首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Noradrenergic regulation of parvocellular neurons in the rat hypothalamic paraventricular nucleus.
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Noradrenergic regulation of parvocellular neurons in the rat hypothalamic paraventricular nucleus.

机译:大鼠下丘脑室旁核中小细胞神经元的去甲肾上腺素调节。

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摘要

Noradrenergic projections to the hypothalamic paraventricular nucleus have been implicated in the secretory regulation of several anterior pituitary hormones, including adrenocorticotropin, thyroid-stimulating hormone, growth hormone and prolactin. In an attempt to elucidate the effects of norepinephrine on the central control of pituitary hormone secretion, we looked at the actions of norepinephrine on the electrical properties of putative parvocellular neurons of the paraventricular nucleus using whole-cell current-clamp recordings in hypothalamic slices. About half (51%) of the putative parvocellular neurons recorded responded to norepinephrine with either a synaptic excitation or a direct inhibition. Norepinephrine (30-300microM) caused a marked increase in the frequency of excitatory postsynaptic potentials in about 36% of the parvocellular neurons recorded. The increase in excitatory postsynaptic potentials was blocked by prazosin (10microM), but not by propranolol (10microM) or timolol (20microM), indicating that it was mediated by alpha(1)-adrenoreceptor activation. It was also blocked by ionotropic glutamate receptor antagonists, suggesting that the excitatory postsynaptic potentials were caused by glutamate release. The increase in excitatory postsynaptic potentials was completely abolished by tetrodotoxin, indicating the spike dependence of the norepinephrine-induced glutamate release. In a separate group comprising 14% of the parvocellular neurons recorded, norepinephrine elicited a hyperpolarization (6.2+/-0.69mV) that was blocked by the beta-adrenoreceptor antagonists, propranolol (10microM) and timolol (20microM), but not by the alpha(1)-receptor antagonist, prazosin (10microM). This response was not blocked by tetrodotoxin (1.5-3microM), suggesting that it was caused by a direct postsynaptic action of norepinephrine. The topographic distribution within the paraventricular nucleus of the norepinephrine-responsive and non-responsive parvocellular neurons was mapped based on intracellular biocytin labeling and neurophysin immunohistochemistry.These data indicate that one parvocellular subpopulation, consisting of about 36% of the paraventricular parvocellular neurons, receives an excitatory input from norepinephrine-sensitive local glutamatergic interneurons, while a second, separate subpopulation, representing about 14% of the parvocellular neurons in the paraventricular nucleus, responds directly to norepinephrine with a beta-adrenoreceptor-mediated inhibition. This suggests that excitatory inputs to parvocellular neurons of the paraventricular nucleus are mediated mainly by an intrahypothalamic glutamatergic relay, and that only a relatively small subset of paraventricular parvocellular neurons receives direct noradrenergic inputs, which are primarily inhibitory.
机译:下丘脑室旁核的去甲肾上腺素能投射与几种垂体前叶激素的分泌调节有关,包括促肾上腺皮质激素,促甲状腺激素,生长激素和催乳激素。为了阐明去甲肾上腺素对垂体激素分泌的中枢控制的作用,我们使用下丘脑片中的全细胞电流钳记录,研究了去甲肾上腺素对室旁核假定的小细胞神经元电学性质的作用。记录的大约一半(51%)的假定的小细胞神经元对去甲肾上腺素有突触刺激或直接抑制作用。去甲肾上腺素(30-300microM)引起记录的约36%的小细胞神经元兴奋性突触后电位的频率显着增加。激动剂突触后电位的增加被哌唑嗪(10microM)阻止,但未被普萘洛尔(10microM)或噻吗洛尔(20microM)阻止,表明它是由α(1)-肾上腺素受体激活介导的。它也被离子型谷氨酸受体拮抗剂所阻断,表明兴奋性突触后电位是由谷氨酸释放引起的。河豚毒素完全消除了兴奋性突触后电位的增加,表明去甲肾上腺素诱导的谷氨酸释放的峰值依赖性。在包含14%记录的细小细胞神经元的一个单独的组中,去甲肾上腺素引起超极化(6.2 +/- 0.69mV),该超极化被β-肾上腺素受体拮抗剂,普萘洛尔(10microM)和噻吗洛尔(20microM)阻止, (1)受体拮抗剂吡唑嗪(10microM)。河豚毒素(1.5-3microM)并未阻断这种反应,表明它是由去甲肾上腺素的直接突触后作用引起的。去甲肾上腺素反应性和非反应性小细胞神经元在室旁核内的地形分布是根据细胞内生物素标记和神经物理免疫组织化学绘制的,这些数据表明一个小细胞亚群(约占36%的室旁小细胞神经元)接受了来自去甲肾上腺素敏感的局部谷氨酸能中间神经元的兴奋性输入,而第二个单独的亚群,代表室旁核中小细胞神经元的约14%,直接响应于β-肾上腺素受体介导的去甲肾上腺素。这表明脑室旁小核细胞神经元的兴奋性输入主要由下丘脑内谷氨酸能中继介导,并且仅相对较小的脑室旁小细胞神经元子集接收直接的去甲肾上腺素能输入,这主要是抑制性的。

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