与低剂量外源性前列腺素E(2)相比,饲料中的花生四烯酸抑制了仔猪的骨转化,而前列腺素E则促进了仔猪的骨形成。

IF 2.9 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Vienna D Lucia, Shirley C Fitzpatrick-Wong, Hope A Weiler
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引用次数: 16

摘要

本研究旨在比较膳食中花生四烯酸(AA)与前列腺素E(2)对骨细胞代谢和骨量的影响。选取7窝28头仔猪,随机分为4组,每组1组,试验期15 d:脂肪酸补充配方(FA占总脂肪酸的0.8%,DHA占总脂肪酸的0.1%)+PGE(2)注射剂(0.1mg/kg/d)、FA+生理盐水注射剂、标准配方(STD: n-6∶n-3∶8:1)+PGE(2)注射剂或STD+生理盐水注射剂。血浆骨钙素显示,PGE(2)导致成骨细胞活性升高,尿钙排泄也减少。通过尿n -末端肽和降低骨PGE,膳食FA导致骨吸收减少(2)。PGE(2)和FA处理分别导致股骨矿物质含量升高,但联合处理导致降低。因此,PGE(2)和FA导致骨量增加的机制是不同的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dietary arachidonic acid suppresses bone turnover in contrast to low dosage exogenous prostaglandin E(2) that elevates bone formation in the piglet.

This study was designed to compare the effects of dietary arachidonic acid (AA) versus prostaglandin E(2) (PGE(2)) on bone cell metabolism and bone mass. Twenty-eight piglets from 7 litters were randomized to 1 of 4 treatments for 15 days: fatty acid supplemented formula (FA: 0.8% of total fatty acids as AA and 0.1% of total fatty acids as DHA)+PGE(2) injections (0.1mg/kg/day), FA+saline injections, standard formula (STD: n-6:n-3 of 8:1) + PGE(2) injections or STD+saline injections. PGE(2) resulted in elevated osteoblast activity as indicated by plasma osteocalcin and also reduced urinary calcium excretion. Dietary FA resulted in reduced bone resorption as indicated by urinary N-telopeptide and reduced bone PGE(2). Both PGE(2) and FA treatments independently lead to elevated femur mineral content, but the combined treatment caused a reduction. Thus the mechanisms by which PGE(2) and FA lead to enhanced bone mass are distinct.

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来源期刊
CiteScore
6.40
自引率
6.70%
发文量
60
审稿时长
13.2 weeks
期刊介绍: The role of lipids, including essential fatty acids and their prostaglandin, leukotriene and other derivatives, is now evident in almost all areas of biomedical science. Cell membrane behaviour and cell signalling in all tissues are highly dependent on the lipid constituents of cells. Prostaglandins, Leukotrienes & Essential Fatty Acids aims to cover all aspects of the roles of lipids in cellular, organ and whole organism function, and places a particular emphasis on human studies. Papers concerning all medical specialties are published. Much of the material is particularly relevant to the development of novel treatments for disease.
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