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首页> 外文期刊>Fish & Shellfish Immunology >Arginine and glutamine supplementation to culture media improves theTI Arginine and glutamine supplementation to culture media improves the performance of various channel catfish immune cells
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Arginine and glutamine supplementation to culture media improves theTI Arginine and glutamine supplementation to culture media improves the performance of various channel catfish immune cells

机译:向培养基中补充精氨酸和谷氨酰胺可改善TI对培养基中补充精氨酸和谷氨酰胺可改善各种channel鱼免疫细胞的性能

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Specific components of both the innate and adaptive immune systems of channel catfish were evaluated after supplementation of culture media with arginine (ARC) and/or glutamine (GLN). Primary cell cultures of head-kidney macrophages (MO) were used for phagocytic and bactericidal assays against Edwardsiella ictaluri. Additionally, proliferation assays were conducted with naive peripheral blood lymphocytes (PBL) exposed to non-specific mitogens. To indirectly assess amino acid utilization of both MO and PBL, amino acid levels, with emphasis on ARC and GLN, were evaluated in the basal medium before and after activation or mitogenic exposure. After bactericidal and proliferation assays, the sum of the media free amino acid pool significantly (P < 0.05) decreased 23% and 45%, respectively. Glutamine levels in medium decreased by 38% and ARC by 18% during the bactericidal assay. Also, decreases of 52 and 46% from initial values were found after the proliferation assay for GLN and ARC, respectively. Macrophage phagocytosis and killing ability was significantly (P < 0.05) enhanced by ARC supplementation to culture media regardless of GLN supplementation. Proliferation of naive T-and Blymphocytes upon mitogenic exposure was significantly (P < 0.05) enhanced by supplementing ARC and GLN to the media, but limited synergistic effects were observed. These results suggest that in vitro, ARC and GLN are important substrates and immunomodulators of both innate and adaptive responses in fish leukocytes, and further highlights the potential use of ARC and GLN as immunonutrients in aquafeeds
机译:在培养基中添加精氨酸(ARC)和/或谷氨酰胺(GLN)后,对channel鱼先天性和适应性免疫系统的特定成分进行了评估。头肾巨噬细胞(MO)的原代细胞培养用于针对伊德氏菌的吞噬和杀菌分析。另外,用暴露于非特异性有丝分裂原的幼稚外周血淋巴细胞(PBL)进行增殖测定。为了间接评估MO和PBL的氨基酸利用率,在激活或有丝分裂暴露前后,在基础培养基中评估了氨基酸含量(重点是ARC和GLN)。经过杀菌和增生试验后,培养基中游离氨基酸库的总和分别显着降低(P <0.05)23%和45%。在杀菌试验中,培养基中的谷氨酰胺水平降低了38%,ARC降低了18%。同样,在GLN和ARC的增殖试验后,分别比初始值降低了52%和46%。不管添加GLN,向培养基中添加ARC均可显着增强巨噬细胞的吞噬作用和杀伤能力(P <0.05)。通过向培养基中补充ARC和GLN,有丝分裂暴露后幼稚T淋巴细胞和淋巴细胞的增殖显着增强(P <0.05),但观察到有限的协同作用。这些结果表明,ARC和GLN在体外是鱼白细胞固有反应和适应性反应的重要底物和免疫调节剂,并进一步突显了ARC和GLN在水产饲料中作为免疫营养物的潜在用途

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