{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,14]],"date-time":"2026-09-14T23:22:51Z","timestamp":1789428171208,"version":"build-2803163510"},"reference-count":87,"publisher":"Wiley","issue":"21","license":[{"start":{"date-parts":[[2021,10,8]],"date-time":"2021-10-08T00:00:00Z","timestamp":1633651200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["physoc.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Physiology"],"published-print":{"date-parts":[[2021,11]]},"abstract":"<jats:sec>\n                    <jats:title>Abstract<\/jats:title>\n                    <jats:p>\n                      Active expiration is essential for increasing pulmonary ventilation during high chemical drive (hypercapnia). The lateral parafacial (pF\n                      <jats:sub>L<\/jats:sub>\n                      ) region, which contains expiratory neurones, drives abdominal muscles during active expiration in response to hypercapnia. However, the electrophysiological properties and synaptic mechanisms determining the activity of pF\n                      <jats:sub>L<\/jats:sub>\n                      expiratory neurones, as well as the specific conditions for their emergence, are not fully understood. Using whole cell electrophysiology and single cell quantitative RT\u2010PCR techniques, we describe the intrinsic electrophysiological properties, the phenotype and the respiratory\u2010related synaptic inputs to the pF\n                      <jats:sub>L<\/jats:sub>\n                      expiratory neurones, as well as the mechanisms for the expression of their expiratory activity under conditions of hypercapnia\u2010induced active expiration, using\n                      <jats:italic>in situ<\/jats:italic>\n                      preparations of juvenile rats. We also evaluated whether these neurones possess intrinsic CO\n                      <jats:sub>2<\/jats:sub>\n                      \/[H\n                      <jats:sup>+<\/jats:sup>\n                      ] sensitivity and burst generating properties. GABAergic and glycinergic inhibition during inspiration and expiration suppressed the activity of glutamatergic pF\n                      <jats:sub>L<\/jats:sub>\n                      expiratory neurones in normocapnia. In hypercapnia, these neurones escape glycinergic inhibition and generate burst discharges at the end of expiration. Evidence for the contribution of post\u2010inhibitory rebound, Ca\n                      <jats:bold>\n                        <jats:sub>V<\/jats:sub>\n                      <\/jats:bold>\n                      3.2 isoform of T\u2010type Ca\n                      <jats:sup>2+<\/jats:sup>\n                      channels and intracellular [Ca\n                      <jats:sup>2+<\/jats:sup>\n                      ] is presented. Neither intrinsic bursting properties, mediated by persistent Na\n                      <jats:sup>+<\/jats:sup>\n                      current, nor CO\n                      <jats:sub>2<\/jats:sub>\n                      \/[H\n                      <jats:sup>+<\/jats:sup>\n                      ] sensitivity or expression of CO\n                      <jats:sub>2<\/jats:sub>\n                      \/[H\n                      <jats:sup>+<\/jats:sup>\n                      ] sensitive ion channels\/receptors (TASK or GPR4) were observed. On the other hand, hyperpolarisation\u2010activated cyclic nucleotide\u2013gated and twik\u2010related K\n                      <jats:sup>+<\/jats:sup>\n                      leak channels were recorded. Post\u2010synaptic disinhibition and the intrinsic electrophysiological properties of glutamatergic neurones play important roles in the generation of the expiratory oscillations in the pF\n                      <jats:sub>L<\/jats:sub>\n                      region during hypercapnia in rats.\n                      <jats:boxed-text content-type=\"graphic\" position=\"anchor\">\n                        <jats:graphic xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" mimetype=\"image\/png\" position=\"anchor\" specific-use=\"enlarged-web-image\" xlink:href=\"graphic\/tjp14834-gra-0001-m.png\">\n                          <jats:alt-text>image<\/jats:alt-text>\n                        <\/jats:graphic>\n                      <\/jats:boxed-text>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Key points<\/jats:title>\n                    <jats:p>\n                      <jats:list list-type=\"bullet\">\n                        <jats:list-item>\n                          <jats:p>\n                            Hypercapnia induces active expiration in rats and the recruitment of a specific population of expiratory neurones in the lateral parafacial (pF\n                            <jats:sub>L<\/jats:sub>\n                            ) region.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Post\u2010synaptic GABAergic and glycinergic inhibition both suppress the activity of glutamatergic pF\n                            <jats:sub>L<\/jats:sub>\n                            neurones during inspiratory and expiratory phases in normocapnia.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Hypercapnia reduces glycinergic inhibition during expiration leading to burst generation by pF\n                            <jats:sub>L<\/jats:sub>\n                            neurones; evidence for a contribution of post\u2010inhibitory rebound, voltage\u2010gated Ca\n                            <jats:sup>2+<\/jats:sup>\n                            channels and intracellular [Ca\n                            <jats:sup>2+<\/jats:sup>\n                            ] is presented.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            pF\n                            <jats:sub>L<\/jats:sub>\n                            glutamatergic expiratory neurones are neither intrinsic burster neurones, nor CO\n                            <jats:sub>2<\/jats:sub>\n                            \/[H\n                            <jats:sup>+<\/jats:sup>\n                            ] sensors, and do not express CO\n                            <jats:sub>2<\/jats:sub>\n                            \/[H\n                            <jats:sup>+<\/jats:sup>\n                            ] sensitive ion channels or receptors.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Post\u2010synaptic disinhibition and the intrinsic electrophysiological properties of glutamatergic neurones both play important roles in the generation of the expiratory oscillations in the pF\n                            <jats:sub>L<\/jats:sub>\n                            region during hypercapnia in rats.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                      <\/jats:list>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1113\/jp281545","type":"journal-article","created":{"date-parts":[[2021,9,12]],"date-time":"2021-09-12T15:05:50Z","timestamp":1631459150000},"page":"4925-4948","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":32,"title":["Intrinsic and synaptic mechanisms controlling the expiratory activity of excitatory lateral parafacial neurones of rats"],"prefix":"10.1113","volume":"599","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5755-6147","authenticated-orcid":false,"given":"Karolyne S.","family":"Magalh\u00e3es","sequence":"first","affiliation":[{"name":"Department of Physiology School of Medicine of Ribeir\u00e3o Preto University of S\u00e3o Paulo  Ribeir\u00e3o Preto SP Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5730-0993","authenticated-orcid":false,"given":"Melina P.","family":"da Silva","sequence":"additional","affiliation":[{"name":"Department of Physiology School of Medicine of Ribeir\u00e3o Preto University of S\u00e3o Paulo  Ribeir\u00e3o Preto SP Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4517-6221","authenticated-orcid":false,"given":"Andr\u00e9 S.","family":"Mecawi","sequence":"additional","affiliation":[{"name":"Department of Biophysics Escola Paulista de Medicina Universidade Federal de S\u00e3o Paulo  S\u00e3o Paulo SP Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7410-2913","authenticated-orcid":false,"given":"Julian F. 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