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Updated: Aug 12, 2026

Induction and Assessment of Ischemia-reperfusion Injury in Langendorff-perfused Rat Hearts
Published on: July 27, 2015
Preconditioning against infarction in the rat heart does not involve a pertussis toxin sensitive G protein
1Department of Physiology, University of South Alabama, Mobile 36688.
Objective:
Adenosine receptor antagonists and pertussis toxin both block the anti-infarct effect of preconditioning in rabbit heart. Because adenosine receptor blockers were found to have no effect against preconditioning in rat heart, a study was performed to test whether ribosylating G proteins with pertussis toxin would block the protection.
Methods:
A branch of the left coronary artery was occluded for 30 min and reperfused for 2 h to produce infarction in open chest rats. Infarct size was assessed by tetrazolium staining. Pertussis toxin was given 48 h before surgery. Preconditioned rats experienced three cycles of 5 min regional ischaemia and 5 min reperfusion before the 30 min occlusion.
Results:
Four groups of rats were studied. Non-treated control rats had 68.8(SEM 2.2)% infarction of the risk zone and preconditioning reduced this to 32.0(6.5)%. Pertussis toxin completely eliminated the G protein mediated bradycardia caused by intravenous acetylcholine or adenosine infusion. Pertussis toxin treatment had no effect on infarct size in non-preconditioned rats [60.9(4.2)% infarction]. Preconditioning the pertussis toxin treated heart reduced infarction to 21.3(5.6)%, an amount comparable to that seen in non-treated rats. Arrhythmias during the 30 min ischaemia were reduced in preconditioned hearts and this protection was not altered by pertussis toxin treatment.
Conclusions:
Preconditioning against either infarction or arrhythmias in the rat does not appear to involve a pertussis toxin sensitive G protein.

