Document Detail


Influence of postnatal-development on I(f) occurrence and properties in neonatal rat ventricular myocytes.
MedLine Citation:
PMID:  10533577     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: I(f) is a hyperpolarization-activated current, which plays a key role in determining the spontaneous rate of cardiac pacemaker cells. We have previously shown that I(f) is also expressed in left ventricular myocytes isolated from spontaneously hypertensive rats; in these cells, its occurrence and density is linearly related with the severity of myocardial hypertrophy. Since hypertrophy induces a re-expression of genes encoding fetal proteins, we investigated changes in I(f) properties during post-natal development.
METHODS: Fresh ventricular myocytes were enzymatically isolated from the heart of 1-2- to 28-day-old Wistar rats. The whole-cell configuration of the patch-clamp technique was employed to record the action potential and I(f).
RESULTS: Membrane capacitance, an index of cell size, progressively increased from 13 +/- 1 pF at 1-2 days to 66 +/- 4 pF at 28 days of age (p < 0.01). At 1-2 days, a cesium-sensitive hyperpolarization-activated inward current (I(f)) was recorded in the majority of tested cells (n = 51). The midpoint of the activation curve (V1/2) was -78 +/- 2 mV (n = 32), and specific current conductance of fully activated I(f) (gf.max) was 60 +/- 11 pS/pF. Reversal potential (Vrev) measured by tail-current analysis was -24 +/- 3 mV (n = 8). Reduction of extracellular Na+ from 140 to 35 mM or extracellular K+ from 25 to 5.4 mM caused a shift of -12 +/- 1 mV (n = 3) or -11 +/- 2 mV (n = 5) of Vrev, respectively. Occurrence of I(f) decreased with aging, being present in 64%, 48% and 32% of cells at 10, 15 and 28 days, respectively. When present, I(f) density was significantly smaller than at 1-2 days (p < 0.05), reaching a value of 8 +/- 2 pS/pF at 28 days. However, V1/2 did not change in the older rats, being -80 +/- 2, -83 +/- 4 and -85 +/- 3 mV at 10, 15 and 28 days, respectively. Vrev at 10 and 15 days was -27 and -28 mV, respectively, thus suggesting that channel selectivity did not change.
CONCLUSIONS: The pacemaker current, I(f), is expressed in ventricular myocytes from neonatal rats and progressively disappears; when present, it shows electrophysiological properties similar to I(f) re-expressed in hypertrophied adult rat ventricular myocytes. Thus, it is likely that the occurrence of I(f) in ventricular myocytes of hypertrophied and failing hearts is due to the re-expression of a fetal gene.
Authors:
E Cerbai; R Pino; L Sartiani; A Mugelli
Related Documents :
6256527 - Maturation of sympathetic neurotransmission in the rat heart. vii. suppression of sympa...
17943427 - P38 mitogen-activated protein kinase inhibition decreases tnfalpha secretion and protec...
9495647 - Comparison of cardiac troponin t and cardiac troponin i concentrations in peripheral bl...
2895737 - Effects of arterial vasodilators on cardiac hypertrophy and sympathetic activity in rats.
23428587 - The beneficial impact of fasudil and sildenafil on monocrotaline-induced pulmonary hype...
9795227 - Priming with l-dopa differently affects dynorphin and substance p mrna levels in the st...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Cardiovascular research     Volume:  42     ISSN:  0008-6363     ISO Abbreviation:  Cardiovasc. Res.     Publication Date:  1999 May 
Date Detail:
Created Date:  1999-11-04     Completed Date:  1999-11-04     Revised Date:  2012-02-22    
Medline Journal Info:
Nlm Unique ID:  0077427     Medline TA:  Cardiovasc Res     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  416-23     Citation Subset:  IM    
Affiliation:
Department of Preclinical and Clinical Pharmacology, University of Firenze, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Action Potentials / physiology*
Analysis of Variance
Animals
Animals, Newborn
Biological Transport, Active / physiology*
Cells, Cultured
Heart / growth & development,  physiology*
Ion Transport
Myocardial Contraction / physiology*
Patch-Clamp Techniques
Rats
Rats, Wistar
Grant Support
ID/Acronym/Agency:
1092//Telethon

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Ionic basis of ventricular arrhythmias in remodeled rat heart during long-term myocardial infarction...
Next Document:  Decreased inward rectifier current in adult rabbit ventricular myocytes maintained in primary cultur...