Obesity is a major risk factor of preventable deaths worldwide, with increasing rates being observed in adults and children. To understand the mechanisms of obesity development, genetically lean (Duroc strain) and obese (Rongchang strain) pigs were used to identify potential differences in muscle and adipose development patterns following consumption of an identical diet for 180 days. Lean pigs had a significantly higher lean percentage (67.79% versus 44.71%) and lower obesity index (0.68 versus 0.84) than obese pigs. They also exhibited significantly lower adipocyte volumes and higher myofibre cross-sectional areas. Quantitative polymerase chain reaction showed that lean pigs had a significantly higher expression of muscle growth-related genes and lower expression of lipogenesis-related genes. By contrast, obese pigs had higher expression of a myostatin-related gene and lower expression of lipolysis-related genes. Additionally, the mitochondrial DNA copy number was higher in the muscle and lower in adipose tissue in lean compared with obese pigs. These results indicate that lean pigs have a distinct development pattern from obese pigs, involving lipogenesis, muscle growth, and energy metabolism. This study provides a basis for exploring the mechanisms of adipose deposition and muscle growth in obesity.

ABSTRACT In this study, a method utilizing PCR-restriction fragment length polymorphism (PCR-RFLP) of a mitochondrial gene was developed for the identification of chicken (Gallus gallus), quail (Coturnix coturnix), and common pigeon (Columba livia) meat. PCR products of ~440 bp were obtained from the 12S rRNA gene of these three birds using a pair of universal primers. The three terrestrial birds can be distinguished using one restriction endonuclease, Alu I, which was selected based on species-specific variations in the mt 12S rRNA gene sequence using 9 newly-obtained and 44 published chicken, quail and pigeon sequences. This method was also successfully used to identify commercial quail and pigeon meat products, which were found to be adulterated with chicken meat. Additionally, our method had relatively high sensitivity for detecting a meat mixture. Ten percent of chicken meat in the mixed quail and pigeon sample was detectable. This assay can be useful for the accurate identification of meats from terrestrial birds, avoiding mislabeling or fraudulent species substitution in meat products.

ABSTRACT The bursa of Fabricius (BF) is the central humoral immune organ unique to birds. The present study investigated the possible difference on a molecular level between two duck breeds. The digital gene expression profiling (DGE) technology was used to enrich the differentially expressed genes (DEGs) in BF between the Jianchang and Nonghua-P strains of ducks. DGE data identified 195 DEGs in the bursa. Gene Ontology (GO) analysis suggested that DEGs were mainly enriched in the metabolic pathways and ribosome components. Pathways analysis identified the spliceosome, RNA transport, RNA degradation process, Jak-STAT signaling pathway, TNF signaling pathway and B cell receptor signaling pathway. The results indicated that the main difference in the BF between the two duck strains was in the capabilities of protein formation and B cell development. These data have revealed the main divergence in the BF on a molecular level between genetically different duck breeds and may help to perform molecular breeding programs in poultry in the future.

ABSTRACT The carbohydrate response element-binding protein (ChREBP) is an important nuclear factor that regulates glycolysis and de novo lipogenesis. However, the role of ChREBP in fatty liver development in geese remains unclear. In order to understand the function of ChREBP in lipid metabolism of geese, we first cloned the complete cDNA of the ChREBP of the Sichuan White goose (Anser cygnoides) using RT-PCR, 5’ RACE and 3’ RACE, and analyzed goose ChREBP expression in nine different tissues using real-time PCR technology. The results showed that the goose ChREBP CDS consists of 945bp nucleotides that encode 314 amino acids, and the sequence has high similarities with the swan goose (Anser cygnoides domesticus) and duck (Anas platyrhynchos) sequences, both at the nucleotide and amino acid levels. The predicted ChREBP protein had a molecular mass of 35.64 kDa with pI value of 5.36. The phylogenetic analysis indicated its evolutionary relationships with corresponding orthologous sequences in swan geese and ducks. The qPCR assays revealed that ChREBP is highly expressed in liver in the Sichuan White goose. Together, these results indicate that goose ChREBP may play an important role in the development of hepatic steatosis.

OBJECTIVE: To evaluate the anatomy and medical imaging characteristics in a study observing the atlanto-axial joint (AAJ) and related structures. METHODS: Eight cadaveric specimens of the AAJ segment were studied with both anatomical and imaging methods. The vertebral arteries of the AAJ segment (VA-A), the first and second cervical nerves (CN1, CN2) and synovial fold (SF) of the AAJ were observed and measured. RESULT: After extending from the vertebral canal, the CN1 goes between the posterior arch of the atlas and VA-A, and the CN2 passes between the posterior arch of the atlas and axis, and is posterior to VA-A. Among the eight cases, six were found in the SF in the central anterior AAJ and five in lateral. The vertebral arteries of the AAJ segment go along the AAJ with four curves, of which the second and fourth are away from the bone structure of the AAJ. The distance from CN1, CN2 to VA-A and that from the second, fourth curve of VA-A to AAJ is 0.0-2.2 mm, 0.0-3.6 mm and 0.0-4.8 mm, 2.0-7.9 mm respectively. There is no significant difference between the measurements made anatomically and those by the imaging method (p > 0.05). CONCLUSION: The anatomical method has advantages in observing the CN and SF, while the imaging method shows clearly and directly the VA-A and AAJ. Both are mutually complementary with consistent measurements. The combined use of the two provides a new way to study the complicated anatomy in this region.

OBJETIVO: Evaluar las características del método anatómico y el uso de la imagen médica en un estudio de observación de la articulación atlanto-axial (AAA) y estructuras relacionadas. MÉTODOS: Se estudiaron ocho especimenes cadavéricos del segmento de la AAA tanto con métodos anatómicos como con métodos de imaginología médica. Las arterias vertebrales del segmento de AAA (AV-A), el primer y el segundo nervios cervicales (NC1, NC2) y los pliegues sinoviales (PS) fueron observados y medidos. RESULTADO: Tras de extenderse desde el canal vertebral, el NC1 se extiende entre el arco posterior del atlas, y el NC2 pasa entre el arco posterior del atlas y el axis, y es posterior a las AV-A. Entre los ocho casos, se encontraron seis en los PS en la AAA anterior central, y cinco en la lateral. Las arterias vertebrales del segmento AAA van junto con la AAA con cuatro curvas, de las cuales la segunda y la cuarta están separadas de la estructura ósea de la AAA. La distancia del NC1 y NC2, a las AV-A, y la de la segunda y cuarta curvas de las AV-A a la AAA es 0.0-2.2 mm, 0.0-3.6 mm y 0.0-4.8 mm, 2.0-7.9 mm respectivamente. No hay ninguna diferencia significativa entre las mediciones realizadas anatómicamente y las hechas mediante métodos de imaginología (p > 0.05). CONCLUSIÓN: El método anatómico tiene ventajas al observar el NC y los PS, mientras que el método imaginológico muestra clara y directamente las AV-A y la AAA. Ambos son mutualmente complementarios con las mediciones. El uso combinado de los dos proporciona una nueva manera de estudiar la complicada anatomía de esta región.