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自发性高血压大鼠和Wistar Kyoto大鼠对可卡因肝毒性的敏感性差异。

Sensitivity difference to hepatotoxicity of cocaine in spontaneously hypertensive and Wistar Kyoto rats.

作者信息

Watanabe H K, Hoskins B, Ho I K

出版信息

Alcohol Drug Res. 1987;7(5-6):363-70.

PMID:3113443
Abstract

Experiments were conducted to determine the hepatic damage of cocaine in spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto (WKY) rats in terms of serum glutamic-oxaloacetic transaminase (SGOT) activity, liver weight/body weight ratio and hepatic microsomal enzyme activity, i.e., N-demethylase activity or UDP-glucuronyltransferase (GT) activity. In subacute experiments, 2, 4 and 10 daily cocaine treatments elevated the level of SGOT activity and reduced the liver weight/body weight ratio in SHR rats. The ethylmorphine N-demethylase activity and the cocaine N-demethylase activity in SHR rats were significantly greater (31% and 26%, respectively) than those in WKY rats. Ten daily treatments with cocaine diminished the ethyl morphine N-demethylase activity and the cocaine N-demethylase activity in SHR and WKY rats. However, attenuation of 4-nitrophenol GT activity was only observed in SHR rats. In acute experiments, a single dose of cocaine, 40 mg/kg, elevated the SGOT activity in SHR rats and reduced the 4-nitrophenol GT activity in SHR rats, but it did not affect the activities of SGOT and 4-nitrophenol GT in WKY rats. A higher dose of cocaine, 60 mg/kg, elevated the SGOT activity and reduced cocaine N-demethylase activity and 4-nitrophenol GT activity in both SHR and WKY rats. The present studies suggest that N-demethylation of cocaine plays an important role in the hepatotoxicity of cocaine in animals.

摘要

开展实验以从血清谷氨酸草酰乙酸转氨酶(SGOT)活性、肝重/体重比及肝微粒体酶活性(即N-脱甲基酶活性或UDP-葡糖醛酸基转移酶(GT)活性)方面确定可卡因对自发性高血压大鼠(SHR)和血压正常的Wistar Kyoto(WKY)大鼠的肝损伤。在亚急性实验中,每日2次、4次和10次给予可卡因处理可提高SHR大鼠的SGOT活性水平并降低其肝重/体重比。SHR大鼠中的乙基吗啡N-脱甲基酶活性和可卡因N-脱甲基酶活性显著高于WKY大鼠(分别高31%和26%)。每日10次给予可卡因处理可降低SHR和WKY大鼠中的乙基吗啡N-脱甲基酶活性和可卡因N-脱甲基酶活性。然而,仅在SHR大鼠中观察到4-硝基苯酚GT活性减弱。在急性实验中,单次给予40mg/kg可卡因可提高SHR大鼠的SGOT活性并降低其4-硝基苯酚GT活性,但对WKY大鼠的SGOT和4-硝基苯酚GT活性无影响。更高剂量的60mg/kg可卡因可提高SHR和WKY大鼠的SGOT活性并降低其可卡因N-脱甲基酶活性和4-硝基苯酚GT活性。本研究提示可卡因的N-脱甲基化在可卡因对动物的肝毒性中起重要作用。

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