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血清素对大鼠脊髓运动神经元的直接兴奋作用。

Direct excitation of rat spinal motoneurones by serotonin.

作者信息

Takahashi T, Berger A J

机构信息

Department of Physiology, Kyoto University Faculty of Medicine, Japan.

出版信息

J Physiol. 1990 Apr;423:63-76. doi: 10.1113/jphysiol.1990.sp018011.

Abstract
  1. The effects of serotonin (5-HT) on visually identified motoneurones were investigated using the whole-cell recording technique in a neonatal rat spinal cord slice preparation. 2. In current-clamp recordings, bath application of 5-HT depolarized motoneurones. This effect was observed after synaptic inputs were abolished by replacing external Ca2+ with Mg2+. 3. In voltage-clamp recordings at holding potentials of -70 to -90 mV, 5-HT induced an inward current (I5-HT) in motoneurones in a Ca2(+)-free-Mg2+ solution containing tetrodotoxin. This inward current was accompanied by an increase in membrane conductance, which was prominent at voltages negative to the holding potential. 4. The inward I5-HT response declined with repeated short applications of 5-HT. I5-HT produced by a single prolonged application (5 min) was only slightly diminished during the application period. 5. The minimum effective dose of 5-HT for initiating the inward I5-HT was less than 10 nM. At 10 microM, I5-HT approached maximal levels. The averaged dissociation constant (Kd) for 5-HT was approximately 120 nM. 6. Application of spiperone, the mixed 5-HT1A, 5-HT2 receptor antagonist, blocked the inward I5-HT. Application of (+)-8-OH-dipropylaminotetralin (8-OHDPAT), a 5-HT1A agonist, mimicked the action of 5-HT. 7. Various K+ channel blockers including tetraethylammonium chloride (30 mM), 4-aminopyridine (4 mM) and apamin (100 nM) did not abolish I5-HT. Application of extracellular Cs+ (10 mM) blocked I5-HT. 8. Peak inward I5-HT became larger with increasing extracellular K+. With low Cl- pipette solution (less than 1 mM), or in low extracellular Na+ solution (26 mM), the inward I5-HT was not abolished. 9. The current-voltage relation of I5-HT displayed inward rectification. In high external K+ concentration (20 mM), the reversal potential was about -29 mV, which is close to that of the inward rectifier evoked in motoneurones by membrane hyperpolarization. 10. The current generated by 5-HT displayed similar characteristics to the inward rectifying current induced in motoneurones by membrane hyperpolarization. It is thus suggested that the 5-HT-induced current is possibly mediated by the intrinsic inward rectifier conductance.
摘要
  1. 采用全细胞记录技术,在新生大鼠脊髓切片标本中研究了5-羟色胺(5-HT)对视觉识别的运动神经元的影响。2. 在电流钳记录中,浴加5-HT使运动神经元去极化。在用Mg2+取代细胞外Ca2+消除突触输入后观察到这种效应。3. 在-70至-90 mV的钳制电位下进行电压钳记录时,5-HT在含有河豚毒素的无Ca2+ - Mg2+溶液中诱导运动神经元产生内向电流(I5-HT)。这种内向电流伴随着膜电导的增加,在低于钳制电位的电压下尤为明显。4. 5-HT的重复短时间应用使内向I5-HT反应减弱。单次长时间应用(5分钟)产生的I5-HT在应用期间仅略有减弱。5. 引发内向I5-HT的5-HT的最小有效剂量小于10 nM。在10 μM时,I5-HT接近最大水平。5-HT的平均解离常数(Kd)约为120 nM。6. 5-HT1A、5-HT2混合受体拮抗剂舒必利的应用阻断了内向I5-HT。5-HT1A激动剂(+)-8-羟基二丙基氨基四氢萘(8-OHDPAT)的应用模拟了5-HT的作用。7. 包括氯化四乙铵(30 mM)、4-氨基吡啶(4 mM)和蜂毒明肽(100 nM)在内的各种钾通道阻滞剂并未消除I5-HT。细胞外Cs+(10 mM)的应用阻断了I5-HT。8. 随着细胞外钾离子浓度增加,内向I5-HT峰值变大。在低Cl-移液管溶液(小于1 mM)或低细胞外Na+溶液(26 mM)中,内向I5-HT并未消除。9. I5-HT的电流-电压关系表现出内向整流。在高细胞外钾离子浓度(20 mM)下,反转电位约为-29 mV,这与运动神经元膜超极化诱发的内向整流器的反转电位相近。10. 5-HT产生的电流与运动神经元膜超极化诱导的内向整流电流表现出相似的特性。因此,提示5-HT诱导的电流可能由内在的内向整流电导介导。

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