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首页> 外文期刊>Journal of animal and veterinary advances >Expression Patterns of the Cannabinoid Receptor 1 Gene in Pig Skeletal Muscle and Skeletal Satellite Muscle Cells
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Expression Patterns of the Cannabinoid Receptor 1 Gene in Pig Skeletal Muscle and Skeletal Satellite Muscle Cells

机译:大麻素受体1基因在猪骨骼肌和骨骼卫星肌细胞中的表达模式

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摘要

The Cannabinoid Receptor type 1 (CNR1) is a key component of the endocannabinoid system which has been reported to play a pivotal role in modulating feeding behavior and energy balance. While a large number of researches have showed clearly that CNR1 is expressed in skeletal muscle of mice and human beings, detailed analysis of CNR1 gene expression in pig muscles and muscle cells has not been reported. Here, quantitative PCR were used to characterize the CNR1 in different muscles of pig and isolation of porcine myogenic satellite cells. Results showed that the expression of CNR1 mRNA was greatest in longissimus dorsi muscle (p<0.01) among that in the gastrocnemius (mix), soleus muscle (slow-type) and longissimus doris muscle (fast-type). As to age-related changes of CNR1 gene in different pig muscles, the higher expression was found at the 30th day, then declined (p<0.05) in all three kinds of muscles to the 90th day. At the 150th day, the expression of CNR1 steadily decreased (p<0.05) in the gastrocnemius compared to the 90th day but not in longissimus doris muscle and soleus. Meanwhile the breed differences in the expression of CNR1 mRNA between Jinhua pig and Landrace were also identified. The mRNA abundance of CNR1 in Landrace was higher compared with that of Jinhua pigs and strong differences were observed in longissimus doris muscle (p<0.05) and soleus (p<0.01). In vitro with the differentiation of the satellite cells, the mRNA expression of the CNR1 was significantly down-regulated (p<0.05). The lowest mRNA expression was observed at the 9th day. These data provide a framework of CNR1 gene expression patterns and implicate a novel gene for regulating muscle fiber types.
机译:1型大麻素受体(CNR1)是内源性大麻素系统的关键组成部分,据报道在调节进食行为和能量平衡方面起着关键作用。尽管大量研究清楚地表明CNR1在小鼠和人的骨骼肌中表达,但是尚未报道对猪肌肉和肌细胞中CNR1基因表达的详细分析。在这里,定量PCR被用来表征猪不同肌肉中的CNR1,并分离出猪成肌卫星细胞。结果表明,CNR1 mRNA的表达在腓肠肌(混合),比目鱼肌(慢型)和背最长肌(快速型)中最大(p <0.01)。至于不同猪肌肉中CNR1基因的年龄相关变化,在第30天时发现较高的表达,然后到第90天时这三种肌肉中的CNR1基因均下降(p <0.05)。在第150天,与第90天相比,腓肠肌CNR1的表达稳定下降(p <0.05),但在背最长肌和比目鱼肌中CNR1的表达却没有下降。同时还鉴定了金华猪与长白猪CNR1 mRNA表达的品种差异。与金华猪相比,长白猪CNR1的mRNA丰度更高,在背最长肌(p <0.05)和比目鱼肌(p <0.01)中观察到强烈差异。在体外随着卫星细胞的分化,CNR1的mRNA表达被显着下调(p <0.05)。在第9天观察到最低的mRNA表达。这些数据提供了CNR1基因表达模式的框架,并暗示了一种调节肌肉纤维类型的新基因。

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