首页> 外文期刊>Journal of biochemical and molecular toxicology >Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and leptin on hypothalamic mRNA expression of factors participating in food intake regulation in a TCDD-sensitive and a TCDD-resistant rat strain.
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Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and leptin on hypothalamic mRNA expression of factors participating in food intake regulation in a TCDD-sensitive and a TCDD-resistant rat strain.

机译:2,3,7,8-四氯二苯并-对-二恶英(TCDD)和瘦素对参与TCDD敏感和TCDD耐药的大鼠食物摄入调节因子的下丘脑mRNA表达的影响。

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摘要

An acutely toxic dose of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) leads to a drastically and permanently reduced feed intake and wasting by an unknown mechanism. We focused on the possible interference of TCDD with hypothalamic factors known to take part in the regulation of eating and metabolism, utilizing the over 1000-fold TCDD-sensitivity difference between Long-Evans (Turku/AB; L-E) and Han/Wistar (Kuopio) rats. The mRNA expression of 18 hypothalamic factors (including NPY, AgRP, and CART) was measured by quantitative RT-PCR at 6, 24 and 96 h after TCDD administration. The effects of TCDD were compared with those of leptin and with feed restriction employing a TCDD dose that elicited a severe reduction of feed intake in L-E rats. TCDD mainly modified expression of orexigenic factors causing an initial suppression followed by reversal to enhanced expression by 96 h. The latter was also seen in feed-restricted controls. In contrast, leptin altered both orexigenic and anorexigenic factor mRNAs in amore even manner and its effects were clustered at 6 h. The transient nature of feeding-promoting factor suppression does not strongly support a key role for this phenomenon in TCDD-induced wasting syndrome. However, the fact that TCDD mainly affected orexigenic factors and the temporal differences in response found between the rat strains warrant further research.
机译:2,3,7,8-四氯二苯并-对-二恶英(TCDD)的剧毒剂量会导致永久性地大幅减少采食量,并通过未知的机制造成浪费。我们利用Long-Evans(Turku / AB; LE)和Han / Wistar(Kuopio)之间超过1000倍的TCDD敏感性差异,着重研究了TCDD对已知参与饮食和代谢调节的下丘脑因子的可能干扰。 )大鼠。 TCDD给药后6、24和96小时,通过定量RT-PCR测量18种下丘脑因子(包括NPY,AgRP和CART)的mRNA表达。将TCDD的效果与瘦素的效果进行了比较,并采用了限制TCDD剂量的饲料限制,该剂量可导致L-E大鼠的采食量大大减少。 TCDD主要修饰致癌因子的表达,引起最初的抑制,随后在96小时内逆转增强表达。后者还出现在限制饲料的对照中。相反,瘦素以更均匀的方式改变了致食性和厌食性因子的mRNAs,并且其作用在6小时时聚集。进食促进因子抑制的短暂性不能强烈支持该现象在TCDD诱导的消耗综合征中的关键作用。但是,TCDD主要影响致癌因素的事实以及大鼠品系之间发现的反应时间差异值得进一步研究。

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