Frings S, Benz S, Lindemann B
Department of Physiology, Universität des Saarlandes, Homburg/Saar, Germany.
J Gen Physiol. 1991 Apr;97(4):725-47. doi: 10.1085/jgp.97.4.725.
Action potential-driven current transients were recorded from sensory cilia and used to monitor the spike frequency generated by olfactory receptor neurons, which were maintained in their natural position in the sensory epithelium. Both basal and messenger-induced activities, as elicited with forskolin or cyclic nucleotides, were dependent on the presence of mucosal Na+. The spike rate decreased to approximately 20% when mucosal Na+ was lowered from 120 to 60 mM (replaced by N-methyl-D-glucamine+), without clear changes in amplitude and duration of the recorded action potential-driven transients. Mucosal Ca2+ and Mg2+ blocked spike discharge completely when increased from 1 to 10 mM in Ringer solution. Lowering mucosal Ca2+ below 1 mM increased the spike rate. These results can be explained by the presence of a cyclic nucleotide-dependent, Ca(2+)-sensitive cation conductance, which allows a depolarizing Na+ inward current to flow through the apical membrane of in situ receptor cells. A conductance with these properties, thought to provide the receptor current, was first described for isolated olfactory cells by Nakamura and Gold (1987. Nature (Lond.). 325:442-444). The forskolin-stimulated spike rate decreased when l-cis-diltiazem, a known blocker of the cyclic nucleotide-dependent receptor current, was added to the mucosal solution. Spike rate also decreased when the mucosal K+ concentration was lowered. Mucosal Ba2+ and 4-aminopyridine, presumably by means of cell depolarization, rapidly increased the spike rate. This suggests the presence of apical K+ channels that render the receptor cells sensitive to the K+ concentration of the olfactory mucus. With a slower time course, mucosal Ba2+ and 4-aminopyridine decreased the amplitude and caused rectification of the fast current transients (prolongation of action potentials). Abolishment of the apical Na+ current (by removal of mucosal Na+), as indicated by a strong decrease in spike rate, could be counteracted by adding 10 mM Ba2+ or 1 mM 4-aminopyridine to the mucosal solution, which re-established spiking. Similarly, blockage of the apical cation conductance with 10 mM Ca could be counteracted by adding 10 mM Ba2+ or by raising the mucosal K+ concentration. Thus mucosal concentrations of Na+, K+, and Ca2+ will jointly affect the sensitivity of odor detection.
从感觉纤毛记录动作电位驱动的电流瞬变,并用于监测嗅觉受体神经元产生的峰频率,这些神经元保持在感觉上皮中的自然位置。基础活性和信使诱导的活性,如用福斯可林或环核苷酸引发的,都依赖于粘膜Na+的存在。当粘膜Na+从120 mM降至60 mM(用N-甲基-D-葡萄糖胺+替代)时,峰频率降至约20%,而记录的动作电位驱动的瞬变的幅度和持续时间没有明显变化。当林格氏液中粘膜Ca2+和Mg2+从1 mM增加到10 mM时,它们会完全阻断峰放电。将粘膜Ca2+降低到1 mM以下会增加峰频率。这些结果可以通过存在一种环核苷酸依赖性、Ca(2+)敏感的阳离子电导来解释,这种电导允许去极化的Na+内向电流流过原位受体细胞的顶端膜。中村和戈尔德(1987年,《自然》(伦敦)。325:442-444)首次描述了一种具有这些特性的电导,被认为可提供受体电流。当将已知的环核苷酸依赖性受体电流阻滞剂l-顺式地尔硫卓添加到粘膜溶液中时,福斯可林刺激的峰频率降低。当粘膜K+浓度降低时,峰频率也会降低。粘膜Ba2+和4-氨基吡啶可能通过细胞去极化,迅速增加峰频率。这表明存在顶端K+通道,使受体细胞对嗅觉粘液的K+浓度敏感。在较慢的时间进程中,粘膜Ba2+和4-氨基吡啶降低了幅度并导致快速电流瞬变的整流(动作电位延长)。通过添加10 mM Ba2+或1 mM 4-氨基吡啶到粘膜溶液中可以抵消顶端Na+电流的消除(通过去除粘膜Na+),这重新建立了峰放电。同样,用10 mM Ca阻断顶端阳离子电导可以通过添加10 mM Ba2+或提高粘膜K+浓度来抵消。因此,粘膜中Na+、K+和Ca2+的浓度将共同影响气味检测的敏感性。