Neuronal pacemaker for breathing visualized in vitro

被引:360
作者
Koshiya, N [1 ]
Smith, JC [1 ]
机构
[1] NINDS, Cellular & Syst Neurobiol Sect, Neural Control Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/22540
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Breathing movements in mammals arise from a rhythmic pattern of neural activity, thought to originate in the pre-Botzinger complex(1) in the lower brainstem. The mechanisms generating the neural rhythm in this region are unknown(2-5). The central question is whether the rhythm is generated by a network of bursting pacemaker neurons coupled by excitatory synapses that synchronize pacemaker activity. Here we visualized the activity of inspiratory pacemaker neurons at single-cell and population levels with calcium-sensitive dye. We developed methods to label these neurons retrogradely with the dye in neonatal rodent brainstem slices that retain the rhythmically active respiratory network We simultaneously used infrared structural imaging to allow patch-damp recording from the identified neurons, After we pharmacologically blocked glutamatergic synaptic transmission, a subpopulation of inspiratory neurons continued to burst rhythmically but asynchronously. The intrinsic bursting frequency of these pacemaker neurons depended on the baseline membrane potential, providing a cellular mechanism for respiratory frequency control. These results provide evidence that the neuronal kernel for rhythm generation consists of a network of synaptically-coupled pacemaker neurons.
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页码:360 / 363
页数:4
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