Neurogenesis of gasping does not require inhibitory transmission using GABAA or glycine receptors

被引:25
作者
St-John, WM [1 ]
Paton, JFR
机构
[1] Dartmouth Hitchcock Med Ctr, Dartmouth Med Sch, Dept Physiol, Hanover, NH 03755 USA
[2] Univ Bristol, Sch Med Sci, Dept Physiol, Bristol BS8 1TD, Avon, England
关键词
control of breathing; gasping; mammals; rat; patterns of breathing; eupnea;
D O I
10.1016/S1569-9048(02)00079-4
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We evaluated the hypothesis that the neurogenesis of gasping is not dependent upon inhibitory synaptic transmission involving GABA(A) or glycine receptors. Activity of the phrenic nerve was recorded in a perfused juvenile rat preparation. The pattern of phrenic activity was altered from eupnea to gasping in severe hypoxia or ischaemia. To block GABAA receptors. bicuculline or picrotoxin was administered. Strychnine was used to block transmission by glycine. Following administrations of bicuculline, picrotoxin or strychnine, the eupneic rhythm was greatly distorted whereas the decrementing pattern of the gasp was maintained. At high concentrations of these antagonists, the frequency of gasps was increased and the peak height of gasps fell, We conclude that the neurogenesis of gasping is not dependent upon fast. chloride-mediated inhibitory synaptic transmission. (C) 2002 Elsevier Science B.V. All rights reserved.
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页码:265 / 277
页数:13
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