Acute intermittent optogenetic stimulation of nucleus tractus solitarius neurons induces sympathetic long-term facilitation

被引:24
作者
Yamamoto, Kenta [1 ]
Lalley, Peter [2 ]
Mifflin, Steve [1 ]
机构
[1] Univ N Texas, Hlth Sci Ctr, Dept Integrat Physiol, Cardiovasc Res Inst, Ft Worth, TX 76107 USA
[2] Univ Wisconsin, Dept Neurosci, Sch Med & Publ Hlth, Madison, WI USA
基金
美国国家卫生研究院;
关键词
nucleus tractus solitarius; optogenetics; sympathetic long-term facilitation; synchronization; OBSTRUCTIVE SLEEP-APNEA; CHRONIC EPISODIC HYPOXIA; NERVE ACTIVITY; BLOOD-PRESSURE; BRAIN-STEM; RESPIRATORY PLASTICITY; PROTEIN-KINASE; RAT; DRIVE; NTS;
D O I
10.1152/ajpregu.00381.2014
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Acute intermittent hypoxia (AIH) induces sympathetic and phrenic long-term facilitation (LTF), defined as a sustained increase in nerve discharge. We investigated the effects of AIH and acute intermittent optogenetic (AIO) stimulation of neurons labeled with AAV-CaMKIIa, hChR2(H134R), and mCherry in the nucleus of the solitary tract (NTS) of anesthetized, vagotomized, and mechanically ventilated rats. We measured renal sympathetic nerve activity (RSNA), phrenic nerve activity (PNA), power spectral density, and coherence, and we made cross-correlation measurements to determine how AIO stimulation and AIH affected synchronization between PNA and RSNA. Sixty minutes after AIH produced by ventilation with 10% oxygen in balanced nitrogen, RSNA and PNA amplitude increased by 80% and by 130%, respectively (P < 0.01). Sixty minutes after AIO stimulation, RSNA and PNA amplitude increased by 60% and 100%, respectively, (P < 0.01). These results suggest that acute intermittent stimulation of NTS neurons can induce renal sympathetic and phrenic LTF in the absence of hypoxia or chemoreceptor afferent activation. We also found that while acute intermittent optogenetic and hypoxic stimulations increased respiration-related RSNA modulation (P < 0.01), they did not increase synchronization between central respiratory drive and RSNA. We conclude that mechanisms that induce LTF originate within the caudal NTS and extend to other interconnecting neuronal elements of the central nervous cardiorespiratory network.
引用
收藏
页码:R266 / R275
页数:10
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