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Preparation and Characterization of Rodent Intestinal Microsomes: Comparative Assessment of Two Methods

机译:啮齿动物肠道微粒体的制备和表征:两种方法的比较评估

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摘要

Small intestine plays an important role in the first-pass metabolism of orally ingested xenobiotics as a result of expression of both Phase I and Phase II metabolic enzymes, together with associated transporters. Intestinal microsomes thus can be used to study susceptibility of compounds to metabolism in vitro. The present study was undertaken to have a comparative assessment between different methods of preparation of rodent intestinal microsomes. Mouse and rat intestinal microsomes were prepared by two methods, in method A intestines were homogenized, while in method B mucosal cells were scrapped followed by homogenization. Further, microsomes were prepared by centrifugation (10000xg) followed by ultra centrifugation (100000×g) of the homogenates. The prepared microsomes were characterized for protein concentration using Bradford's method and CYP450 content using carbon monoxide bubbling method. The protein concentration and CYP450 content in microsomes prepared by method B was significantly higher than method A. In conclusion, superior quality intestinal microsomes can be obtained from rodents by using scrapped intestinal mucosal cells as compared to the intestinal homogenates.
机译:由于I期和II期代谢酶以及相关转运蛋白的表达,小肠在口服摄入的异物的首过代谢中起着重要作用。因此,肠微粒体可用于研究化合物对体外代谢的敏感性。进行本研究是为了对啮齿动物肠道微粒体的不同制备方法进行比较评估。通过两种方法制备小鼠和大鼠的肠微粒体,在方法A中肠均质化,而在方法B中刮除粘膜细胞,然后均质化。此外,通过将匀浆物离心(10000xg)然后超离心(100000×g)来制备微粒体。使用Bradford方法表征制备的微粒体的蛋白质浓度,使用一氧化碳鼓泡方法表征CYP450的含量。通过方法B制备的微粒体中的蛋白质浓度和CYP450含量显着高于方法A。总之,与肠匀浆相比,使用报废的肠粘膜细胞可以从啮齿类动物中获得优质肠微粒体。

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