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      Curcumin reduces enteric isoprostane 8-iso-PGF2α and prostaglandin GF2α in specific pathogen-free Leghorn chickens challenged with Eimeria maxima

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          Abstract

          The purpose of this pilot study was to evaluate and determine the concentration of prostaglandin GF2α (PGF2α) and isoprostane 8‐iso‐PGF2α in plasma and intestine of specific pathogen-free (SPF) Leghorn chickens challenged with Eimeria maxima, with or without dietary supplementation of curcumin using solid‐phase microextraction and ultra‐performance liquid chromatography/tandem mass spectrometry. Eighty 1-day-old male SPF chickens were randomly allocated to one of four groups with four replicates (n = 5 chickens/replicate). Groups consisted of: (1) Control (no challenge), (2) Curcumin (no challenge), (3) Eimeria maxima (challenge), and (4) Eimeria maxima (challenge) + curcumin. At day 28 of age, all chickens in the challenge groups were orally gavaged with 40,000 sporulated E. maxima oocysts. No significant differences ( P > 0.05) were observed in the groups regardless of the treatment or challenge with E. maxima. Enteric levels of both isoprostane 8‐iso‐PGF2α and PGF2α at 7 days and 9 days post-challenge were significantly increased ( P < 0.01) compared to the non-challenge control chickens. Interestingly, the enteric levels of both isoprostane 8‐iso‐PGF2α and PGF2α at 7 days post-challenge were significantly reduced in chickens fed curcumin, compared to control chickens challenge with E. maxima. At 9 days post-challenge, only levels of isoprostane 8‐iso‐PGF2α in the enteric samples were significantly reduced in chickens challenged with E. maxima supplemented with curcumin, compared with E. maxima challenge chickens. No differences of isoprostane 8‐iso‐PGF2α or PGF2α were observed in plasma at both days of evaluation. Similarly, no significant differences were observed between the challenge control or chickens challenge with E. maxima and supplemented with curcumin at both times of evaluation. The results of this pilot study suggests that the antioxidant anti-inflammatory properties of curcumin reduced the oxidative damage and subsequent intestinal mucosal over-production of lipid oxidation products. Further studies to confirm and extend these results in broiler chickens are required.

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          Prostaglandins and inflammation.

          Prostaglandins are lipid autacoids derived from arachidonic acid. They both sustain homeostatic functions and mediate pathogenic mechanisms, including the inflammatory response. They are generated from arachidonate by the action of cyclooxygenase isoenzymes, and their biosynthesis is blocked by nonsteroidal antiinflammatory drugs, including those selective for inhibition of cyclooxygenase-2. Despite the clinical efficacy of nonsteroidal antiinflammatory drugs, prostaglandins may function in both the promotion and resolution of inflammation. This review summarizes insights into the mechanisms of prostaglandin generation and the roles of individual mediators and their receptors in modulating the inflammatory response. Prostaglandin biology has potential clinical relevance for atherosclerosis, the response to vascular injury and aortic aneurysm.
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            AIM2 recognizes cytosolic dsDNA and forms a caspase-1 activating inflammasome with ASC

            The innate immune system senses nucleic acids via germ-line encoded pattern recognition receptors. RNA is sensed via Toll-like receptor (TLR)−3, −7 and −8 or by the RNA helicases RIG-I and MDA-51. Little is known about sensors for cytoplasmic DNA which trigger antiviral and/or inflammatory responses2–6. The best characterized of these responses involves activation of the TANK-binding kinase (TBK1)-Interferon Regulatory Factor (IRF)-3 signaling axis to trigger transcriptional induction of IFN〈/® genes2,3. A second, less well-defined pathway leads to the activation of an ‘inflammasome’ which via caspase-1, controls the catalytic cleavage of the pro-forms of the cytokines IL-1β and IL-186,7. Here we identify the IFI20X/IFI16 (PYHIN) family member8, absent in melanoma 2 (AIM2), as a receptor for cytosolic DNA which regulates caspase-1. The HIN200 domain of AIM2 binds to DNA, while the PYD domain (but not that of the other PYHIN family members) associates with the adapter molecule ASC to activate both NF-κB and caspase-1. Knockdown of AIM2 abrogates caspase-1 activation in response to cytoplasmic dsDNA and the dsDNA virus, vaccinia. Collectively, these observations identify AIM2 as a novel receptor for cytoplasmic DNA, which forms an inflammasome with the ligand and ASC to activate caspase-1.
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              Poultry coccidiosis: recent advancements in control measures and vaccine development.

