Timing of xenon-induced delayed postconditioning to protect against spinal cord ischaemia-reperfusion injury in rats

British Journal of Anaesthesia

Volumn 113, Issue 1, 2014, Pages 168-176

  Yang, Y W ^a   Cheng, W P ^a   Lu, J K ^a   Dong, X H ^a   Wang, C B ^a   Zhang, J ^a   Zhao, L Y ^a   Gao, Z F ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

neuroprotectant; spinal cord, ischaemia reperfusion injury; xenon, delayed postconditioning

Indexed keywords

NITROGEN; OXYGEN; XENON;

ANIMAL EXPERIMENT; ANIMAL MODEL; AORTA OCCLUSION; APOPTOSIS; ARTICLE; CONTROLLED STUDY; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; IN VIVO STUDY; ISCHEMIC POSTCONDITIONING; MALE; NERVE CELL; NEUROPROTECTION; NICK END LABELING; NISSL STAINING; NONHUMAN; PRIORITY JOURNAL; RAT; REPERFUSION; SPINAL CORD ISCHEMIA;

NEUROPROTECTANT; SPINAL CORD, ISCHAEMIA-REPERFUSION INJURY; XENON, DELAYED POSTCONDITIONING;

ANIMALS; APOPTOSIS; CARBON DIOXIDE; DRUG ADMINISTRATION SCHEDULE; ISCHEMIC POSTCONDITIONING; LOCOMOTION; MALE; NEURONS; NEUROPROTECTIVE AGENTS; OXYGEN; PARTIAL PRESSURE; RATS; RATS, SPRAGUE-DAWLEY; REPERFUSION INJURY; SPINAL CORD; SPINAL CORD ISCHEMIA; XENON;

EID: 84903989616     PISSN: 00070912     EISSN: 14716771     Source Type: Journal    
DOI: 10.1093/bja/aet352     Document Type: Article

References (39)

