Substance P Modulation of Hypoglossal Motoneuron Excitability During Development: Changing Balance Between Conductances

被引:12
作者
Adachi, Tadafumi [1 ,2 ]
Huxtable, Adrianne G. [1 ]
Fang, X. [1 ]
Funk, Gregory D. [1 ,2 ]
机构
[1] Univ Alberta, Dept Physiol, Sch Mol & Syst Med, Fac Med & Dent, Edmonton, AB T6G 2H7, Canada
[2] Univ Auckland, Dept Physiol, Fac Med & Hlth Sci, Auckland, New Zealand
基金
加拿大健康研究院;
关键词
THYROTROPIN-RELEASING-HORMONE; IMMUNOREACTIVE NERVE-TERMINALS; TRIGEMINAL MOTOR NUCLEUS; PRE-BOTZINGER COMPLEX; FREELY MOVING CATS; DOMAIN K+ CHANNEL; RAT-BRAIN-STEM; MICE IN-VITRO; BINDING-SITES; SPINAL-CORD;
D O I
10.1152/jn.00016.2010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adachi T, Huxtable AG, Fang X, Funk GD. Substance P Modulation of Hypoglossal Motoneuron Excitability During Development: Changing Balance Between Conductances. J Neurophysiol 104: 854-872, 2010. First published June 10, 2010; doi: 10.1152/jn.00016.2010. Although Substance P (SP) acts primarily through neurokinin 1 (NK1) receptors to increase the excitability of virtually all motoneurons (MNs) tested, the ontogeny of this transmitter system is not known for any MN pool. Hypoglossal (XII) MNs innervate tongue protruder muscles and participate in several behaviors that must be functional from birth including swallowing, suckling and breathing. We used immunohistochemistry, Western immunoblotting, and whole cell recording of XII MNs in brain stem slices from rats ranging in age from postnatal day zero (P0) to P23 to explore developmental changes in: NK1 receptor expression; currents evoked by SPNK1 (an NK1-selective SP receptor agonist) and; the efficacy of transduction pathways transforming ligand binding into channel modulation. Despite developmental reductions in XII MN NK1 receptor expression, SPNK1 current density remained constant at 6.1 +/- 1.0 (SE) pA/pF. SPNK1 activated at least two conductances. Activation of a pH-insensitive Na+ conductance dominated in neonates (P0-P5), but its contribution fell from similar to 80 to similar to 55% in juveniles (P14-P23). SPNK1 also inhibited a pH-sensitive, two-pore domain K+ (TASK)-like K+ current. Its contribution increased developmentally. First, the density of this pH-sensitive K+ current doubled between P0 and P23. Second, SPNK1 did not affect this current in neonates, but reduced it by 20% at P7-P10 and 80% in juveniles. In addition, potentiation of repetitive firing was greatest in juveniles. These data establish that despite apparent reductions in NK1 receptor density, SP remains an important modulator of XII MN excitability throughout postnatal development due, in part, to increased expression of a pH-sensitive, TASK-like conductance.
引用
收藏
页码:854 / 872
页数:19
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