The effect of dietary supplementation of Eucalyptus leaves (EL) powder on productive performance and immune response in 2 varieties of Japanese quail was investigated. A total of 180 twelve-week-old laying Japanese quails from 2 color varieties (gray and white) were randomly assigned and distributed according to a completely randomized design in a 3 × 2 factorial arrangement (dietary treatment × variety) forming 6 subgroups (30 each). EL were mixed with the diet in 3 levels (0, 0.1, and 0.2%). Each hen was individually housed in a wire cage of laying batteries and kept in an open house under hot environmental temperature. Productive traits were determined for an experimental period of 6 wk. Egg quality, carcass traits, blood parameters, and immune response were also determined. The results indicated that the productive traits were not significantly affected by EL supplementation. Shell quality and broken eggs significantly improved in quails fed a diet containing EL compared with those in the control. The quails fed a diet supplemented with 0.1% EL exhibited significantly higher cellular mediated and humoral immune responses than those in the other treatment groups. Glutathione peroxidase activity tended to be significantly increased by the dietary administration of EL at the level of 0.2%. Concerning quail varieties, it could be noticed that the gray quails exhibited higher productive performance, shell quality, and cellular immunity than the white counterparts. It could be concluded that supplementing a diet with 0.1 EL as a natural feed additive greatly enhances eggshell quality and immunocompetence and reduces number of broken eggs of Japanese quails raised under high environmental temperature.
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http://dx.doi.org/10.1016/j.psj.2019.09.001 | DOI Listing |
Background: The key advantage of active immunization is the induction of sustained, polyclonal antibody responses that are readily boosted by occasional immunizations. Recent clinical trial outcomes for monoclonal antibodies lecanemab and donanemab, establish the relevance of targeting pathological Abeta for clearing amyloid plaques in Alzheimer's disease. ACI-24.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Columbia University Irving Medical Center, New York, NY, USA.
Background: Genetic studies indicate a causal role for microglia, the innate immune cells of the central nervous system (CNS), in Alzheimer's disease (AD). Despite the progress made in identifying genetic risk factors, such as CD33, and underlying molecular changes, there are currently limited treatment options for AD. Based on the immune-inhibitory function of CD33, we hypothesize that inhibition of CD33 activation may reverse microglial suppression and restore their ability to resolve inflammatory processes and mitigate pathogenic amyloid plaques, which may be neuroprotective.
View Article and Find Full Text PDFBackground: A large body of evidence now indicates that the most pathogenic species of Aß in Alzheimer's disease (AD) consist of soluble toxic oligomers (AßO) as opposed to insoluble fibrils and monomers. Using our computational platform, we identified 4 different AßO-restricted conformational B cell epitopes (300, 301, 303, 305) that were tested as vaccines for their ability to induce an antibody response that selectively targets toxic AßO, without inducing potentially detrimental B or T cell responses against plaque or normal Aß. A novel ex vivo approach was then used to select an optimal vaccine configuration amongst the 15 possible combinations of the 4 epitopes to provide maximal binding to a toxic oligomer-enriched low molecular weight (LMW) fraction of soluble AD brain extracts.
View Article and Find Full Text PDFHistol Histopathol
December 2024
Laboratory of Anatomy, Department of Basic Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.
Sex hormones regulate gut function and mucosal immunity; however, their specific effects on the mucosa-associated lymphoid tissue (MALT) in the rectum of mammals remain unclear. Here, we aimed to investigate the influence of sex on MALT in the rectum of mammals by focusing on the rectal mucosa-associated lymphoid tissues (RMALTs) of C57BL/6NCrSIc mice. Histological analysis revealed that RMALTs were predominantly located in the lamina propria and submucosa of the rectal mucosa, with a significant sex-related difference in the distance from the anorectal junction to the first appearance of the RMALT.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Inserm, Sorbonne Université, Centre de Recherche Saint-Antoine, Immune System and Neuroinflammation Laboratory, Hôpital Saint-Antoine, Paris, France.
Background: Chronic innate neuroinflammation mediated by microglia and astrocytes in response to Aβ and pathological Tau species is a cardinal feature of AD that contributes to disease pathogenesis. Accumulating evidence now also highlight an instrumental role of T cells and peripheral-central immune crosstalk in the pathophysiology of AD. Both preclinical and clinical reports suggest the potential therapeutic interest of peripheral immunomodulatory approaches aimed at amplifying regulatory T cells (Tregs), e.
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