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泌乳兔乳腺上皮细胞中花生四烯酸代谢与酪蛋白分泌:前列腺素和白三烯合成抑制剂的作用

Arachidonic acid metabolism and casein secretion in lactating rabbit mammary epithelial cells: effects of inhibitors of prostaglandins and leukotrienes synthesis.

作者信息

Blachier F, Lacroix M C, Ahmed A M, Léger C, Ollivier-Bousquet M

机构信息

Laboratoire de Physiologie de la Lactation INRA-CRJ, Jouy-en-Josas, France.

出版信息

Prostaglandins. 1988 Feb;35(2):259-76. doi: 10.1016/0090-6980(88)90092-5.

Abstract

The metabolism of arachidonic acid (AA) in fragments of lactating rabbit mammary glands in vitro was studied by considering the distribution of 13-[14C]AA in the cells, and the effects of inhibitors of cyclooxygenase and lipoxygenase pathway on the basal and prolactin (PRL)-stimulated casein secretion. 13-[14C]AA was incorporated in all classes of lipids and PRL increased transiently the percentage of free fatty acid after 1 and 5 min. Ten microM ETYA (5,8,11,14-Eicosatetraynoic acid), a tetrayne analogue of AA inhibited prostaglandins F2 alpha (PGF2 alpha) production but not leukotrienes B4 and C4 (LTB4 and LTC4) production and increased basal casein secretion. 10(-4) M DCHA (Docosahexaenoic acid) a competitive inhibitor of prostaglandin-synthetase inhibited PGF2 alpha production but did not affect basal nor PRL-stimulated casein secretion. Fourteen microM indomethacin inhibited PGF2 alpha and LTC4 production and PRL-stimulated casein secretion. Ten microM NdgA (nordihydroguaiaretic acid) an inhibitor of lipoxygenase pathway, inhibited LTB4 and LTC4 production, increased basal level of casein secretion and inhibited PRL-stimulated casein secretion. Hundred microM caffeic acid, an inhibitor of glutathione-S-transferase (GST), a class of enzymes implied in the transformation of LTA4 into LTC4, had the same effect that NDGA on basal and PRL-stimulated casein secretion. These findings show that inhibitors of AA metabolites alter casein secretion.

摘要

通过考虑13-[14C]花生四烯酸(AA)在细胞中的分布,以及环氧合酶和脂氧合酶途径抑制剂对基础和催乳素(PRL)刺激的酪蛋白分泌的影响,研究了体外泌乳兔乳腺组织碎片中AA的代谢。13-[14C]AA被整合到所有脂质类别中,PRL在1分钟和5分钟后短暂增加了游离脂肪酸的百分比。10微摩尔ETYA(5,8,11,14-二十碳四烯酸),一种AA的四炔类似物,抑制前列腺素F2α(PGF2α)的产生,但不抑制白三烯B4和C4(LTB4和LTC4)的产生,并增加基础酪蛋白分泌。10(-4)M DCHA(二十二碳六烯酸),一种前列腺素合成酶的竞争性抑制剂,抑制PGF2α的产生,但不影响基础或PRL刺激的酪蛋白分泌。14微摩尔消炎痛抑制PGF2α和LTC4的产生以及PRL刺激的酪蛋白分泌。10微摩尔去甲二氢愈创木酸(NdgA),一种脂氧合酶途径抑制剂,抑制LTB4和LTC4的产生,增加酪蛋白分泌的基础水平并抑制PRL刺激的酪蛋白分泌。100微摩尔咖啡酸,一种谷胱甘肽-S-转移酶(GST)抑制剂,一类参与LTA4转化为LTC4的酶,对基础和PRL刺激的酪蛋白分泌具有与NdgA相同的作用。这些发现表明AA代谢物抑制剂会改变酪蛋白分泌。

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