Controlled low-pressure perfusion at the beginning of reperfusion attenuates neurologic injury after spinal cord ischemia

Journal of Thoracic and Cardiovascular Surgery

Volumn 133, Issue 4, 2007, Pages 942-948

  Shi, Enyi ^a,c   Jiang, Xiaojing ^b   Kazui, Teruhisa ^a   Washiyama, Naoki ^a   Yamashita, Katsushi ^a   Terada, Hitoshi ^a   Bashar, Abul Hasan Muhammad ^a  

^a First Department of Surgery   (Japan)

^b HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c CHINA MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PRECURSOR PROTEIN; MALONALDEHYDE;

ABDOMINAL AORTA ANEURYSM; ANEURYSM SURGERY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BALLOON CATHETER; CONTROLLED STUDY; FUNCTIONAL ASSESSMENT; HISTOPATHOLOGY; IMMUNOREACTIVITY; LUMBAR SPINAL CORD; NEUROPROTECTION; NONHUMAN; PERFUSION PRESSURE; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; RABBIT; REPERFUSION INJURY; SCORING SYSTEM; SPINAL CORD INJURY; SPINAL CORD ISCHEMIA; THORACIC AORTA ANEURYSM;

ANIMALS; BLOOD PRESSURE; DISEASE MODELS, ANIMAL; OXIDATIVE STRESS; PERFUSION; RABBITS; REPERFUSION INJURY; SPINAL CORD; SPINAL CORD ISCHEMIA;

EID: 33947226115     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtcvs.2006.12.017     Document Type: Article

References (29)

