玉米赤霉烯酮对蛋鸡肝脏损伤作用的研究
Study on the effect of zearalenone on liver damage in laying hens
-
摘要: 为了了解玉米赤霉烯酮(zearalenone, ZEN)对肝脏结构和功能的损伤作用,试验将75只270日龄海兰粉蛋鸡随机分成3组,每组25只,空白对照组饲喂全价基础日粮,试验Ⅰ、Ⅱ组分别将1,2 mg/kg ZEN混入全价基础日粮中饲喂,连续饲喂90 d后剖杀,各组选取6只蛋鸡采集血清检测肝脏功能,肉眼观察肝脏病变并评分,石蜡切片观察肝脏组织学变化。结果表明:与空白对照组比较,试验Ⅰ组蛋鸡血清中天门冬氨酸氨基转移酶(AST)活性极显著升高(P<0.01),试验Ⅱ组天门冬氨酸氨基转移酶、丙氨酸氨基转移酶(ALT)、碱性磷酸酶(ALP)活性极显著升高(P<0.01),总蛋白(TP)和白蛋白(ALB)含量显著降低(P<0.05);与空白对照组比较,试验Ⅰ、Ⅱ组蛋鸡肝脏病变评分极显著升高(P<0.01);在肝脏病理组织切片中,试验Ⅰ组蛋鸡肝脏出现小泡性脂肪变性,而试验Ⅱ组以肝细胞坏死和纤维化为主。说明ZEN可严重损伤肝脏结构,引起肝细胞变性、坏死和纤维化,并出现相应的肝功能下降。Abstract: In order to understand the damage effect of zearalenone(ZEN) on liver structure and function, 75 270-day-old Hailan pink layers were randomly divided into 3 groups, each with 25 chickens. The blank control group was fed the full basal diet, and the test groups Ⅰ and Ⅱ were fed with 1,2 mg/kg ZEN mixed with the full basal diet respectively; and those groups were fed continuously for 90 days and then killed. Serum was collected from 6 laying hens in each group to detect liver function, the visually observed and scored of liver disease, and paraffin sections were used to observe the histological changes of the liver. The results showed that compared with the blank control group, the activity of aspartate aminotransferase(AST) in the serum of the laying hens in the test group Ⅰ was extremely significantly increased(P<0.01);in the test group Ⅱ,aspartate aminotransferase, alanine aminotransferase(ALT),alkaline phosphatase(ALP) activities were extremely significantly increased(P<0.01),and the contents of total protein(TP) and albumin(ALB) were significantly reduced(P<0.05). Compared with the blank control group, the lesion scores of the laying hens in the test groups Ⅰ and Ⅱ increased extremely significantly(P<0.01);in the liver pathological tissue sections, the liver of the laying hens in the test group Ⅰ showed vesicular steatosis, while in the test group Ⅱ,it was dominated by hepatocyte necrosis and fibrosis. The results suggested that ZEN can severely damage the liver structure, cause liver cell degeneration, necrosis and fibrosis, and cause corresponding liver function decline.