The effect of volatile anaesthetics on the relative sensitivity of facial and distal thoracic limb muscles to vecuronium in dogs

ObjectiveTo compare n. facialis-m. nasolabialis (nF-mNL) and n. ulnar-mm. carpi flexorii (nU-mCF) sensitivity to vecuronium during halothane or isoflurane anaesthesia.Study designRandomized, prospective, experimental study.AnimalsForty-four client-owned dogs (19 male, 25 female) undergoing surgery; mean age: 5.0 years; mean body mass: 24.7 kg.MethodsThirty minutes after acepromazine (0.05 mg kg^?1) and morphine (0.5 mg kg^?1), anaesthesia was induced with intravenous (IV) thiopental and maintained with either halothane (n = 22) or isoflurane (randomly allocated) in oxygen. The lungs were mechanically ventilated and end-tidal inhaled anaesthetic (Fe’_IAA) maintained at 1.2 × MAC values. Neuromuscular transmission at nF-uNL and nU-mCF was monitored using the train of four count. Vecuronium (50 μg kg^?1 IV) was injected (t = 0) after 15 trains, 50-60 minutes after inhalational anaesthesia began, when Fe’_IAA had been constant for >15 minutes. Times of the disappearance (-) and reappearance (+) of the fourth (T4) and first twitch (T1) were recorded allowing the calculation of: latent (t = 0 to T4-) and manifest onset times (t = 0 to T1-) duration of blockade (T1- to T1+) and drug effect (T4- to T4+) and recovery time (T1+-T4+). Student’s paired t-test was used to compare simultaneous responses at nF-uNL and nU-mCF. An unpaired t-test was used to compare anaesthetic effects.ResultsLatent and manifest onset times were significantly (p < 0.05) briefer, blockade and drug effects were significantly longer and recovery from blockade were significantly slower in the nF-mNL unit in both halothane and isoflurane recipients. Profound block duration and drug action were significantly longer and recovery from blockade were significantly slower in halothane recipients at both nerve-muscle units.Conclusion and clinical relevanceThe nF-mNL was more sensitive than nU-mCF to vecuronium, particularly in halothane-anaesthetized dogs.     

Effects of high and low inspired fractions of oxygen on horse erythrocyte membrane properties, blood viscosity and muscle oxygenation during anaesthesia

ObjectivesTo evaluate whether a period of hyperoxia or after a period of hypoxia produced changes attributable to reactive oxygen species in anaesthetized horses.Study designProspective randomized experimental study.AnimalsSix healthy (ASA I) geldings, aged 4.5–9.5 years and weighing 510–640 kg^?1.MethodsAfter 30 minutes breathing air as carrier gas for isoflurane, horses were assigned randomly to breathe air as carrier gas (CG0.21) or oxygen as carrier gas (CG1.00) for a further 90 minutes. After an interval of 1 month each horse was re-anaesthetized with the other carrier gas for the 90 minute test period. Ventilation was controlled throughout anaesthesia. Arterial blood was sampled to measure gas tensions, lactate, cholesterol, vitamin E, 4-hydroxy-alkenals, 8-epi-PGF_2α, half haemolysis time, half erythrolysis time, and erythrocyte membrane fluidity. Muscle blood flow and oxygenation were evaluated by near infrared spectroscopy and coloured Doppler.ResultsAfter the first 30 minutes horses were hypoxemic. Subsequently the CG1.00 group became hyperoxaemic (PaO₂～240 mmHg) whereas the CG0.21 group remained hypoxaemic (PaO₂～60 mmHg) and had increased lactate concentration. No significant changes in vitamin E, 4-hydroxy-alkenals, or 8-epi-PGF_2α concentrations were detected. During the 90 minute test period the CG0.21 group had increased resistance to free-radical-mediated lysis in erythrocytes, whereas the CG1.00 group had slightly decreased resistance of whole blood to haemolysis. CG0.21 induced a progressive muscle deoxygenation whereas CG1.00 induced an increase in muscle oxygen saturation followed by progressive deoxygenation towards baseline.Conclusions and clinical relevanceDuring isoflurane anaesthesia in horses, the hyperoxia induced by changing from air to oxygen induced minimal damage from reactive oxygen species. Using air as the carrier gas decreased skeletal muscle oxygenation compared with using oxygen.     

哺乳动物成体干细胞的研究进展

干细胞具有自我更新能力,能够产生高度分化的功能细胞。干细胞按照发育阶段分为胚胎干细胞和成体干细胞。根据干细胞的发育潜能分为三类：全能干细胞、多能干细胞和单能干细胞。胚胎干细胞的发育等级较高,是全能干细胞,而成体干细胞的发育等级较低,是多能或单能干细胞。一般认为成年组织或器官内的干细胞具有组织特异性,只能分化成特定的细胞或组织,然而,研究结果表明,组织特异性干细胞同样具有分化成其他细胞或组织的潜能,这为干细胞的应用开创了更广泛的空间。作者主要综述了干细胞的研究进展及几种成体干细胞的诱导分化。     

