참고문헌
- Aronowski, J., and Hall, C.E. (2005). New horizons for primary intracerebral hemorrhage treatment: experience from preclinical studies. Neurol Res. 27, 268-279. https://doi.org/10.1179/016164105X25225
- Balami, J.S., and Buchan, A.M. (2012). Complications of intracerebral haemorrhage. Lancet Neurol. 11, 101-118. https://doi.org/10.1016/S1474-4422(11)70264-2
- Beckman, J.S., and Koppenol, W.H. (1996). Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. Am. J. Physiol. 271, C1424-1437. https://doi.org/10.1152/ajpcell.1996.271.5.C1424
- Bhasin, R.R., Xi, G., Hua, Y., Keep, R.F., and Hoff, J.T. (2002). Experimental intracerebral hemorrhage: effect of lysed erythrocytes on brain edema and blood-brain barrier permeability. Acta Neurochir. Suppl. 81, 249-251.
- Candelise, L., Gattinoni, M., Bersano, A., Micieli, G., Sterzi, R., and Morabito, A. (2007). Stroke-unit care for acute stroke patients: an observational follow-up study. Lancet 369, 299-305. https://doi.org/10.1016/S0140-6736(07)60152-4
- Chen, M., Li, X., Zhang, X., He, X., Lai, L., Liu, Y., Zhu, G., Li, W., Li, H., Fang, Q., Wang, Z., and Duan, C. (2015). The inhibitory effect of mesenchymal stem cell on blood-brain barrier disruption following intracerebral hemorrhage in rats: contribution of TSG-6. J. Neuroinflammation 12, 61. https://doi.org/10.1186/s12974-015-0284-x
- Di Nicola, M., Carlo-Stella, C., Magni, M., Milanesi, M., Longoni, P.D., Matteucci, P., Grisanti, S., and Gianni, A.M. (2002). Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli. Blood 99, 3838-3843. https://doi.org/10.1182/blood.V99.10.3838
- Ding, R., Chen, Y., Yang, S., Deng, X., Fu, Z., Feng, L., Cai, Y., Du M, Zhou, Y., and Tang, Y. (2014). Blood-brain barrier disruption induced by hemoglobin in vivo: Involvement of up-regulation of nitric oxide synthase and peroxynitrite formation. Brain Res. 1571, 25-38. https://doi.org/10.1016/j.brainres.2014.04.042
- Ding, R., Feng, L., He, L., Chen, Y., Wen, P., Fu, Z., Lin, C., Yang, S., Deng, X., Zeng, J., and Sun, G. (2015). Peroxynitrite decomposition catalyst prevents matrix metalloproteinase-9 activation and neurovascular injury after hemoglobin injection into the caudate nucleus of rats. Neuroscience 297, 182-193. https://doi.org/10.1016/j.neuroscience.2015.03.065
- Fatar, M., Stroick, M., Griebe, M., Marwedel, I., Kern, S., Bieback, K., Giesel, F.L., Zechmann, C., Kreisel, S., Vollmar, F., et al., (2008). Lipoaspirate-derived adult mesenchymal stem cells improve functional outcome during intracerebral hemorrhage by proliferation of endogenous progenitor cells stem cells in intracerebral hemorrhages. Neurosci Lett. 443, 174-178. https://doi.org/10.1016/j.neulet.2008.07.077
- Gong, C., Hoff, J.T., and Keep, R.F. (2000). Acute inflammatory reaction following experimental intracerebral hemorrhage in rat. Brain Res. 871, 57-65. https://doi.org/10.1016/S0006-8993(00)02427-6
- Hermann, A., Gastl, R., Liebau, S., Popa, M.O., Fiedler, J., Boehm, B.O., Maisel, M., Lerche, H., Schwarz, J., Brenner, R., et al. (2004). Efficient generation of neural stem cell-like cells from adult human bone marrow stromal cells. J. Cell Sci. 117, 4411-4422. https://doi.org/10.1242/jcs.01307
- Hirabayashi, H., Takizawa, S., Fukuyama, N., Nakazawa, H., and Shinohara, Y. (2000). Nitrotyrosine generation via inducible nitric oxide synthase in vascular wall in focal ischemia-reperfusion. Brain Res. 852, 319-325. https://doi.org/10.1016/S0006-8993(99)02117-4