1. Cambria RP, Clouse WD, Davison JK, Dunn PF, Corey M, Dorer D. Thoracoabdominal aneurysm repair: results with 337 operations performed over a 15-year interval. Ann Surg 2002; 236: 471-9
2. Zhao ZQ, Corvera JS, Halkos ME, et al. Inhibition ofmyocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning.AmJ Physiol Heart Circ Physiol 2003; 285: 579-88
3. Obal D, Dettwiler S, Favoccia C, Scharbatke H, Preckel B, Schlack W. The influence of mitochondrial KATP-channels in the cardioprotection of preconditioning and postconditioning by sevoflurane in the rat in vivo. Anesth Analg 2005; 101: 1252-60
4. Kin H, Zatta AJ, Lofye MT, et al. Postconditioning reduces infarct size via adenosine receptor activation by endogenous adenosine. Cardiovasc Res 2005; 67: 124-33
5. Yellon DM, Opie LH. Postconditioning for protection of the infarcting heart. Lancet 2006; 367: 456-8
6. Staat P, Rioufol G, Piot C, et al. Postconditioning the human heart. Circulation 2005; 112: 2143-8
7. Wang Q, Chen Q, Ding Q, et al. Sevoflurane postconditioning attenuates spinal cord reperfusion injury through free radicals-mediated up-regulation of antioxidant enzymes in rabbits. J Surg Res 2011; 169: 292-300
8. David HN, Haelewyn B, Rouillon C, et al. Neuroprotective effects of xenon: a therapeutic window of opportunity in rats subjected to transient cerebral ischemia. FASEB J 2008; 22: 1275-86
9. Lee JJ, Li L, Jung HH, Zuo Z. Postconditioningwith isofluranereduced ischemia-induced brain injury in rats. Anesthesiology 2008; 108: 1055-62
10. Roubille F, Franck-Miclo A, Covinhes A, et al. Delayed postconditioning in the mouse heart in vivo. Circulation 2011; 124: 1330-6
11. Ren C, Gao X, Niu G, Yan Z, Chen X, Zhao H. Delayed postconditioning protects against focal ischemic brain injury in rats. PLoS One 2008; 3: 3851
12. Tian F, Xu LH, Zhao W, Tian LJ, Ji XL. The optimal therapeutic timing and mechanism of puerarin treatment of spinal cord ischemia- reperfusion injury in rats. J Ethnopharmacol 2011; 134: 892-6
13. Wang Q, Ding Q, Zhou Y, et al. Ethyl pyruvate attenuates spinal cord ischemic injury with a wide therapeutic window through inhibiting high-mobility group box 1 release in rabbits. Anesthesiology 2009; 110: 1279-86
14. Derwall M, Coburn M, Rex S, Hein M, Rossaint R, Fries M. Xenon: recent developments and future perspectives. Minerva Anestesiol 2009; 75: 37-45
15. Fries M, Nolte KW, Coburn M, et al. Xenon reduces neurohistopathological damage and improves the early neurological deficit after cardiac arrest in pigs. Crit Care Med 2008; 36: 2420-6
16. Yang YW, Lu JK, Cheng WP, et al. Post-conditioning by xenon reduces ischaemia-reperfusion injury of the spinal cord in rats. Acta Anaesthesiol Scand 2012; 56: 1325-31
17. Basso DM, Beattie MS, Bresnahan JC. A sensitive and reliable locomotor rating scale for open field testing in rats. Neurotrauma 1995; 12: 1-21
18. Fan L, Wang K, Shi Z, Die J, Wang C, Dang X. Tetramethylpyrazine protects spinal cord and reduces inflammation in a rat model of spinal cord ischemia-reperfusion injury. J Vasc Surg 2011; 54: 192-200
19. Taira Y, Marsala M. Effect of proximal arterial perfusion pressure on function, spinal cord blood flow, and histopathologic changes after increasing intervals of aortic occlusion in the rat. Stroke 1996; 27: 1850-8
20. Yamamoto Y, Kawaguchi M, Kurita N, Kakimoto M, Inoue S, Furuya H. Effects of xenon on ischemic spinal cord injury in rabbits: a comparison with propofol. Acta Anaesthesiol Scand 2010; 54: 337-42
21. Zhou C, Tu J, Zhang Q, et al. Delayed ischemic postconditioning protects hippocampal CA1 neurons by preserving mitochondrial integrity via Akt/GSK3b signaling. NeurochemInt 2011; 59: 749-58
22. Fries M, Coburn M, Nolte KW, et al. Early administration of xenon or isoflurane may not improve functional outcome and cerebral alterations in a porcine model of cardiac arrest. Resuscitation 2009; 80: 584-90
23. Karin M, Ben-Neriah Y. Phosphorylation meets ubiquitination: the controlofNF-[kappa]Bactivity.AnnuRev Immunol2000;18: 621-63
24. Kanoh M, Takemura G, Misao J, et al. Significance of myocytes with positiveDNAin situ nick end-labeling (TUNEL) in hearts with dilated cardiomyopathy: not apoptosis but DNA repair. Circulation 1999; 99: 2757-64
25. Didenko VV, Hornsby PJ. Presence of double-strand breaks with single-base 3' overhangs in cells undergoing apoptosis but not necrosis. J Cell Biol 1996; 135: 1369-76
26. Gold R, Schmied M, Giegerich G, et al. Differentiation between cellular apoptosis and necrosis by the combined use of in situ tailing and nick translation techniques. Lab Invest 1994; 71: 219-25
27. Saraste A. Morphologic criteria and detection of apoptosis. Herz 1999; 24: 189-95
28. Kroemer G, Galluzzi L, Vandenabeele P, et al. Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009. Cell Death Differ 2009; 16: 3-11
29. Fan LH, Wang KZ, Cheng B. Effects of Ginkgo biloba extract on lipid peroxidation and apoptosis after spinal cord ischemia/reperfusion in rabbits. Chin J Traumatol 2006; 9: 77-81
30. Fan LH, Wang KZ, Cheng B, Wang CS, Dang XQ. Anti-apoptotic and neuroprotective effects of Tetramethylpyrazine following spinal cord ischemia in rabbits. BMC Neurosci 2006; 7: 48
31. Garrido R, Mattson MP, Hennig B, Toborek M. Nicotine protects against arachidonic-acid-induced caspase activation, cytochrome c release and apoptosis of cultured spinal cord neurons. J Neurochem 2001; 76: 1395-403
32. Sîrbulescu RF, Zupanc GK. Inhibition of caspase-3-mediated apoptosis improves spinal cord repair in a regeneration-competent vertebrate system. Neuroscience 2010; 171: 599-612
33. Cattano D, Williamson P, Fukui K, et al. Potential of xenon to induce or to protect against neuroapoptosis in the developing mouse brain. Can J Anaesth 2008; 55: 429-36
34. Hardingham GE, Bading H. The Yin and Yang of NMDA receptor signalling. Trends Neurosci 2003; 26: 81-9
35. Neal MJ, Cunningham JR, Hutson PH, Hogg J. Effects of ischaemia on neurotransmitter release from the isolated retina. J Neurochem 1994; 62: 1025-33
36. An G, Lin TN, Liu JS, Xue JJ, He YY, Hsu CY. Expression of c-fos and c-jun family genes after focal cerebral ischemia. Ann Neurol 1993; 33: 457-64
37. Shima Y, Tajiri T, Taguchi T, Suita S. Increased expression of c-fos and c-jun in the rat small intestinal epithelium after ischemia- reperfusion injury: a possible correlation with the proliferation or apoptosis of intestinal epithelial cells. J Pediatr Surg 2006; 41: 830-6
38. Lin Y, Mather LE, Power I, Cousins MJ. The effect of diclofenac on the expression of spinal cord c-fos-like immunoreactivityafter ischemia- reperfusion-induced acute hyperalgesia in the rat tail. Anesth Analg 2000; 90: 1141-5
39. Mio Y, Shim YH, Richards E, Bosnjak ZJ, Pagel PS, Bienengraeber M. Xenon preconditioning: the role of prosurvival signaling, mitochondrialpermeability transitionandbioenergetics in rats. Anesth Analg 2009; 108: 858-66