Mashek D G, Grummer R R
Department of Dairy Science, University of Wisconsin, Madison 53706, USA.
J Dairy Sci. 2004 Jan;87(1):67-72. doi: 10.3168/jds.S0022-0302(04)73143-4.
The objective was to determine the effects of linoleic acid and different isomers of conjugated linoleic acid (CLA) at different concentrations on hepatic lipid and glucose metabolism in the bovine. Monolayer cultures of hepatocytes obtained from 7- to 10-d-old Holstein bull calves were exposed to treatments from 16 to 64 h after plating. The treatments included 1.0 mM palmitic acid plus either 0.1 or 1.0 mM of cis-9, cis-12 linoleic acid, cis-9, trans-11 CLA, or trans-10, cis-12 CLA. Metabolism of palmitic acid to cellular triacylglycerol (TAG) was decreased when media contained cis-9, trans-11 compared with trans-10, cis-12 CLA. Total cellular TAG content was increased for the CLA isomers compared to cis-9, cis-12 linoleic acid. Both CLA isomers increased palmitic acid incorporation into phospholipids, cholesterol, and media triacylglycerol compared with cis-9, cis-12 linoleic acid at a concentration of 1.0 mM. Increasing the concentration of treatment fatty acids from 0.1 to 1.0 mM decreased oxidation of palmitic acid to acid-soluble products, but no effects of fatty acids were observed. There was no treatment effect on rates of gluconeogenesis from propionic acid. Overall, CLA isomers elicited changes in palmitic acid metabolism to cellular and media triacylglycerol, and cellular phospholipids and cholesterol, but had little or no effect on other measured pathways of lipid metabolism or gluconeogenesis in bovine hepatocytes.
目的是确定不同浓度的亚油酸和共轭亚油酸(CLA)的不同异构体对牛肝脏脂质和葡萄糖代谢的影响。从7至10日龄的荷斯坦公牛犊获得的肝细胞单层培养物在接种后16至64小时接受处理。处理包括1.0 mM棕榈酸加0.1或1.0 mM的顺式-9,顺式-12亚油酸、顺式-9,反式-11 CLA或反式-10,顺式-12 CLA。与反式-10,顺式-12 CLA相比,当培养基含有顺式-9,反式-11时,棕榈酸向细胞三酰甘油(TAG)的代谢减少。与顺式-9,顺式-12亚油酸相比,CLA异构体的总细胞TAG含量增加。与浓度为1.0 mM的顺式-9,顺式-12亚油酸相比,两种CLA异构体均增加了棕榈酸掺入磷脂、胆固醇和培养基三酰甘油中的量。将处理脂肪酸的浓度从0.1 mM增加到1.0 mM可减少棕榈酸向酸溶性产物的氧化,但未观察到脂肪酸的影响。丙酸糖异生速率没有处理效应。总体而言,CLA异构体引起棕榈酸代谢向细胞和培养基三酰甘油以及细胞磷脂和胆固醇的变化,但对牛肝细胞中其他测量的脂质代谢途径或糖异生几乎没有影响。