Autonomic control of the cardiovascular system in the cat during hypoxemia

Auton Neurosci. 2013 Mar;174(1-2):21-30. doi: 10.1016/j.autneu.2012.11.005. Epub 2012 Dec 21.

Abstract

This study aimed to determine the roles played by the autonomic interoreceptors, the carotid bodies (cbs) and the aortic bodies (abs) in anesthetized, paralyzed, artificially ventilated cats' response to systemic hypoxemia. Four 15min challenges stimulated each of 15 animals: (1) hypoxic hypoxia (10%O₂ in N₂; HH) in the intact (int) cat where both abs and cbs sent neural traffic to the nucleus tractus solitarius (NTS); (2) carbon monoxide hypoxia (30%O₂ in N₂ with the addition of CO; COH) in the intact cat where only the abs sent neural traffic to the NTS; (3) HH in the cat after transection of both aortic depressor nerves, resecting the aortic bodies (HHabr), where only the cbs sent neural traffic to the NTS; (4) COH to the abr cat where neither abs nor cbs sent neural traffic to the NTS. Cardiac output (C.O.), contractility (dP/dt(MAX)), systolic/diastolic pressures, aortic blood pressure, total peripheral resistance, pulmonary arterial pressure, and pulmonary vascular resistance (PVR) were measured. When both cbs and abs were active the maximum increases were observed except for PVR which decreased. Some variables showed the cbs to have a greater effect than the abs. The abs proved to be important during some challenges for maintaining blood pressure. The data support the critically important role for the chemoreceptor-sympathetic nervous system connection during hypoxemia for maintaining viable homeostasis, with some differences between the cbs and the abs.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Aorta / innervation
  • Aorta / physiopathology
  • Aortic Bodies / metabolism*
  • Aortic Bodies / physiopathology
  • Aortic Bodies / surgery
  • Autonomic Nervous System / metabolism*
  • Autonomic Nervous System / physiopathology
  • Blood Pressure
  • Cardiac Output, High / etiology
  • Cardiovascular System / innervation*
  • Cardiovascular System / physiopathology
  • Carotid Body / metabolism*
  • Carotid Body / physiopathology
  • Cats
  • Female
  • Hypoxia / chemically induced
  • Hypoxia / metabolism*
  • Hypoxia / physiopathology
  • Male
  • Myocardial Contraction
  • Neural Pathways / metabolism
  • Neural Pathways / physiopathology
  • Pulmonary Artery / innervation
  • Pulmonary Artery / physiopathology
  • Pulmonary Circulation
  • Respiratory System / innervation*
  • Respiratory System / physiopathology
  • Solitary Nucleus / metabolism
  • Solitary Nucleus / physiopathology
  • Synaptic Transmission*
  • Vascular Resistance