Lumbar interbody expanding cage. A preliminary study on an animal model

Interbody fusion devices are used in human medicine for treating degenerative diseases of the spine. Currently, there is not a universally accepted assessment tool for determining fusion, and the definitive criteria for diagnosing a successful interbody fusion remain controversial. The aim of this study was to describe microscopic and helical computed tomography (CT) imaging in the assessment of lumbar interbody fusion using cylindrical threaded titanium expanding cage in sheep. One cylindrical threaded expanding titanium cage (Proconcept--SA, Orange, France) was inserted through a transperitoneal approach after radical discectomy and packed with cancellous bone autograft in five adult sheep. The subjects were euthanatized after three, six, 12, 18 and 24 months. CT images revealed lumbar fusion at 12 months post operation, whereas microscopic evaluations indicated the presence of lumbar fusion at 18 months. CT and histological grades were the same in 65% of the cases observed. There were not a significant difference between CT, histological and micro radiographic grades. Helical CT scanning can be considered to be a suitable method for the monitoring of lumbar fusion as it enables observation of the deposition of bony bridging within the cage.     

Evaluation of cross-protection by immunization with an experimental trivalent companion animal periodontitis vaccine in the mouse periodontitis model

Companion animal periodontal disease is one of the most prevalent diseases seen by veterinarians. The goal of this study was to evaluate the vaccine performance of a trivalent canine periodontitis vaccine in the mouse oral challenge model of periodontitis. Mice vaccinated subcutaneously with an inactivated, whole-cell vaccine preparation of Porphyromonas denticanis, Porphyromonas gulae, and Porphyromonas salivosa displayed significantly reduced alveolar bone loss in response to heterologous and cross-species challenges as compared to sham vaccinated animals. Based on the results of these studies, a periodontitis vaccine may be a useful tool in preventing the initiation and progression of periodontitis caused by the most commonly isolated pigmenting anaerobic bacteria in animals.     

Campylobacter jejuni infection in the ferret: an animal model of human campylobacteriosis

Campylobacter infection in weanling ferrets (Mustela putorius furo) was studied as an animal model for enteric campylobacteriosis in persons. The screening of fecal cultures on selective campylobacter media showed that Campylobacter jejuni/coli was not present in the normal enteric flora. Intragastric feeding of a mixture of cat feed and 2.5 X 10(8) C jejuni isolated from ferrets with naturally occurring proliferative colitis was accomplished. All ferrets (n = 8) became infected on 3 days after they were inoculated, and at 5 to 7 days, they had bile-tinged, liquid feces with excessive mucus and blood. Ferrets gradually recovered from the diarrhea, and feces were normal 10 to 14 days after inoculation was done. Feces contained C jejuni at 14, 23, 28, 39, 46, 60, 91, 101, 109 and 144 days. In the second experiment, weanling ferrets initially were treated with 10% sodium bicarbonate, and 1 X 10(10) C jejuni organisms were administered in the cat feed. Diarrhea with fecal leukocytes and occult blood with occasional mucus appeared in almost all of the 21 ferrets from days 4 through 7. Campylobacter jejuni was isolated from the blood of 11 ferrets between 3 hours and 14 days after they were inoculated. Campylobacter jejuni bactericidal antibodies were present in serum samples at 14 days, with titers of 1:16 to 1:32. Intestinal lesions including cellular infiltration with mononuclear and polymorphonuclear leukocytes were in the lamina propria of the pyloric mucosa and small intestine of infected and control ferrets. The colon of 3 infected ferrets had small focal infiltrates of neutrophils on the lamina propria; one ferret had perivascular cuffing.(ABSTRACT TRUNCATED AT 250 WORDS)     

Equine synovial tendon sheaths and bursae: an histological and scanning electron microscopical study

