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首页> 外文期刊>Neuroendocrinology: International Journal for Basic and Clinical Studies on Neuroendocrine Relationships >Hypothalamo-pituitary-adrenal axis-regulated stress response and negative feedback sensitivity is altered by prenatal morphine exposure in adult female rats.
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Hypothalamo-pituitary-adrenal axis-regulated stress response and negative feedback sensitivity is altered by prenatal morphine exposure in adult female rats.

机译:下丘脑-垂体-肾上腺轴调节的应激反应和负反馈敏感性被成年雌性大鼠的产前吗啡暴露所改变。

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It has been shown that adult female rats react to stressors more intensely than adult male rats. Our previous work demonstrated that the adrenocorticotropic hormone (ACTH) but not corticosterone (CORT) response to stress is altered by prenatal morphine exposure in adult male rats. Response of the hypothalamo-pituitary-adrenal (HPA) axis to stress is known to be sex specific and dependent on the hormonal fluctuation of the estrous cycle. Therefore, the present study examined the effect of prenatal morphine exposure on the levels of ACTH and CORT before and after restraint stress in adult female rats. Experiment 1 tested ACTH and CORT plasma levels before and after restraint stress in prenatally morphine- and saline-exposed, adult diestrus and proestrus female rats. Prenatal morphine exposure suppressed the restraint stress-induced ACTH levels in both diestrus and proestrus females, but did not have any effects on the basal or stress-induced CORT levels. Experiment 2 examined the sensitivity of negative feedback using the dexamethasone (DEX) (0.001, 0.01, 0.1 and 1.0 mg/kg) suppression test in adult, prenatally morphine- and saline-exposed female rats. In saline-exposed, proestrus but not diestrus females, all doses of DEX were effective in suppressing the restraint stress-induced increase in CORT levels. In both diestrus and proestrus, morphine-exposed females, only the two highest doses of DEX (0.1 and 1.0 mg/kg) were successfully suppressing the stress-induced CORT levels. The stress-induced increase in the ACTH level was suppressed only by the highest dose of DEX (1.0 mg/kg) in both saline- and morphine-exposed, diestrus and proestrus females. Thus, the present study demonstrates that prenatal morphine exposure alters the HPA axis-regulated stress response and the sensitivity of negative feedback that are affected by the fluctuation of ovarian hormones.
机译:已经显示成年雌性大鼠对应激源的反应比成年雄性大鼠更强烈。我们以前的工作表明成年雄性大鼠的产前吗啡暴露改变了促肾上腺皮质激素(ACTH)而非皮质酮(CORT)对压力的反应。已知下丘脑-垂体-肾上腺(HPA)轴对压力的反应是性别特异性的,并取决于发情周期的激素波动。因此,本研究探讨了成年雌性大鼠在限制应激前后,产前吗啡暴露对ACTH和CORT水平的影响。实验1测试了在产前暴露于吗啡和盐水的成年雌性和成年雌性大鼠的束缚应激前后,ACTH和CORT血浆水平。产前吗啡暴露抑制了雌性和雌性雌性的束缚应激诱导的ACTH水平,但是对基础或应激诱导的CORT水平没有任何影响。实验2使用地塞米松(DEX)(0.001、0.01、0.1和1.0 mg / kg)抑制试验在成年,出生前吗啡和盐水暴露的雌性大鼠中检查了负反馈的敏感性。在暴露于生理盐水的雌激素前体而不是雌性雌激素中,所有剂量的DEX均可有效抑制束缚应激诱导的CORT水平升高。在雌性吗啡暴露的雌激素和雌激素中,只有两种最高剂量的DEX(0.1和1.0 mg / kg)成功抑制了压力诱导的CORT水平。应力诱导的ACTH水平的升高仅在暴露于盐水和吗啡的雌性,雌性和发情期雌性中最高剂量的DEX(1.0 mg / kg)被抑制。因此,本研究表明,产前吗啡暴露改变了受卵巢激素波动影响的HPA轴调节的应激反应和负反馈的敏感性。

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