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排序方式: 共有84条查询结果,搜索用时 15 毫秒
41.
Sumit Rawal Miranda M. Bauer Kristelle M. Mendoza Hani El-Nezami Jeffery R. Hall Ji Eun Kim John R. Stevens Kent M. Reed Roger A. Coulombe Jr. 《Research in veterinary science》2014
Turkeys are extremely sensitive to aflatoxin B1 (AFB1) which causes decreased growth, immunosuppression and liver necrosis. The purpose of this study was to determine whether probiotic Lactobacillus, shown to be protective in animal and clinical studies, would likewise confer protection in turkeys, which were treated for 11 days with either AFB1 (AFB; 1 ppm in diet), probiotic (PB; 1 × 1011 CFU/ml; oral, daily), probiotic + AFB1 (PBAFB), or PBS control (CNTL). The AFB1 induced drop in body and liver weights were restored to normal in CNTL and PBAFB groups. Hepatotoxicity markers were not significantly reduced by probiotic treatment. Major histocompatibility complex (MHC) genes BG1 and BG4, which are differentially expressed in liver and spleens, were not significantly affected by treatments. These data indicate modest protection, but the relatively high dietary AFB1 treatment, and the extreme sensitivity of this species may reveal limits of probiotic-based protection strategies. 相似文献
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阿维菌素类药物兽医临床驱虫应用研究进展 总被引:1,自引:0,他引:1
综述了阿维菌素类药物的药理作用、应用、耐药性、使用注意事项、毒理学及其残留等方面的研究进展。 相似文献
43.
冰草提取物对桃蚜的杀虫活性及对体内两种酶活性的影响 总被引:5,自引:0,他引:5
重点介绍了冰草的不同溶剂提取物对桃蚜的杀虫活性及其对蚜虫体内蛋白酶、谷胱甘肽-S-转移酶活性的影响。结果表明,冰草氯仿和水提取物对桃蚜有较好的内吸活性,并对桃蚜体内蛋白酶、谷胱甘肽-S-转移酶活性均有明显抑制作用,而在触杀处理中,提取物对蚜虫各酶系活性的影响不明显。 相似文献
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《农业科学与技术》2013,(10):1403-1408
Advanced glycation end-products (AGEs) are products of non-enzymatic glycation of proteins, lipids or nucleic acids and other macromolecules. To be spe- cific, Nε-(carboxymethyl)-Iysine (CML) is one of the most important components of AGEs, which is wildly distributed in the body and can be formed in vivo or in food processing and heating processes. Previous studies have shown that CML is a ma- jor immunological epitope in AGEs and plays an important role in diabetes and its complications, as well as in the development and progression of aging. This review summarized recent advances in major source, toxicological hazard and control mea- sures of CML. 相似文献
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The in vivo metabolism of [14CH3S]- and [14CH3O]O,O,S-trimethyl phosphorothioate (OOS) was followed in rats after oral administration of threshold or LD50 toxic doses of 20 or 60 mg/kg. Similar metabolic studies were conducted with coadministration of 1% O,O,O-trimethyl phosphorothionate (OOO), which prevented all signs of delayed toxicity, including weight loss. When administered alone, OOS was metabolized mainly (50–60%) via removal of the CH3S moiety, which was largely converted to expired CO2. Approximately 20% of the compound was O-demethylated, presumably by conjugation with glutathione, and then further metabolized to CO2. Major urinary products were identified as O,O-dimethyl phosphoric acid (50–60%) and O,S-dimethyl phosphorothioic acid (~20%). Coadministration of OOO caused a slight decrease (~5%) in the cleavage of the CH3S moiety, indicated by a reduction in 14CO2 from [14CH3S]OOS and a quantitatively similar increase in the formation of O,S-dimethyl phosphoric acid. Limited pharmacokinetic studies indicated that OOS was rapidly absorbed and distributed throughout the body. Coadministration of 1% OOO caused a slight increase in the blood half-life of parent OOS when administered at 60 mg/kg. It was concluded that a small proportion of the cleavage of the CH3S moiety from OOS is involved in the intoxication process, and that this intoxication reaction is specifically inhibited by OOO. 相似文献
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