Monckton James E, McCormick David A
Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
J Neurophysiol. 2002 Apr;87(4):2124-36. doi: 10.1152/jn.00650.2001.
Serotonergic fibers broadly innervate the thalamus and may influence the sleep wake cycle, attention, and other processes through modulation of neurons in this structure. However, the actions of serotonin in the dorsal thalamus have been investigated in detail only in the dorsal lateral geniculate nucleus. In the present study, we examined the action of serotonin in several different regions of the ferret dorsal thalamus, including the associative nuclei, using the in vitro slice preparation and intracellular recording techniques. In nearly all nuclei examined, the predominant action of serotonin was one of hyperpolarization and inhibition of the tonic firing mode. The magnitude of the hyperpolarizing response decreased with age and varied greatly across and somewhat within nuclei maintaining the following relationship (in descending order of magnitude): lateral posterior, lateral dorsal, pulvinar, mediodorsal, center median, anteroventral, central lateral, ventral basal, and medial geniculate. This hyperpolarization is elicited through two mechanisms: one direct and the other via local interneurons. The direct action occurs through an increase in potassium conductance mediated through the 5-HT(1A) receptor. This conclusion is supported by the findings that it persists in the presence of tetrodotoxin and block of GABAergic synaptic transmission, the reversal potential shifts in a Nernstian fashion with changes in extracellular potassium concentration, and the response is antagonized by the 5-HT(1A) antagonist WAY100635 and mimicked by the application of the 5-HT(1A)-selective agonist 8-OH DPAT. The second mechanism by which 5-HT evoked a hyperpolarization was through the activation of local interneurons. In slices in which GABA receptors were not blocked, 5-HT application increased the frequency and amplitude of spontaneous inhibitory postsynaptic potentials (IPSPs) occurring in thalamocortical neurons. Application of 5-HT to physiologically or morphologically identified interneurons evoked a prolonged suprathreshold depolarization. Our results suggest that serotonergic inputs act differentially across the thalamus in a complex manner involving direct and indirect mechanisms. It appears that 5-HT has a greater direct postsynaptic inhibitory influence in the posterior, medial, and intralaminar nuclei than in the primary sensory nuclei.
5-羟色胺能纤维广泛地支配丘脑,并可能通过调节该结构中的神经元来影响睡眠-觉醒周期、注意力及其他生理过程。然而,5-羟色胺在背侧丘脑中的作用仅在背外侧膝状核中得到了详细研究。在本研究中,我们使用体外脑片制备和细胞内记录技术,研究了5-羟色胺在雪貂背侧丘脑的几个不同区域(包括联合核)中的作用。在几乎所有被检测的核团中,5-羟色胺的主要作用是超极化并抑制紧张性放电模式。超极化反应的幅度随年龄增长而降低,并且在不同核团之间以及同一核团内部存在很大差异,呈现以下关系(按幅度降序排列):外侧后核、外侧背核、枕核、背内侧核、中央中核、前腹核、中央外侧核、腹侧基底核和内侧膝状核。这种超极化是通过两种机制引发的:一种是直接机制,另一种是通过局部中间神经元介导。直接作用是通过5-HT(1A)受体介导的钾电导增加而发生的。这一结论得到以下发现的支持:在存在河豚毒素和GABA能突触传递被阻断的情况下,该作用仍然持续;反转电位随细胞外钾浓度的变化呈能斯特式移动;该反应被5-HT(1A)拮抗剂WAY100635拮抗,并被5-HT(1A)选择性激动剂8-OH DPAT模拟。5-羟色胺引发超极化的第二种机制是通过激活局部中间神经元。在未阻断GABA受体的脑片中,应用5-羟色胺会增加丘脑皮质神经元中自发抑制性突触后电位(IPSPs)的频率和幅度。将5-羟色胺应用于生理或形态学上已鉴定的中间神经元会引发长时间的阈上 depolarization 。我们的结果表明,5-羟色胺能输入以涉及直接和间接机制的复杂方式在丘脑中发挥不同作用。看来,5-羟色胺在后部、内侧和板内核中的直接突触后抑制作用比在主要感觉核中更大。 (注:原文中“Application of 5-HT to physiologically or morphologically identified interneurons evoked a prolonged suprathreshold depolarization.”中的“depolarization”未翻译完整,推测可能是“去极化”,但需结合完整语境进一步确认。)