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Sources of Extramitochondrial Corticoidogenic Cholesterol in the Adrenal Cortex

机译:肾上腺皮质线粒体皮质类固醇的来源

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References(21) Cited-By(5) Intracellular sources of extramitochondrial corticoidogenic cholesterol in bovine, rat and hamster adrenocortical cells were examined in vitro by comparing the species differences in the effects of various inhibitors on the adrenocorticotropic hormone (ACTH)-induced corticoidogenesis. The inhibitors were ML-236B (3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor), W-7 (N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide; calmodulin inhibitor), dichlorvos (0, 0-dimethyl-2, 2-dichlorovinyl phosphate; organic phosphorylation inhibitor), chloroquine ((7-chloro-4-4-diethylamino-1-methyl-butylamino) quinoline; lysosomal enzyme inhibitor) and cycloheximide (protein synthesis inhibitor). During 2 to 3 hr incubation periods, the ACTH-induced corticoidogenesis was not inhibited by ML-236B (100 μM) in the bovine and rat adrenocortical cells. In the hamster adrenocortical cells, ML-236B (100 μM) did not affect the ACTH-induced corticoidogenesis during the initial 1 hr incubation periods; but thereafter, the ACTH-induced corticoidogenesis during the subsequent 2 hr incubation periods was completely blocked by ML-236B. The ACTH-induced corticoidogenesis was inhibited by W-7 (up to 25 μM) in the bovine and rat adrenocortical cells, but this was not the case in the hamster cells. Chloroquine (up to 400 μM) inhibited the ACTH-induced corticoidogenesis in the adrenocortical cells of three different species, but the hamster adrenal cells were much more vulnerable than the bovine and rat cells. The ACTH-induced corticoidogenesis in the adrenocortical cells of three different species were equally inhibited by cycloheximide (up to 1 mM). It could be deduced from the present data that intracellular sources of corticoidogenic cholesterol during the ACTH-induced corticoidogenesis in vitro are mainly lysosomes and de novo synthetized cholesterol in the hamster cells, and the main sources are lipid droplets and lysosomes in the rat and bovine cells, respectively.
机译:参考文献(21)(5)牛,大鼠和仓鼠肾上腺皮质细胞中线粒体皮质类固醇生成胆固醇的细胞内来源,通过比较各种抑制剂对促肾上腺皮质激素(ACTH)诱导的皮质类固醇生成作用的物种差异,在体外进行了检查。抑制剂为ML-236B(3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂),W-7(N-(6-氨基己基)-5-氯-1-萘磺酰胺;钙调蛋白抑制剂),敌敌畏(0,0-二甲基-2,2-二氯乙烯基磷酸;有机磷酸化抑制剂),氯喹((7-氯-4-4-二乙基氨基-1-甲基丁基氨基)喹啉;溶酶体酶抑制剂)和环己酰亚胺(蛋白质合成)抑制剂)。在2至3小时的潜伏期中,牛和大鼠肾上腺皮质细胞中ML-236B(100μM)不会抑制ACTH诱导的皮质激素生成。在仓鼠肾上腺皮质细胞中,ML-236B(100μM)在最初的1小时潜伏期中不影响ACTH诱导的皮质激素生成。但是此后,ML-236B完全阻止了ACTH诱导的随后2个小时潜伏期的皮质激素生成。 W-7(最高达25μM)在牛和大鼠肾上腺皮质细胞中抑制了ACTH诱导的皮质激素生成,但在仓鼠细胞中却并非如此。氯喹(最高达400μM)在三种不同物种的肾上腺皮质细胞中抑制了ACTH诱导的皮质类固醇生成,但是仓鼠肾上腺细胞比牛和大鼠细胞更易受伤害。在三种不同物种的肾上腺皮质细胞中,ACTH诱导的皮质类固醇生成均受到环己酰亚胺的抑制(最高1 mM)。从目前的数据可以推断,ACTH诱导的体外皮质激素生成过程中,皮质激素生成胆固醇的细胞内来源主要是溶酶体和从头开始合成的仓鼠细胞中胆固醇,主要来源是大鼠和牛细胞中的脂质滴和溶酶体。 , 分别。

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