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首页> 外文期刊>Journal of neuroendocrinology >Presynaptic noradrenergic regulation of glutamate inputs to hypothalamic magnocellular neurones.
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Presynaptic noradrenergic regulation of glutamate inputs to hypothalamic magnocellular neurones.

机译:谷氨酸输入到下丘脑大细胞神经元的突触前去甲肾上腺素调节。

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摘要

Glutamate and norepinephrine transmitter systems play critical roles in the synaptic control of hypothalamic magnocellular neurones. We recently reported on a norepinephrine-sensitive glutamate circuit within the paraventricular nucleus (PVN) that projects to magnocellular neurones. Here, we present evidence for norepinephrine regulation of glutamate release in the PVN and supraoptic nucleus (SON) via actions on presynaptic terminals. Whole-cell synaptic currents were recorded in magnocellular neurones of the SON and PVN in an acute slice preparation. Bath application of norepinephrine (100 micro m) caused a robust, reversible increase in the frequency of spontaneous glutamatergic excitatory postsynaptic currents in 100% of SON neurones (246%) and in 88% of PVN magnocellular neurones (259%). The norepinephrine-induced increase in glutamate release was mediated by activation of both presynaptic alpha1 receptors and alpha2 receptors, but the alpha1-receptor component was the predominant component of the response. The presynaptic actions of norepinephrine were predominantly, although not completely, resistant to blockade of Na-dependent spikes, implicating a presynaptic terminal locus of action. Interestingly, the spike-dependent component of the response was greater in PVN than in SON magnocellular neurones. This robust presynaptic facilitation of glutamate release by norepinephrine, combined with the known excitatory postsynaptic actions of norepinephrine, activational effects on local glutamate circuits, and inhibitory effects on gamma-aminobutyric acid release, indicate a strong excitatory role of norepinephrine in the regulation of oxytocin and vasopressin release during physiological stimulation.
机译:谷氨酸和去甲肾上腺素递质系统在下丘脑大细胞神经元的突触控制中起关键作用。我们最近报道了脑室旁核(PVN)中去甲肾上腺素敏感的谷氨酸回路,该回路投射到大细胞神经元。在这里,我们提供证据表明去甲肾上腺素通过突触前末端的作用调节PVN和视上核(SON)中的谷氨酸释放。在急性切片制剂中,在SON和PVN的大细胞神经元中记录了全细胞突触电流。浴中使用去甲肾上腺素(100微米)导致100%的SON神经元(246%)和88%的PVN巨细胞神经元(259%)的自发性谷氨酸能兴奋性突触后突触电流的频率发生强劲,可逆的增加。去甲肾上腺素诱导的谷氨酸释放增加是由突触前α1受体和α2受体的激活介导的,但α1受体成分是该反应的主要成分。去甲肾上腺素的突触前作用主要(尽管不完全)对Na依赖性刺突的阻滞有抵抗力,这暗示着突触前的终末作用位点。有趣的是,PVN中应答的峰值依赖性成分要比SON巨细胞神经元大。去甲肾上腺素对谷氨酸释放的这种强大的突触前促进作用,与去甲肾上腺素的已知兴奋性突触后突触作用,对局部谷氨酸循环的激活作用以及对γ-氨基丁酸释放的抑制作用,表明去甲肾上腺素在催产素和催产素的调节中具有强烈的兴奋作用。在生理刺激过程中释放加压素。

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