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首页> 外文期刊>Mycotoxin Research >Urinary deoxynivalenol (DON) and zearalenone (ZEA) as biomarkers of DON and ZEA exposure of pigs
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Urinary deoxynivalenol (DON) and zearalenone (ZEA) as biomarkers of DON and ZEA exposure of pigs

机译:尿中的脱氧雪腐酚(DON)和玉米赤霉烯酮(ZEA)作为猪DON和ZEA暴露的生物标志物

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摘要

Four diets contaminated with 1.1 to 5.0 mg/kg deoxynivalenol (DON) and 0.4 to 2.4 mg/kg zearalenone (ZEA) were fed to four groups of six growing Large White pigs. Urine samples were collected after 3 to 4 days and again after 6 to 7 days on the diets.On each sampling day, half of the animals were sampled in the morning, after an 8-h fast, and the other half were sampled in the afternoon, after 7 h of ad libitum access to feed. The urinary concentrations of DON, DON-glucuronide, DON-3-sulphate, de-epoxy-DON, as well as of ZEA, ZEA-14-glucuronide, a-zearalenol and a-zearale4ol-14-glucuronide, analysed using LC-MS/MS, were used to calculate urinary DON and ZEA equivalent concentrations (DONe and ZEAe). The urinary concentration of DONe (/><0.001), butnot of ZEAe (P=0.31), was lower in the fasted than that in the fed animals. The urinary DONe/ creatinine and ZEAe/creatinine ratios were highly correlated with DON and ZEA intake per kg body weight the day preceding sampling (r=0.76 and 0.77; P<0.001).The correlations between DON intake during the 7 h preceding urine sampling in the afternoon and urinary DONe/creatinine ratio (r= 0.88) as well as between mean ZEA intake during 3 days preceding urine sampling and urinary ZEAe/creatinine ratio(r=0.84) were even higher, reflecting the plasma elimination half-time of several hours for DON and of more than 3 days for ZEA. ZEAe analysed in enzymatically hydrolysed urine using an ELISA kit was highly correlated with the LC-MS/ MS data (r = 0.94).The urinary DONe and ZEAe to creatinine ratios, analysed in pooled urine samples of several pigs fed the same diet, can be used to estimate their exposure to DON and ZEA.
机译:将四只日粮饲喂四组受1.1至5.0 mg / kg脱氧雪茄烯醇(DON)和0.4至2.4 mg / kg玉米赤霉烯酮(ZEA)污染的日粮。在饮食中3-4天后和6-7天后再次收集尿液样本。在每个采样日,禁食8小时后,早上对一半的动物进行采样,而对另一半则进行采样。下午,随意采食7小时后。使用LC-HPLC分析的DON,DON-葡萄糖醛酸苷,DON-3-硫酸盐,脱环氧DON以及ZEA,ZEA-14-葡萄糖醛酸,α-玉米赤霉烯醇和a-zearale4ol-14-葡萄糖醛酸尿样的尿液浓度MS / MS用于计算尿中DON和ZEA的当量浓度(DONe和ZEAe)。空腹的DONe(/><0.001),而不是ZEAe(P = 0.31)的尿液浓度低于喂食动物的尿液浓度。尿DONe /肌酐和ZEAe /肌酐的比值与采样前一天DON和ZEA摄入量/千克体重高度相关(r = 0.76和0.77; P <0.001)。尿液采样前7 h DON摄入量之间的相关性。下午和尿中DONe /肌酐之比(r = 0.88)以及尿液采样前3天的平均ZEA摄入量与尿ZEAe /肌酐之比(r = 0.84)甚至更高,反映了血浆清除半衰期DON需要几个小时,而ZEA需要超过3天。使用ELISA试剂盒对酶解尿液中的ZEAe进行分析与LC-MS / MS数据高度相关(r = 0.94)。在饲喂相同日粮的几只猪的合并尿液样品中分析的尿中DONe和ZEAe与肌酐的比率可以用于估计他们在DON和ZEA中的暴露程度。

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