Isoflurane postconditioning improved long-term neurological outcome possibly via inhibiting the mitochondrial permeability transition pore in neonatal rats after brain hypoxia-ischemia

Neuroscience

Volumn 280, Issue , 2014, Pages 193-203

  Zhao, P ^a,b   Ji, G ^a,b   Xue, H ^a,b   Yu, W ^a,b   Zhao, X ^a,b   Ding, M ^a,b   Yang, Y ^a,b   Zuo, Z ^a,b  

^a CHINA MEDICAL UNIVERSITY   (China)

^b UNIVERSITY OF VIRGINIA   (United States)

Author keywords

Hypoxic ischemic brain injury; Isoflurane; Mitochondrial permeability transition pore; Neonatal rat; Postconditioning

Indexed keywords

ATRACTYLOSIDE; CYCLOSPORIN A; ISOFLURANE; MITOCHONDRIAL PERMEABILITY TRANSITION PORE; CARRIER PROTEIN; CENTRAL NERVOUS SYSTEM AGENTS; CYCLOSPORIN; NEUROPROTECTIVE AGENT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN ATROPHY; BRAIN WEIGHT; COMPARATIVE STUDY; CONTROLLED STUDY; DRUG MECHANISM; FEMALE; HIPPOCAMPAL CA3 REGION; HISTOPATHOLOGY; HYPOTHALAMUS VENTROMEDIAL NUCLEUS; HYPOXIC ISCHEMIC ENCEPHALOPATHY; ISCHEMIC POSTCONDITIONING; LATENT PERIOD; LEFT HEMISPHERE; MALE; MITOCHONDRIAL PERMEABILITY; MORRIS WATER MAZE TEST; MORTALITY; NERVOUS SYSTEM PARAMETERS; NEURONAL DENSITY RATIO; NEWBORN; NONHUMAN; OPTICAL DENSITY; ORIENTING RESPONSE; OUTCOME ASSESSMENT; RAT; RIGHT HEMISPHERE; ANIMAL; ANTAGONISTS AND INHIBITORS; COMMON CAROTID ARTERY; DISEASE MODEL; DRUG EFFECTS; HYPOXIA-ISCHEMIA, BRAIN; MAZE TEST; METABOLISM; MITOCHONDRION; MOTOR ACTIVITY; PATHOLOGY; PATHOPHYSIOLOGY; RANDOMIZATION; SPATIAL MEMORY; SPRAGUE DAWLEY RAT; THALAMUS VENTRAL NUCLEUS;

ANIMALS; ANIMALS, NEWBORN; ATRACTYLOSIDE; CA3 REGION, HIPPOCAMPAL; CAROTID ARTERY, COMMON; CENTRAL NERVOUS SYSTEM AGENTS; CYCLOSPORINE; DISEASE MODELS, ANIMAL; HYPOXIA-ISCHEMIA, BRAIN; ISOFLURANE; MAZE LEARNING; MITOCHONDRIA; MITOCHONDRIAL MEMBRANE TRANSPORT PROTEINS; MOTOR ACTIVITY; NEUROPROTECTIVE AGENTS; RANDOM ALLOCATION; RATS, SPRAGUE-DAWLEY; SPATIAL MEMORY; VENTRAL THALAMIC NUCLEI;

EID: 84907701229     PISSN: 03064522     EISSN: 18737544     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2014.09.006     Document Type: Article

References (45)