The structure of equine synovial tendon sheaths and bursae has been examined by light and scanning electron microscopy. Tissue samples were obtained from horses of various types and ages with no clinical evidence of sheath or bursal disorders. The interior of both structures was lined by a cellular layer superimposed on a vascular zone supported by a fibrous layer. The pattern of cell distribution of the lining varied from site to site within the same structure depending on the nature of the underlying tissue and on the amount of movement to which the structure was subjected. The cellular layer was predominantly fibrous in nature with scanty, widely separated fibroblasts (eg where it lines the palmar ligament, tendons and paratendons). In the mesotendon and bursal extremities, where the lining is subjected to a positive degree of movement, the cellular layer was areolar in type with well established folds populated by abundant cells oval to round in shape. In foals and yearlings, the supportive layer was mainly around the areolar with patches of adipose tissue; which were gradually replaced by fibrous tissue as the animal grew.     

A histological study of the effect of cortisol and some six steroids on the immune response to sheep erythrocytes by the mouse.

Sections of the spleen, thymus, lymph nodes and liver, collected from mice at various time intervals after injection with either steroid hormones only, sheep red blood cells (SRBC) only, or SRBC plus steroid hormones, were compared by histological examination. A regimen of 3 injections of 4 mg of cortisol given at 24 hourly intervals was shown to have a more severe effect than 3 injections of 1 mg given at the same times irrespective of whether SRBC were injected or not. The thymic cortex showed rapid and extensive depletion of lymphocytes very soon after corticosteroid treatment and did not recover until about the 8th day. The medulla was affected to a lesser extent. Spleens and lymph nodes showed early lymphocyte destruction, active ingestion of debris by macrophages, and germinal centres were considerably decreased in number and less clearly demarcated in corticosteroid-treated animals than in SRBC immunized controls. Spleens and lymph nodes of mice that received SRBC only exhibited the characteristic morphology of active germinal centre development associated with the immune response. Corticosteroid treatment of mice sensitized with SRBC caused an increase in neutrophilic promyelocytes in bone marrow smears to the 4th day, whereafter their numbers returned to normal. The normoblasts were decreased on the 2nd and 3rd days whereafter they increased to normal. Plasma cells were increased in SRBC injected animals in bone marrow smears. Of the effects of the sex steroids studied the most notable was a drastic effect of estradiol on the thymus; both the cortex and medulla were completely depleted of lymphocytes and could hardly be distinguished.     

小鼠SMC1A基因原核表达系统的构建及其生物信息学探讨

为了探讨SMC1A基因特点及其蛋白的结构和功能,通过PCR扩增SMC1A基因,将其构建至pET-28a(+)原核表达载体上,经PCR鉴定及测序鉴定后,对SMC1A基因的相关生物信息学特性进行初步探讨.结果 显示:克隆获得的小鼠SMC1A基因可编码1233个氨基酸,同源性分析发现,其与大鼠源、恒河猴源和人源的SMC1A基...     

A quantitative study of the histological morphology of the endometrium of normal and barren mares.

The density of uterine glands, height of surface epithelium, numbers of hemosiderin laden macrophages, inflammatory cells and layers of periglandular fibrosis were evaluated in uterine biopsies from 40 mares. These features were found to be highly variable in normal equine endometrium. Minor pathological changes appeared to be masked by this normal variability. Atrophy of uterine glands was recognized in mares which had been barren for more than three years. No significant differences were found between barren and normal mares in the height of epithelium, number of hemosiderin laden macrophages, inflammatory cells or layers of collagen surrounding glands in the superficial portion of endometrium. The number of layers of fibrosis surrounding glands in the deep part of lamina propria were found to be correlated with years of barrenness. This finding appears to have prognostic potential.     