- Hua, Y., Schallert, T., Keep, R.F., Wu, J., Hoff, J.T., and Xi, G. (2002). Behavioral tests after intracerebral hemorrhage in the rat. Stroke 33, 2478-2484. https://doi.org/10.1161/01.STR.0000032302.91894.0F
- Huang, F.P., Xi, G., Keep, R.F., Hua, Y., Nemoianu, A., and Hoff, J.T. (2002). Brain edema after experimental intracerebral hemorrhage: role of hemoglobin degradation products. J. Neurosurg. 96, 287-93. https://doi.org/10.3171/jns.2002.96.2.0287
- Jiang, Y., Jahagirdar, B.N., Reinhardt, R.L., Schwartz, R.E., Keene, C.D., Ortiz-Gonzalez, X.R., Reyes, M., Lenvik, T., Lund, T., Blackstad, M., et al. (2002). Pluripotency of mesenchymal stem cells derived from adult marrow. Nature 418, 41-49. https://doi.org/10.1038/nature00870
- Jin, S.Z., Meng, X.W., Sun, X., Han, M.Z., Liu, B.R., Wang, X.H., and Pei, F.H. (2011). Hepatocyte growth factor promotes liver regeneration induced by transfusion of bone marrow mononuclear cells in a murine acute liver failure model. J. Hepatobiliary Pancreat. Sci. 18, 397-405. https://doi.org/10.1007/s00534-010-0343-8
- Jung, K.H., Chu, K., Jeong, S.W., Han, S.Y., Lee, S.T., Kim, J.Y., Kim, M., and Roh, J.K. (2004). HMG-CoA reductase inhibitor, atorvastatin, promotes sensorimotor recovery, suppressing acute inflammatory reaction after experimental intracerebral hemorrhage. Stroke 35, 1744-9. https://doi.org/10.1161/01.STR.0000131270.45822.85
- Katsu, M., Niizuma, K., Yoshioka, H., Okami, N., Sakata, H., and Chan, P.H. (2010). Hemoglobin-induced oxidative stress contributes to matrix metalloproteinase activation and blood-brain barrier dysfunction in vivo. J. Cereb. Blood Flow Metab. 30, 1939-1950. https://doi.org/10.1038/jcbfm.2010.45
- Khan, M., Dhammu, T.S., Sakakima, H., Shunmugavel, A., Gilg, A.G., Singh, A.K., and Singh, I. (2012). The inhibitory effect of Snitrosoglutathione on blood-brain barrier disruption and peroxynitrite formation in a rat model of experimental stroke. J. Neurochem. 123 Suppl 2, 86-97. https://doi.org/10.1111/j.1471-4159.2012.07947.x
- Kim, D.W., Im, S.H., Kim, J.Y., Kim, D.E., Oh, G.T., and Jeong, S.W. (2009). Decreased brain edema after collagenase-induced intracerebral hemorrhage in mice lacking the inducible nitric oxide synthase gene. Laboratory investigation. J. Neurosurg. 111, 995-1000. https://doi.org/10.3171/2009.3.JNS081285
- Liang, H., Yin, Y., Lin, T., Guan, D., Ma, B., Li, C., Wang, Y., and Zhang, X. (2013). Transplantation of bone marrow stromal cells enhances nerve regeneration of the corticospinal tract and improves recovery of neurological functions in a collagenase-induced rat model of intracerebral hemorrhage. Mol. Cells 36, 17-24. https://doi.org/10.1007/s10059-013-2306-9
- Liao, W., Zhong, J., Yu, J., Xie, J., Liu, Y., Du L, Yang, S., Liu, P., Xu, J., Wang, J., Han, Z., and Han, Z.C. (2009). Therapeutic benefit of human umbilical cord derived mesenchymal stromal cells in intracerebral hemorrhage rat: implications of anti-inflammation and angiogenesis. Cell. Physiol. Biochem. 24, 307-316. https://doi.org/10.1159/000233255
- Masada, T., Hua, Y., Xi, G., Yang, G.Y., Hoff, J.T., and Keep, R.F. (2001). Attenuation of intracerebral hemorrhage and thrombininduced brain edema by overexpression of interleukin-1 receptor antagonist. J. Neurosurg. 95, 680-686. https://doi.org/10.3171/jns.2001.95.4.0680
