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C57B1/6小鼠肝脏亚细胞组分的制备与表征,特别强调其在环氧水解酶活性研究中的适用性。

Preparation and characterization of subcellular fractions from the liver of C57B1/6 mice, with special emphasis on their suitability for use in studies of epoxide hydrolase activities.

作者信息

Meijer J, Bergstrand A, DePierre J W

出版信息

Biochem Pharmacol. 1987 Apr 1;36(7):1139-51. doi: 10.1016/0006-2952(87)90425-4.

DOI:10.1016/0006-2952(87)90425-4
PMID:3566808
Abstract

The present study was designed to prepare and characterize subcellular fractions from the liver of male C57B1/6 mice, with special emphasis on their suitability for use in studies of epoxide hydrolase isozymes. The effects of different washing and pelleting procedures on the mitochondrial, microsomal and cytosolic fractions were studied. It was found that 133,000 gav for 60 min (i.e. more extensive force than the usual 105,000 gav for 60 min) was necessary to obtain a membrane-free cytosolic fraction, while one wash for microsomes and two washes for mitochondria yielded reasonably pure fractions. The purity of the different fractions obtained by differential centrifugation was then determined using established enzyme markers and morphological examination with the electron microscope. Several enzymes involved in drug metabolism were also measured in these fractions. The subcellular distributions obtained here for marker enzymes closely resemble those reported for rat liver. Starvation had no significant effect on the epoxide hydrolase activities nor did the addition of mouse bile or rat liver cytosol, which might contain inhibitors. The change in epoxide hydrolase activities with time after preparation of the subcellular fractions was studied, as well as the effect of freeze-thawing. The subfractions prepared here are suitable for the further characterization of the different forms of epoxide hydrolase present in mouse liver, as well as for other studies requiring well-characterized subfractions.

摘要

本研究旨在制备雄性C57B1/6小鼠肝脏的亚细胞组分并对其进行表征,特别强调其在环氧化物水解酶同工酶研究中的适用性。研究了不同洗涤和离心程序对线粒体、微粒体和胞质组分的影响。发现为获得无膜胞质组分,需要133,000 gav离心60分钟(即比通常的105,000 gav离心60分钟施加更大的力),而微粒体洗涤一次、线粒体洗涤两次可得到纯度合理的组分。然后使用既定的酶标志物并通过电子显微镜进行形态学检查,测定通过差速离心获得的不同组分的纯度。还测定了这些组分中几种参与药物代谢的酶。此处获得的标记酶的亚细胞分布与大鼠肝脏报道的非常相似。饥饿对环氧化物水解酶活性没有显著影响,添加可能含有抑制剂的小鼠胆汁或大鼠肝脏胞质溶胶也没有显著影响。研究了亚细胞组分制备后环氧化物水解酶活性随时间的变化以及冻融的影响。此处制备的亚组分适用于进一步表征小鼠肝脏中存在的不同形式的环氧化物水解酶,以及适用于其他需要特征明确的亚组分的研究。

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