1. Coselli J.S., LeMaire S.A., Miller III C.C., Schmittling Z.C., Koksoy C., Pagan J., et al. Mortality and paraplegia after thoracoabdominal aortic aneurysm repair: a risk factor analysis. Ann Thorac Surg 69 (2000) 409-414
2. Estrera A.L., Garami Z., Miller III C.C., Sheinbaum R., Huynh T.T., Porat E.E., et al. Distal aortic perfusion and cerebrospinal fluid drainage for thoracoabdominal and descending thoracic aortic repair: ten years of organ protection. Ann Surg 238 (2003) 372-380
3. Zhao Z.Q., and Vinten-Johansen J. Postconditioning: reduction of reperfusion-induced injury. Cardiovasc Res 70 (2006) 200-211
4. Zhao Z.Q., Corvera J.S., Halkos M.E., Kerendi F., Wang N.P., Guyton R.A., et al. Inhibition of myocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol 285 (2003) H579-H588
5. Argaud L., Gateau-Roesch O., Raisky O., Loufouat J., Robert D., and Ovize M. Postconditioning inhibits mitochondrial permeability transition. Circulation 111 (2005) 194-197
6. Tsang A., Hausenloy D.J., Mocanu M.M., and Yellon D.M. Postconditioning: a form of "modified reperfusion" protects the myocardium by activating the phosphatidylinositol 3-kinase-Akt pathway. Circ Res 95 (2004) 230-232
7. Kin H., Zhao Z.Q., Sun H.Y., Wang N.P., Corvera J.S., Halkos M.E., et al. Postconditioning attenuates myocardial ischemia-reperfusion injury by inhibiting events in the early minutes of reperfusion. Cardiovasc Res 62 (2004) 74-85
8. Staat P., Rioufol G., Piot C., Cottin Y., Cung T.T., L'Huillier I., et al. Postconditioning the human heart. Circulation 112 (2005) 2143-2148
9. Zhao H., Sapolsky R.M., and Steinberg G.K. Interrupting reperfusion as a stroke therapy: ischemic postconditioning reduces infarct size after focal ischemia in rats. J Cereb Blood Flow Metab 26 (2006) 1114-1121
10. Jiang X., Shi E., Nakajima Y., and Sato S. Postconditioning, a series of brief interruptions of early reperfusion, prevents neurologic injury after spinal cord ischemia. Ann Surg 244 (2006) 148-153
11. Suzuki K., Kazui T., Terada H., Umemura K., Ikeda Y., Bashar A.H., et al. Experimental study on the protective effects of edaravone against ischemic spinal cord injury. J Thorac Cardiovasc Surg 130 (2005) 1586-1592
12. Tarlov I.M. Acute spinal cord compression paralysis. J Neurosurg 36 (1972) 10-20
13. Mutch W.A., Graham M.R., Halliday W.C., Thiessen D.B., and Girling L.G. Use of neuroanesthesia adjuncts (hyperventilation and mannitol administration) improves neurological outcome after thoracic aortic cross-clamping in dogs. Stroke 24 (1993) 1204-1210
14. Kurita N., Kawaguchi M., Kakimoto M., Yamamoto Y., Inoue S., Nakamura M., et al. Reevaluation of gray and white matter injury after spinal cord ischemia in rabbits. Anesthesiology 105 (2006) 305-312
15. Honda F., Imai H., Ishikawa M., Kubota C., Shimizu T., Fukunaga M., et al. Cilostazol attenuates gray and white matter damage in a rodent model of focal cerebral ischemia. Stroke 37 (2006) 223-228
16. Jean W.C., Spellman S.R., Nussbaum E.S., and Low W.C. Reperfusion injury after focal cerebral ischemia: the role of inflammation and the therapeutic horizon. Neurosurgery 43 (1998) 1382-1396
17. Hossmann K.A. Reperfusion of the brain after global ischemia: hemodynamic disturbances. Shock 8 (1997) 95-101
18. Okamoto F., Allen B.S., Buckberg G.D., Bugyi H., and Leaf J. Reperfusion conditions: importance of ensuring gentle versus sudden reperfusion during relief of coronary occlusion. J Thorac Cardiovasc Surg 92 (1986) 613-620
19. Sato H., Jordan J.E., Zhao Z.Q., Sarvotham S.S., and Vinten-Johansen J. Gradual reperfusion reduces infarct size and endothelial injury but augments neutrophil accumulation. Ann Thorac Surg 64 (1997) 1099-1107
20. Herkert O., Diebold I., Brandes R.P., Hess J., Busse R., and Gorlach A. NADPH oxidase mediates tissue factor-dependent surface procoagulant activity by thrombin in human vascular smooth muscle cells. Circulation 105 (2002) 2030-2036
21. Saito A., Maier C.M., Narasimhan P., Nishi T., Song Y.S., Yu F., et al. Oxidative stress and neuronal death/survival signaling in cerebral ischemia. Mol Neurobiol 31 (2005) 105-116
22. Zhang N., Komine-Kobayashi M., Tanaka R., Liu M., Mizuno Y., and Urabe T. Edaravone reduces early accumulation of oxidative products and sequential inflammatory responses after transient focal ischemia in mice brain. Stroke 36 (2005) 2220-2225
23. Takahashi G., Sakurai M., Abe K., Itoyama Y., and Tabayashi K. MCI-186 reduces oxidative cellular damage and increases DNA repair function in the rabbit spinal cord after transient ischemia. Ann Thorac Surg 78 (2004) 602-607
24. Penna C., Rastaldo R., Mancardi D., Raimondo S., Cappello S., Gattullo D., et al. Post-conditioning induced cardioprotection requires signaling through a redox-sensitive mechanism, mitochondrial ATP-sensitive K+ channel and protein kinase C activation. Basic Res Cardiol 101 (2006) 180-189
25. Kanellopoulos G.K., Xu X.M., Hsu C.Y., Lu X., Sundt T.M., and Kouchoukos N.T. White matter injury in spinal cord ischemia: protection by AMPA/kainate glutamate receptor antagonism. Stroke 31 (2000) 1945-1952
26. Kurita N., Kawaguchi M., Horiuchi T., Inoue S., Sakamoto T., Nakamura M., et al. An evaluation of white matter injury after spinal cord ischemia in rats: a comparison with gray matter injury. Anesth Analg 100 (2005) 847-854
27. Follis F., Scremin O.U., Blisard K.S., Scremin A.M., Pett S.B., Scott W.J., et al. Selective vulnerability of white matter during spinal cord ischemia. J Cereb Blood Flow Metab 13 (1993) 170-178
28. Pantoni L., Garcia J.H., and Gutierrez J.A. Cerebral white matter is highly vulnerable to ischemia. Stroke 27 (1996) 1641-1646
29. Imai H., McCulloch J., Graham D.I., Masayasu H., and Macrae I.M. New method for the quantitative assessment of axonal damage in focal cerebral ischemia. J Cereb Blood Flow Metab 22 (2002) 1080-1089