首页> 外文期刊>British Poultry Science >Muscle structure and gene expression in pectoralis major muscle in response to deep pectoral myopathy induction in fast- and slow-growing commercial broilers
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Muscle structure and gene expression in pectoralis major muscle in response to deep pectoral myopathy induction in fast- and slow-growing commercial broilers

机译:胸部主要肌肉中的肌肉结构和基因表达,响应于生长缓慢和缓慢的商业肉鸡的深层胸膜疗法诱导

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1. The objective of this study was to determine muscle structure and gene expression in pectoralis major (p. major) muscle of broilers in response to deep pectoral myopathy (DPM) induction.2. A total of 160 chickens from slow- and fast-growing broilers were raised under same conditions. Half of the broilers from each strain were encouraged to wing flap when they reached 2800g body weight. Pectoralis minor (p. minor) muscle of the broilers was inspected for the occurrence of DPM and p. major samples were collected from broilers with or without DPM. The muscle fibre area and number, capillary number and the signalling pathways of vascular development (vascular endothelial growth factor A, VEGFA) and muscle contraction regulation (actin alpha 1, ACTA1; myosin light chain kinase 2, MYLK2 and ATPase Ca+2 transporting gene 1, ATP2A1) were studied in p. major muscle.3. DPM induction increased fibre area of p. major muscle with a greater rate in the slow-growing strain compared with fast-growing line. Although the capillary number was higher in slow-growing compared with fast-growing broilers, in the case of DPM induction, the number of capillaries was similar between strains.4. Expression of VEGFA, MYLK2 and ATP2A1 was greater in slow- than in fast-growing broilers. DPM induction increased expression of ACTA1, VEGFA and ATP2A1 in p. major muscle of broilers from both strains; however, MYLK2 expression was downregulated.5. Changes in capillary density and expression of VEGFA found in the p. major muscle of broilers with DPM suggest increased blood flow to increase oxygen availability. The upregulation of ATP2A1 by DPM induction could be attributable to alterations in calcium ion transportation from the cytoplasm into the sarcoplasmic reticulum.6. The results are evidence of changes in muscle structure and gene expression pathways in p. major muscle of broilers with DPM.
机译:本研究的目的是在肉鸡的胸椎肌肉肌肉(P.MOT)肌肉中的肌肉结构和基因表达响应深胸肌肌病(DPM)诱导。在相同的条件下,共增加了来自慢速和快速增长的肉鸡的160只鸡。当它们达到2800克的体重时,鼓励每个菌株的一半肉鸡。胸肌次要(p.次要)肉鸡的肌肉被检查了DPM和P的发生。从有或没有DPM的肉鸡收集主要样品。肌纤维面积和数量,毛细血管数和血管发育的信号通路(血管内皮生长因子A,VEGFA)和肌肉收缩调节(Actin alpha 1,Acta1;肌蛋白轻链激酶2,MyLK2和ATP酶Ca + 2输送基因1,ATP2A1)在p中进行了研究。主要肌肉。 DPM诱导增加的p。与快速生长线相比,具有较高速度的主要肌肉具有更高的速率。虽然与快速生长的肉鸡相比,毛细数量较高,但在DPM诱导的情况下,毛细血管的数量在菌株之间相似。 VEGFA,MYLK2和ATP2A1的表达速度较慢,而不是快速生长的肉鸡。 DPM诱导acta1,VEGFA和ATP2A1在p中的表达增加。来自两种菌株的肉鸡的主要肌肉;但是,MyLK2表达下调了。毛细血管密度的变化和VEGFA在p中的表达。具有DPM的肉鸡的主要肌肉表明增加了血流以增加氧气可用性。 DPM诱导的ATP2A1的上调可归因于从细胞质进入肌上网的钙离子输送的变化。结果是p中肌肉结构和基因表达途径变化的证据。肉鸡的主要肌肉与DPM。

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