4.6 Article

Peripheral chemoreflex activation induces expiratory but not inspiratory excitation of C1 pre-sympathetic neurones of rats

期刊

ACTA PHYSIOLOGICA
卷 235, 期 4, 页码 -

出版社

WILEY
DOI: 10.1111/apha.13853

关键词

breathing; C1 pre-sympathetic neurones; optogenetics; peripheral chemoreceptors; sympathetic activity and Kolliker-Fuse

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [313719/2020-9, 437375/2018-8]
  2. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2018/07027-5, 2019/11863-6, 2020/03955-5, 2021/06886-7]
  3. Marsden Fund
  4. Royal Society of New Zealand and Health Research Council of New Zealand

向作者/读者索取更多资源

Activation of peripheral chemoreceptors increases sympathetic activity during expiration by exciting expiratory neurons antecedent to C1 pre-sympathetic neurons. However, activation of inspiratory neurons does not trigger an increase in sympathetic activity.
Aims Stimulation of peripheral chemoreceptors, as during hypoxia, increases breathing and respiratory-related sympathetic bursting. Activation of catecholaminergic C1 neurones induces sympathoexcitation, while its ablation reduces the chemoreflex sympathoexcitatory response. However, no study has determined the respiratory phase(s) in which the pre-sympathetic C1 neurones are recruited by peripheral chemoreceptor and whether C1 neurone activation affects all phases of respiratory modulation of sympathetic activity. We addressed these unknowns by testing the hypothesis that peripheral chemoreceptor activation excites pre-sympathetic C1 neurones during inspiration and expiration. Methods Using the in situ preparation of rat, we made intracellular recordings from baroreceptive pre-sympathetic C1 neurones during peripheral chemoreflex stimulation. We optogenetically activated C1 neurones selectively and compared any respiratory-phase-related increases in sympathetic activity with that which occurs following stimulation of the peripheral chemoreflex. Results Activation of peripheral chemoreceptors using cytotoxic hypoxia (potassium cyanide) increased the firing frequency of C1 neurones and both the frequency and amplitude of their excitatory post-synaptic currents during the phase of expiration only. In contrast, optogenetic stimulation of C1 neurones activates inspiratory neurones, which secondarily inhibit expiratory neurones, but produced comparable increases in sympathetic activity across all phases of respiration. Conclusion Our data reveal that the peripheral chemoreceptor-mediated expiratory-related sympathoexcitation is mediated through excitation of expiratory neurones antecedent to C1 pre-sympathetic neurones; these may be found in the Kolliker-Fuse nucleus. Despite peripheral chemoreceptor excitation of inspiratory neurones, these do not trigger C1 neurone-mediated increases in sympathetic activity. These studies provide compelling novel insights into the functional organization of respiratory-sympathetic neural networks.

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