Selenium deficiency-induced multiple tissue damage with dysregulation of immune and redox homeostasis in broiler chicks under heat stress

Broiler chicks are fast-growing and susceptible to dietary selenium(Se) deficiency. This study sought to reveal the underlying mechanisms of how Se deficiency induces key organ dysfunctions in broilers. Day-old male chicks(n=6 cages/diet, 6 chicks/cage) were fed with a Se-deficient diet(Se-Def, 0.047 mg Se/kg) or the Se-Def+0.3 mg Se/kg(Control, 0.345 mg Se/kg) for 6weeks. The serum, liver, pancreas, spleen, heart, and pectoral muscle of the broilers were collected at week 6 to assay for Se concentration, histopathology, serum metabolome, and tissue transcriptome. Compared with the Control group, Se deficiency induced growth retardation and histopathological lesions and reduced Se concentration in the five organs. Integrated transcriptomics and metabolomics analysis revealed that dysregulation of immune and redox homeostasis related biological processes and pathways contributed to Se deficiency-induced multiple tissue damage in the broilers. Meanwhile, four metabolites in the serum, daidzein, epinephrine, L-aspartic acid and 5-hydroxyindoleacetic acid, interacted with differentially expressed genes with antioxidative effects and immunity among all the five organs, which contributed to the metabolic diseases induced by Se deficiency. Overall, this study systematically elucidated the underlying molecular mechanisms in the pathogenesis of Se deficiency-related diseases, which provides a better understanding of the significance of Se-mediated heath in animals.

Protective Effects of Radix Astragali Injection on Multiple Organs of Rats with Obstructive Jaundice

Objective： To investigate the protective effects and mechanisms of Radix Astragali Injection on multiple organs of rats with obstructive jaundice（OJ）. Methods： A total of 180 rats were randomly divided into the sham-operated, model control and treated groups（60 in each group）. On 7, 14, 21 and 28 days after operation, the serum contents of alanine aminotransferase（ALT）, aspartate aminotransferase（AST）, r-glutamyl transpeptidase（r-GT）, total bilirubin（TBil）, direct bilirubin（DBil）, blood urine nitrogen（BUN）, and creatinine（CREA） were determined. And the pathological changes of livers, kidneys and lungs, and protein expressions of toll-like receptor-4（TLR-4） of livers, intercellular adhesion molecule-1（ICAM-1） of lungs, Bax and nuclear factor-kappa B（NF-κB）, as well as apoptotic indexes of multiple organs were observed, respectively. Results： The pathological severity scores of multiple organs（including livers on 7, 14, 21 and 28 days, kidneys on 14 and 28 days, and lungs on 14 days）, serum contents of ALT（14 and 21 days）, AST（14 days）, TBil（7, 14, 21 and 28 days）, DBil（14 and 21 days）, BUN（28 days）, protein expressions of TLR-4（in livers, 28 days）, Bax（in livers and kidneys, 21 days）, and apoptotic indexes in livers（7 and 21 days） in the treated group were significantly lower than those in the model control group（P〈0.05 or P〈0.01）. Conclusion： Radix Astragali Injection exerts protective effects on multiple organs of OJ rats by improving the pathological changes of lung, liver and kidney, decreasing the serum index of hepatic and renal function as well as inhibiting the protein expression of TLR-4 and Bax in the livers and Bax in the kidneys.

Dynamic microenvironment and multiple damaged tissue regeneration in a de novo and synchronized manner

Regenerative medicine has rapidly developed over the past decade and created new opportunities to repair or replace tissue or organ function lost because of congenital defects, age, diseases, or serious damage （Cheng et al., 2016a; Cheng et al., 2016b）. Regenerative medicine strategies in- clude the transplantation of bioactive factors, stem cells, or biomaterials, even the induced regeneration in a de novo, depending on the application （Fu, 2014a; Huang and Fu, 2014）. However, there are several limitations to the use of regenerative medicine in the clinic with respect to using stem cells and biomaterials.