Copper-induced hepatitis: the COMMD1 deficient dog as a translational animal model for human chronic hepatitis

Chronic inflammatory liver disease regardless of aetiology leads to failing regeneration and fibrosis, ending in cirrhosis. Both in man and in animals this worldwide health problem has no definitive cure. Chronic liver injury causes hepatic stellate cells to proliferate and differentiate into matrix-producing cells. New therapeutic options will be developed upon detailed understanding of the molecular mechanisms driving liver fibrosis. This may lead to new anti-fibrotic therapies which need to be tested in suitable models before application in the veterinary and human clinic. On the other side, to restore the failing regenerative capacity of the diseased liver cells, adult progenitor cells are of interest, as an alternative to whole organ transplantation. In order to find the most suitable large animal model it is important to recognise that the typical histopathological reaction pattern of the liver can differ between mammalian species. It is therefore imperative that specialists in veterinary internal medicine and pathology, being familiar with the diseases and pathologies of the liver in different animal species, are teaming-up in finding the best models for veterinary and human liver diseases. Several large animal models have been mentioned, like pigs, sheep, and dogs. Based on the observations that man and dog share the same hepatopathies and have identical clinical, pathological and pathogenetic reaction patterns during the development of liver disease, the dog seems to be a properly suited species to test new therapeutic strategies for pets and their best friends.     

常见几种微量元素与健康的研究进展

人体及畜禽的必须微量元素现代人多称之为“生命元素” ,它在人体及动物有机体中起着重要的作用 ,维护机体的健康乃至生命的作用是不可替代的 ,它几乎参与人及动物有机体的全部生理活动过程。必需微量元素的摄取不足或吸收失衡都直接影响到机体的正常运作 ,有些营养学家称微量元素是比蛋白质、脂肪、糖和维生素更重要的营养素。目前 ,对人及动物的微量元素摄入量及营养需要量和耐受量在国内外都做了大量的研究 ,并研制了大量的微量元素保健产品 ,如富硒蛋、高碘蛋、高锌蛋、富硒大米、富硒茶等。1　微量元素的生物功能1 1　营养功能必需微…     

The pentobarbital anesthetized dog: an animal model for assessing chemically induced changes in renal function and ultrastructure

An experimental procedure was devised using the pentobarbital-anesthetized dog that could be used for the comprehensive evaluation of the renal effects of chemicals. After IV or renal arterial administration of 0.9% saline solution (vehicle), 12 renal function determinants were continuously monitored for periods of 2 and 6 hours. At the completion of the 2 or 6 hours of study, the kidneys of a number of dogs (usually between 1 and 7) in each vehicle-treated group were subjected to a modification of the intravascular perfusion-of-fixative technique to evaluate the ultrastructural status of the outer cortical, inner cortical, and outer medullary tissue. The remaining dogs (at least 3) in each vehicle-treated group were given a nonnephrotoxic, but maximally effective, diuretic dose of ethacrynic acid, which enabled an assessment of the functional integrity of the thick ascending limb of Henle's loop. Renal function and glomerular and tubular ultrastructure remained stable in the pentobarbital-anesthetized dog for up to 6 hours after administration of vehicle. Sustained infusion of inulin (included in the procedure to estimate glomerular filtration rate) throughout the duration of the experiments, and pentobarbital anesthesia of various durations did not alter the morphologic status of the canine nephron. The procedure used for the renal perfusion of fixative circumvented any manipulation of the kidneys before fixation and allowed for the acquisition of normal (unaltered) appearing tissue from all areas of the kidneys. The responses of pentobarbital-anesthetized dogs to ethacrynic acid administration were similar when given 2 and 6 hours after the vehicle administration.(ABSTRACT TRUNCATED AT 250 WORDS)     

Construction and analysis of a Mannheimia haemolytica A1 luxS mutant

Mannheimia haemolytica A1 is the causative agent of bovine pneumonic pasteurellosis, a major cause of sickness, death, and economic loss to the feedlot cattle industry. M. haemolytica A1 produces autoinducer-2 (AI-2) like molecules that are capable of inducing quorum sensing system 2 of Vibrio harveyi. This interspecies quorum sensing system has been shown to regulate the expression of virulence genes in several pathogenic bacteria. The protein central to the production of AI-2 is LuxS. To determine if quorum sensing is involved in the regulation of virulence genes in M. haemolytica A1, a luxS mutant was constructed by replacing luxS with a cat cassette. This mutant was verified by PCR analysis, Southern hybridization, as well as its inability to induce bioluminescence in the V. harveyi reporter strain. RT-PCR analysis showed there was no difference in leukotoxin (lktC) mRNA levels, however there were increased mRNA levels of putative virulence associated genes, transferrin binding protein B (tbpB), adhesin (ahs) and capsule biosynthesis (nmaA). Electron microscopy showed that the level of encapsulation in the mutant is higher than the parent. Additionally, the mutant was slightly more adherent to bovine tracheal cells than the parent. In vitro competition assays showed the mutant out-competed the parent under iron-restricted conditions. However, in a calf challenge, the parent was the dominant isolate recovered.     

