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Alterations in circulating cyclic guanosine monophosphate (c-GMP) during short and long ischemia in preconditioning

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Abstract

The aim of this study was to investigate if levels of circulating cyclic guanosine monophosphate (c-GMP) alter, in preconditioning. Twenty-eight rabbits were divided into four groups. In vivo hearts were preconditioned, either with 5 min (group A, n=8) or with 1 min (group B, n=8) ischemia, followed by 10 min reperfusion, while groups C (n=7) and D (n=5) had no interventions. Protection was determined by subjecting groups A, B and C (but not D) to 30 min regional ischemia which was followed (including group D) by 2h reperfusion. Seven blood samples were collected for the assessment of circulating c-GMP at different points of time. All results were expressed in pmol/ml using radioimmunoassay and the infarcted to risk area in percent using fluorescent particles and tetrazolium chloride (TTC). Circulating c-GMP increased during long ischemia only in group A (baseline value 47±4, long ischemic values 60.5±4 and 60.4±4, p<0.05). Circulating c-GMP in group A was significantly higher in the middle of the long ischemia in comparison to the groups B, C and D (60.5±4 vs 43.9±4, 45.8±5 and 43.6±4, p<0.05). Infarcted to risk ratio was lower in group A than in groups B and C (12.2±4 vs 29.6±6 and 34.2±6, respectively, p<0.05). Circulating c-GMP is increased in classically preconditioned in comparison to ineffectively preconditioned hearts or to control groups. This elevation may be related to the protective effect of this phenomenon.

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Iliodromitis, E.K., Papadopoulos, C.C., Markianos, M. et al. Alterations in circulating cyclic guanosine monophosphate (c-GMP) during short and long ischemia in preconditioning. Basic Res Cardiol 91, 234–239 (1996). https://doi.org/10.1007/BF00788909

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  • DOI: https://doi.org/10.1007/BF00788909

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