              Coccidiosis is recognized as the major parasitic disease of poultry and is caused by the apicomplexan protozoan Eimeria. Coccidiosis seriously impairs the growth and feed utilization of infected animals resulting in loss of productivity. Conventional disease control strategies rely heavily on chemoprophylaxis and, to a certain extent, live vaccines. Combined, these factors inflict tremendous economic losses to the world poultry industry in excess of USD 3 billion annually. Increasing regulations and bans on the use of anticoccidial drugs coupled with the associated costs in developing new drugs and live vaccines increases the need for the development of novel approaches and alternative control strategies for coccidiosis. This paper aims to review the current progress in understanding the host immune response to Eimeria and discuss current and potential strategies being developed for coccidiosis control in poultry.
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                Author and article information

                Contributors
                gtellez@uark.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                2 June 2021
                2 June 2021
                2021
                : 11
                : 11609
                Affiliations
                [1 ]GRID grid.9486.3, ISNI 0000 0001 2159 0001, Programa de Doctorado en Ciencias de la Salud y Producción Animal, , Universidad Nacional Autonoma de Mexico, ; Cuautitlan Izcalli, Estado de Mexico Mexico
                [2 ]GRID grid.9486.3, ISNI 0000 0001 2159 0001, Laboratorio No 5: LEDEFAR, Unidad de Investigacion Multidisciplinaria, Facultad de Estudios Superiores Cuautitlan, , Universidad Nacional Autonoma de Mexico, ; Cuautitlan Izcalli, Estado de Mexico Mexico
                [3 ]GRID grid.441048.d, ISNI 0000 0004 1755 8342, Division de Ingenieria en Nanotecnologia, , Universidad Politecnica del Valle de Mexico, ; Tultitlan, Estado de Mexico Mexico
                [4 ]GRID grid.9486.3, ISNI 0000 0001 2159 0001, Departamento de Medicina y Zootecnia de Aves, Facultad de Medicina Veterinaria y Zootecnia, , UNAM, ; Mexico, Mexico
                [5 ]GRID grid.9486.3, ISNI 0000 0001 2159 0001, Departamento de Ciencias Biologicas, Facultad de Estudios Superiores Cuautitlan, , Universidad Nacional Autonoma de Mexico, ; Cuautitlan Izcalli, Estado de Mexico Mexico
                [6 ]GRID grid.411017.2, ISNI 0000 0001 2151 0999, Department of Poultry Science, , University of Arkansas, ; Fayetteville, AR USA
                Article
                90679
                10.1038/s41598-021-90679-5
                8172875
                34078952
                7499dc3f-2b70-42f4-83fa-e5180a0cb68c
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 2 March 2021
                : 10 May 2021
                Funding
                Funded by: PAPIIT IT201620 project of DGAPA‐UNAM, Universidad Nacional Autónoma de México. The authors thank CONACyT for the doctoral grant number 494367PAPIIT IT201620 project of DGAPA‐UNAM, Universidad Nacional Autónoma de México. The authors thank CONACyT for the doctoral grant number 494367
                Award ID: 494367
                Funded by: USDA-NIFA Sustainable Agriculture Systems.Title of Project: Empowering U.S. Broiler Production for Transformation and Sustainability
                Award ID: 2019-69012-2905
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                biological techniques,immunology,microbiology,gastroenterology
                Uncategorized
                biological techniques, immunology, microbiology, gastroenterology

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