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Correlations between Low Doses of Zearalenone Its Carryover Factor and Estrogen Receptor Expression in Different Segments of the Intestines in Pre-Pubertal Gilts—A Study Protocol

机译:百育肠道肠道肠道不同区段中低剂量酸碱酮携带因子和雌激素受体表达的相关性 - A研究方案

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摘要

Plant materials can be contaminated with Fusarium mycotoxins and their derivatives, whose toxic effects on humans and animals may remain subclinical. Zearalenone (ZEN), a low-molecular-weight compound, is produced by molds in crop plants as a secondary metabolite. The objective of this study will be to analyze the in vivo correlations between very low monotonic doses of ZEN (5, 10, and 15 μg ZEN/kg body weight—BW for 42 days) and the carryover of this mycotoxin and its selected metabolites from the intestinal contents to the intestinal walls, the mRNA expression of estrogen receptor alfa (ERα) and estrogen receptor beta (ERβ) genes, and the mRNA expression of genes modulating selected colon enzymes (CYP1A1 and GSTP1) in the intestinal mucosa of pre-pubertal gilts. An in vivo experiment will be performed on 60 clinically healthy animals with initial BW of 14.5 ± 2 kg. The gilts will be randomly divided into a control group (group C, n = 15) and three experimental groups (group ZEN5, group ZEN10, and group ZEN15; n = 15). Group ZEN5 will be administered per os 5 μg ZEN/kg BW (MABEL), group ZEN10—10 μg ZEN/kg BW (NOAEL), and group ZEN15—15 µg ZEN/kg BW (low LOAEL). In each group, five animals will be euthanized on analytical dates 1 (exposure day 7), 2 (exposure day 21), and 3 (exposure day 42). Samples for in vitro analyses will be collected from an intestinal segment resected from the following regions: the third (horizontal) part of the duodenum, jejunum, ileum, cecum, ascending colon, transverse colon, and descending colon. The experimental material will be collected under special conditions, and it will be transported to specialist laboratories where samples will be obtained for further analyses.
机译:植物材料可以污染镰刀菌霉菌毒素及其衍生物,其对人类和动物的毒性影响可能是亚临床的。 Zearalenone(ZEN),一种低分子量化合物,通过作物植物中的模具作为次级代谢物生产。本研究的目的是分析非常低单调剂量的ZEN(5,10和15μg/ kg体重-BW 42天)之间的体内相关性以及该霉菌毒素的携带及其选定的代谢物肠壁的肠含量,雌激素受体Alfa(ERα)和雌激素受体β(ERβ)基因的mRNA表达,以及在Pre-pubertal的肠粘膜中调节所选结肠酶(Cyp1a1和Gstp1)的基因的mRNA表达吉尔茨。体内实验将在60名临床健康的动物上进行,初始BW为14.5±2千克。胃肠将随机分为对照组(组,N = 15)和三个实验组(组ZEN5,组ZEN10和ZEN15组; n = 15)。 Group Zen5将由OS5μgZEN / kg BW(MABEL),组ZEN10-10μgZEN / kg BW(NOAEL)组和ZEN15-15μgZEN / kg BW(低宽松琴)给药。在每组中,五只动物将在分析日期1(暴露第7天),2(暴露日21)和3(暴露日42)上被安乐死。用于体外分析的样品将从从以下地区切除的肠段收集:十二指肠,Jejunum,Hileum,Cecum,升序结肠,横向结肠和下降结肠的第三(水平)部分。实验材料将在特殊条件下收集,并将其运输到专业实验室,其中将获得进一步分析的样品。

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