<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pereyra KV</submitter><funding>Fondecyt</funding><funding>NHLBI NIH HHS</funding><funding>NIH HHS</funding><pagination>113-127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12804341</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121(1)</volume><pubmed_abstract>Central chemoreflex activation worsens cardiorespiratory dysfunction in high-output heart failure (HO-HF). Recently, interdependence between both peripheral and central chemoreceptors has been linked to alterations in cardiorespiratory regulation. Whether central chemoreflex potentiation in HO-HF requires sensory inputs from peripheral chemoreceptors remains completely unknown. Accordingly, we hypothesized that peripheral-central chemoreceptor interaction promotes cardiorespiratory dysfunction in non-ischemic HO-HF. We used male Sprague-Dawley rats to investigate the role of carotid bodies (CBs), the main peripheral chemoreceptors, on autonomic, respiratory, and cardiac function alterations during the progression of HO-HF. CB denervation (CBD) was used to eliminate CB inputs in HO-HF rats. The effect of CBD on HO-HF related cardiac, autonomic, and ventilatory function was measured using echocardiography, pressure-volume loop analysis, electrocardiography, plethysmography, and telemetry. HO-HF rats exhibited enhanced central chemoreflex drive, irregular breathing, autonomic imbalance, cardiac electrophysiological abnormalities, cardiac diastolic dysfunction, and cardiac hypertrophy. Remarkably, CBD completely normalized central chemoreflex function in HO-HF rats, restored ventilatory stability, reduced apnea-hypopnea incidence, improved heart rate variability, shortened QRS and PR intervals, attenuated collagen deposition, and ameliorated diastolic dysfunction. Additionally, CBD also corrected respiratory-cardiovascular coupling abnormalities in HO-HF rats. These findings demonstrate that an intact and functional CB is necessary for the development of cardiorespiratory disturbances in non-ischemic HO-HF. Targeting CB-central chemoreceptor interdependence may represent a novel therapeutic approach for non-ischemic HO-HF.</pubmed_abstract><journal>Basic research in cardiology</journal><pubmed_title>Peripheral chemoreceptors sustain central chemoreflex potentiation and cardiorespiratory abnormalities in high-output heart failure.</pubmed_title><pmcid>PMC12804341</pmcid><funding_grant_id>R01HL176779</funding_grant_id><funding_grant_id>R01 HL176779</funding_grant_id><funding_grant_id>1180172</funding_grant_id><funding_grant_id>1220950</funding_grant_id><pubmed_authors>Pereyra KV</pubmed_authors><pubmed_authors>Del Rio R</pubmed_authors><pubmed_authors>Toledo C</pubmed_authors><pubmed_authors>Bernal-Santander I</pubmed_authors><pubmed_authors>Schwarz KG</pubmed_authors><pubmed_authors>Vicencio SC</pubmed_authors><pubmed_authors>Diaz-Jara E</pubmed_authors><pubmed_authors>Ortiz FC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Peripheral chemoreceptors sustain central chemoreflex potentiation and cardiorespiratory abnormalities in high-output heart failure.</name><description>Central chemoreflex activation worsens cardiorespiratory dysfunction in high-output heart failure (HO-HF). Recently, interdependence between both peripheral and central chemoreceptors has been linked to alterations in cardiorespiratory regulation. Whether central chemoreflex potentiation in HO-HF requires sensory inputs from peripheral chemoreceptors remains completely unknown. Accordingly, we hypothesized that peripheral-central chemoreceptor interaction promotes cardiorespiratory dysfunction in non-ischemic HO-HF. We used male Sprague-Dawley rats to investigate the role of carotid bodies (CBs), the main peripheral chemoreceptors, on autonomic, respiratory, and cardiac function alterations during the progression of HO-HF. CB denervation (CBD) was used to eliminate CB inputs in HO-HF rats. The effect of CBD on HO-HF related cardiac, autonomic, and ventilatory function was measured using echocardiography, pressure-volume loop analysis, electrocardiography, plethysmography, and telemetry. HO-HF rats exhibited enhanced central chemoreflex drive, irregular breathing, autonomic imbalance, cardiac electrophysiological abnormalities, cardiac diastolic dysfunction, and cardiac hypertrophy. Remarkably, CBD completely normalized central chemoreflex function in HO-HF rats, restored ventilatory stability, reduced apnea-hypopnea incidence, improved heart rate variability, shortened QRS and PR intervals, attenuated collagen deposition, and ameliorated diastolic dysfunction. Additionally, CBD also corrected respiratory-cardiovascular coupling abnormalities in HO-HF rats. These findings demonstrate that an intact and functional CB is necessary for the development of cardiorespiratory disturbances in non-ischemic HO-HF. Targeting CB-central chemoreceptor interdependence may represent a novel therapeutic approach for non-ischemic HO-HF.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-06-06T17:14:24.833Z</modification><creation>2026-06-03T03:09:54.241Z</creation></dates><accession>S-EPMC12804341</accession><cross_references><pubmed>41449201</pubmed><doi>10.1007/s00395-025-01154-5</doi></cross_references></HashMap>