Acoustic structure of vocalization and stapedius muscle activity during vocal development in chickens (Gallus gallus)

The link between stapedius muscle activity and acoustic structure of vocalization was analysed in cocks of age 20–30 to 90–100 days old. The results show that stapedius muscle activation depends on the acoustic structure of vocalization and changes during vocal development. This dependence was observed in spontaneous calls and in vocalizations elicited by stimulating the mesencephalic calling area. In 30-day-old cocks stapedius muscle EMG response is never associated with vocalizations with an acoustic energy content which is always distributed at frequencies higher than 2000 Hz. The coupling between vocalization and stapedius muscle activity begins later, when birds produce vocalizations with acoustic energy shifted towards lower frequencies. Overall, stapedius muscle activity is related to a bird's production of high amplitude low frequencies. These results support the hypothesis that the primary role of the stapedius muscle during normal vocal development is to dampen the amplitude of low frequency energy that reaches the cochlea during vocalization.     

Isolation and culture of rat superior mesenteric artery smooth muscle cells

Summary The structure and function of vascular smooth muscle cells have been extensively investigated with the aid of in vitro culture techniques. The majority of studies have utilized aortic tissue as the source of cells. We present here a method for isolating and culturing smooth muscle cells of the rat superior mesenteric artery, an elasto-muscular vessel that is structurally and functionally different from the aorta. Cells were isolated from partially digested explants and characterized by immunochemical and biochemical techniques. Unlike cultured fibroblasts, the cultured cells stained positive for smooth muscle specific actin. The cells also produced laminin and type IV collagen in culture. This method provides a means for the isolation of large numbers of viable smooth muscle cells from the superior mesenteric artery which can be propagated in culture for in vitro study.     

组织器官通讯对骨骼肌发育的作用及调控机制研究进展

骨骼肌是动物机体最重要的器官之一,研究骨骼肌发育调控机制对于肌肉相关疾病的诊断以及家畜肉质的改善都有着重要意义。骨骼肌发育调控是一个复杂的过程,受到大量肌肉分泌因子和信号通路的调节。此外,为了维持体内代谢稳态并最大限度地利用能量,机体协调多个组织器官形成了复杂而又精密的代谢调控网络,对于调控骨骼肌发育也发挥着重要的作用。随着组学技术的发展,人们对于组织器官通讯的潜在机制进行了深入研究。本文综述了脂肪组织、神经组织、肠道等组织器官通讯对于骨骼肌发育的影响,以期为靶向调控骨骼肌发育提供理论基础。     

Refined structure of bovine carbonic anhydrase III at 2.0 Å resolution

The three-dimensional structure of bovine carbonic anhydrase III (BCA III) from red skeletal muscle cells has been determined by molecular replacement methods. The structure has been refined at 2.0 Å resolution by both constrained and restrained structure-factor least squares refinement. The current crystallographic R-value is 19.2% and 121 solvent molecules have so far been found associated with the protein. The structure is highly similar to the refined structure of human carbonic anhydrase II. Some differences in amino acid sequence and structure between the two isoenzymes are discussed. In BCA III, Lys 64 and Arg 91 (His 64 and Ile 91 in HCA II) are both pointing out from the active site cavity forming salt bridges with Glu 4 and Asp 72 (His 4 and Asp 72 in HCA II), respectively. However, Arg 67 and Phe 198 (Asn 67 and Leu 198 in HCA II) are oriented towards the zinc ion and significantly reduce the volume of the active site cavity. Phe 198 particularly reduces the size of the substrate binding region at the “deep water” position at the bottom of the cavity and we sugest that this is one of the major reasons for the differences in catalytic properties of isoenzyme III as compared to isozyme II. © 1993 Wiley-Liss, Inc.     

Murine FGF-4 gene expression is spatially restricted within embryonic skeletal muscle and other tissues

Fibroblast growth factors are believed to play many distinct roles in vertebrate development, owing to their ability to stimulate cell growth, prevent cell death, determine cell fate, and inhibit terminal differentiation in a variety of in vitro culture systems. We have used in situ hybridization to localize fibroblast growth factor-4 (FGF-4, also termed HST and K-FGF) gene expression in 7.5 to 16.5 day gestation mouse embryos. Seven discrete sites of gene expression were detected: (1) primitive streak (E7.5–8.5); (2) paraxial presomitic mesoderm in the trunk (E7.5–11.5); (3) primitive neuroectoderm (E8.0–8.5); (4) pharyngeal pouch endoderm (E8.5–9.5); (5) branchial arch ectoderm (E8.5–9.5); (6) limb apical ectoderm (E10.5–12.5), and (7) skeletal myoblast groups (E9.5–13.5). FGF-4 gene expression is spatially restricted within many of these sites. The profile of FGF-4 gene expression among skeletal muscle groups is overlapping, but distinct, from that of FGF-5, thereby revealing myoblast heterogeneity at the molecular level and suggesting distinct roles for multiple FGFs in muscle development.     

人类小腿肌肉对运动训练生理响应的电学特性研究

目的 运动训练已被证明能够改善许多慢性肌肉功能疾病,被用于治疗衰老型肌萎缩。本文采用电阻抗成像(electrical impedance tomography,EIT)研究人类小腿肌肉对运动训练生理响应的电学特性,旨在使用EIT方法可视化运动训练对人类小腿响应肌肉隔室内肌肉纤维体积增加的效果。方法 实验对象被要求在连续5个实验日进行左、右腿单侧提踵训练,应用EIT检测每日运动训练前和运动训练后小腿肌肉的电导率分布。为了定量分析运动训练对响应肌肉隔室的作用,使用配对样本t检验分析EIT重建图像的空间平均电导率<σ>。结果 运动训练后,由小腿腓肠肌组成的M₁肌肉隔室空间平均电导率<σ>_M1显著增加。此外,连续5个实验日的EIT测量结果显示,运动训练前的空间平均电导率<σ^pre>_M1呈上升趋势。所有实验对象在实验日1早晨进行实验前的腿部瘦体重与<σ>_M1呈线性关系,即<σ>_M1随腿部瘦体重增加而增加;运...     

神经肌肉电刺激下小腿肌肉的电学特性研究

目的 采用电阻抗成像（electrical impedance tomography,EIT）方法研究神经肌肉电刺激（neuromuscular electrical stimulation,NMES）下小腿肌肉的电学特性,旨在将EIT作为一种长期监测方法,从而可视化NMES训练对人类小腿肌肉的训练效果。方法 16名实验对象被随机分配到对照组（control group,CG,n=8）和最佳电压强度的NMES训练组（optimal voltage intensity training group,OG,n=8）。对照组保持正常生活方式并不进行NMES和其他的肌肉训练;NMES训练组中使用商业NMES设备对实验对象右小腿进行23 min的NMES训练,每周3次,为期5周。应用EIT测量在每周一训练开始前的电导率分布。并且采用生物电阻抗分析（bioelectrical impedance analysis,BIA）方法测量右腿细胞外含水量与身体总含水量的比率（ECW/TBW） βrl,及身体总含水量（TBW）τ。为了量化NMES在肌肉训练过程中的作用,使用配对样本t检验分析EIT重建图像的...