RGD Reference Report - Dynamic changes in HCN2, HCN4, KCNE1, and KCNE2 expression in ventricular cells from acute myocardial infarction rat hearts. - Rat Genome Database

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Dynamic changes in HCN2, HCN4, KCNE1, and KCNE2 expression in ventricular cells from acute myocardial infarction rat hearts.

Authors: Xia, S  Wang, Y  Zhang, Y  Deng, SB  Du, JL  Wang, XC  She, Q 
Citation: Xia S, etal., Biochem Biophys Res Commun. 2010 May 7;395(3):330-5. doi: 10.1016/j.bbrc.2010.04.003. Epub 2010 Apr 8.
RGD ID: 7242918
Pubmed: PMID:20381460   (View Abstract at PubMed)
DOI: DOI:10.1016/j.bbrc.2010.04.003   (Journal Full-text)

AIMS: To investigate dynamic changes in the expression of HCN2, HCN4, as well as KCNE1, and KCNE2 mRNA and protein levels in ventricular cells from acute myocardial infarction (AMI) rat hearts. MAIN METHODS: An AMI model was induced by ligating the left anterior descending coronary artery (LAD) of Sprague-Dawley rats. The rats were randomly divided into four experimental groups: 24-hour (24h) post-AMI, 1-week (1w) post-AMI, 2-week (2w) post-AMI, and 4-week (4w) post-AMI; sham-operated control rat groups were established in parallel for each time point. HCN2, HCN4, KCNE1, and KCNE2 mRNA and protein levels were measured by reverse transcription-polymerase chain reaction (RT-PCR) and by immunohistochemistry and Western blot, respectively. Key FINDINGS: Ventricular arrhythmias occurred in all the post-AMI groups, particularly in the 1w and 2w post-AMI groups. Although HCN2, HCN4, KCNE1, and KCNE2 genes were expressed in the left ventricular myocardium of sham-operated control rats, their expression increased in rat ischemic left ventricular myocardium, with dynamic changes in expression observed 4 weeks after AMI. HCN2, HCN4, and KCNE2 protein levels were highest at 1w and KCNE2 protein levels peaked at 2w post-AMI. SIGNIFICANCE: The expression of the HCN2, HCN4, as well as KCNE1, and KCNE2 genes in ventricular cells from AMI rat hearts underwent dynamic changes, reaching peak levels at 1 or 2weeks post-AMI. The increased expression maybe related to ventricular arrhythmogenesis after AMI.




  
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Original Reference(s)
KCNE1HumanCardiac Arrhythmias  ISOKcne1 (Rattus norvegicus)associated with Myocardial InfarctionRGD 
KCNE2HumanCardiac Arrhythmias  ISOKcne2 (Rattus norvegicus)associated with Myocardial InfarctionRGD 
Kcne1RatCardiac Arrhythmias  IEP associated with Myocardial InfarctionRGD 
Kcne1MouseCardiac Arrhythmias  ISOKcne1 (Rattus norvegicus)associated with Myocardial InfarctionRGD 
Kcne2RatCardiac Arrhythmias  IEP associated with Myocardial InfarctionRGD 
Kcne2MouseCardiac Arrhythmias  ISOKcne2 (Rattus norvegicus)associated with Myocardial InfarctionRGD 


Genes (Rattus norvegicus)
Kcne1  (potassium voltage-gated channel subfamily E regulatory subunit 1) Kcne2  (potassium voltage-gated channel subfamily E regulatory subunit 2)

Genes (Mus musculus)
Kcne1  (potassium voltage-gated channel, Isk-related subfamily, member 1) Kcne2  (potassium voltage-gated channel, Isk-related subfamily, gene 2)

Genes (Homo sapiens)
KCNE1  (potassium voltage-gated channel subfamily E regulatory subunit 1) KCNE2  (potassium voltage-gated channel subfamily E regulatory subunit 2)