- Meirelles, L.S., Fontes, A.M., Covas, D.T., and Caplan, A.I. (2009). Mechanisms involved in the therapeutic properties of mesenchymal stem cells. Cytokine Growth Factor Rev. 20, 419-427. https://doi.org/10.1016/j.cytogfr.2009.10.002
- Moncada, S., and Bolanos, J.P. (2006). Nitric oxide, cell bioenergetics and neurodegeneration. J. Neurochem. 97, 1676-1689. https://doi.org/10.1111/j.1471-4159.2006.03988.x
- Murphy, T.H., and Corbett, D. (2009). Plasticity during stroke recovery: from synapse to behaviour. Nat. Rev. Neurosci. 10, 861-872. https://doi.org/10.1038/nrn2735
- Nagai, A., Kim, W.K., Lee, H.J., Jeong, H.S., Kim, K.S., Hong, S.H., Park, I.H., and Kim, S.U. (2007). Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow. PLoS One 2, e1272. https://doi.org/10.1371/journal.pone.0001272
- Nogawa, S., Forster, C., Zhang, F., Nagayama, M., Ross, M.E., and Iadecola, C. (1998). Interaction between inducible nitric oxide synthase and cyclooxygenase-2 after cerebral ischemia. Proc. Natl. Acad. Sci. USA 95, 10966-10971. https://doi.org/10.1073/pnas.95.18.10966
- Ocarino, N.M., Bozzi, A., Pereira, R.D., Breyner, N.M., Silva, V.L., Castanheira, P., Goes, A.M., and Serakides, R., (2008). Behavior of mesenchymal stem cells stained with 4', 6-diamidino-2-phenylindole dihydrochloride (DAPI) in osteogenic and non osteogenic cultures. Biocell 32, 175-183.
- Pacher, P., Beckman, J.S., and Liaudet, L. (2007). Nitric oxide and peroxynitrite in health and disease. Physiol. Rev. 87, 315-424. https://doi.org/10.1152/physrev.00029.2006
- Pannu, R., and Singh, I., (2006). Pharmacological strategies for the regulation of inducible nitric oxide synthase: neurodegenerative versus neuroprotective mechanisms. Neurochem. Int. 49, 170-182. https://doi.org/10.1016/j.neuint.2006.04.010
- Pittenger, M.F., Mackay, A.M., Beck, S.C., Jaiswal, R.K., Douglas, R., Mosca, J.D., Moorman, M.A., Simonetti, D.W., Craig, S., and Marshak, D.R. (1999). Multilineage potential of adult human mesenchymal stem cells. Science 284, 143-147. https://doi.org/10.1126/science.284.5411.143
- Qureshi, A.I., Mendelow, A.D., and Hanley, D.F. (2009). Intracerebral haemorrhage. Lancet 373, 1632-1644. https://doi.org/10.1016/S0140-6736(09)60371-8
- Seyfried, D.M., Han, Y., Yang, D., Ding, J., Shen, L.H., Savant-Bhonsale, S., and Chopp, M. (2010). Localization of bone marrow stromal cells to the injury site after intracerebral hemorrhage in rats. J. Neurosurg. 112, 329-335. https://doi.org/10.3171/2009.2.JNS08907
- Steinberg, G.K., Kondziolka, D., Wechsler, L.R., Lunsford, L.D., Coburn, M.L., Billigen, J.B., Kim, A.S., Johnson, J.N., Bates, D., King, B., et al. (2016). Clinical outcomes of transplanted modified bone marrow-derived mesenchymal stem cells in stroke: a phase 1/2a study. Stroke 47, 1817-1824. https://doi.org/10.1161/STROKEAHA.116.012995
- Suofu, Y., Clark, J., Broderick, J., Wagner, K.R., Tomsick, T., Sa, Y., and Lu, A. (2010). Peroxynitrite decomposition catalyst prevents matrix metalloproteinase activation and neurovascular injury after prolonged cerebral ischemia in rats. J. Neurochem. 115, 1266-1276. https://doi.org/10.1111/j.1471-4159.2010.07026.x
- Tejima, E., Zhao, B.Q., Tsuji, K., Rosell, A., van Leyen, K., Gonzalez, R.G., Montaner, J., Wang, X., and Lo, E.H., (2007). Astrocytic induction of matrix metalloproteinase-9 and edema in brain hemorrhage. J. Cereb. Blood Flow Metab. 27, 460-468. https://doi.org/10.1038/sj.jcbfm.9600354
