首页> 美国卫生研究院文献>The Journal of Physiology >The osmoreceptor complex in the rat: evidence for interactions between the supraoptic and other diencephalic nuclei.
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The osmoreceptor complex in the rat: evidence for interactions between the supraoptic and other diencephalic nuclei.

机译:大鼠中的渗透压感受器复合物:视超视核与其他双脑核之间相互作用的证据。

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摘要

1. Experiments were undertaken to provide evidence for the existence of a circuit of neuronal interconnections between the supraoptic nucleus (SON), the ventral anteroventral third ventricular region (including the organum vasculosum of the lamina terminalis; ventral AV3V) and the median preoptic nucleus (MnPO), and to determine the importance of these connections in the osmotic control of the neuronal activity of the SON. Extracellular recordings were made in the urethane-anaesthetized male rat from neurones in one of these three sites, while the other two sites were electrically stimulated. 2. During recording from the SON, electrical stimulus pulses applied either to the ventral AV3V or to the MnPO were followed by orthodromic excitation (OD+) or initial short-duration inhibition followed by long-duration excitation (OD- +) of most SON neurones (44/48). The latency of OD+ or OD+ component of OD- + response produced by electrical stimulation of the MnPO was significantly (paired t test, P less than 0.01) shorter than that by the stimulation of the ventral AV3V. None of the neurones we recorded in the SON was activated antidromically by stimulation of either the ventral AV3V or the MnPO. Pressure injection of lidocaine (10%, 50 nl) into the MnPO reversibly depressed the OD+ effect after stimulation of the ventral AV3V in all the SON neurones tested (11/11), while injection of lidocaine into the ventral AV3V did not affect the OD+ effect after stimulation of the MnPO in most neurones (7/9). Both types of observation are consistent with the presence of an excitatory input to SON through the MnPO. 3. Pressure injection of lidocaine into both the ventral AV3V and the MnPO reversibly blocked the activation of SON neurones following an I.P. injection of 1.5 M-NaCl (1 ml) (ventral AV3V 11/11; MnPO, 10/10 cells tested). Injection of lidocaine at both sites, however, did not prevent activation of SON neurones by hypovolaemia (2 ml of blood was withdrawn through a cannula in the right atrium: ventral AV3V, 4/5; MnPO, 4/4 cells tested). The integrity of connections in the ventral AV3V and MnPO thus appeared to be essential for osmotic activation of the SON. 4. Of the 119 ventral AV3V neurones which were tested for their response to electrical stimulation of the SON, forty-nine neurones showed orthodromic excitation (OD+; n = 33) or initial inhibition followed by excitation (OD- +; n = 16). Thirty of the forty-nine OD+ or OD- + neurones also showed antidromic excitation (AD) after electrical stimulation of the MnPO.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.进行实验以提供证据,证明在视上核(SON),腹侧前腹第三室区(包括椎板末端的器官血管;腹侧AV3V)和正中视前核( MnPO),并确定这些连接在SON神经元活性渗透控制中的重要性。在尿烷麻醉的雄性大鼠中,从这三个部位之一的神经元中进行细胞外记录,而另外两个部位被电刺激。 2.在从SON进行记录的过程中,对大多数SON神经元施加正弦激励(OD +)或最初的短时抑制,然后进行长时程激励(OD- +),然后施加到腹侧AV3V或MnPO上的电刺激脉冲(44/48)。 MnPO电刺激产生的OD +或OD- +反应的OD +组分的潜伏期显着(配对t检验,P小于0.01)比腹侧AV3V刺激的潜伏期短。我们在SON中记录的神经元均未通过刺激腹侧AV3V或MnPO来抗激活。在所有测试的SON神经元(11/11)中,在刺激腹侧AV3V后,向MnPO中加压注射利多卡因(10%,50 nl)可逆地降低了OD +效应,而向腹侧AV3V注射利多卡因并不影响OD +刺激大多数神经元中的MnPO后效果(7/9)。两种观察类型均与通过MnPO向SON的兴奋性输入相一致。 3.腹膜内注射后向腹腔AV3V和MnPO加压注射利多卡因可逆地阻断SON神经元的激活。注射1.5 M-NaCl(1 ml)(腹腔AV3V 11/11; MnPO,测试了10/10个细胞)。然而,在两个部位注射利多卡因并不能防止低血容量引起SON神经元的激活(通过右心房中的插管抽取2毫升血液:腹侧AV3V,4/5; MnPO,4/4细胞)。因此,腹侧AV3V和MnPO的连接完整性对于SON的渗透激活至关重要。 4.在测试的119个腹侧AV3V神经元对SON的电刺激反应中,有49个神经元表现出原位刺激(OD +; n = 33)或最初的抑制作用,然后是兴奋性刺激(OD- +; n = 16)。 。在对MnPO进行电刺激后,四十九个OD +或OD- +神经元也显示出反线激发(AD)。(摘要截断为400字)

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