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[环核苷酸对海胆早期胚胎对细胞毒性神经药理学制剂敏感性的影响]

[Effect of cyclic nucleotides on the sensitivity of early sea urchin embryos to cytotoxic neuropharmacological preparations].

作者信息

Shmukler Iu B, Buznikov G A, Grigor'ev N G, Mal'chenko L A

出版信息

Biull Eksp Biol Med. 1984 Mar;97(3):354-5.

PMID:6322883
Abstract

It has been shown that cytotoxic action of neuropharmacological drugs (transmitter antagonists) on early urchin embryos is reduced or abolished by cyclic nucleotides and sodium fluoride. Such a protective action differs in cAMP and dibutyryl analogs of cyclic nucleotides, depending on the chemical structure of an embryotoxic substance. It is suggested that, endogenous intracellular "prenervous" transmitters and cyclic nucleotides are interrelated in the regulation of cell division in urchin embryos.

摘要

研究表明,环核苷酸和氟化钠可降低或消除神经药理学药物(递质拮抗剂)对海胆早期胚胎的细胞毒性作用。这种保护作用在环磷酸腺苷(cAMP)和环核苷酸的二丁酰类似物中有所不同,这取决于胚胎毒性物质的化学结构。有人提出,内源性细胞内“神经前体”递质和环核苷酸在海胆胚胎细胞分裂的调节中相互关联。

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