afferent activation
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Author(s):  
Kristi A Streeter ◽  
Michael D. Sunshine ◽  
Paul W. Davenport ◽  
David D. Fuller

Phrenic afferents project to brainstem areas responsible for cardiorespiratory control and the mid-cervical spinal cord containing the phrenic motor nucleus. Our purpose was to quantify the impact of small and large diameter phrenic afferent activation on phrenic motor output. Anesthetized and ventilated rats received unilateral phrenic nerve stimulation while contralateral phrenic motor output and blood pressure were recorded. Twelve currents of 40Hz inspiratory-triggered stimulation were delivered (20 seconds on, 5 minutes off) to establish current response curves. Stimulation pulse width was varied to preferentially activate large diameter phrenic afferents (narrow pulse width) and recruit small diameter fibers (wide pulse width). Contralateral phrenic amplitude was elevated immediately post-stimulation at currents above 35 µA for wide, and 70 µA for narrow pulse stimulation when compared to animals not receiving stimulation (time controls). Wide pulse width stimulation also increased phrenic burst frequency at currents ≥35 µA, caused a transient decrease in mean arterial blood pressure at currents ≥50 µA, and resulted in a small change in heart rate at 300 µA. Unilateral dorsal rhizotomy attenuated stimulation-induced cardiorespiratory responses, indicating phrenic afferent activation is required. Additional analyses compared phrenic motor amplitude to output before stimulation and showed that episodic activation of phrenic afferents with narrow pulse stimulation can induce short-term plasticity. We conclude that activation of phrenic afferents: 1) enhances contralateral phrenic motor amplitude when large diameter afferents are activated, and 2) when small diameter fibers are recruited the amplitude response is associated with changes in burst frequency and cardiovascular parameters.


2021 ◽  
Vol 12 (2) ◽  
pp. e00313
Author(s):  
Vincent Cibert-Goton ◽  
Ching Lam ◽  
Melanie Lingaya ◽  
Yirga Falcone ◽  
John N. Wood ◽  
...  

2021 ◽  
Vol 76 (1) ◽  
pp. 83-88
Author(s):  
Jeffrey Cayaban Pagaduan ◽  
Sam Shi Xuan Wu ◽  
James William Fell ◽  
Yung-Sheng Chen

Abstract Heart rate variability biofeedback (HRV BFB) is paced breathing scheme that stimulates resonance in the cardiovascular system. This study aimed to investigate the effect of a single-session HRV BFB on Hoffman reflex (H-reflex) of the soleus muscle. Twelve healthy males (height: 173.7 ± 7.18 cm; weight: 72.7 ± 17.7 kg; age: 24.0 ± 5.02 yrs) completed a randomized-crossover intervention involving a 10-minute HRV BFB and normal breathing (CON) separated by 48 hours. Results revealed significantly lower 1a afferent activation after HRV BFB. Similarly, the HRV BFB also demonstrated lower proportion of activated motor neurons from 1a afferents. In conclusion, an acute HRV BFB influenced the reduction in motoneuron excitability at resting condition.


2020 ◽  
Vol 13 (2) ◽  
pp. 149-157 ◽  
Author(s):  
Anika Bytomski ◽  
Gerhard Ritschel ◽  
Antonie Bierling ◽  
Johanna Bendas ◽  
Kerstin Weidner ◽  
...  

Author(s):  
Kevin K. W. Ng ◽  
Christoffer Olausson ◽  
Richard M. Vickery ◽  
Ingvars Birznieks

AbstractWe have previously described a novel temporal encoding mechanism in the somatosensory system, where mechanical pulses grouped into periodic bursts create a perceived tactile frequency based on the duration of the silent gap between bursts, rather than the mean rate or the periodicity. This coding strategy may offer new opportunities for transmitting information to the brain using various sensory neural prostheses and haptic interfaces. However, it was not known whether the same coding mechanisms apply when using electrical stimulation, which recruits a different spectrum of afferents. Here, we demonstrate that the predictions of the burst gap coding model for frequency perception apply to burst stimuli delivered with electrical pulses, re-emphasising the importance of the temporal structure of spike patterns in neural processing and perception of tactile stimuli. Reciprocally, the electrical stimulation data confirm that the results observed with mechanical stimulation do indeed depend on neural processing mechanisms in the central nervous system, and are not due to skin mechanical factors and resulting patterns of afferent activation.


2018 ◽  
Vol 73 ◽  
pp. 441-449 ◽  
Author(s):  
Evilin Naname Komegae ◽  
David George Stephen Farmer ◽  
Virginia Leah Brooks ◽  
Michael Joseph McKinley ◽  
Robin Michael McAllen ◽  
...  

2018 ◽  
Vol 6 (12) ◽  
pp. e13742 ◽  
Author(s):  
Julia Shanks ◽  
Zhiqiu Xia ◽  
Steven J. Lisco ◽  
George J. Rozanski ◽  
Harold D. Schultz ◽  
...  

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