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给予α-六氯环己烷后,大鼠肝脏中用于合成胞苷核苷酸的[2-¹⁴C]乳清酸利用率降低。

Decreased utilization of [2-14C]orotic acid for the synthesis of cytidine nucleotides in rat liver after administration of alpha-hexachlorocyclohexane.

作者信息

Seifert J, Vácha J

出版信息

Toxicology. 1977 Apr;7(2):155-61. doi: 10.1016/0300-483x(77)90060-9.

Abstract

Administration of alpha-1,2,3,4,5,6-hexachlorocyclohexane (alpha-HCH) to rats decreased the utilization of [2-14C]orotic acid for the synthesis of liver cytidine nucleotides. The specific radioactivities of uridine components of the acid-soluble pool and rRNA increased during the first hours of treatment with the drug. Later on the specific radioactivities of uridine nucleotides remained unchanged, while those of cytidine components decreased gradually. Administration of hydrocortisone increased the incorporation of labelled orotic acid into rRNA cytidylic acid.

摘要

给大鼠施用α-1,2,3,4,5,6-六氯环己烷(α-六氯环己烷)会降低[2-¹⁴C]乳清酸用于合成肝脏胞嘧啶核苷酸的利用率。在药物治疗的最初几个小时内,酸溶性池和rRNA中尿苷成分的比放射性增加。随后,尿苷核苷酸的比放射性保持不变,而胞嘧啶成分的比放射性逐渐降低。施用氢化可的松会增加标记乳清酸掺入rRNA胞苷酸的量。

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