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Neuroprotective Effects of Ischemic Preconditioning and Postconditioning on Global Brain Ischemia in Rats through the Same Effect on Inhibition of Apoptosis

DOI: 10.3390/ijms13056089

Keywords: brain ischemic injury, ischemic preconditioning, ischemic postconditioning, apoptosis, neuroprotection

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Abstract:

Transient forebrain or global ischemia induces neuronal death in vulnerable CA1 pyramidal cells with many features. A brief period of ischemia, i.e., ischemic preconditioning, or a modified reperfusion such as ischemic postconditioning, can afford robust protection of CA1 neurons against ischemic challenge. Therefore, we investigated the effect of ischemic preconditioning and postconditioning on neural cell apoptosis in rats. The result showed that both ischemic preconditioning and postconditioning may attenuate the neural cell death and DNA fragment in the hippocampal CA1 region. Further western blot study suggested that ischemic preconditioning and postconditioning down-regulates the protein of cleaved caspase-3, caspase-6, caspase-9 and Bax, but up-regulates the protein Bcl-2. These findings suggest that ischemic preconditioning and postconditioning have a neuroprotective role on global brain ischemia in rats through the same effect on inhibition of apoptosis.

 References

[1]  Wardlaw, J.M.; von Kummer, R.; Farrall, A.J.; Chappell, F.M.; Hill, M.; Perry, D. A large web-based observer reliability study of early ischaemic signs on computed tomography. The Acute Cerebral CT Evaluation of Stroke Study (ACCESS). PLoS One 2010, 5, doi:10.1371/journal.pone.0015757.
[2]  Sinanovic, O. Neuropsychology of acute stroke. Psychiatr. Danubina 2010, 22, 278–281.
[3]  Van Bel, F.; Groenendaal, F. Long-term pharmacologic neuroprotection after birth asphyxia: Where do we stand? Neonatology 2008, 94, 203–210.
[4]  Mantz, J.; Degos, V.; Laigle, C. Recent advances in pharmacologic neuroprotection. Eur. J. Anaesth 2010, 27, 6–10.
[5]  Chavez, J.C.; Hurko, O.; Barone, F.C.; Feuerstein, G.Z. Pharmacologic interventions for stroke: Looking beyond the thrombolysis time window into the penumbra with biomarkers, not a stopwatch. Stroke J. Cereb. Circ 2009, 40, e558–e563.
[6]  Durukan, A.; Tatlisumak, T. Preconditioning-induced ischemic tolerance: A window into endogenous gearing for cerebroprotection. Exp. Transl. Stroke Med 2010, 2, doi:10.1186/2040-7378-2-2.
[7]  Bhuiyan, M.I.H.; Kim, Y.J. Mechanisms and prospects of ischemic tolerance induced by cerebral preconditioning. Int. Neurourol. J 2010, 14, 203–212.
[8]  Lehotsky, J.; Burda, J.; Danielisova, V.; Gottlieb, M.; Kaplan, P.; Saniova, B. Ischemic tolerance: The mechanisms of neuroprotective strategy. Anat. Rec. (Hoboken) 2009, 292, 2002–2012.
[9]  Ferrara, A.; El Bejaoui, S.; Seyen, S.; Tirelli, E.; Plumier, J.-C. The usefulness of operant conditioning procedures to assess long-lasting deficits following transient focal ischemia in mice. Behav. Brain Res 2009, 205, 525–534.
[10]  Stenzel-Poore, M.P.; Stevens, S.L.; King, J.S.; Simon, R.P. Preconditioning reprograms the response to ischemic injury and primes the emergence of unique endogenous neuroprotective phenotypes: A speculative synthesis. Stroke J.Cereb. Circ 2007, 38, 680–685.
[11]  Miao, Y.; Zhang, W.; Lin, Y.; Lu, X.; Qiu, Y. Neuroprotective effects of ischemic preconditioning on global brain ischemia through up-regulation of acid-sensing ion channel 2a. Int. J. Mol. Sci 2010, 11, 140–153.
