Site of origin and molecular substrate of atrioventricular junctional rhythm in the rabbit heart

Circ Res. 2003 Nov 28;93(11):1102-10. doi: 10.1161/01.RES.0000101913.95604.B9. Epub 2003 Oct 16.

Abstract

During failure of the sinoatrial node, the heart can be driven by an atrioventricular (AV) junctional pacemaker. The position of the leading pacemaker site during AV junctional rhythm is debated. In this study, we present evidence from high-resolution fluorescent imaging of electrical activity in rabbit isolated atrioventricular node (AVN) preparations that, in the majority of cases (11 out of 14), the AV junctional rhythm originates in the region extending from the AVN toward the coronary sinus along the tricuspid valve (posterior nodal extension, PNE). Histological and immunohistochemical investigation showed that the PNE has the same morphology and unique pattern of expression of neurofilament160 (NF160) and connexins (Cx40, Cx43, and Cx45) as the AVN itself. Block of the pacemaker current, If, by 2 mmol/L Cs+ increased the AV junctional rhythm cycle length from 611+/-84 to 949+/-120 ms (mean+/-SD, n=6, P<0.001). Immunohistochemical investigation showed that the principal If channel protein, HCN4, is abundant in the PNE. As well as the AV junctional rhythm, the PNE described in this study may also be involved in the slow pathway of conduction into the AVN as well as AVN reentry, and the predominant lack of expression of Cx43 as well as the presence of Cx45 in the PNE shown could help explain its slow conduction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Atrial Function / drug effects
  • Atrial Function / physiology
  • Atrioventricular Node / drug effects
  • Atrioventricular Node / metabolism
  • Atrioventricular Node / physiology*
  • Biological Clocks / drug effects
  • Biological Clocks / physiology
  • Body Surface Potential Mapping
  • Cesium / pharmacology
  • Connexin 43 / analysis
  • Connexins / biosynthesis
  • Cyclic Nucleotide-Gated Cation Channels
  • Electrophysiologic Techniques, Cardiac
  • Gap Junction alpha-5 Protein
  • Heart Atria / metabolism
  • Heart Rate* / drug effects
  • Heart Rate* / physiology
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • In Vitro Techniques
  • Ion Channels / biosynthesis
  • Muscle Proteins / biosynthesis
  • Neurofilament Proteins / biosynthesis
  • Optics and Photonics
  • Periodicity*
  • Potassium Channels
  • Pyridinium Compounds
  • Rabbits
  • Sinoatrial Node / physiology

Substances

  • Connexin 43
  • Connexins
  • Cyclic Nucleotide-Gated Cation Channels
  • HCN4 protein, human
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • Ion Channels
  • Muscle Proteins
  • Neurofilament Proteins
  • Potassium Channels
  • Pyridinium Compounds
  • connexin 45
  • Cesium
  • 1-(3-sulfonatopropyl)-4-(beta)(2-(di-n-butylamino)-6-naphthylvinyl)pyridinium betaine