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Results Microsomal protein of adult worms can degrade the heme in vitro , the activity being 56.7 nmol bilirubin/.

结果 成虫的微粒体蛋白可在体外将血红素降解为胆红素,酶活性为 5 6 7nmol/,最适 pH为 8 7。

At a concentration of 10-6 mol·L-1, compound 4 showed antioxidative activity inhibiting Fe+2-cystine induced rat liver microsomal lipid peroxidation with inhibitory rate of 60%.

在10-6 mol·L-1浓度下,化合物4对Fe2+-Cys诱导大鼠肝微粒体丙二醛生成抑制率为60%。

With activities of the elderlyliver microsomal enzyme bring down,which dru9S dosage should be reduced?

老年人肝微粒体酶活性降低,因此服用下列哪些药物时要适当减量?

Liver neoplasms;Polymorphism, genetic;Life style;Microsomal epoxide hydrolase

肝肿瘤 多态现象,遗传生活方式微粒体环氧化物水解酶

In present study, we observed effect of taurine on liver lipid metabolism in rat, an animal capable of synthesizing substantial amount of taurine and extensively used in studies on lipid metabolism, and tried to explain its biochemical basis by investigating several hepatic microsomal membrane-bound enzymes activities related to lipid metabolism.

本实验中,我们将观察牛磺酸对大鼠肝脂质代谢的影响,并观察牛磺酸对大鼠肝脏微粒体脂质代谢酶活力的影响,以探讨牛磺酸影响肝脏脂质代谢的可能机制。

The metabolism of nimodipine in human liver microsomes was studied in vitro to identify its metabolites and metabolic pathway.

采用人肝微粒体在体外研究尼莫地平在人体内的代谢物及代谢途径。

Objective To establish the UV determination methodology of protein concentration in liver microsomes of Sprague-Dawley rats.

目的 建立Sprague-Dawley大鼠肝微粒体蛋白浓度测定的紫外分光光度检测法。

Through a multidimensional compared to prove the feasibility and reliability of in vitro drug metabolism platform of human and rat liver microsomes.

通过多方面的比较,证明了本研究建立的人、鼠肝微粒体体外药物代谢平台的可行性和可靠性。

Objective To explore the inhibitive effects of 1, 3, 8-trihydroxy-5-methoxyxanthone on cytochrome P450s (CYP450s) in human liver microsomes.

目的:在人肝微粒体中研究1,3,8-三羚基-5-甲氧基山酮(1,3,8-trihydroxy-5-methoxyx-anthone,TMX)对细胞色素P450酶(CYP450s)的抑制作用。

In addition,the result of HPLC shows that WLP-S-10 200mg/kg inhibited metabolism of acetaminophen in liver microsomes.

HPLC结果显示,WLP-S-10可以抑制肝微粒体对扑热息痛的代谢。

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呼气,收缩臀部肌肉;拱起身体,尽量抬起头来,右腿伸直朝向天花板(膝微屈,以避免肌肉紧张)。

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