摩杂一代水牛脑垂体前叶的超微结构研究

利用超薄切片对摩杂一代水牛脑垂体前叶的腺细胞进行透射电镜观察,发现5种腺细胞各有其超微结构特征：促性腺激素细胞胞体呈圆形,直径为7.6～9.0 μm;分泌颗粒分为明显的大小2种颗粒,且电子密度高。促甲状腺激素细胞的直径为6.0～7.5 μm;分泌颗粒少而最小,且大小无显著差异,多沿质膜分布;细胞核小,多位于中央。促肾上腺皮质激素细胞多在邻近垂体神经部的腺体前叶中,细胞核不规则,常偏向一侧,分泌颗粒常于细胞周边或一端;胞体直径为7.1～8.5 μm。促生长激素细胞数量多,核大而圆,分泌颗粒多且均一,充满胞质。催乳素细胞胞体最大,直径为11.2～13.4 μm,数量多,核小,常偏于一侧;分泌颗粒多而大小不等,充满胞质。旨在为研究摩杂一代水牛生殖泌乳的内分泌调控机制提供形态学基础资料。     

骨骼肌电穿孔转基因技术研究进展

目前,在大动物模型试验中,骨骼肌电穿孔转基因技术已被广泛用于转染一些功能基因,并能显著提高非病毒载体基因的转染效率。笔者就电穿孔促进基因通过细胞膜的可能机理及影响骨骼肌电穿孔转基因效率的关键因素（如物种、细胞直径、场强、脉冲参数、电极和电脉冲仪等）进行了综述。     

养殖花羔红点鲑营养价值分析

本文对人工养殖的花羔红点鲑的肌肉组成进行了分析。花羔红点鲑的水分、粗脂肪、粗蛋白、粗灰分含量十分丰富。不同年龄花羔红点鲑肌肉氨基酸含量有一定差异。花羔红点鲑肌肉脂肪酸含量高,并随年龄增长成升高趋势。花羔红点鲑有较高的营养价值,是一种可大力推广的优良品种。     

肌球蛋白重链基因与肉品质的关系

肌纤维是构成肌肉的基本单位,肌纤维的特性直接影响猪肉品质.猪的肌纤维根据肌球蛋白重链(MyHC)的多态性可分为1、2a、2b和2x 4种类型,在代谢上分别与慢速氧化型、快速氧化型、快速酵解型和中间类型相对应.肌纤维的生成在分子水平上受到肌细胞生成素基因的精确调控,肌纤维的类型在生长过程中不断发生转化,并受遗传、生长、性别和营养等多因素的影响.     

蓝狐消化道5-羟色胺和生长抑素免疫组化定位

采用免疫组织化学SP法.研究蓝狐消化道内5-羟色胺和生长抑素2种免疫阳性细胞的形态结构与分布密度.结果表明,消化道中这2种免疫阳性细胞形态多呈圆形、椭圆形或锥体形,主要集中分布在胃腺上皮、肠上皮及肠腺上皮细胞之间.5-HT免疫阳性细胞数量以结肠最多,直肠和空肠次之,胃底腺区、十二指肠、回肠和幽门腺区较少,食管、贲门腺区和盲肠中未见:SS免疫阳性细胞大量出现于幽门腺区,食管、责门腺区和盲肠中未见;根据其形态推测,蓝狐消化道这2种免疫阳性细胞有内、外2种分泌功能.     

Histological and immunohistochemical evaluation of duodenal and colonic biopsies after oral bovine lactoferrin supplementation in beagle puppies

Lactoferrin is a natural compound in the milk of mammals and was shown to influence the intestinal micro‐flora and the immune system in mice, calves, dogs and man. The present study was carried out to investigate the effect of orally administered bovine lactoferrin (0, 30, 60 and 120 mg/kg DM feed) on the intestinal morphology and lymphocyte colonization in 36 motherless raised puppies. Endoscopic biopsies from duodenum and colon, taken in week 14, were scored histologically after staining with haematoxylin and eosin (H&E) and lymphocytes (CD3⁺, CD4⁺, CD8⁺) and plasma cells (IgA⁺, IgG⁺, IgM⁺) were enumerated after immunohistochemical staining by computer‐aided quantification. Histological scoring revealed no significant differences amongst the groups. IgG⁺ plasma cells were reduced (p < 0.05) in the lamina propria of the colon of the 30 and the 60 mg group. The number of CD8⁺ lymphocytes was higher (p < 0.05) in the epithelium of the colon of the lactoferrin groups. In conclusion, this study indicated only minimal effects of bovine lactoferrin on the population of selected immune cells in the gut mucosa of puppies. More investigations are needed to describe the impact of lactoferrin on the digestive physiology of puppies.     

Symmorphosis and livestock bioenergetics: production animal muscle has low mitochondrial volume fractions

A comparative analysis of skeletal muscle structure reveals that production species (nine species, representing three mammalian families and an avian family) have mitochondrial volume fractions (MVF) 37% lower than the non‐production species at equivalent size (17 species, with representatives from 10 mammalian families) ( Fig. 1 ; F_1,25 = 4.79; p = 0.039). As MVF provides evidence of oxidative capacity, this comparative analysis indicates that production animals share an exceptionally low oxidative capacity muscle phenotype. A possible bioenergetic reason for this observation, relating to a reduction in the cost of maintaining trans‐membrane ion gradients is briefly discussed. This discussion is framed within a biological economic design theory called symmorphosis and makes predictions about avenues for improvements in livestock bioenergetics.

Figure 1 Open in figure viewer PowerPoint The scaling of log skeletal muscle mitochondrial volume density (MVF) with log endotherm size. Production species (PS) (red circles, red line) have a 37% lower MVF than non‐production species (NPS) (blue circles, blue line). NPS log MVF = ?0.11 log M_b + 0.88 (r² = 0.48, n = 17). PS log MVF = ?0.11 log M_b + 0.74 (r² = 0.69, n = 9).