<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Tompkins JD</submitter><funding>NHLBI NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>Intrinsic cardiac neurons (ICNs) play a crucial role in the proper functioning of the heart; yet a paucity of data pertaining to human ICNs exists. We took a multidisciplinary approach to complete a detailed cellular comparison of the structure and function of ICNs from mice, pigs, and humans. Immunohistochemistry of whole and sectioned ganglia, transmission electron microscopy, intracellular microelectrode recording and dye filling for quantitative morphometry were used to define the neurophysiology, histochemistry, and ultrastructure of these cells across species. The densely packed, smaller ICNs of mouse lacked dendrites, formed axosomatic connections, and had high synaptic efficacy constituting an obligatory synapse. At Pig ICNs, a convergence of subthreshold cholinergic inputs onto ex</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.04.04.588174</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11030249</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative specialization of intrinsic cardiac neurons in humans, mice, and pigs.</pubmed_title><pmcid>PMC11030249</pmcid><funding_grant_id>P01 HL164311</funding_grant_id><funding_grant_id>OT2 OD023848</funding_grant_id><funding_grant_id>OT2 OD026585</funding_grant_id><pubmed_authors>Patel JC</pubmed_authors><pubmed_authors>Cho Y</pubmed_authors><pubmed_authors>Ardell JL</pubmed_authors><pubmed_authors>Hoover DB</pubmed_authors><pubmed_authors>Smith EH</pubmed_authors><pubmed_authors>Shivkumar K</pubmed_authors><pubmed_authors>Biscola NP</pubmed_authors><pubmed_authors>Ajijola OA</pubmed_authors><pubmed_authors>Tompkins JD</pubmed_authors><pubmed_authors>Havton LA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative specialization of intrinsic cardiac neurons in humans, mice, and pigs.</name><description>Intrinsic cardiac neurons (ICNs) play a crucial role in the proper functioning of the heart; yet a paucity of data pertaining to human ICNs exists. We took a multidisciplinary approach to complete a detailed cellular comparison of the structure and function of ICNs from mice, pigs, and humans. Immunohistochemistry of whole and sectioned ganglia, transmission electron microscopy, intracellular microelectrode recording and dye filling for quantitative morphometry were used to define the neurophysiology, histochemistry, and ultrastructure of these cells across species. The densely packed, smaller ICNs of mouse lacked dendrites, formed axosomatic connections, and had high synaptic efficacy constituting an obligatory synapse. At Pig ICNs, a convergence of subthreshold cholinergic inputs onto ex</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-04-08T19:47:46.047Z</modification><creation>2026-04-08T14:32:57.99Z</creation></dates><accession>S-EPMC11030249</accession><cross_references><pubmed>38645175</pubmed><doi>10.1101/2024.04.04.588174</doi></cross_references></HashMap>