Suppr超能文献

佛波酯抑制激动剂诱导的大鼠海马切片中[3H]肌醇-1-磷酸的积累。

Phorbol esters inhibit agonist-induced [3H] inositol-1-phosphate accumulation in rat hippocampal slices.

作者信息

Labarca R, Janowsky A, Patel J, Paul S M

出版信息

Biochem Biophys Res Commun. 1984 Sep 17;123(2):703-9. doi: 10.1016/0006-291x(84)90286-9.

Abstract

In rat hippocampal slices, carbachol and norepinephrine induce an accumulation of [3H]-inositol-1-phosphate which is markedly amplified in the presence of lithium. The tumor-promoting agents phorbol 12,13-dibutyrate (PDB) and 4 beta phorbol, 12 beta-myristate, 13 alpha-acetate (PMA) have no effect on [3H] inositol-1-phosphate accumulation alone, but when preincubated with hippocampal slices significantly inhibit the accumulation of [3H]-inositol-1-phosphate induced by carbachol and norepinephrine. The IC50 values for PDB and PMA are 0.2 microM and 25 microM respectively. In contrast, the weak tumor promoting agents 4-O-methylphorbol 12 myristate 13 acetate (MPMA) and phorbol 13,20-diacetate (P 13,20 DA) only slightly attenuate the agonist-induced response at concentrations less than or equal to 100 microM, whereas 4 alpha-phorbol (4 alpha-PHR), a biologically inactive phorbol, has no effect. These data suggest that phorbol ester receptor-mediated events may be negatively coupled to agonist-induced phosphatidylinositol hydrolysis.

摘要

在大鼠海马切片中,卡巴胆碱和去甲肾上腺素可诱导[3H]-肌醇-1-磷酸积累,在锂存在的情况下这种积累会显著增强。促肿瘤剂佛波醇12,13-二丁酸酯(PDB)和4β-佛波醇、12β-肉豆蔻酸酯、13α-乙酸酯(PMA)单独对[3H]肌醇-1-磷酸积累无影响,但与海马切片预孵育后可显著抑制卡巴胆碱和去甲肾上腺素诱导的[3H]-肌醇-1-磷酸积累。PDB和PMA的IC50值分别为0.2微摩尔和25微摩尔。相比之下,弱促肿瘤剂4-O-甲基佛波醇12-肉豆蔻酸酯13-乙酸酯(MPMA)和佛波醇13,20-二乙酸酯(P 13,20 DA)在浓度小于或等于100微摩尔时仅轻微减弱激动剂诱导的反应,而生物活性无的佛波醇4α-佛波醇(4α-PHR)则无作用。这些数据表明佛波醇酯受体介导的事件可能与激动剂诱导的磷脂酰肌醇水解呈负偶联。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验