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本文引用的文献

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Rat supraoptic neurones: the effects of locally applied hypertonic saline.大鼠视上核神经元:局部应用高渗盐水的影响。
J Physiol. 1980 Jul;304:405-14. doi: 10.1113/jphysiol.1980.sp013332.
2
Supraoptic neurones of rat hypothalamus are osmosensitive.大鼠下丘脑的视上核神经元对渗透压敏感。
Nature. 1980 Sep 11;287(5778):154-7. doi: 10.1038/287154a0.
3
Ionic mechanism for the osmotically-induced depolarization in neurones of the guinea-pig supraoptic nucleus in vitro.豚鼠视上核神经元体外渗透压诱导去极化的离子机制。
J Physiol. 1982 Jun;327:157-71. doi: 10.1113/jphysiol.1982.sp014225.
4
Lesions of the organum vasculosum of the lamina terminalis (OVLT) attenuate osmotically-induced drinking and vasopressin secretion in the dog.终板血管器(OVLT)损伤会减弱犬因渗透压诱导的饮水和抗利尿激素分泌。
Endocrinology. 1982 May;110(5):1837-9. doi: 10.1210/endo-110-5-1837.
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Effect of anteroventral third ventricle lesions on vasopressin release by organ-cultured hypothalamo-neurohypophyseal explants.
Neuroendocrinology. 1983 Jul;37(1):78-84. doi: 10.1159/000123519.
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Deficits in drinking and vasopressin secretion after lesions of the nucleus medianus.正中核损伤后饮水及抗利尿激素分泌的缺陷
Neuroendocrinology. 1983 Jul;37(1):73-7. doi: 10.1159/000123518.
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The organization of forebrain afferents to the paraventricular and supraoptic nuclei of the rat.大鼠前脑传入纤维至室旁核和视上核的组织架构
J Comp Neurol. 1983 Aug 1;218(2):121-44. doi: 10.1002/cne.902180202.
8
Subfornical organ--supraoptic nucleus connections: an electrophysiologic study in the rat.穹窿下器-视上核连接:大鼠的电生理研究
Brain Res. 1984 Jun 11;303(1):7-13. doi: 10.1016/0006-8993(84)90205-1.
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The organum vasculosum laminae terminalis: a critical area for osmoreception.终板血管器:渗透压感受的关键区域。
Prog Brain Res. 1983;60:91-8. doi: 10.1016/S0079-6123(08)64377-0.
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Role for the subfornical organ in vasopressin release.穹窿下器在血管加压素释放中的作用。
Brain Res Bull. 1984 Jul;13(1):43-7. doi: 10.1016/0361-9230(84)90006-6.

大鼠的渗透压感受器复合体:视上核与其他间脑核之间相互作用的证据。

The osmoreceptor complex in the rat: evidence for interactions between the supraoptic and other diencephalic nuclei.

作者信息

Honda K, Negoro H, Dyball R E, Higuchi T, Takano S

机构信息

Department of Physiology, Fukui Medical School, Matsuoka, Japan.

出版信息

J Physiol. 1990 Dec;431:225-41. doi: 10.1113/jphysiol.1990.sp018328.

DOI:10.1113/jphysiol.1990.sp018328
PMID:2100308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181772/
Abstract
  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)
摘要
  1. 开展实验以提供证据,证明视上核(SON)、腹侧前腹侧第三脑室区域(包括终板血管器;腹侧AV3V)和视前正中核(MnPO)之间存在神经元相互连接回路,并确定这些连接在SON神经元活动的渗透压控制中的重要性。在经氨基甲酸乙酯麻醉的雄性大鼠中,从这三个部位之一的神经元进行细胞外记录,同时对另外两个部位进行电刺激。2. 在从SON记录期间,向腹侧AV3V或MnPO施加电刺激脉冲后,大多数SON神经元(44/48)出现顺向兴奋(OD+)或初始短时间抑制后长时间兴奋(OD- +)。由MnPO电刺激产生的OD- +反应的OD+或OD+成分的潜伏期明显(配对t检验,P小于0.01)短于腹侧AV3V刺激产生的潜伏期。我们在SON中记录的神经元没有一个因腹侧AV3V或MnPO的刺激而出现逆向激活。向MnPO压力注射利多卡因(10%,50 nl)在所有测试的SON神经元(11/11)中,可逆地抑制了腹侧AV3V刺激后的OD+效应,而向腹侧AV3V注射利多卡因在大多数神经元(7/9)中不影响MnPO刺激后的OD+效应。这两种观察结果均与通过MnPO向SON存在兴奋性输入一致。3. 向腹侧AV3V和MnPO两者压力注射利多卡因,可逆地阻断了腹腔注射1.5 M - NaCl(1 ml)后SON神经元的激活(腹侧AV3V,11/11;MnPO,10/10个测试细胞)。然而,在两个部位注射利多卡因并不能阻止低血容量引起的SON神经元激活(通过右心房插管抽出2 ml血液:腹侧AV3V,4/5;MnPO,4/4个测试细胞)。因此,腹侧AV3V和MnPO中连接的完整性似乎是SON渗透压激活所必需的。4. 在测试的119个腹侧AV3V神经元中,有49个神经元对SON的电刺激表现出顺向兴奋(OD+;n = 33)或初始抑制后兴奋(OD- +;n = 16)。这49个OD+或OD- +神经元中的30个在MnPO电刺激后也表现出逆向兴奋(AD)。(摘要截断于400字)