No loss of cardioprotection by postconditioning in connexin 43-deficient mice.

Abstract:

:In situ hearts and isolated cardiomyocytes from heterozygous connexin 43-deficient (Cx43+/-) mice cannot be protected by ischemic preconditioning or diazoxide. We have now addressed the role of connexin 43 in ischemic postconditioning (PC). Wild type (WT) and Cx43+/- mice were subjected to 30 min coronary occlusion and 120 min reperfusion, with and without a PC protocol of three cycles of 10 s coronary occlusion/10 s reperfusion. Infarct size (TTC staining) was reduced by PC from 54+/-5 to 37+/-3% of area at risk in WT. Likewise, infarct size was reduced by PC from 53+/-4 to 34+/-3% of area at risk in Cx43+/-. We conclude that connexin 43 is no prerequisite for PC's protection. To this end, the signal transduction of ischemic preconditioning and postconditioning differs.

journal_name

Basic Res Cardiol

authors

Heusch G,Büchert A,Feldhaus S,Schulz R

doi

10.1007/s00395-006-0589-0

keywords:

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

354-6

issue

4

eissn

0300-8428

issn

1435-1803

journal_volume

101

pub_type

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