized that inhibitors of esterases such as tri-o-tolyl phosphate (TOTP) can modulate the formation of FAMEs. To test this, four groups of rats were used. Group 1 served as control (vehicle only). Group 2 was treated with methanol only (3 g/kg via gavage), group 3 was given TOTP only (100 mg/kg i.p. in corn oil), and group 4 was administered TOTP as in group 3, followed by methanol after 18 h. Three hours after exposure, animals were sacrificed and FAEES activity and FAME levels were measured in blood, liver, pancreas, and brown fat. About 95% of FAEES activity was inhibited in the liver and whole blood of TOTP-treated rats (group 3) but no inhibition was observed in the pancreas or brown fat. Total hepatic FAMEs were found to be lowest for the TOTP-treated group (3) and highest in the methanol-treated animals (group 2). Total pancreatic FAMEs in different groups were not statistically different, while significant increases were observed in the brown fat in both methanol-treated groups. To verify that the oxidative metabolism of methanol was unaffected by TOTP, alcohol dehydrogenase activity was also measured and found to be unchanged in any group as compared to control. These results demonstrate that the formation of FAMEs can be modulated in the liver and probably in blood, but not in the pancreas or brown fat by the inhibitors of FAEES.
脂肪酸甲酯(FAMEs)的形成及其毒性在体外和体内均有报道。在先前的研究中,已表明催化FAMEs形成的脂肪酸乙酯合酶(FAEES)也具有酯酶活性。因此,有人推测酯酶抑制剂如磷酸三邻甲苯酯(TOTP)可以调节FAMEs的形成。为了验证这一点,使用了四组大鼠。第1组作为对照组(仅给予赋形剂)。第2组仅用甲醇处理(经口灌胃3 g/kg),第3组仅给予TOTP(100 mg/kg腹腔注射于玉米油中),第4组与第3组一样给予TOTP,18小时后再给予甲醇。暴露3小时后,处死动物,测定血液、肝脏、胰腺和棕色脂肪中的FAEES活性和FAME水平。在TOTP处理的大鼠(第3组)的肝脏和全血中,约95%的FAEES活性受到抑制,但在胰腺或棕色脂肪中未观察到抑制作用。发现TOTP处理组(第3组)的肝脏总FAMEs最低,而甲醇处理的动物(第2组)中最高。不同组的胰腺总FAMEs无统计学差异,而在两个甲醇处理组的棕色脂肪中均观察到显著增加。为了验证甲醇的氧化代谢不受TOTP影响,还测定了乙醇脱氢酶活性,发现与对照组相比,任何组的该活性均未改变。这些结果表明,FAEES抑制剂可以调节肝脏中FAMEs的形成,可能也能调节血液中的形成,但不能调节胰腺或棕色脂肪中的形成。