首页> 外文期刊>Journal of dairy science >Differential Effects of n-3 and n-6 Fatty Acids on Prostaglandin F_(2α) Production by Bovine Endometrial Cells
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Differential Effects of n-3 and n-6 Fatty Acids on Prostaglandin F_(2α) Production by Bovine Endometrial Cells

机译:n-3和n-6脂肪酸对牛子宫内膜细胞产生前列腺素F_(2α)的差异作用

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Recent studies have implicated n-3 polyunsaturated fatty acids in the reduction of eicosanoid production in the bovine uterus. The objective of this study was to determine whether the effect of eicosapentaenoic acid (EPA; C_(20:5), n-3) on PGF_(2α) production by bovine endometrial (BEND) cells is influenced by the quantity of linoleic acid (C_(18:2), n-6) in the incubation medium. Confluent BEND cells were incubated in the absence (control) or presence of 100 μM of EPA for 24 h. After incubation, cells were rinsed and then stimulated with phorbol 12,13-dibutyrate (PDBu; 100 ng/mL) for 6 h. Additional sets of culture dishes were treated with a combination of EPA and increasing n-6-3 fatty acid ratios for 24 h and then challenged with PDBu for 6 h. The PDBu stimulated PGF_(2α) secretion and upregulated steady-state concentrations of prostaglandin endoperoxide synthase-2 and peroxisome proliferator-activated receptor delta mRNA within 6 h. Preincubation of BEND cells with EPA for 24 h decreased PGF_(2α) response to phorbol ester, but had no detectable effects on prostaglandin endoperoxide synthase-2 or peroxisome proliferator-activated receptor delta mRNA abundance in PDBu-stimulated BEND cells. The inhibitory effect of EPA on PGF_(2α) production was reverted in BEND cells treated with an increasing n-6-to-n-3 fatty acid ratio. Findings indicate that the net inhibition of endometrial PGF_(2α) bioynthesis by n-3 fatty acids may vary depending on the ratio of n-6 to n-3 fatty acids in the uterus.
机译:最近的研究表明,n-3多不饱和脂肪酸可减少牛子宫中类花生酸的产生。这项研究的目的是确定二十碳五烯酸(EPA; C_(20:5),n-3)对牛子宫内膜(BEND)细胞生产PGF_(2α)的影响是否受亚油酸( C_(18:2),n-6)在孵育培养基中。在不存在(对照)或存在100μMEPA的情况下,将融合的BEND细胞孵育24小时。孵育后,漂洗细胞,然后用佛波醇12,13-二丁酸酯(PDBu; 100 ng / mL)刺激6小时。用EPA和增加n-6 / n-3脂肪酸比例的组合处理其他培养皿24小时,然后用PDBu攻击6 h。 PDBu在6小时内刺激了PGF_(2α)的分泌,并升高了前列腺素内过氧化物合酶2和过氧化物酶体增殖物激活的受体delta mRNA的稳态浓度。 BEND细胞与EPA预孵育24小时可降低对佛波酯的PGF_(2α)反应,但对PDBu刺激的BEND细胞中的前列腺素内过氧化物合酶2或过氧化物酶体增殖物激活的受体δmRNA丰度没有可检测的影响。在以增加的n-6-n-3脂肪酸比例处理的BEND细胞中,EPA对PGF_(2α)产生的抑制作用得以恢复。结果表明,n-3脂肪酸对子宫内膜PGF_(2α)生物合成的净抑制作用可能会根据子宫中n-6与n-3脂肪酸的比例而变化。

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