J. Anim Sci.
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Published online first on June 25, 2007
J. Anim Sci. 1990. doi:10.2527/jas.2007-0062
© 2007 American Society of Animal Science

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J. Anim Sci., doi: 10.2527/jas.2007-0062
©Copyright, 2007, The American Society of Animal Science


ARTICLE

Glucose-6-phosphate dehydrogenase and leptin are related to marbling differences among Limousin and Angus or Japanese Black x Angus steers

M. Bonnet 1, Y. Faulconnier 1, C. Leroux 1, C. Jurie 1, I. Cassar-Malek 1, D. Bauchart 1, P. Boulesteix 2, D. Pethick 3, J. F. Hocquette 1, Y. Chilliard 1*

1 INRA, UR1213 Unité de Recherche sur les Herbivores, F-63122 St Genès Champanelle, France
2 UPRA France Limousin Sélection, Lanaud, F-87220 Boisseuil, France
3 Murdoch University, Division of Veterinary and Biomedical Sciences Perth, Australia 6150

* To whom correspondence should be addressed. E-mail: chilliar{at}clermont.inra.fr.


   Abstract

This work aimed to investigate 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 and/or mRNA levels of enzymes involved in de novo lipogenesis [acetyl-coA carboxylase (ACC), fatty acid synthase (FAS), glucose-6-phosphate dehydrogenase (G6PDH), malic enzyme], circulating triacylglycerol (TAG) uptake [lipoprotein lipase (LPL)], and fatty acid esterification [glycerol-3-phosphate dehydrogenase (G3PDH)], as well as 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 (RA), and the glycolytic Semitendinosus (STN) 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 ≤ 0.02) FAS and G6PDH activities in s.c. AT. In RA and STN, the 75 % less (P < 0.001) TAG content was concomitant with a 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 10-mo finished Angus steers. 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 ≤ 0.02) mRNA levels and/or activities of ACC, G6PDH, LPL and G3PDH 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 ≤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.

Key Words: Adipose tissue, bovine, leptin, lipogenic activities, muscles







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