长时间给药促肾上腺皮质激素对大鼠肾上腺微粒体和可溶性细胞组分[14C]甘氨酸结合活性的影响

Robert V. Farese
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引用次数: 8

摘要

1.1. 在ACTH给药的前几天,用于支持[14C]甘氨酸在体外并入大鼠肾上腺蛋白的105000 × g上清和微粒体的活性增加。与此同时,肾上腺重量、蛋白质含量和RNA含量逐渐增加,而DNA含量几乎没有变化。在ACTH给药后的几天内,出现一段时间的DNA复制,并伴有以下变化:(a)肾上腺总rna含量降低;(b)微粒体rna浓度降低;(c)阻断ACTH对肾上腺重量和净蛋白合成的影响;(d) 105 × 000 g支持[14C]甘氨酸掺入的上清液和微粒体的活性降低。这些抑制变化随后随着ACTH的进一步施用和dna复制期的完成而逆转。有人建议可溶性的(?转运酶)和微粒体(增加的核糖体和信使RNA)因子负责ACTH对肾上腺蛋白合成的影响是代谢不稳定的,ACTH诱导这些因子是通过(或需要)dna定向RNA合成介导的。
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Changes in [14C]glycine-incorporating activities of rat-adrenal microsomes and soluble cell fraction during prolonged adrenocorticotropin administration

  • 1.

    1. During the first several days of ACTH administration the activities of the 105 000 × g supernatant and microsomes for supporting incorporation of [14C]glycine in vitro into rat adrenal protein are increased. Concomitantly, there are progressive increases in adrenal weight, protein content and RNA content, with little or no change in DNA content.

  • 2.

    2. Over the next several days of ACTH administration a period of DNA replication occurs accompanied by the following changes: (a) a decrease in total adrenal-RNA content; (b) a decrease in microsomal-RNA concentration; (c) an interruption of the effect of ACTH on adrenal weight and net protein synthesis; and (d) a decrease in activities of the 105 × 000 g supernatant and microsomes for supporting [14C]glycine incorporation. These inhibitory changes are subsequently reversed with further ACTH administration and completion of the DNA-replication period.

  • 3.

    3. It is suggested that the soluble (? transfer enzyme) and microsomal (increased ribosomal and messenger RNA) factors responsible for the effects of ACTH on adrenal protein synthesis are metabolically unstable, and that the induction of these factors by ACTH is mediated through (or requires) DNA-directed RNA synthesis.

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Author index Erratum Subject index Changes in sedimentation properties of ribosomal ribonucleic acids during the course of ribosome formation in Escherichia coli The inhibition of deoxyribonucleotidyl transferase, DNAase and RNAase by sodium poly ethenesulfonic acid. Effect of the molecular weight of the inhibitor
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