- Vaquero, J., Otero, L., Bonilla, C., Aguayo, C., Rico, M.A., Rodriguez, A., and Zurita, M. (2013). Cell therapy with bone marrow stromal cells after intracerebral hemorrhage: impact of platelet-rich plasma scaffolds. Cytotherapy 15, 33-43. https://doi.org/10.1016/j.jcyt.2012.10.005
- Virag, L., Szabo, E., Gergely, P., and Szabo, C. (2003). Peroxynitriteinduced cytotoxicity: mechanism and opportunities for intervention. Toxicol. Lett. 140-141, 113-124. https://doi.org/10.1016/S0378-4274(02)00508-8
- Wang, J., and Dore, S. (2008). Heme oxygenase 2 deficiency increases brain swelling and inflammation after intracerebral hemorrhage. Neuroscience 155, 1133-1141. https://doi.org/10.1016/j.neuroscience.2008.07.004
- Wang, J., Fields, J., Zhao, C., Langer, J., Thimmulappa, R.K., Kensler, T.W., Yamamoto, M., Biswal, S., and Dore, S. (2007). Role of Nrf2 in protection against intracerebral hemorrhage injury in mice. Free Radic. Biol. Med. 43, 408-414. https://doi.org/10.1016/j.freeradbiomed.2007.04.020
- Wang, S.P., Wang, Z.H., Peng, D.Y., Li, S.M., Wang, H., and Wang, X.H. (2012). Therapeutic effect of mesenchymal stem cells in rats with intracerebral hemorrhage: reduced apoptosis and enhanced neuroprotection. Mol. Med. Rep. 6, 848-854. https://doi.org/10.3892/mmr.2012.997
- Wu, B., Ma, Q., Suzuki, H., Chen, C., Liu, W., Tang, J., and Zhang, J. (2011). Recombinant osteopontin attenuates brain injury after intracerebral hemorrhage in mice. Neurocrit. Care 14, 109-117. https://doi.org/10.1007/s12028-010-9372-z
- Xi, G., Keep, R.F., and Hoff, J.T. (1998). Erythrocytes and delayed brain edema formation following intracerebral hemorrhage in rats. J. Neurosurg. 89, 991-6. https://doi.org/10.3171/jns.1998.89.6.0991
- Xi, G., Hua, Y., Bhasin, R.R., Ennis, S.R., Keep, R.F., and Hoff, J.T. (2001). Mechanisms of edema formation after intracerebral hemorrhage: effects of extravasated red blood cells on blood flow and blood-brain barrier integrity. Stroke 32, 2932-2938. https://doi.org/10.1161/hs1201.099820
- Yan, K., Zhang, R., Sun, C., Chen, L., Li, P., Liu, Y., Peng, L., Sun, H., Qin, K., Chen, F., et al. (2013). Bone marrow-derived mesenchymal stem cells maintain the resting phenotype of microglia and inhibit microglial activation. PLoS One 8, e84116. https://doi.org/10.1371/journal.pone.0084116
- Yang, S., Chen, Y., Deng, X., Jiang, W., Li, B., Fu, Z., Du, M., and Ding, R. (2013). Hemoglobin-induced nitric oxide synthase overexpression and nitric oxide production contribute to blood-brain barrier disruption in the rat. J. Mol. Neurosci. 51, 352-363. https://doi.org/10.1007/s12031-013-9990-y
- Zhang, L., Schallert, T., Zhang, Z.G., Jiang, Q., Arniego, P., Li, Q., Lu, M., and Chopp, M. (2002). A test for detecting long-term sensorimotor dysfunction in the mouse after focal cerebral ischemia. J. Neurosci. Methods 117, 207-214. https://doi.org/10.1016/S0165-0270(02)00114-0
- Zhang, R., Liu, Y., Yan, K., Chen, L., Chen, X.R., Li, P., Chen, F.F., and Jiang, X.D. (2013). Anti-inflammatory and immunomodulatory mechanisms of mesenchymal stem cell transplantation in experimental traumatic brain injury. J. Neuroinflammation 10, 106.
- Zhao, X., Zhang, Y., Strong, R., Zhang, J., Grotta, J.C., and Aronowski, J. (2007). Distinct patterns of intracerebral hemorrhageinduced alterations in NF-kappaB subunit, iNOS, and COX-2 expression. J. Neurochem. 101, 652-663.
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