Endogenous rhythm generation in the pre-Botzinger complex and ionic currents:: modelling and in vitro studies

被引:100
作者
Rybak, IA
Shevtsova, NA
St-John, WM
Paton, JFR
Pierrefiche, O
机构
[1] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
[2] Dartmouth Coll Sch Med, Dept Physiol, Lebanon, NH 03756 USA
[3] Univ Bristol, Sch Med Sci, Dept Physiol, Bristol BS8 1TD, Avon, England
[4] UFR Med, Neurophysiol Lab, ETP APC, F-80036 Amiens, France
关键词
computational modelling; potassium channels; rat; respiratory rhythm; transverse slices; PERSISTENT SODIUM CURRENT; BRAIN-STEM SLICE; ROSTRAL VENTROLATERAL MEDULLA; THALAMIC RELAY NEURONS; RAT SPINAL-CORD; RESPIRATORY RHYTHM; NEONATAL-RAT; PACEMAKER NEURONS; CELLULAR MECHANISMS; POTASSIUM CHANNELS;
D O I
10.1046/j.1460-9568.2003.02739.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The pre-Botzinger complex is a small region in the mammalian brainstem involved in generation of the respiratory rhythm. As shown in vitro , this region, under certain conditions, can generate endogenous rhythmic bursting activity. Our investigation focused on the conditions that may induce this bursting behaviour. A computational model of a population of pacemaker neurons in the pre-Botzinger complex was developed and analysed. Each neuron was modelled in the Hodgkin-Huxley style and included persistent sodium and delayed-rectifier potassium currents. We found that the firing behaviour of the model strongly depended on the expression of these currents. Specifically, bursting in the model could be induced by a suppression of delayed-rectifier potassium current (either directly or via an increase in extracellular potassium concentration, [K+ ](o) ) or by an augmentation of persistent sodium current. To test our modelling predictions, we recorded endogenous population activity of the pre-Botzinger complex and activity of the hypoglossal (XII) nerve from in vitro transverse brainstem slices (700 mum) of neonatal rats (P0-P4). Rhythmic activity was absent at 3 mm[K+ ](o) but could be triggered by either the elevation of [K+ ](o) to 5-7 mm or application of potassium current blockers (4-AP, 50-200 mum, or TEA, 2 or 4 mm), or by blocking aerobic metabolism with NaCN (2 mm). This rhythmic activity could be abolished by the persistent sodium current blocker riluzole (25 or 50 mum). These findings are discussed in the context of the role of endogenous bursting activity in the respiratory rhythm generation in vivo vs. in vitro and during normal breathing in vivo vs. gasping.
引用
收藏
页码:239 / 257
页数:19
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