首页> 美国卫生研究院文献>American Journal of Physiology - Regulatory Integrative and Comparative Physiology >Early life stress downregulates endothelin receptor expression and enhances acute stress-mediated blood pressure responses in adult rats
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Early life stress downregulates endothelin receptor expression and enhances acute stress-mediated blood pressure responses in adult rats

机译:生命早期应激下调成年大鼠内皮素受体的表达并增强急性应激介导的血压反应

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摘要

We hypothesized that early life stress enhances endothelin (ET-1)-dependent acute stress responses in adulthood. We utilized a unique rat model, wild-type (WT) and ETB receptor-deficient spotting lethal (sl/sl) rats, as well as pharmacological blockade of ET receptors, in a model of early life stress, maternal separation (MS). MS was performed in male WT and sl/sl rats 3 h/day from day 2 to 14 of life. Acute air jet stress (AJS)-induced responses (elevation in blood pressure, plasma corticosterone, and plasma ET-1) were evaluated in adult MS rats compared with the nonhandled littermate (control) rats. MS significantly augmented the acute AJS-induced blood pressure response (area under the curve) in WT rats compared with control, while the AJS-induced pressor responses were similar in sl/sl MS and control rats. ET receptor blockade significantly blunted the AJS-induced pressor response in WT MS and control rats. Moreover, AJS-induced plasma corticosterone levels in control rats were sensitive to ET receptor blockade, yet, AJS did not alter plasma corticosterone levels in MS rats. MS significantly increased circulating ET-1 levels, and AJS-induced plasma ET-1 levels were similarly increased in control and MS rats. MS induced a significant downregulation in expression of ETA and ETB receptors in aortic tissue compared with control rats. These results indicate that early life stress reduced expression of ETA and ETB receptors, leading to alterations in the ET pathway, and an exaggerated acute stress-mediated pressor response in adulthood.
机译:我们假设,成年早期的应激会增强内皮素(ET-1)依赖性的急性应激反应。在早期应激,母体分离(MS)模型中,我们利用了独特的大鼠模型,野生型(WT)和ETB受体缺陷型致死性(sl / sl)大鼠,以及ET受体的药理阻断作用。从生命的第二天到第14天,每天3小时/天在雄性WT和sl / sl大鼠中进行MS。与未处理的同窝幼仔(对照)大鼠相比,评估了成年MS大鼠的急性喷气压力(AJS)诱导的反应(血压,血浆皮质酮和血浆ET-1升高)。与对照组相比,MS显着增强了WT大鼠的急性AJS诱发的血压反应(曲线下的面积),而sl / sl MS和对照组大鼠的AJS诱发的升压反应相似。 ET受体阻滞显着减弱了WT MS和对照大鼠中AJS诱导的升压反应。此外,AJS诱导的对照组大鼠血浆皮质酮水平对ET受体阻滞敏感,但AJS并未改变MS大鼠血浆皮质酮水平。 MS显着增加了循环ET-1水平,而对照组和MS大鼠中AJS诱导的血浆ET-1水平也同样升高。与对照组相比,MS诱导主动脉组织中ETA和ETB受体表达的显着下调。这些结果表明,早期生活压力会降低ETA和ETB受体的表达,从而导致ET途径的改变,并在成年期夸大急性压力介导的升压反应。

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