Ischemic preconditioning may be transferable via whole blood transfusion: Preliminary evidence

Citation
Ew. Dickson et al., Ischemic preconditioning may be transferable via whole blood transfusion: Preliminary evidence, J THROMB TH, 8(2), 1999, pp. 123-129
Citations number
30
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
JOURNAL OF THROMBOSIS AND THROMBOLYSIS
ISSN journal
09295305 → ACNP
Volume
8
Issue
2
Year of publication
1999
Pages
123 - 129
Database
ISI
SICI code
0929-5305(199908)8:2<123:IPMBTV>2.0.ZU;2-1
Abstract
This research was designed to test the hypothesis that ischemic preconditio ning can be transferred between animals via whole blood transfusion. Precon ditioning at a distance refers to the reduction in myocardial infarct size seen when coronary artery occlusion is preceded by brief ischemic episodes of noncardiac tissue. Isolation of the trigger signal responsible for this effect maybe useful in the diagnosis and treatment of acute coronary occlus ive syndromes. Rabbits were paired by crossmatching blood samples prior to experimentation. Crossmatched pairs were placed into either preconditioned (P) or control sets. Rabbits in the preconditioned sets were further divide d into donor (PD) and acceptor (PA) animals. PD animals underwent five epis odes of circumflex and renal artery occlusion followed by reperfusion. Befo re and after each preconditioning episode, a whole blood exchange was perfo rmed between PD and PA animals. Alternatively, control rabbits underwent th e same surgical procedures and time-sequenced transfusion without precondit ioning. All animals then underwent prolonged circumflex occlusion (60 minut es) followed by reperfusion (30 minutes). The area of myocardium at risk (R ) was determined by isotope-labeled microsphere injection. Infarct size (I) was determined by NBT staining. The percent infarct within the risk area ( I/R) was then compared. The I/R was significantly lower in the PA (14.0% +/ - 12.2) and PD (14.3% +/- 11.2) groups as compared with controls (61% +/- 2 0.6). There was no significant difference between the PA and PD groups. In conclusion, the ischemic preconditioning effect can be transferred to nonpr econditioned animals via whole blood transfusion, suggesting a humoral mech anism for preconditioning at a distance.