首页> 美国卫生研究院文献>Physiological Reports >Expression of genes involved in carbohydrate‐lipid metabolism in muscle and fat tissues in the initial stage of adult‐age obesity in fed and fasted mice
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Expression of genes involved in carbohydrate‐lipid metabolism in muscle and fat tissues in the initial stage of adult‐age obesity in fed and fasted mice

机译:进食和禁食小鼠成年肥胖初期肌肉和脂肪组织中糖脂代谢相关基因的表达

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摘要

C57Bl mice exhibit impaired glucose metabolism by the late adult age under standard living conditions. The aim of this study was to evaluate white adipose tissue (WAT), brown adipose tissue (BAT), and skeletal muscle expression of genes involved in carbohydrate‐lipid metabolism at postpubertal stages preceding the late adult age in C57Bl mice. Muscle mRNA levels of uncoupling protein 3 (Ucp3) and carnitine palmitoyltransferase 1 (Cpt1) (indicators of FFA oxidation), WAT mRNA levels of hormone‐sensitive lipase (Lipe) and lipoprotein lipase (Lpl) (indicators of lipolysis and lipogenesis), muscle and WAT mRNA levels of the type 4 glucose transporter Slc2a4 (indicators of insulin‐dependent glucose uptake), and BAT mRNA levels of uncoupling protein 1 (Ucp1) (indicator of thermogenesis) were measured in fed and 16 h‐fasted mice in three age groups: 10‐week‐old (young), 15‐week‐old (early adult), and 30‐week‐old (late adult). Weight gain from young to early adult age was not accompanied by changes in WAT and BAT indexes and biochemical blood parameters. Weight gain from early to late adult age was accompanied by increased WAT and BAT indexes and decreased glucose tolerance. Muscle Ucp3 and Cpt1 mRNA levels and WAT Lipe and Slc2a4 mRNA levels increased from young to early adult age and then sharply decreased by the late adult age. Moreover, BAT Ucp1 mRNA level decreased in the late adult age. Fasting failed to increase muscle Cpt1 style="fixed-case">mRNA levels in late adult mice. These transcriptional changes could contribute to impaired glucose metabolism and the onset of obesity in late adult mice during normal development.
机译:在标准生活条件下,到成年后期,C57B1小鼠的葡萄糖代谢受损。这项研究的目的是评估C57B1小鼠成年后期青春期后糖脂代谢相关基因的白色脂肪组织(WAT),棕色脂肪组织(BAT)和骨骼肌表达。解偶联蛋白3(Ucp3)和肉碱棕榈酰转移酶1(Cpt1)的肌肉mRNA水平(FFA氧化指标),激素敏感性脂肪酶(Lipe)和脂蛋白脂肪酶(Lpl)的WAT mRNA水平(脂解和脂肪生成指标),肌肉在三个年龄的进食和16小时禁食小鼠中测量了4型葡萄糖转运蛋白Slc2a4(胰岛素依赖性葡萄糖摄取的指标)和WAT mRNA水平以及解偶联蛋白1(Ucp1)的BAT mRNA水平(生热指标)年龄组:10周龄(年轻),15周龄(成年早期)和30周龄(成年晚期)。从年轻到成年体重增加并没有伴随WAT和BAT指数以及生化血液参数的变化。从成年早期到晚期体重增加,同时伴随着WAT和BAT指数增加以及葡萄糖耐量降低。肌肉Ucp3和Cpt1 mRNA水平以及WAT Lipe和Slc2a4 mRNA水平从年轻到成年早期就升高,而到成年后期则急剧下降。此外,BAT Ucp1 mRNA水平在成年后期下降。空腹未能增加成年后期小鼠的肌肉Cpt1 style =“ fixed-case”> mRNA 水平。这些转录变化可能会导致葡萄糖代谢受损和成年后期正常发育期间肥胖的发作。

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