1. Akhavan M.M., Foroutan T., Safari M., Sadighi-Moghaddam B., Emami-Abarghoie M., Rashidy-Pour A. Prenatal exposure to maternal voluntary exercise during pregnancy provides protection against mild chronic postnatal hypoxia in rat offspring. Pak J Pharm Sci 2012, 25(1):233-238.
2. Argaud L., Gateau-Roesch O., Raisky O., Loufouat J., Robert D., Ovize M. Postconditioning inhibits mitochondrial permeability transition. Circulation 2005, 111(2):194-197.
3. Bona E., Johansson B.B., Hagberg H. Sensorimotor function and neuron pathology five to six weeks after hypoxia-ischemia in seven-day-old rats. Pediatr Res 1997, 42:678-683.
4. Brosnan H., Bickler P.E. Xenon neurotoxicity in rat hippocampal slice cultures is similar to isoflurane and sevoflurane. Anesthesiology 2013, 119(2):335-344.
5. Bryce J., Boschi-Pinto C., Shibuya K., Black R.E. WHO estimates of the causes of death in children. Lancet 2005, 365(9465):1147-1152.
6. Christophe M., Nicolas S. Mitochondria: a target for neuroprotective interventions in cerebral ischemia-reperfusion. Curr Pharm Des 2006, 12(6):739-757.
7. Cooper D.J. Induced hypothermia for neonatal hypoxic-ischemic encephalopathy: pathophysiology, current treatment, and nursing considerations. Neonatal Netw 2011, 30(1):29-35.
8. Dixon C.E., Lyeth B.G., Povlishock J.T., Finding R.L., Hamm R.J., Marmarou A., et al. A fluid percussion model of experimental brain injury in the rat. J Neurosurg 1987, 67:110-119.
9. Dobbing J., Sands J. The brain growth spurt in various mammalian species. Early Hum Dev 1979, 3:79-84.
10. Fang J., Wu L., Chen L. Postconditioning attenuates cardiocyte ultrastructure injury and apoptosis by blocking mitochondrial permeability transition in rats. Acta Cardiol 2008, 63(3):377-387.
11. Feng J., Lucchinetti E., Ahuja P., Pasch T., Perriard J.C., Zauqq M. Isoflurane postconditioning prevents opening of the mitochondrial permeability transition pore through inhibition of glycogen synthase kinase 3beta. Anesthesiology 2005, 103:987-995.
12. Gross G.J., Hsu A., Pfeiffer A.W., Nithipatikom K. Roles of endothelial nitric oxide synthase (eNOS) and mitochondrial permeability transition pore (MPTP) in epoxyeicosatrienoic acid (EET)-induced cardioprotection against infarction in intact rat hearts. J Mol Cell Cardiol 2013, 59:20-29.
13. Hagberg H., Bona E., Gilland E., Puka-Sundvall M., et al. Hypoxia-ischaemia model in the 7-day-old rat: possibilities and shortcomings. Acta Paediatr Suppl 1997, 422(suppl. 2):85-88.
14. Handelmann G.E., Olton D.S. Spatial memory following damage to hippocampal CA3 pyramidal cells with kainic acid: impairment and recovery with preoperative training. Brain Res 1981, 217:41-58.
15. Kann O., kovacs R., Njunting M., Behren C.J., Otanal J., Lehmann T.N., et al. Metabolic dysfunction during neuronal activation in the vivo hippocampus from chronic epileptic rats and humans. Brain 2005, 128:2396-2407.
16. Kong F.J., Ma L.L., Hu W.W., Wang W.N., Lu H.S., Chen S.P. Fetal exposure to high isoflurane concentration induces postnatal memory and learning deficits in rats. Biochem Pharmacol 2012, 84(4):558-563.
17. Jiang C., Xia M., Wang M., Chen S. Dexmedetomidine preconditioning protects isolated rat hearts against ischemia/reperfusion injuries and its mechanism. Zhejiang Da Xue Xue Bao Yi Xue Ban 2013, 42(3):326-330.
18. Li Q., Guo H.C., Maslov L.N., Qiao X.W., Zhou J.J., Zhang Y. Mitochondrial permeability transition pore plays a role in the cardioprotection of CB2 receptor against ischemia-reperfusion injury. Can J Physiol Pharmacol 2014, 92(3):205-214.
19. Lynch J.K., Nelson K.B. Epidemiology of perinatal stroke. Curr Opin Pediatr 2001, 13(6):499-505.
20. Nuñez J.L., McCarthy M.M. Estradiol exacerbates hippocampal damage in a model of preterm infant brain injury. Endocrinology 2003, 144(6):2350-2359.
21. Puka-Sundvall M., Wallina C., Gilland E., Hallinb U., Wang X., Sandberg M. Impairment of mitochondrial respiration after cerebral hypoxia-ischemia in immature rats: relationship to activation of caspase-3 and neuronal injury. Dev Brain Res 2000, 125:43-50.
22. Mancuso C., Scapagini G., Curro D., Gluffrida Stella A.M., De Marco C., Butterfiled D.A., et al. Mitochondrial dysfunction, free radical generation and cellular stress response in neurodegenerative disorders. Front Biosci 2007, 12:1107-1123.
23. McDonald J.W., Johnston M.V. Physiological and pathophysiological roles of excitatory amino acids during central nervous system development. Brain Res Rev 1990, 15:41-70.
24. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. Neurosci Methods 1984, 11:47-60.
25. Osman M.M., Lulic D., Glover L., Stahl C.E., Lau T., van Loveren H. Cyclosporine-A as a neuroprotective agent against stroke: its translation from laboratory research to clinical application. Neuropeptides 2011, 45(6):359-368.
26. Otellin V.A., Khozhaï L.I., Vataeva L.A., Shishko T.T. The remote consequences of hypoxia influence in perinatal development period on structurally functional characteristics of the rat brain. Ross Fiziol Zh Im I M Sechenova 2011, 97(10):1092-1100.
27. Pagel P.S., Krolikowski J.G., Neff D.A., Weihrauch D., Beinenqraeber M., Kersten J.R., et al. Inhibition of glycogen synthase kinase enhances isoflurane-induced protection against myocardial infarction during early reperfusion in vivo. Anesth Analg 2006, 102:1348-1354.
28. Piot C., Croisille P., Staat P., Thibault H., Rioufol G., Mewton N. Effect of cyclosporine on reperfusion injury in acute myocardial infarction. N Engl J Med 2008, 359(5):473-481.
29. Rodriguez V.M., Carrizales L., Mendoza M.S., Fajardo O.R., Giordano M. Effects of sodium arsenite exposure on development and behavior in the rat. Neurotoxicol Teratol 2003, 24:743-750.
30. Rybnikova E., Glushchenko T., Tyulkova E., Baranova K., Samoilov M. Mild hypobaric hypoxia preconditioning up-regulates expression of transcription factors c-Fos and NGFI-A in rat neocortex and hippocampus. Neurosci Res 2009, 65(4):360-366.
31. Sanches E.F., Arteni N.S., Scherer E.B., Kolling J., Nicola F., Willborn S. Are the consequences of neonatal hypoxia-ischemia dependent on animals' sex and brain lateralization?. Brain Res 2013, 1507:105-114.
32. Sanches E.F., Arteni N.S., Nicola F., Boisserand L., Willborn S., Netto C.A. Early hypoxia-ischemia causes hemisphere and sex-dependent cognitive impairment and histological damage. Neuroscience 2013, 237:208-215.
33. Song R., Bian H., Huang X., Zhao K.S. Atractyloside induces low contractile reaction of arteriolar smooth muscle through mitochondrial damage. J Appl Toxicol 2012, 32:402-408.
34. Sullivan P.G., Rabchevsky A.G., Waldmeier P.C., Springer J.E. Mitochondrial permeability transition in CNS trauma: cause or effect of neuronal cell death?. J Neurosci Res 2005, 79(1-2):231-239.
35. Sun J., Luan Q., Dong H., Song W., Xie K., Hou L. Inhibition of mitochondrial permeability transition pore opening contributes to the neuroprotective effects of ischemic postconditioning in rats. Brain Res 2012, 1436:101-110.
36. +-ATPase activity is reduced in hippocampus of rats submitted to an experimental model of depression: effect of chronic lithium treatment and possible involvement in learning deficits. Neurobiol Learn Mem 2005, 84:102-110.
37. Weis S.N., Pettenuzzo L.F., Krolow R., Valentim L.M., Mota C.S., Dalmaz C. Neonatal hypoxia-ischemia induces sex-related changes in rat brain mitochondria. Mitochondrion 2012, 12(2):271-279.
38. Wu B., Yu Z., You S., Zheng Y., Liu J., Gao Y. Physiological disturbance may contribute to neurodegeneration induced by isoflurane or sevoflurane in 14day old rats. PLoS One 2014, 9(1):e84622.
39. + channel is mediated by inhibiting the mitochondrial permeability transition pore. Neurosci Lett 2006, 402:184-189.
40. Zhao X., Yang Z., Liang G., Zhen W., Peng Y., Donald J.J. Dual effects of isoflurane on proliferation, differentiation and survival in human neural progenitor cells. Anesthesiology 2013, 118(3):537-549.
41. Zhao P., Zuo Z. Isoflurane preconditioning induces neuroprotection that is inducible nitric oxide synthase-dependent in the neonatal rats. Anesthesiology 2004, 101:695-702.
42. Zhao P., Peng L., Li L., Xu X., Zuo Z. Isoflurane preconditioning improves long-term neurologic outcome after hypoxic-ischemic brain injury in neonatal rats. Anesthesiology 2007, 107:963-970.
43. Zhao P., Chai J., Long B. Protective effect of isoflurane postconditioning on reducing hypoxic-ischemic brain injury in neonatal rats. J China Med Univ 2012, 41:5-7.
44. Zhao P., Yu W., Long B., Chai J. The neuroprotective effects of isoflurane on neonatal hypoxic-ischemic brain injury in the rats in various time points. Chin J Anesthiol 2012, 32:979-981.
45. Zhu W., Wang L., Zhang L. Isoflurane preconditioning neuroprotection in experimental focal stroke is androgen-dependent in male mice. Neuroscience 2010, 169:758-769.