[12]  Xing, B.; Chen, H.; Zhang, M.; Zhao, D.; Jiang, R.; Liu, X.; Zhang, S. Ischemic postconditioning inhibits apoptosis after focal cerebral ischemia/reperfusion injury in the rat. Stroke J. Cereb. Circ 2008, 39, 2362–2369.
[13]  Hausenloy, D.J.; Yellon, D.M. Preconditioning and postconditioning: Underlying mechanisms and clinical application. Atherosclerosis 2009, 204, 334–341.
[14]  Pignataro, G.; Scorziello, A.; di Renzo, G.; Annunziato, L. Post-ischemic brain damage: Effect of ischemic preconditioning and postconditioning and identification of potential candidates for stroke therapy. FEBS J 2009, 276, 46–57.
[15]  Durukan, A.; Tatlisumak, T. Acute ischemic stroke: Overview of major experimental rodent models, pathophysiology, and therapy of focal cerebral ischemia. Pharmacol. Biochem. Behav 2007, 87, 179–197.
[16]  Plum, F. Neuroprotection in acute ischemic stroke. J. Am. Med. Assoc 2001, 285, 1760–1761.
[17]  Ginsberg, M.D. Current status of neuroprotection for cerebral ischemia. Synoptic overview. Stroke 2009, 40, 111–114.
[18]  Gladstone, D.J.; Black, S.E.; Hakim, A.M. Toward wisdom from failure-Lessons from neuroprotective stroke trials and new therapeutic directions. Stroke 2002, 33, 2123–2136.
[19]  Kirino, T. Ischemic tolerance. J. Cereb. Blood Flow Metab 2002, 22, 1283–1296.
[20]  Hausenloy, D.J.; Yellon, D.M. The therapeutic potential of ischemic conditioning: An update. Nat. Rev. Cardiol 2011, 8, 619–629.
[21]  Kardesoglu, E.; Isilak, Z.; Uz, O.; Yiginer, O. Ischemic conditioning: A current concept in reducing reperfusion injury. Chin. Med. J 2011, 124, 480.
[22]  Zhang, W.; Miao, Y.; Zhou, S.; Jiang, J.; Luo, Q.; Qiu, Y. Neuroprotective effects of ischemic postconditioning on global brain ischemia in rats through upregulation of hippocampal glutamine synthetase. J. Clin. Neurosci 2011, 18, 685–689.
[23]  Kocher, A.A.; Schuster, M.D.; Szabolcs, M.J.; Takuma, S.; Burkhoff, D.; Wang, J.; Homma, S.; Edwards, N.M.; Itescu, S. Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function. Nat. Med 2001, 7, 430–436.
[24]  Vohra, H.A.; Galinanes, M. Effect of the degree of ischaemic injury and reoxygenation time on the type of myocardial cell death in man: Role of caspases. BMC Physiol 2005, 5, doi:10.1186/1472-6793-5-14.
[25]  Prunell, G.F.; Arboleda, V.A.; Troy, C.M. Caspase function in neuronal death: Delineation of the role of caspases in ischemia. CNS Neurol. Disord. Curr. Drug Target 2005, 4, 51–61.
[26]  Yang, X.-Y.; Liu, Q.-N.; Zhang, L.; Jiang, S.-Q.; Gong, P.-L. Neuroprotective effect of dauricine after transient middle cerebral artery occlusion in rats: Involvement of Bcl-2 family proteins. Am. J. Chin. Med 2010, 38, 307–318.
[27]  Koubi, D.; Jiang, H.; Zhang, L.; Tang, W.; Kuo, J.; Rodriguez, A.I.; Hunter, T.J.; Seidman, M.D.; Corcoran, G.B.; Levine, R.A. Role of Bcl-2 family of proteins in mediating apoptotic death of PC12 cells exposed to oxygen and glucose deprivation. Neurochem. Int 2005, 46, 73–81.
[28]  Lim, S.Y.; Hausenloy, D.J. Remote ischemic conditioning: From bench to bedside. Front. Physiol 2012, 3, doi:10.3389/fphys.2012.00027.
[29]  Thielmann, M. Remote ischemic preconditioning in cardiac surgery: Caught between clinical relevance and statistical significance? Basic Res. Cardiol 2012, 107, 1–4.
[30]  Yagi, T.; Yoshioka, H.; Wakai, T.; Kato, T.; Horikoshi, T.; Kinouchi, H. Activation of signal transducers and activators of transcription 3 in the hippocampal CA1 region in a rat model of global cerebral ischemic preconditioning. Brain Res 2011, 1422, 39–45.
[31]  Hossmann, K.A. Cerebral ischemia: Models, methods and outcomes. Neuropharmacology 2008, 55, 257–270.

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