Zha Ding-Jun, Wang Zhi-Ming, Lin Ying, Liu Tao, Qiao Li, Lu Lian-Jun, Li Yun-Qing, Qiu Jian-Hua
Department of Otorhinolaryngology, Affiliated Xijing Hospital, The Fourth Military Medical University, Xi'an, China.
J Neurochem. 2007 Oct;103(1):57-66. doi: 10.1111/j.1471-4159.2007.04776.x. Epub 2007 Jul 20.
In the present study, the modulatory effects of noradrenaline (NA) on the GABA response were investigated in the isolated cultured spiral ganglion neurons of rat by using nystatin perforated patch recording configuration under voltage-clamp conditions. NA reversibly depressed GABA response in a concentration-dependent manner and neither changed the reversal potential of the GABA response nor affected the apparent affinity of GABA to its receptor. alpha2-adrenoceptor agonist and antagonist, clonidine and yohimbine mimicked and blocked the NA action on the GABA response, respectively. N-[2(methylamino)ethyl]-5-isoquinoline sulfonamide dihydrochloride (H-89), a protein kinase A inhibitor, mimicked the effect of NA on the GABA response. NA failed to affect the GABA response in the presence of both cAMP and protein kinase A modulator. However, NA still depressed the GABA response even in the presence of both phorbol-12-myristate-13-acetate, a protein kinase C activator and chelerythrine, a protein kinase C inhibitor. These results suggest that the NA suppression of the GABA response is mediated by alpha2-adrenoceptor which reduces intracellular cAMP formation through the inhibition of adenylyl cyclase. Therefore, NA input to the spiral ganglion neurons may modulate the auditory transmission by affecting the GABA response.
在本研究中,采用制霉菌素穿孔膜片钳记录模式,在电压钳条件下,研究了去甲肾上腺素(NA)对大鼠离体培养螺旋神经节神经元GABA反应的调节作用。NA以浓度依赖的方式可逆性地抑制GABA反应,既不改变GABA反应的反转电位,也不影响GABA与其受体的表观亲和力。α2-肾上腺素能受体激动剂和拮抗剂可乐定和育亨宾分别模拟和阻断了NA对GABA反应的作用。蛋白激酶A抑制剂N-[2(甲氨基)乙基]-5-异喹啉磺酰胺二盐酸盐(H-89)模拟了NA对GABA反应的作用。在同时存在cAMP和蛋白激酶A调节剂的情况下,NA未能影响GABA反应。然而,即使在同时存在蛋白激酶C激活剂佛波酯-12-肉豆蔻酸酯-13-乙酸酯和蛋白激酶C抑制剂白屈菜红碱的情况下,NA仍能抑制GABA反应。这些结果表明,NA对GABA反应的抑制作用是由α2-肾上腺素能受体介导的,该受体通过抑制腺苷酸环化酶减少细胞内cAMP的形成。因此,螺旋神经节神经元的NA输入可能通过影响GABA反应来调节听觉传导。