Damanhouri Z A, Tayeb O S
Department of Pharmacology, Faculty of Medicine and Allied Sciences, King Fahad Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
Comp Biochem Physiol Biochem Mol Biol. 1994 Jul;108(3):349-55. doi: 10.1016/0305-0491(94)90086-8.
The activities of the conjugative enzymes, glutathione S-transferase and UDP-glucuronyl-transferase, have been measured in vitro in the livers of camels, guinea-pigs and rats. Some sex differences were observed in the levels of these conjugative enzymes. In rats and guinea-pigs, females had higher UDP-glucuronyltransferase activity than males. In camels, females had higher glutathione S-transferase activity than males. In these species, the cytochrome P-450 isozymes observed between the 50,000 and 60,000 mol. wt regions have been separated and characterized by SDS-polyacrylamide gel electrophoresis. Camels showed lower levels of all types of cytochrome P-450 isozymes, while guinea-pigs showed higher levels of most of these isozymes. In general, camels seemed to have the lowest drug-metabolizing enzyme activity when compared to rats and guinea-pigs.
已在体外测定了骆驼、豚鼠和大鼠肝脏中结合酶谷胱甘肽S-转移酶和UDP-葡萄糖醛酸基转移酶的活性。在这些结合酶的水平上观察到了一些性别差异。在大鼠和豚鼠中,雌性的UDP-葡萄糖醛酸基转移酶活性高于雄性。在骆驼中,雌性的谷胱甘肽S-转移酶活性高于雄性。在这些物种中,通过SDS-聚丙烯酰胺凝胶电泳分离并鉴定了在50,000至60,000摩尔分子量区域之间观察到的细胞色素P-450同工酶。骆驼的所有类型细胞色素P-450同工酶水平较低,而豚鼠的大多数这些同工酶水平较高。总体而言,与大鼠和豚鼠相比,骆驼的药物代谢酶活性似乎最低。