Key result
Acute intermittent optogenetic stimulation of nucleus tractus solitarius neurons increased renal sympathetic nerve activity amplitude by 60% and phrenic nerve activity by 100% compared to baseline.
Absolute Event Rate: 60% vs 80%
p-value: p=<0.01
Acute intermittent optogenetic stimulation of NTS neurons induces sympathetic and phrenic long-term facilitation independently of hypoxia, highlighting the role of the caudal NTS in cardiorespiratory network plasticity.
Should not change practice; hypothesis-generating for NTS plasticity in cardiorespiratory control.
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.
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Yamamoto et al. (2014) studied Normal physiology (animal model) (n=23). Acute intermittent optogenetic (AIO) stimulation vs. Acute intermittent hypoxia (AIH) and control (stimulation outside NTS) was evaluated on Increase in renal sympathetic nerve activity (RSNA) amplitude at 60 minutes (p=<0.01). Acute intermittent optogenetic stimulation of nucleus tractus solitarius neurons increased renal sympathetic nerve activity amplitude by 60% and phrenic nerve activity by 100% compared to baseline.
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