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激素和药物对成骨样细胞原代培养物中花生四烯酸代谢的刺激作用。

Stimulation of arachidonic acid metabolism in primary cultures of osteoblast-like cells by hormones and drugs.

作者信息

Feyen J H, van der Wilt G, Moonen P, Di Bon A, Nijweide P J

出版信息

Prostaglandins. 1984 Dec;28(6):769-81. doi: 10.1016/0090-6980(84)90034-0.

Abstract

The effects of parathyroid hormone (PTH), dihydroxycholecalciferol (1,25-(OH)2 D3), thrombin, epidermal growth factor (EGF) and 12-o-tetradecanoylphorbol-13-acetate (PMA) on the biosynthesis and release of arachidonic acid metabolites were studied in primary cultures of osteoblast-like cells isolated from 18-day-old chick embryo calvaria. Cells were labelled with (14C)-arachidonic acid for 30 h. The radioactive eicosanoids were extracted from the cell culture media after a further 30 h stimulation period and analysed on a PRP-1 column by HPLC. The radioactive products were characterized by co-elution of (3H) standard prostanoids. Osteoblasts showed a basal release of the prostanoids 6-keto-PGF1 alpha, TXB2, PGF2 alpha, PGE2, PGD2 and PGB2, the latter being the most abundant one. Indomethacin (10(-5) M) effectively inhibited the basal release, but not that of an as yet unidentified compound. The release of prostanoids was stimulated by PTH (2 U/ml), thrombin (0.4 NIH/ml), EGF (50 ng/ml) and PMA (25 ng/ml), the latter being by far the most potent one. 1,25-(OH)2D3 was found to slightly inhibit the prostanoid release. These results indicate: (1) primary cultures of osteoblasts synthesize several prostaglandins, thromboxane B2 and one unidentified product. (2) the action on bone of PTH and the various drugs tested may be, at least partly, mediated by an increased prostaglandin production by osteoblasts. Clearly this does not apply to 1,25-(OH)2D3.

摘要

在从18日龄鸡胚颅骨分离的成骨细胞样细胞原代培养物中,研究了甲状旁腺激素(PTH)、二羟胆钙化醇(1,25-(OH)₂D₃)、凝血酶、表皮生长因子(EGF)和12-O-十四烷酰佛波醇-13-乙酸酯(PMA)对花生四烯酸代谢产物生物合成和释放的影响。细胞用(¹⁴C)-花生四烯酸标记30小时。在进一步的30小时刺激期后,从细胞培养基中提取放射性类二十烷酸,并通过高效液相色谱在PRP-1柱上进行分析。放射性产物通过(³H)标准前列腺素的共洗脱进行表征。成骨细胞显示出前列腺素6-酮-PGF₁α、TXB₂、PGF₂α、PGE₂、PGD₂和PGB₂的基础释放,其中PGB₂含量最高。吲哚美辛(10⁻⁵M)有效抑制基础释放,但对一种尚未鉴定的化合物的释放没有抑制作用。PTH(2 U/ml)、凝血酶(0.4 NIH/ml)、EGF(50 ng/ml)和PMA(25 ng/ml)刺激前列腺素的释放,其中PMA的刺激作用最强。发现1,25-(OH)₂D₃略微抑制前列腺素的释放。这些结果表明:(1)成骨细胞原代培养物合成几种前列腺素、血栓素B₂和一种未鉴定的产物。(2)PTH和所测试的各种药物对骨骼的作用可能至少部分是由成骨细胞前列腺素产生增加介导的。显然,这不适用于1,25-(OH)₂D₃。

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