INRA, UMR 1213 Herbivores, Equipe Alimentation Génomique Lactation, Site de Theix, F-63122 Saint-Genès-Champanelle, France.
J Dairy Sci. 2012 Nov;95(11):6755-9. doi: 10.3168/jds.2012-5620. Epub 2012 Sep 7.
This study was conducted in lactating goats with the aim of measuring the deposition of trans-11 18:1 (vaccenic acid, VA) and the product of its Δ(9)-desaturation, cis-9, trans-11 18:2 (rumenic acid, RA), in the major tissues that are involved in lipid metabolism in the lactating ruminant (i.e., mammary secretory tissue, liver, and omental and perirenal adipose tissues) and examining its potential link with variations in the expression of genes encoding Δ(9)-desaturase [stearoyl-CoA desaturases 1 and 5 (SCD1 and SCD5)]. Eight lactating goats were fed a diet supplemented with sunflower oil (n=4) or sunflower oil plus fish oil and additional starch (n=4), based on the hypothesis that these dietary treatments could affect Δ(9)-desaturase gene expression in specific tissues. A chemical tracer, 1.5 g of [1-13C]VA as nonesterified fatty acid, was delivered by jugular injection. Goats were slaughtered 4 d later, and tissue samples were collected for the measurement of [13C]VA and [13C]RA enrichment and SCD1 and SCD5 expression. The addition of fish oil and additional starch to a diet containing sunflower oil was associated with several changes in [13C]VA and [13C]RA enrichment. These results support previous studies suggesting that mammary secretory tissue is the primary site of Δ(9)-desaturation in lactating goats. In adipose tissues, the [13C]VA + [13C]RA enrichment was consistent with a net uptake of circulating fatty acids to reconstitute body reserves at the end of the lactation cycle. The putative uptake of [13C]RA synthesized by other tissues precludes any conclusion from being drawn regarding potential Δ(9)-desaturation in the liver of goats, despite the detection of SCD1 and SCD5 mRNA in this tissue. Finally, no significant effect of dietary treatment was observed for SCD1 or SCD5 mRNA abundance in the mammary secretory tissue or other body tissues.
本研究旨在测量反式 11 18:1(油酸,VA)和其 Δ(9)-去饱和产物顺式 9, 反式 11 18:2(蓖麻酸,RA)在泌乳反刍动物中参与脂质代谢的主要组织(即乳腺分泌组织、肝脏、网膜和肾周脂肪组织)中的沉积,并研究其与编码 Δ(9)-去饱和酶的基因表达变化的潜在联系[硬脂酰辅酶 A 去饱和酶 1 和 5(SCD1 和 SCD5)]。8 只泌乳山羊分别喂食添加葵花籽油(n=4)或葵花籽油加鱼油和额外淀粉(n=4)的日粮,基于这些日粮处理可能会影响特定组织中 Δ(9)-去饱和酶基因表达的假设。通过颈静脉注射 1.5 克[1-13C]VA 作为非酯化脂肪酸提供化学示踪剂。4 天后山羊被屠宰,收集组织样本测量[13C]VA 和[13C]RA 富集度以及 SCD1 和 SCD5 表达。在含有葵花籽油的日粮中添加鱼油和额外的淀粉与[13C]VA 和[13C]RA 富集的几个变化有关。这些结果支持了之前的研究,表明乳腺分泌组织是泌乳山羊中 Δ(9)-去饱和的主要部位。在脂肪组织中,[13C]VA + [13C]RA 富集与循环脂肪酸的净摄取一致,以在泌乳周期结束时重新构成身体储备。其他组织合成的[13C]RA 的潜在摄取排除了从肝脏中进行潜在的 Δ(9)-去饱和得出任何结论的可能性,尽管在该组织中检测到了 SCD1 和 SCD5 mRNA。最后,在乳腺分泌组织或其他身体组织中,日粮处理对 SCD1 或 SCD5 mRNA 丰度没有显著影响。