Pathogenesis of encephalomyocarditis experimental infection in young piglets: a potential animal model to study viral myocarditis

The pathogenesis of encephalomyocarditis (EMC) due to the EMC virus (EMCV) was studied in 24 piglets oro-nasally infected with the field isolate B279/95. Two pigs were kept as negative controls and were euthanised at hour 0. The remaining 24 were euthanised every 6 h up to 78-h post infection (hpi). Virus isolation, histological examination and EMCV immunodetection were performed on the spleen, intestine, pancreas, liver, kidneys, heart, lungs, lymph nodes, tonsils and brain. EMCV was isolated at 6-hpi from the intestine and lymph nodes and at 12-hpi from the heart. From 6 to 12-hpi, scattered degenerate myocardiocytes were immunolabelled. Subsequently, myocarditis developed and progressively worsened. Immunopositive reaction in tonsil macrophages, observed in the early stage of infection (6-hpi), suggests that tonsils are the portal of entry, and by mean of wandering macrophages the EMC virus is then distributed through the body. Afterwards, EMCV-B279/95 replicates intensively in the cytoplasm of myocardiocytes and the acute myocarditis is strictly related to the tropism of these cells. Four pigs died spontaneously. In three animals no post mortem lesions or virus were isolated/detected, although all of them showed mild myocarditis. The experimental infection with EMCV B279/95 indicates: (i) the experimental protocol mimics the individual variability observed in natural disease, (ii) tonsils are the portal of entry of infection and the heart is the target organ, (iii) EMCV provides a valuable animal model for comparative studies on progressive viral myocarditis.     

A quantitative histological study of changes in the bovine testis and epididymis associated with age.

Quantitative histological studies were performed on the testis and epididymis of 80 normal bulls from beef herds in tropical Australia. Four age groups, ranging from nine months to over 10 years were established. Volumetric proportions of parenchymal and collagenous tissues, and tubular or duct surface to tissue volume ratios were determined at the dorsal, middle and ventral testicular regions and at the head, body and tail of the epididymis for each group. Detailed volumetric analyses of the relative volumes of particular parenchymal and stromal elements were made a the middle testicular region. Lymphoid and plasma cell populations were compared in all regions, including the efferent ducts. Differences in the distribution of testicular parenchyma and collagen were found; the dorsal region had more parenchyma and less collagen than the middle and ventral areas. Progressive intertubular fibrosis attributed to age was quantified; it was most marked ventrally. Reductions in the relative volumes of germinal cells, Sertoli cells, tubular cytoplasm and parenchyma, and in tubular surface to testis volume ratios with advancing age, indicated a decrease in the capacity per unit volume of testis to produce sperm. Increased immunocyte populations in the efferent duct region in young bulls were attributed to initial antigenic exposure. Increased antigenic exposure, in association with senile degenerative changes of the genitalia, might have caused the increased immunocyte populations seen in very old bulls.     

Divergent selection for immune responsiveness in chickens: estimation of realized heritability with an animal model.

With the aim of improving general disease resistance, chickens were divergently selected for their antibody titers 5 d after immunization with sheep red blood cells for nine generations. Selected and control lines differed significantly for primary and secondary responses after three generations. Heritability of the antibody titer was estimated by REML fitting an animal model using a derivative-free algorithm. The heritability estimate using data on all lines simultaneously was .31. Realized heritability of the antibody titer in the selected lines was estimated by using either the phenotypic cumulative response as the deviation from the control line or the mean breeding values obtained with an animal model. Values from the two methods were consistent, giving a realized heritability of .21 and .25 in the high and low lines, respectively. The genetic trend was not linear and the response to selection tended to accelerate over generations.     

