The content and distribution of body lipids are of special interest for production efficiency and meat quality in the farm animal industry. Triglycerides represent the most variable fraction of tissue lipids, and are mainly stored in adipocytes. Although several studies have reported regional differences in the expression of genes and their products in adipocytes from various species, the characteristics of i.m. adipocytes remain poorly described. To evaluate adipocyte features according to muscle and other fat locations, adipocyte proteins were isolated from trapezius skeletal muscle, and intermuscular, s.c., or perirenal adipose tissues from 6 female pigs (80 d of age). Protein extracts were labeled and analyzed by 2-dimensional, fluorescent, differential gel electrophoresis. The comparisons revealed that 149 spots were always differentially expressed (P < 0.05, ratio exceeding |2|-fold difference) between i.m. adipocytes and the fat cells derived from the 3 other adipose locations. The proteins that were downregulated in i.m. fat cells belonged to various metabolic pathways, such as lipogenesis (cytosolic malate dehydrogenase and isocitrate dehydrogenase, P < 0.01), glycolysis (enolases and aldolase, P = 0.01), lipolysis (perilipin, P < 0.01), fatty acid oxidation (long-chain fatty-acyl CoA dehydrogenase, P < 0.01), and energy transfer (catalase, voltage-dependent anion channel 1, and electron-transfer flavoprotein, P < 0.05). In contrast, both prohibitin-1 and cell division cycle 42 homolog, with possible roles in cell growth, were up-regulated (P < 0.05) in i.m. adipocytes compared with other fat cells. Fewer differences were observed when adipocytes isolated from s.c., perirenal, and intermuscular fat tissues were compared, with a maximum of 17 spots differing significantly in abundance between perirenal and s.c. adipose tissues. The findings that proteins involved in both anabolic and energy-yielding catabolic pathways are downregulated in i.m. adipocytes compared with s.c., visceral, or intermuscular adipocytes, suggest that the metabolic activity of i.m. adipocytes is low. Thus, triggering adipogenesis rather than cell metabolism per se might be a valuable strategy to control lipid deposition in pig skeletal muscles.
ABSTRA ABSTRA ABSTRA ABSTRA ABSTRACT CT CT CT CT: A quality index method (QIM) was dev : A quality index method (QIM) was dev : A quality index method (QIM) was dev : A quality index method (QIM) was dev : A quality index method (QIM) was developed for far eloped for far eloped for far eloped for far eloped for farmed A med A med A med A med Atlantic halibut, and together with instr tlantic halibut, and together with instr tlantic halibut, and together with instr tlantic halibut, and together with instr tlantic halibut, and together with instrumenumen-umen-umenumental, chemical, sensor tal, chemical, sensor tal, chemical, sensor tal, chemical, sensor tal, chemical, sensory y y y y, and bacter , and bacter , and bacter , and bacter , and bacteriological analysis iological analysis iological analysis iological analysis iological analysis, quality changes of halibut stor , quality changes of halibut stor , quality changes of halibut stor , quality changes of halibut stor , quality changes of halibut stored on ice for 26 d was ev ed on ice for 26 d was ev ed on ice for 26 d was ev ed on ice for 26 d was ev ed on ice for 26 d was evaluated. aluated. aluated. aluated. aluated.
fed either a recommended humantype diet (NF; n ϭ 4) or were overfed a western-type diet with saturated fat and high-glycemic index carbohydrates (OF, n ϭ 4). Muscle samples (biceps femoris) were histochemically stained for the identification of intramuscular adipocytes, intramyocellular lipid aggregates (oil red O), and myofiber types (myosin ATPase, succinate dehydrogenase). Gene expressions and/or activities of factors involved in lipogenesis, lipolysis, or energetic metabolism were quantified in muscle. Results: Cross-sectional areas of myofibers paralleled pig body weight (r ϭ 0.86, p Ͻ 0.01). The size of intramuscular adipocytes, the relative proportion of oil red O-stained fibers, and total muscle lipid content tended (p Յ 0.10) to increase in response to OF diet. Hormone-sensitive lipase, carnitine palmityl transferase-I, and uncoupling protein 2 mRNA levels were lower (p Ͻ 0.05) in OF pigs than in NF pigs. Activities of -hydroxyacyl-coenzyme A dehydrogenase and citrate synthase assessing post-carnitine palmityl transferase I events and the proportion of oxidative myofibers were not altered by OF diet. Activity and gene expression of fatty acid synthase were lower (p Ͻ 0.02) in OF pigs than in NF pigs. Discussion: Overfeeding in Yucatan minipigs reduced the expression levels of three catabolic steps in skeletal muscle that are involved also in the etiology of human obesity.
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