참고문헌
- Lajtha A. Handbook of neurochemistry. 2nd, Vol 3. Plenum Press 1985:501-3
- Oja SS, Kontro P, Lahdesmaki P. Amino acids as inhibitory neurotransmitters. Prog Pharmaol 1997;1:1-119
- Shuaib A. The role of taurine in cerebral ischemia: studies in transient forebrain ischemia and embolic focal ischemia in rodents. Adv Exp Med Biol 2003;526:421-31
- French ED, Vezzani A, Whetsell WO Jr, Schwarcz R. Anti- excitotoxic actions of taurine in the rat hippocampus studied in vivo and in vitro. Adv Exp Med Biol 1986;203:349-62
- Trenkner E. The role of taurine and glutamate during early postnatal cerebellar development of normal and weaver mutant mice. Adv Exp Med Biol 1990;268:239-44
- Schurr A, Tseng MT, West CA, Rigor BM. Taurine improves the recovery of neuronal function following cerebral hypoxia: an in vitro study. Life Sci 1987;40:2059-66 https://doi.org/10.1016/0024-3205(87)90098-1
-
Lehmann A, Hagberg H, Nystr
$\ddot{o}$ m B, Sandberg M, Hamberger A. In vivo regulation of extracellular taurine and other neuroactive amino acids in the rabbit hippocampus. Prog Clin Biol Res 1985;179:289-311 - Sun GC, Wang D, Tao C. Effects of taurine on the levels of prostaglandins in brain tissue during cerebral ischemia/reperfusion in rats. Chinese Pharmaceutical J 2000;35:815-7
- Watson RW, Redmond HP, Wang JH, Bouchier-Hayes D. Mechanisms involved in sodium arsenite-induced apoptosis of human neutrophils. J Leukoc Biol 1996;60:625-32 https://doi.org/10.1002/jlb.60.5.625
- Wang JH, Redmond HP, Watson RW, Condron C, Bouchier- Hayes D. The beneficial effect of taurine on the prevention of human endothelial cell death. Shock 1996;6:331-8 https://doi.org/10.1097/00024382-199611000-00006
- Refik Mas M, Comert B, Oncu K, Vural SA, Akay C, Tasci I, et al. The effect of taurine treatment on oxidative stress in experimental liver fibrosis. Hepatol Res 2004;28:207-15 https://doi.org/10.1016/j.hepres.2003.11.012
- Dell'Anna ME, Calzolari S, Molinari M, Iuvone L, Calimici R. Neonatal anoxia induces transitory hyperactivity, permanent spatial memory deficits and CA1 cell density reduction in developing rats. Behav Brain Res 1991;45:125-34 https://doi.org/10.1016/S0166-4328(05)80078-6
- Ferriero DM, Holtzman DM, Black SM. Neonatal mice lacking neuronal nitric oxide synthase are less vulnerable to hypoxic-ischemic injury. Neurobiol Dis 1996;3:64-71 https://doi.org/10.1006/nbdi.1996.0006
- Levine S. Anoxic-ischemic encephalopathy in rats. Am J Pathol 1960;36:1-17
- Pulsinelli WA, Brierley JB, Plum F. Temporal profile of neuronal damage in a model of transient forebrain ischemia. Ann Neurol 1982;11:491-8 https://doi.org/10.1002/ana.410110509
- Rice JE 3rd, Vannucci RC, Brierley JB. The influence of immaturity on hypoxic-ischemic brain damage in the rat. Ann Neurol 1981;9:131-41 https://doi.org/10.1002/ana.410090206
- Alimi CR, Yundt KD, Wheeler ME, Rosenbaum J, Altman DI, Powers WJ. Neonatal cerebral blood flow (PET) and childhood relational memory performance. Soc Neurosci Abstr 1997;23:490
- Rosenbaum JL, Almli CR, Yundt KD, Altman DI, Powers WJ. Higher neonatal cerebral blood flow correlates with worse childhood neurological outcome. Neurology 1997;49:1035-41 https://doi.org/10.1212/WNL.49.4.1035
- Vanucci RC. Experimental biology of cerebral hypoxia-ischemia: Relation to perinatal brain damage. Pediatr Res 1990; 27:317-26 https://doi.org/10.1203/00006450-199004000-00001
- Vargha-Khadem F, Gadian DG, Watkins KE, Connelly W, Van Paesschen W, Mishkin M. Differential effects of early hippocampal pathology on episodic and semantic memory. Science 1997;277:376-80 https://doi.org/10.1126/science.277.5324.376
- Volpe JJ. Neurology of the Newborn, 3rd ed. Philadelphia: WB Saunders, 1995
- Ashwal S, Pearce WJ. Animal models of neonatal stroke. Curr Opin Pediatr 2001;13:506-16 https://doi.org/10.1097/00008480-200112000-00003
- Brewer GJ. Isolation and culture of adult rat hippocampal neurons. J Neurosci Methods 1997;71:143-55 https://doi.org/10.1016/S0165-0270(96)00136-7
- Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 1983;65:55-63 https://doi.org/10.1016/0022-1759(83)90303-4
