Protection from preconditioning can be reinstated at various reperfusion intervals
- PMID: 8877077
- DOI: 10.1007/BF02627958
Protection from preconditioning can be reinstated at various reperfusion intervals
Abstract
The aim of this study was to evaluate the way in which short-term protection declines and is eventually lost in preconditioning and to determine the efficacy of a second preconditioning at various reperfusion intervals. Male rabbits were divided into six groups. Forty-five minutes (sustained) ischemia followed by 120 minutes reperfusion was applied 60, 65, 70, 75, and 80 minutes after a 5 minute preconditioning (groups A, B, C, D, and E) and in a control group (F) after no preconditioning. The infarct to risk ratio (I/R) was 38.3 +/- 3.5% in group A, 46.0 +/- 7.8% in B, 61.6 +/- 9.7% in C, 68.1 +/- 4.2% in D, 64.5 +/- 7.8% in E, and 61.0 +/- 7.7% in F. Group A had a smaller I/R compared with groups C, D, E, and F (p < 0.05). In another series, groups G, H, and I were exposed to two 5-minute preconditioning stimuli, separated, respectively, by 45, 60, and 75 minutes of reperfusion; 10 minutes after the last preconditioning, the animals were exposed to 45-minutes ischemia and 120 minutes reperfusion. Groups A and D (with the smaller and higher I/R ratio) were also incorporated into this protocol in order to compare the effect of the additional preconditioning with the single one. The I/R ratio was 25.4 +/- 8.5% in group G, 22.8 +/- 7.0% in group H, and 14.7 +/- 4.0% in group I (p = NS). Group D showed a higher I/R compared with groups G, A, and H (p < 0.01), and group I had a smaller I/R compared with groups A (p < 0.01) and D (p < 0.001). Cardioprotection after a first preconditioning declines gradually and is eventually lost. An additional preconditioning is always effective, and the longer the interval from the first preconditioning, the more potent is the effect.
Similar articles
-
The re-introduction of ischemic preconditioning is able to protect myocardium after repeated long reperfusion intervals.Cardioscience. 1994 Dec;5(4):277-81. Cardioscience. 1994. PMID: 7742487
-
Oxygen radicals can induce preconditioning in rabbit hearts.Circ Res. 1997 May;80(5):743-8. doi: 10.1161/01.res.80.5.743. Circ Res. 1997. PMID: 9130455
-
A comparison of adenosine-induced cardioprotection and ischemic preconditioning in dogs. Efficacy, time course, and role of KATP channels.Circulation. 1994 Mar;89(3):1229-36. doi: 10.1161/01.cir.89.3.1229. Circulation. 1994. PMID: 8124811
-
[Postconditioning: a brief review].Herz. 2006 Sep;31(6):600-6. doi: 10.1007/s00059-006-2842-6. Herz. 2006. PMID: 17036192 Review. German.
-
Realizing the clinical potential of ischemic preconditioning and postconditioning.Nat Clin Pract Cardiovasc Med. 2005 Nov;2(11):568-75. doi: 10.1038/ncpcardio0346. Nat Clin Pract Cardiovasc Med. 2005. PMID: 16258568 Review.
Cited by
-
Two episodes of remote ischemia preconditioning improve motor and sensory function of hind limbs after spinal cord ischemic injury.J Spinal Cord Med. 2020 Nov;43(6):878-887. doi: 10.1080/10790268.2019.1600829. Epub 2019 Apr 15. J Spinal Cord Med. 2020. PMID: 30985269 Free PMC article.
-
Oral nicorandil recaptures the waned protection from preconditioning in vivo.Br J Pharmacol. 2003 Mar;138(6):1101-6. doi: 10.1038/sj.bjp.0705149. Br J Pharmacol. 2003. PMID: 12684266 Free PMC article.
-
Ischemic preconditioning: protection against myocardial necrosis and apoptosis.Vasc Health Risk Manag. 2007;3(5):629-37. Vasc Health Risk Manag. 2007. PMID: 18078014 Free PMC article. Review.
References
Publication types
MeSH terms
LinkOut - more resources
Medical
Miscellaneous