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血清素和去甲肾上腺素可兴奋豚鼠和猫丘脑网状核的γ-氨基丁酸能神经元。

Serotonin and noradrenaline excite GABAergic neurones of the guinea-pig and cat nucleus reticularis thalami.

作者信息

McCormick D A, Wang Z

机构信息

Section of Neurobiology, Yale University School of Medicine, New Haven, CT 06510.

出版信息

J Physiol. 1991 Oct;442:235-55. doi: 10.1113/jphysiol.1991.sp018791.

Abstract
  1. The actions of serotonin (5-HT) and noradrenaline (NA) in the cat perigeniculate nucleus (PGN) and the guinea-pig nucleus reticularis thalami (NRT) were investigated with extracellular and intracellular recordings obtained from neurones in thalamic slices maintained in vitro. 2. Single, local application of either 5-HT or NA resulted in pronounced (5-50 Hz) and prolonged (2-10 min) excitation associated with the occurrence of single-spike activity. Serotoninergic excitation was specifically blocked by the 5-HT2/5-HT1C antagonists ketanserin and ritanserin, but not by the 5-HT1A antagonist pindolol or the 5-HT3 antagonist ICS 205-930. Furthermore, the 5-HT response was mimicked by alpha-methyl-5-HT, but not by the 5-HT1A agonist 8-hydroxydipropylaminotetralin (8-OHDPAT) or the 5-HT3 agonist 2-methyl-5-HT. Together, these results indicate that this excitatory response is mediated through 5-HT2 receptors with the possible involvement of 5-HT1C receptors. 3. Noradrenergic excitation was specifically blocked by the alpha 1-antagonist prazosin, but not by the beta-antagonist propranolol or the alpha 2-antagonist yohimbine. Similarly, the response was mimicked by the alpha-agonist phenylephrine, but not by the beta-agonist isoprenaline. These results indicate that the noradrenergic excitation is mediated by alpha 1-adrenoceptors. 4. Block of synaptic transmission either by lowering external calcium concentration ([Ca2+]o) to 0.5 mM and raising external magnesium concentration ([Mg2+]o) to 10 mM or by local application of tetrodotoxin failed to block the excitatory or depolarizing response to 5-HT or NA indicating that these responses are direct and not mediated through the release of other neurotransmitters. 5. Intracellular recordings revealed that the 5-HT- and NA-induced excitations are mediated by a pronounced slow depolarization associated with an apparent decrease in input conductance and an increase in the membrane time constant. Current versus voltage plots obtained under voltage clamp before and during the presence of 5-HT and NA revealed that these neurotransmitters induced an inward current which reversed to an outward current at -107 and -110 mV, respectively, in 2.5 mM external potassium concentration ([K+]o). This reversal potential was identical to that associated with an increase in potassium conductance activated by acetylcholine (-110 mV) in the same neurones. Plots of the amplitude of the 5-HT- or NA-induced current versus membrane potential revealed a linear relationship in the voltage range from -140 to -60 mV.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用细胞外和细胞内记录技术,从体外培养的丘脑切片中的神经元获取数据,研究了5-羟色胺(5-HT)和去甲肾上腺素(NA)在猫的外侧膝状体周围核(PGN)和豚鼠丘脑网状核(NRT)中的作用。2. 单独局部应用5-HT或NA会导致明显的(5-50赫兹)且持续时间较长的(2-10分钟)兴奋,并伴有单峰活动的出现。5-羟色胺能兴奋被5-HT2/5-HT1C拮抗剂酮色林和利坦色林特异性阻断,但不被5-HT1A拮抗剂吲哚洛尔或5-HT3拮抗剂ICS 205-930阻断。此外,5-HT反应可被α-甲基-5-HT模拟,但不能被5-HT1A激动剂8-羟基二丙基氨基四氢萘(8-OHDPAT)或5-HT3激动剂2-甲基-5-HT模拟。这些结果共同表明,这种兴奋性反应是通过5-HT2受体介导的,可能还涉及5-HT1C受体。3. 去甲肾上腺素能兴奋被α1拮抗剂哌唑嗪特异性阻断,但不被β拮抗剂普萘洛尔或α2拮抗剂育亨宾阻断。同样,该反应可被α激动剂去氧肾上腺素模拟,但不能被β激动剂异丙肾上腺素模拟。这些结果表明,去甲肾上腺素能兴奋是由α1肾上腺素能受体介导的。4. 通过将细胞外钙浓度([Ca2+]o)降至0.5毫摩尔/升并将细胞外镁浓度([Mg2+]o)升至10毫摩尔/升,或局部应用河豚毒素来阻断突触传递,均未能阻断对5-HT或NA的兴奋性或去极化反应,这表明这些反应是直接的,并非通过其他神经递质的释放介导。5. 细胞内记录显示,5-HT和NA诱导的兴奋是由明显的缓慢去极化介导的,这与输入电导的明显降低和膜时间常数的增加有关。在5-HT和NA存在之前和期间,通过电压钳获得的电流-电压图显示,这些神经递质诱导了内向电流,在2.5毫摩尔/升的细胞外钾浓度([K+]o)下,该内向电流分别在-107毫伏和-110毫伏时反转成外向电流。这种反转电位与同一神经元中由乙酰胆碱激活的钾电导增加相关的反转电位(-110毫伏)相同。5-HT或NA诱导的电流幅度与膜电位的关系图在-140至-60毫伏的电压范围内显示出线性关系。(摘要截选至400字)

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