Substance P modulation of TRPC3/7 channels improves respiratory rhythm regularity and ICAN-dependent pacemaker activity

被引:39
作者
Ben-Mabrouk, Faiza [1 ]
Tryba, Andrew K. [1 ]
机构
[1] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
关键词
mice; CPG; ICAN; pacemaker; pre-Botzinger complex; substance P; TRPC; MOUSE PREBOTZINGER COMPLEX; PRE-BOTZINGER COMPLEX; RETT-SYNDROME; IN-VITRO; NEURAL-NETWORK; SODIUM CURRENT; TRP CHANNELS; NEONATAL-RAT; BIOGENIC-AMINES; NEURONS;
D O I
10.1111/j.1460-9568.2010.07156.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuromodulators, such as substance P (SubP), play an important role in modulating many rhythmic activities driven by central pattern generators (e.g. locomotion, respiration). However, the mechanism by which SubP enhances breathing regularity has not been determined. Here, we used mouse brainstem slices containing the pre-Botzinger complex to demonstrate, for the first time, that SubP activates transient receptor protein canonical (TRPC) channels to enhance respiratory rhythm regularity. Moreover, SubP enhancement of network regularity is accomplished via selective enhancement of ICAN (inward non-specific cation current)-dependent intrinsic bursting properties. In contrast to INaP (persistent sodium current)-dependent pacemakers, ICAN-dependent pacemaker bursting activity is TRPC-dependent. Western Blots reveal TRPC3 and TRPC7 channels are expressed in rhythmically active ventral respiratory group island preparations. Taken together, these data suggest that SubP-mediated activation of TRPC3/7 channels underlies rhythmic ICAN-dependent pacemaker activity and enhances the regularity of respiratory rhythm activity.
引用
收藏
页码:1219 / 1232
页数:14
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