- Franconi F, Bennardini F, Mattana A, Miceli M, Ciuti M, Mian M, et al. Plasma and platelet taurine are reduced in subjects with insulin-dependent diabetes mellitus: effects of taurine supplementation. Am J Clin Nutr 1995;61:1115-9 https://doi.org/10.1093/ajcn/61.5.1115
- Bouckenooghe T, Remacle C, Reusens B. Is taurine a functional nutrient? Curr Opin Clin Nutr Metab Care 2006;9:728- 33 https://doi.org/10.1097/01.mco.0000247469.26414.55
- Stapleton PP, O'Flaherty L, Redmond HP, Bouchier-Hayes DJ. Host defense-a role for the amino acid taurine? JPEN J Parenter Enteral Nutr 1998;22:42-8 https://doi.org/10.1177/014860719802200142
- Huxtable RJ. Physiological actions of taurine. Physiol Rev 1992;72:101-63 https://doi.org/10.1152/physrev.1992.72.1.101
- Northington FJ, Ferriero DM, Martin LJ. Neurodegeneration in the thalamus following neonatal hypoxia-ischemia is programmed cell death. Dev Neurosci 2001;23:186-91 https://doi.org/10.1159/000046141
- Fariello RG, Golden GT, Pisa M. Homotaurine (3 aminopropanesulfonic acid; 3APS) protects from the convulsant and cytotoxic effect of systemically administered kainic acid. Neurology 1982;32:241-5 https://doi.org/10.1212/WNL.32.3.241
- Matsumoto K, Ueda S, Hashimoto T, Kuriyama K. Ischemic neuronal injury in the rat hippocampus following transient forebrain ischemia: evaluation using in vivo microdialysis. Brain Res 1991;543:236-42 https://doi.org/10.1016/0006-8993(91)90033-R
- Boldyrev AA, Johnson P, Wei Y, Tan Y, Carpenter DO. Carnosine and taurine protect rat cerebellar granular cells from free radical damage. Neurosci Lett 1999;263:169-72 https://doi.org/10.1016/S0304-3940(99)00150-0
- Uchiyama-Tsuyuki Y, Araki H, Yae T, Otomo S. Changes in the extracellular concentrations of amino acids in the rat striatum during transient focal cerebral ischemia. J Neurochem 1994;62:1074-8 https://doi.org/10.1046/j.1471-4159.1994.62031074.x
- Matsumoto K, Lo EH, Pierce AR, Halpern EF, Newcomb R. Secondary elevation of extracellular neurotransmitter amino acids in the reperfusion phase following focal cerebral ischemia. J Cereb Blood Flow Metab 1996;16:114-24 https://doi.org/10.1097/00004647-199601000-00014
- Simpson RK Jr, Robertson CS, Goodman JC. Spinal cord ischemia-induced elevation of amino acids: extracellular measurement with microdialysis. Neurochem Res 1990;15:635-9 https://doi.org/10.1007/BF00973755
- Lekieffre D, Callebert J, Plotkine M, Boulu RG. Concomitant increases in the extracellular concentrations of excitatory and inhibitory amino acids in the rat hippocampus during forebrain ischemia. Neurosci Lett 1992;137:78-82 https://doi.org/10.1016/0304-3940(92)90303-O
- Ooboshi H, Sadoshima S, Yao H, Ibayashi S, Matsumoto T, Uchimura H, et al. Ischemia-induced release of amino acids in the hippocampus of aged hypertensive rats. J Cereb Blood Flow Metab 1995;15:227-34 https://doi.org/10.1038/jcbfm.1995.28
- Shimada N, Graf R, Rosner G, Heiss WD. Ischemia-induced accumulation of extracellular amino acids in cerebral cortex, white matter, and cerebrospinal fluid. J Neurochem 1993;60: 66-71 https://doi.org/10.1111/j.1471-4159.1993.tb05823.x
- Mankovskaya IN, Serebrovskaya TV, Swanson RJ, Vavilova GL, Kharlamova ON. Mechanisms of taurine antihypoxic and antioxidant action. High Alt Med Biol 2000;1:105-10 https://doi.org/10.1089/15270290050074242
- Nakajima W, Ishida A, Lange MS, Gabrielson KL, Wilson MA, Martin LJ, et al. Apoptosis has a prolonged role in the neurodegeneration after hypoxic ischemia in the newborn rat. J Neurosci 2000;20:7994-8004
피인용 문헌
- Reversal of the Caspase-Dependent Apoptotic Cytotoxicity Pathway by Taurine from Lycium barbarum (Goji Berry) in Human Retinal Pigment Epithelial Cells: Potential Benefit in Diabetic Retinopathy vol.2012, pp.None, 2012, https://doi.org/10.1155/2012/323784
- Effects of Dizocilpine (MK-801) via Up-modulation of N-methyl-D-aspartate (NMDA) Receptors on Hypoxic-Ischemic Brain Injury in Neonatal Rats vol.25, pp.3, 2009, https://doi.org/10.14734/kjp.2014.25.3.166
- Chinese herbal drugs for the treatment of diabetic retinopathy vol.69, pp.3, 2017, https://doi.org/10.1111/jphp.12683
- Expedition into Taurine Biology: Structural Insights and Therapeutic Perspective of Taurine in Neurodegenerative Diseases vol.10, pp.6, 2009, https://doi.org/10.3390/biom10060863