Ventilatory responses to acute hypoxia in neurokinin-1 receptor deficient mice

被引:4
作者
Grasemann, Hartmut
Gerard, Norma P.
De Sanctis, George T.
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Pulm & Crit Care Div, Cambridge, MA 02138 USA
[2] Childrens Hosp, Perlmutter Lab, Boston, MA 02115 USA
关键词
control of breathing; chemoreceptor; hypoxic responses;
D O I
10.1016/j.resp.2007.07.012
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
The regulatory effect of substance P on respiration is mediated via neurokinin (NK) receptors. While previous studies suggest that NK-1 receptors are involved, little is known about the role NK-2 receptors in ventilatory responses to hypoxia. Ventilatory responses to acute hypoxia (8% O-2 in N-2) were measured by indirect plethysmography in unanaesthetized, unrestrained NK-1 receptor gene deficient (NK-1-/-) and wild-type mice. In additional experiments mice were treated with an NK-2 receptor antagonist prior to hypoxic challenge. Resting ventilatory parameters were not different between groups. NK-1-/- mice displayed significantly greater shortening of expiratory time and higher increase of breathing frequency during hypoxia than wild-type mice. Treatment with the NK-2 receptor antagonist SR 48968 (1 mg/kg) resulted in a further shortening of inspiratory and expiratory time in NK-1-/- but not wild-type mice. These results demonstrate that both NK-1 and NK-2 receptors are involved in the modification of ventilation in response to acute hypoxia. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:227 / 231
页数:5
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