Bonnet M, Faulconnier Y, Leroux C, Jurie C, Cassar-Malek I, Bauchart D, Boulesteix P, Pethick D, Hocquette J F, Chilliard Y
INRA, UR1213 Herbivores, Site de Theix, F-63122 St Genès Champanelle, France.
J Anim Sci. 2007 Nov;85(11):2882-94. doi: 10.2527/jas.2007-0062. Epub 2007 Jun 25.
This work investigated the metabolic basis for the variability of carcass and i.m. adiposity in cattle. Our hypothesis was that the comparison of extreme breeds for adiposity might allow for the identification of some metabolic pathways determinant for carcass and i.m. adiposity. Thus, 23- to 28-mo-old steers of 3 breeds, 2 with high [Angus or Japanese Black x Angus (J. Black cross)] and 1 with low (Limousin) i.m. and carcass adiposity, were used to measure activities or mRNA levels, or both, of enzymes involved in de novo lipogenesis [acetyl-coA carboxylase, fatty acid synthase (FAS), glucose-6-phosphate dehydrogenase (G6PDH), malic enzyme], circulating triacylglycerol (TAG) uptake (lipoprotein lipase), and fatty acid esterification (glycerol-3-phosphate dehydrogenase), as well as the mRNA level of leptin, an adiposity-related factor. In a first study, enzyme activities were assayed in the s.c. adipose tissue (AT), the oxidative rectus abdominis, and the glycolytic semitendinosus muscles from steers finished for 6 mo. Compared with Angus or J. Black cross, Limousin steers had a 27% less (P = 0.003) rib fat thickness, and 23 and 29% less (P < or = 0.02) FAS and G6PDH activities in s.c. AT. In rectus abdominis and semitendinosus, the 75% less (P < 0.001) TAG content was concomitant with 50% less (P < 0.001) G6PDH activity. In a second study, enzyme activities plus mRNA levels were assayed in an oxido-glycolytic muscle, the longissimus thoracis (LT), in the i.m. AT dissected from LT, and in s.c. AT from the same Limousin steers and from Angus steers finished for 10 mo. Compared with Angus, the 50% less (P < 0.001) rib fat thickness in Limousin contrasted with the 1.1- to 5.8-fold greater (P < or = 0.02) mRNA levels or activities, or both, of acetyl-coA carboxylase, G6PDH, lipoprotein lipase, and glycerol-3-phosphate dehydrogenase in s.c. AT. Conversely, the 90% less (P < 0.001) TAG content in Limousin LT was concomitant to the 79 and 83% less (P < or = 0.002) G6PDH activity and leptin mRNA level. Such differences could arise from a greater number of adipocytes in LT from Angus steers because no difference was found between Limousin and Angus for G6PDH activity and leptin mRNA in i.m. AT. We conclude that FAS and G6PDH in s.c. AT could be involved in differences in carcass adiposity, but this relationship disappeared when the fatness increased strongly. Leptin and G6PDH are related to the expression of marbling whatever the body condition and thus could be relevant indicators of marbling in beef cattle.
本研究探讨了牛胴体及肌内脂肪沉积变异的代谢基础。我们的假设是,比较脂肪沉积差异极大的品种,或许能够确定一些决定胴体及肌内脂肪沉积的代谢途径。因此,选用了3个品种23至28月龄的阉牛,其中2个品种脂肪沉积高(安格斯牛或日本黑牛×安格斯牛(日本黑牛杂交种)),1个品种脂肪沉积低(利木赞牛),用于测定参与从头脂肪生成的酶(乙酰辅酶A羧化酶、脂肪酸合酶(FAS)、葡萄糖-6-磷酸脱氢酶(G6PDH)、苹果酸酶)的活性或mRNA水平,或两者皆测,同时测定循环三酰甘油(TAG)摄取(脂蛋白脂肪酶)和脂肪酸酯化(甘油-3-磷酸脱氢酶),以及肥胖相关因子瘦素的mRNA水平。在第一项研究中,对育肥6个月的阉牛的皮下脂肪组织(AT)、氧化型腹直肌和糖酵解型半腱肌中的酶活性进行了测定。与安格斯牛或日本黑牛杂交种相比,利木赞阉牛的肋部脂肪厚度减少了27%(P = 0.003),皮下AT中的FAS和G6PDH活性分别降低了23%和29%(P≤0.02)。在腹直肌和半腱肌中,TAG含量减少75%(P < 0.001)的同时,G6PDH活性降低了50%(P < 0.001)。在第二项研究中,对育肥10个月的利木赞阉牛和安格斯阉牛的氧化糖酵解型肌肉——胸最长肌(LT)、从LT中分离出的肌内AT以及皮下AT中的酶活性和mRNA水平进行了测定。与安格斯牛相比,利木赞牛的肋部脂肪厚度减少了50%(P < 0.001),而皮下AT中乙酰辅酶A羧化酶、G6PDH、脂蛋白脂肪酶和甘油-3-磷酸脱氢酶的mRNA水平或活性,或两者皆有,比安格斯牛高1.1至5.8倍(P≤0.02)。相反,利木赞牛LT中的TAG含量减少了90%(P < 0.001),同时G6PDH活性和瘦素mRNA水平分别降低了79%和83%(P≤0.002)。这种差异可能是由于安格斯阉牛LT中的脂肪细胞数量较多,因为在肌内AT中,利木赞牛和安格斯牛的G6PDH活性及瘦素mRNA水平没有差异。我们得出结论,皮下AT中的FAS和G6PDH可能与胴体脂肪沉积差异有关,但当脂肪过度沉积时,这种关系消失。无论体况如何,瘦素和G6PDH都与大理石花纹的表达有关,因此可能是肉牛大理石花纹的相关指标。