Vokhmintseva L V
Eksp Klin Farmakol. 2008 May-Jun;71(3):40-2.
Cytochrome P4502E1 levels in microsomal and lysosomal liver fractions was studied in Wistar rats treated with epinephrine (5.5 x 10(-6) mole/g, i.p., 1 h before test) on the background of isoniazid administration (daily dose 250 mg/kg, i.p., for 3 days). Epinephrine administration resulted in increased cytochrome P4502E1 level in the vacuole/lysosome apparatus of rat liver. On the background of isoniazid administration, cytochrome P4502E1 level and p-nitrophenol-hydroxylase activity in both low- and high-density lysosomes were decreased. Epinephrine administration under these conditions increased the cytochrome P-4502E1 level in lysosomes due to autophagy.
在异烟肼给药(每日剂量250mg/kg,腹腔注射,持续3天)的背景下,对用肾上腺素(5.5×10⁻⁶摩尔/克,腹腔注射,在测试前1小时)处理的Wistar大鼠的微粒体和溶酶体肝脏组分中的细胞色素P4502E1水平进行了研究。给予肾上腺素导致大鼠肝脏液泡/溶酶体装置中细胞色素P4502E1水平升高。在异烟肼给药的背景下,低密度和高密度溶酶体中的细胞色素P4502E1水平和对硝基苯酚羟化酶活性均降低。在这些条件下给予肾上腺素由于自噬作用增加了溶酶体中细胞色素P - 4502E1的水平。