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Fastigial inputs to paraventricular neurosecretory neurones studied by extra- and intracellular recordings in rats.

机译:通过大鼠的细胞外和细胞内记录研究脑室旁神经分泌神经元的小脑输入。

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摘要

1. The effects of stimulation of the cerebellar fastigial nucleus (FN) on the activity of neurosecretory neurones in the hypothalamic paraventricular nucleus (PVN) of rats, anaesthetized with urethane and alpha-chloralose, were investigated by extracellular and intracellular recordings. 2. With extracellular recording, 139 PVN neurosecretory neurones were identified by antidromic activation following stimulation of the pituitary stalk, of which 120 were spontaneously firing and 19 were silent. Three types of responses to FN stimulation (1 or 2 pulses at 333 Hz) were observed in 43% of spontaneously firing PVN neurosecretory neurones: inhibition (type I) with a latency of 4.3 +/- 4.1 ms (mean +/- S.D., 32 of 120 neurones, 27%); excitation (type E) with 22.3 +/- 8.1 ms latency (14 of 120, 11%); and inhibition-excitation type (I-E) with 5.5 +/- 3.4 ms latency (6 of 120, 5%). Silent neurosecretory neurones did not respond to FN stimulation. Twelve per cent of non-neurosecretory cells (three out of twenty-six tested) responded to FN stimulation (one was inhibited, and two were excited). 3. Repetitive stimulation (60 Hz, 10 s) of the FN, which evoked a stimulus-locked pressor response, suppressed on-going activity of PVN neurosecretory neurones in 43% (twenty-nine of sixty-eight) of neurones tested. In 40% of these neurones, the activity was also inhibited by intravenous injection of phenylephrine (3 micrograms in 0.3 ml Ringer solution), while in other neurones the injection had no effect. Rebound excitation of neurone activity lasting for 1-5 min after termination of repetitive stimulation was observed in 28% of the neurones. Ten neurones (14%) were excited by repetitive stimulation. 4. Successful intracellular recordings were made from seventy-two PVN neurones, of which thirty-seven were neurosecretory cells. The mean resting membrane potential was -51 mV (n = 72; range from -40 to -75 mV). The input resistance of neurosecretory cells was 117 +/- 21 M omega (range 93-153 M omega; n = 8). This value was higher than that for non-neurosecretory cells which was found to be 53 +/- 10 M omega (range 35-72 M omega; n = 9). The difference was statistically significant (P less than 0.01, Student's t test). 5. In response to FN stimulation, sixteen (43%) of the thirty-seven neurosecretory neurones showed IPSPs with latencies of 7.4 +/- 2.8 ms and three (8%) exhibited EPSPs with latencies of 13.3 +/- 4.2 ms.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.通过细胞外和细胞内记录研究了刺激小脑小脑顶核(FN)对大鼠下丘脑室旁核(PVN)中神经分泌神经元活性的影响,并用氨基甲酸乙酯和α-氯草胺麻醉。 2.通过细胞外记录,在垂体柄刺激后通过抗蠕动激活鉴定出139个PVN神经分泌神经元,其中120个是自发放电的,19个是沉默的。在43%的自发发射的PVN神经分泌神经元中观察到对FN刺激的三种类型的响应(在333 Hz处有1或2个脉冲):抑制(I型),潜伏期为4.3 +/- 4.1 ms(平均+/- SD, 120个神经元中的32个,占27%);激发(E型),潜伏期为22.3 +/- 8.1毫秒(120的14,11%);以及抑制激发类型(I-E),潜伏期为5.5 +/- 3.4毫秒(6 / 120,5%)。沉默的神经分泌神经元对FN刺激无反应。百分之十二的非神经糖化细胞(测试的二十六个中的三个)对FN刺激有反应(一个被抑制,两个被兴奋)。 3. FN的重复刺激(60 Hz,10 s)引起刺激锁定的加压反应,抑制了43%(68个中的29个)神经元中PVN神经分泌神经元的持续活动。在40%的这些神经元中,静脉注射去氧肾上腺素(在0.3 ml林格溶液中3微克)也抑制了该活性,而在其他神经元中,注射没有作用。在28%的神经元中观察到重复刺激终止后,神经元活动的反弹刺激持续1-5分钟。十个神经元(14%)被重复刺激而兴奋。 4.成功的细胞内记录来自72个PVN神经元,其中37个是神经分泌细胞。平均静息膜电位为-51 mV(n = 72;范围为-40至-75 mV)。神经分泌细胞的输入阻力为117 +/- 21 MΩ(范围93-153 MΩ; n = 8)。该值高于非神经糖化细胞的53 +/- 10 MΩ(范围35-72 MΩ; n = 9)。差异具有统计学意义(P小于0.01,Student's t检验)。 5.响应FN刺激,在37个神经分泌神经元中,有十六个(43%)的IPSP潜伏期为7.4 +/- 2.8毫秒,而三个(8%)的EPSP潜伏期为13.3 +/- 4.2毫秒。(摘要以400字截断)

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