Kang Yu-Ming, Chen Jian-Yong, Ouyang Wei, Qiao Jian-Tian, Reyes-Vazquez Cruz, Dafny Nachum
Department of Neurobiology, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Int J Neurosci. 2004 Mar;114(3):299-319. doi: 10.1080/00207450490264115.
Effects of serotonin (5-HT) on electrophysiological activities of single hypothalamic arcuate neurons in rat brain slices were observed by extracellular recording. The results showed that (1) of 385 arcuate neurons observed, the patterns of spontaneous firing were divided into 3 categories: "slow irregular" (46.0%), "fast continuous" (22.6%), and "bursting" firing (31.4%); (2) of 149 neurons tested for 5-HT, most (55.0%) responded to the drug by decreasing firing rate, 22.2% by increasing firing rate, 11.4% exhibit biphasic pattern, and 11.4% did not respond to 5-HT application; (3) substitution of low Ca2-high Mg2+ artificial cerebrospinal fluid (ACSF) for normal ACSF did not abolish the 5-HT-induced excitatory effect while it did abolish the 5-HT-induced inhibitory effect, suggesting the effect in latter cases was elicited by a Ca2+-dependent release of neuroactive substances; (4) cyproheptadine, a non-selective 5-HT receptor antagonist, antagonized the 5-HT-induced excitatory effect in all neurons tested, while pindolol, a 5-HT1A/1B receptor antagonist, antagonized the 5-HT-induced excitatory effect in 50% of neurons tested; (5) both cyproheptadine and pindolol antagonized the 5-HT-induced inhibitory effect; and (6) bicuculline, a GABAA receptor antagonist, antagonized the 5-HT-induced inhibitory effect. These results suggest that 5-HT may exert its excitatory effects directly through 5-HT1A/1B and other subtypes of 5-HT-receptors located on the surface of the neurons recorded, while its inhibitory effects are mediated indirectly through the activation of a local inhibitory GABAergic interneuron.
通过细胞外记录观察了血清素(5-羟色胺,5-HT)对大鼠脑片单个下丘脑弓状核神经元电生理活动的影响。结果表明:(1)在观察的385个弓状核神经元中,自发放电模式分为3类:“缓慢不规则型”(46.0%)、“快速连续型”(22.6%)和“爆发型”放电(31.4%);(2)在149个接受5-HT检测的神经元中,大多数(55.0%)对该药物的反应是放电频率降低,22.2%是放电频率增加,11.4%呈现双相模式,11.4%对5-HT应用无反应;(3)用低Ca2+高Mg2+人工脑脊液(ACSF)替代正常ACSF并未消除5-HT诱导的兴奋作用,但消除了5-HT诱导的抑制作用,提示后一种情况下的作用是由神经活性物质的Ca2+依赖性释放引起的;(4)非选择性5-HT受体拮抗剂赛庚啶在所有检测的神经元中均拮抗5-HT诱导的兴奋作用,而5-HT1A/1B受体拮抗剂吲哚洛尔在50%检测的神经元中拮抗5-HT诱导的兴奋作用;(5)赛庚啶和吲哚洛尔均拮抗5-HT诱导的抑制作用;(6)GABAA受体拮抗剂荷包牡丹碱拮抗5-HT诱导的抑制作用。这些结果表明,5-HT可能通过记录的神经元表面上的5-HT1A/1B和其他5-HT受体亚型直接发挥其兴奋作用,而其抑制作用则通过激活局部抑制性GABA能中间神经元间接介导。