Absorption of equations for non-parents for an animal model with maternal effects and genetic groups

Rules for forming the mixed-model equations for the reduced animal model with all relationships and including maternal effects have been set out by Quaas and Pollak. They also have shown how to simplify the mixed-model equations when genetic group effects are included in the model with what has become known as the Q-P transformation. Westell has given rules for calculating the coefficients for the Q-P transformed equations that are associated with the inverse of the numerator relationship matrix and genetic group effects. Those rules can be extended to include maternal effects and genetic groups for maternal as well as direct effects. As with the rules of Quaas and Pollak for the equations for the reduced animal model, a similar set of rules can be obtained for the genetic groups model after the Q-P transformation. The rules are derived easily by examining the algebraic results of absorbing the direct and maternal breeding value equations for non-parents into the parent breeding value, group and fixed effects equations. These rules involve Westell's rules and the inverse elements of the genetic (co)variance matrix for direct and maternal additive genetic effects. The rules make calculation of breeding values for parents for models including direct and maternal genetic group effects nearly as easy as for models without genetic group effects. Back solution for direct and maternal breeding values of non-parents similarly is as simple as when genetic group effects are not in the model.     

Autophagic response in the Rabbit Hemorrhagic Disease,an animal model of virally-induced fulminant hepatic failure

The Rabbit Hemorrhagic Disease Virus (RHDV) induces a severe disease that fulfils many requirements of an animal model of fulminant hepatic failure. However, a better knowledge of molecular mechanisms contributing to liver damage is required, and it is unknown whether the RHDV induces liver autophagy and how it relates to apoptosis. In this study, we attempted to explore which signalling pathways were involved in the autophagic response induced by the RHDV and to characterize their role in the context of RHDV pathogenesis. Rabbits were infected with 2 × 10⁴ hemmaglutination units of a RHDV isolate. The autophagic response was measured as presence of autophagic vesicles, LC3 staining, conversion of LC3-I to autophagosome-associated LC3-II and changes in expression of beclin-1, UVRAG, Atg5, Atg12, Atg16L1 and p62/SQSTM1. RHDV-triggered autophagy reached a maximum at 24 hours post-infection (hpi) and declined at 30 and 36 hpi. Phosphorylation of mTOR also augmented in early periods of infection and there was an increase in the expression of the endoplasmic reticulum chaperones BiP/GRP78, CHOP and GRP94. Apoptosis, measured as caspase-3 activity and expression of PARP-1, increased significantly at 30 and 36 hpi in parallel to the maximal expression of the RHDV capsid protein VP60. These data indicate that RHDV infection initiates a rapid autophagic response, perhaps in an attempt to protect liver, which associates to ER stress development and is independent from downregulation of the major autophagy suppressor mTOR. As the infection continues and the autophagic response declines, cells begin to exhibit apoptosis.     

A study of the transfer of tetracycline resistance genes between Escherichia coli in the intestinal tract of a mouse and a chicken model

Experiments to demonstrate the transfer of genes within a natural environment are technically difficult because of the unknown numbers and strains of bacteria present, as well as difficulties designing adequate control experiments. The results of such studies should be viewed within the limits of the experimental design. Most experiments to date have been based on artificial models, which only give approximations of the real-life situation. The current study uses more natural models and provides information about tetracycline resistance as it occurs in wild-type bacteria within the environment of the normal intestinal tract of an animal. Tetracycline sensitive, nalidixic acid resistant Escherichia coli isolates of human origin were administered to mice and chicken animal models. They were monitored for acquisition of tetracycline resistance from indigenous or administered donor E. coli. Five sets of in vivo experiments demonstrated unequivocal transfer of tetracycline resistance to tetracycline sensitive recipients. The addition of tetracycline in the drinking water of the animals increased the probability of transfer between E. coli strains originating from the same animal species. The co-transfer of unselected antibiotic resistance in animal models was also demonstrated.