首页> 外文期刊>Stress: the international journal on the biology of stress >Activation of 5-HT1A receptors in the rat dorsomedial hypothalamus inhibits stress-induced activation of the hypothalamic-pituitary-adrenal axis
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Activation of 5-HT1A receptors in the rat dorsomedial hypothalamus inhibits stress-induced activation of the hypothalamic-pituitary-adrenal axis

机译:大鼠背体下丘脑中的5-HT1A受体的激活抑制了下丘脑 - 垂体 - 肾上腺轴的应力诱导的活化

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Acute activation of the hypothalamic-pituitary-adrenal (HPA) axis, leading to the release of corticosteroid hormones into the circulation, is an adaptive response to perceived threats. Persistent activation of the HPA axis can lead to impaired physiological or behavioral function with maladaptive consequences. Thus, efficient control and termination of stress responses is essential for well-being. However, inhibitory control mechanisms governing the HPA axis are poorly understood. Previous studies suggest that serotonergic systems, acting within the medial hypothalamus, play an important role in inhibitory control of stress-induced HPA axis activity. To test this hypothesis, we surgically implanted chronic jugular cannulae in adult male rats and conducted bilateral microinjection of vehicle or the 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino) tetralin hydrobromide (8-OH-DPAT; 8nmol, 0.2L, 0.1L/min, per side) into the dorsomedial hypothalamus (DMH) immediately prior to a 40min period of restraint stress. Repeated blood sampling was conducted using an automated blood sampling system and plasma corticosterone concentrations were determined using enzyme-linked immunosorbent assay. Bilateral intra-DMH microinjections of 8-OH-DPAT suppressed stress-induced increases in plasma corticosterone within 10min of the onset of handling prior to restraint and, as measured by area-under-the-curve analysis of plasma corticosterone concentrations, during the 40min period of restraint. These data support an inhibitory role for serotonergic systems, acting within the DMH, on stress-induced activation of the HPA axis.Lay summary: Inhibitory control of the hypothalamic-pituitary-adrenal (HPA) stress hormone response is important for well-being. One neurochemical implicated in inhibitory control of the HPA axis is serotonin. In this study we show that activation of serotonin receptors, specifically inhibitory 5-HT1A receptors in the dorsomedial hypothalamus, is sufficient to inhibit stress-induced HPA axis activity in rats.
机译:急性激活下丘脑 - 垂体 - 肾上腺(HPA)轴,导致皮质类固醇激素释放到循环中,是对感知威胁的适应性。 HPA轴的持续激活可导致生理或行为功能受损,具有适应不良后果。因此,有效的控制和应力响应的终止对于福祉至关重要。然而,控制HPA轴的抑制控制机制很差。以前的研究表明,在内侧下丘脑中作用的血清onergics系统在应激诱导的HPA轴活性的抑制控制中起重要作用。为了测试这一假设,我们在成年雄性大鼠中手术植入慢性颈痈,并进行了载体的双侧微注射或5-HT1A受体激动剂,8-羟基-2-(DI-N-丙基氨基)四rollin氢溴酸萘(8-OH-DPAT ;在40分钟约束应力之前,在40分钟内立即进入背体下丘脑(DMH)中的8nmol,0.2L,0.1L / min。使用自动血液采样系统进行重复血液取样,使用酶联免疫吸附测定测定血浆皮质酮浓度。在克制之前,在处理前10分钟内抑制8-OH-DPAT的双侧DMH抑制应激诱导的血浆皮质酮内的增加,并且通过血浆皮质酮浓度的面积曲线分析测量,在40分钟内测量克制的时期。这些数据支持在DMH内作用的血清奈良能系统的抑制作用,在DMH内作用于应激诱导的HPA轴的活化。缺乏肝癌 - 垂体 - 肾上腺(HPA)胁迫激素响应对福祉至关重要。涉及HPA轴抑制控制的一种神经化学物质是血清素。在该研究中,我们表明,血清素受体的激活,特异性抑制在背体下丘脑中的抑制5-HT1A受体,足以抑制大鼠中应激诱导的HPA轴活性。

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