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咪达唑仑对大鼠海马CA1区突触传递的影响
引用本文:魏辉明,麻伟青,李治贵,于涛,王慧明,张承华.咪达唑仑对大鼠海马CA1区突触传递的影响[J].中华麻醉学杂志,2009,29(11).
作者姓名:魏辉明  麻伟青  李治贵  于涛  王慧明  张承华
作者单位:成都军区昆明总医院麻醉科,650032
摘    要:目的 探讨咪达唑仑对大鼠海马CA1区突触传递的影响.方法 成年雄性Wistar大鼠35只,体重190~220 g,随机分为7组(n=5),单刺激下4组:对照组(C_1组)、荷包牡丹碱组(B_1组)、咪达唑仑组(M_1组)和荷包牡丹碱+咪达唑仑组(BM组);配对刺激下3组:对照组(C_2组)、荷包牡丹碱组(B_2组)和咪达唑仑组(M_2组).单刺激条件:刺激方波波宽0.1 ms、频率0.033 Hz,配对刺激条件:刺激方波波宽0.1 ms、频率0.033 Hz,两个配对刺激间隔30 ms,刺激强度为诱发兴奋性突触后电位(EPSP)峰值刺激强度的50%.C_(1,2)组和M_(1,2)组记录EPSP幅值的基础值,随后分别腹腔注射生理盐水3 ml/kg和咪达唑仑3 mg/kg;B_(1,2)组和BM组记录EPSP幅值的基础值,随后腹腔注射荷包牡丹碱2 mg/kg,20 min后BM组腹腔注射咪达唑仑3 mg,/kg.各组给药结束后再记录60 min,每10 min为一时段.单刺激下计算各时间段EPSP幅值与基础值的比值即相对幅值,配对刺激下记录两个配对刺激下的EPSP幅值(分别为E_1和E_2),计算E_2/E_1.结果 与C_1组比较,M_1组EPSP相对幅值降低(P<0.05或0.01),B_1组和BM组差异无统计学意义(P>0.05);与C_2组比较,B_2组E_2及E_2/E_1升高(P<0.05),E_1差异无统计学意义(P>0.05),M_2组E_1、E_2及E_2/E1_均降低(P<0.05);与B_2组比较,M_2组E_1、E_2及E_2/E_1均降低(P<0.05).结论 咪达唑仑可抑制大鼠海马CA1区兴奋性突触传递,呈可逆性,其机制可能与增强γ-氨基丁酸(GABA)能性突触前抑制性回路的兴奋性有关,而非直接影响GABA_A受体功能状态.

关 键 词:咪达唑仑  突触传递  海马

Effect of midazolam on synaptic transmission in rat hippocampal CA1 area
Abstract:Objective To investigate the effect of midazolam on synaptic transmission in stratum radiatum of CA1 area of rat hippocampus and the underlying mechanism. Methods Thirty-five adult male Wistar rats weighing 190-220 g were randomly divided into 7 groups ( n = 5 each) . Two types of stimulation were used: single stimulation and paired pulse stimulation. Four groups under single stimulation: control group (group C_1), bicuculline group (group B_1 ), midazolam group (group M_1) and bicuculline + midazolam group (group BM). Three groups under paired pulse stimulation: control group ( group C_2 ), bicuculline group (group B_2 ) and midazolam group (group M_2 ) . The animals were anesthetized with intraperitoneal (IP) pentobarbital 50 mg/kg. The stimulating and recording electrodes were inserted into the stratum radiatum of CA1 area of the hippocampus. The interval between the 2 pulse stimulation was 30 ms. Excitatory post-synaptic potential (EPSP) was elicited before (baseline) and after IP bicuculline (2 mg/kg) or/and midazolam (3 mg/kg) administration. The EPSP amplitude was recorded during single stimulation. EPSP_2 /EPSP_1 ( E_2 /E_1 ) ratio was recorded during paired pulse stimulation. Results Compared with group C, , the EPSP amplitude was significantly decreased in group M, ( P < 0.05 or 0.01) , but no significant change was found in group B, and BM ( P > 0.05) . Compared with group C_2 , E_2 and E_2/E_1, ratio were significantly increased in group B_2 , while E_1 , E_ 2, and E_2/E_1, ratio were significantly decreased in group M2 ( P < 0.05). E_1, E_2 and E_2 /E_1, ratio were significantly lower in group M_2 than in group B_2 (P < 0.05) . Conclusion Midazolam can reversibly depress the excitatory synaptic transmission efficacy in the CA1 area of the rat hippocampus through presynaptic inhibitory circuit. CABA_A receptor is not directly disturbed.
Keywords:Midazolam  Synaptic transmission  Hippocampus
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