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Vasopressin receptors of the vasopressor (V1) type in the nucleus of the solitary tract of the rat mediate direct neuronal excitation

机译:大鼠孤束核中血管加压素(V1)型的加压素受体介导直接神经元兴奋

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摘要

The existence of vasopressin-sensitive neurons in the nucleus of the solitary tract of the rat and the presence in this brain area of vasopressin binding sites were investigated using extracellular single- unit recordings from brain-stem slices and light microscopic autoradiography. About 45% of the recorded neurons responded to vasopressin at 5–2000 nM by a reversible, concentration-dependent increase in firing rate. The action of vasopressin was direct, was suppressed by a vasopressor antagonist, and was mimicked by a vasopressor agonist. Oxytocin was 10–100 times less efficient than vasopressin and a specific antidiuretic agonist was without effect. Using light microscopic autoradiography and 3H-arginine vasopressin as a ligand, high-affinity vasopressin binding sites were found distributed over the whole rostrocaudal extent of the nucleus of the solitary tract. Binding was displaced by unlabeled vasopressor agonist but not by unlabeled antidiuretic agonist. Thus, the nucleus of the solitary tract contains V1-type vasopressin receptors which are, at least in part, located on neuronal membranes and whose activation generates bioelectrical signals. Solitary tract vasopressin-sensitive neurons may be the target of a vasopressinergic innervation originating in the hypothalamic paraventricular nucleus and could be involved in the central regulation of cardiovascular functions.
机译:使用脑干切片的细胞外单细胞记录和光学显微放射照相技术,研究了大鼠孤立道核中是否存在加压素敏感神经元,以及在该脑区中是否存在加压素结合位点。约45%的记录神经元在5–2000 nM时对血管加压素的反应是可逆的,浓度依赖性的放电速率增加。加压素的作用是直接的,被加压素拮抗剂抑制,并被加压素激动剂模拟。催产素的效率比加压素低10-100倍,而特定的抗利尿激动剂无效。使用光学显微放射自显影术并以3H-精氨酸加压素为配体,发现高亲和力加压素结合位点分布在孤束核的整个后额尾区域。结合被未标记的血管升压激动剂取代,但未被未标记的抗利尿剂激动剂取代。因此,孤立道的核包含至少部分位于神经元膜上并且其激活产生生物电信号的V1型加压素受体。孤束加压素敏感神经元可能是源自下丘脑室旁核的加压素神经支配的靶标,并且可能参与心血管功能的中央调节。

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