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Volumn 110, Issue 3, 2005, Pages 232-238

Redox metals and oxidative abnormalities in human prion diseases

Author keywords

Creutzfeld Jakob disease; Gerstmann Straussler Scheinker syndrome; Oxidative damage; Prion; Redox metals

Indexed keywords

8 HYDROXYGUANINE; AMYLOID BETA PROTEIN; HEME OXYGENASE 1; INDUCIBLE NITRIC OXIDE SYNTHASE; LIPID; METAL DERIVATIVE; PRION PROTEIN;

EID: 26444549058     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-005-1034-4     Document Type: Article
Times cited : (55)

References (42)
  • 6
    • 0034110873 scopus 로고    scopus 로고
    • Cerebral amyloidosis in prion diseases
    • 10842694
    • DeArmond SJ (2000) Cerebral amyloidosis in prion diseases. Amyloid 7:3-6 10842694
    • (2000) Amyloid , vol.7 , pp. 3-6
    • DeArmond, S.J.1
  • 7
    • 13844292518 scopus 로고    scopus 로고
    • Changed iron regulation in scrapie-infected neuroblastoma cells
    • 10.1016/j.molbrainres.2004.10.018
    • Fernaeus S, Halldin J, Bedecs K, Land T (2005) Changed iron regulation in scrapie-infected neuroblastoma cells. Brain Res Mol Brain Res 133:266-273 10.1016/j.molbrainres.2004.10.018
    • (2005) Brain Res. Mol. Brain Res. , vol.133 , pp. 266-273
    • Fernaeus, S.1    Halldin, J.2    Bedecs, K.3    Land, T.4
  • 8
    • 0033002350 scopus 로고    scopus 로고
    • Nuclear DNA fragmentation in Creutzfeldt-Jakob disease: Does a mere positive in situ nuclear end-labeling indicate apoptosis?
    • 9930889
    • Ferrer I (1999) Nuclear DNA fragmentation in Creutzfeldt-Jakob disease: does a mere positive in situ nuclear end-labeling indicate apoptosis? Acta Neuropathol 97:5-12 9930889
    • (1999) Acta Neuropathol. , vol.97 , pp. 5-12
    • Ferrer, I.1
  • 9
    • 0141514771 scopus 로고    scopus 로고
    • Sporadic and familial CJD: Classification and characterisation
    • 10.1093/bmb/66.1.213
    • Gambetti P, Kong Q, Zou W, Parchi P, Chen SG (2003) Sporadic and familial CJD: Classification and characterisation. Br Med Bull 66:213-239 10.1093/bmb/66.1.213
    • (2003) Br. Med. Bull. , vol.66 , pp. 213-239
    • Gambetti, P.1    Kong, Q.2    Zou, W.3    Parchi, P.4    Chen, S.G.5
  • 12
    • 0032726882 scopus 로고    scopus 로고
    • Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases
    • 10550300
    • Guentchev M, Wanschitz J, Voigtlander T, Flicker H, Budka H (1999) Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases. Am J Pathol 155:1453-1457 10550300
    • (1999) Am. J. Pathol. , vol.155 , pp. 1453-1457
    • Guentchev, M.1    Wanschitz, J.2    Voigtlander, T.3    Flicker, H.4    Budka, H.5
  • 15
    • 0842332840 scopus 로고    scopus 로고
    • Silent prions lying in wait: A two-hit model of prion/amyloid formation and infection
    • 10.1016/j.jmb.2003.12.004
    • Hall D, Edskes H (2004) Silent prions lying in wait: A two-hit model of prion/amyloid formation and infection. J Mol Biol 336:775-786 10.1016/ j.jmb.2003.12.004
    • (2004) J. Mol. Biol. , vol.336 , pp. 775-786
    • Hall, D.1    Edskes, H.2
  • 18
    • 0345621492 scopus 로고    scopus 로고
    • Pathology of variant Creutzfeldt-Jakob disease
    • Ironside JW (2000) Pathology of variant Creutzfeldt-Jakob disease. Arch Virol Suppl (16):143-151
    • (2000) Arch. Virol. Suppl. , Issue.16 , pp. 143-151
    • Ironside, J.W.1
  • 21
    • 17144456296 scopus 로고    scopus 로고
    • Diagnosis of prion diseases
    • 10.1093/bmb/66.1.267
    • Kubler E, Oesch B, Raeber AJ (2003) Diagnosis of prion diseases. Br Med Bull 66:267-279 10.1093/bmb/66.1.267
    • (2003) Br. Med. Bull. , vol.66 , pp. 267-279
    • Kubler, E.1    Oesch, B.2    Raeber, A.J.3
  • 22
    • 0030908160 scopus 로고    scopus 로고
    • Internucleosomal breakdown of the DNA of brain cortex in human spongiform encephalopathy
    • 10.1016/S0197-0186(96)00153-2
    • Lucas M, Izquierdo G, Munoz C, Solano F (1997) Internucleosomal breakdown of the DNA of brain cortex in human spongiform encephalopathy. Neurochem Int 31:241-244 10.1016/S0197-0186(96)00153-2
    • (1997) Neurochem. Int. , vol.31 , pp. 241-244
    • Lucas, M.1    Izquierdo, G.2    Munoz, C.3    Solano, F.4
  • 23
    • 10644241804 scopus 로고    scopus 로고
    • Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: Implications for species barrier in prion uptake from the intestine
    • 10.1523/JNEUROSCI.2864-04.2004
    • Mishra RS, Basu S, Gu Y, Luo X, Zou WQ, Mishra R, Li R, Chen SG, Gambetti P, Fujioka H, Singh N (2004) Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. J Neurosci 24:11280-11290 10.1523/JNEUROSCI.2864-04.2004
    • (2004) J. Neurosci. , vol.24 , pp. 11280-11290
    • Mishra, R.S.1    Basu, S.2    Gu, Y.3    Luo, X.4    Zou, W.Q.5    Mishra, R.6    Li, R.7    Chen, S.G.8    Gambetti, P.9    Fujioka, H.10    Singh, N.11
  • 24
  • 26
    • 0036113819 scopus 로고    scopus 로고
    • The role of iron and copper in the aetiology of neurodegenerative disorders: Therapeutic implications
    • 11994023
    • Perry G, Sayre LM, Atwood CS, Castellani RJ, Cash AD, Rottkamp CA, Smith MA (2002) The role of iron and copper in the aetiology of neurodegenerative disorders: Therapeutic implications. CNS Drugs 16:339-352 11994023
    • (2002) CNS Drugs , vol.16 , pp. 339-352
    • Perry, G.1    Sayre, L.M.2    Atwood, C.S.3    Castellani, R.J.4    Cash, A.D.5    Rottkamp, C.A.6    Smith, M.A.7
  • 28
    • 0032506187 scopus 로고    scopus 로고
    • Prions
    • 10.1073/pnas.95.23.13363
    • Prusiner SB (1998) Prions. Proc Natl Acad Sci USA 95:13363-13383 10.1073/ pnas.95.23.13363
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 13363-13383
    • Prusiner, S.B.1
  • 29
    • 0037715143 scopus 로고    scopus 로고
    • Expression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper delivery
    • 10.1074/jbc.M211830200
    • Rachidi W, Vilette D, Guiraud P, Arlotto M, Riondel J, Laude H, Lehmann S, Favier A (2003) Expression of prion protein increases cellular copper binding and antioxidant enzyme activities but not copper delivery. J Biol Chem 278:9064-9072 10.1074/jbc.M211830200
    • (2003) J. Biol. Chem. , vol.278 , pp. 9064-9072
    • Rachidi, W.1    Vilette, D.2    Guiraud, P.3    Arlotto, M.4    Riondel, J.5    Laude, H.6    Lehmann, S.7    Favier, A.8
  • 30
    • 0346729697 scopus 로고    scopus 로고
    • Neuroprotective functions of prion protein
    • 10.1002/jnr.10864
    • Roucou X, Gains M, LeBlanc AC (2004) Neuroprotective functions of prion protein. J Neurosci Res 75:153-161 10.1002/jnr.10864
    • (2004) J. Neurosci. Res. , vol.75 , pp. 153-161
    • Roucou, X.1    Gains, M.2    LeBlanc, A.C.3
  • 31
    • 0030989545 scopus 로고    scopus 로고
    • 4-Hydroxynonenal-derived advanced lipid peroxidation end products are increased in Alzheimer's disease
    • 9109537
    • Sayre LM, Zelasko DA, Harris PL, Perry G, Salomon RG, Smith MA (1997) 4-Hydroxynonenal-derived advanced lipid peroxidation end products are increased in Alzheimer's disease. J Neurochem 68:2092-2097 9109537
    • (1997) J. Neurochem. , vol.68 , pp. 2092-2097
    • Sayre, L.M.1    Zelasko, D.A.2    Harris, P.L.3    Perry, G.4    Salomon, R.G.5    Smith, M.A.6
  • 32
    • 0032847544 scopus 로고    scopus 로고
    • In situ methods for detection and localization of markers of oxidative stress: Application in neurodegenerative disorders
    • 10507022
    • Sayre LM, Perry G, Smith MA (1999) In situ methods for detection and localization of markers of oxidative stress: Application in neurodegenerative disorders. Methods Enzymol 309:133-152 10507022
    • (1999) Methods Enzymol. , vol.309 , pp. 133-152
    • Sayre, L.M.1    Perry, G.2    Smith, M.A.3
  • 36
    • 0030885482 scopus 로고    scopus 로고
    • Iron accumulation in Alzheimer disease is a source of redox-generated free radicals
    • 10.1073/pnas.94.18.9866
    • Smith MA, Harris PL, Sayre LM, Perry G (1997) Iron accumulation in Alzheimer disease is a source of redox-generated free radicals. Proc Natl Acad Sci USA 94:9866-9868 10.1073/pnas.94.18.9866
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 9866-9868
    • Smith, M.A.1    Harris, P.L.2    Sayre, L.M.3    Perry, G.4
  • 37
    • 0037083888 scopus 로고    scopus 로고
    • Metal imbalance and compromised antioxidant function are early changes in prion disease
    • 11829763
    • Thackray AM, Knight R, Haswell SJ, Bujdoso R, Brown DR (2002) Metal imbalance and compromised antioxidant function are early changes in prion disease. Biochem J 362:253-258 11829763
    • (2002) Biochem. J. , vol.362 , pp. 253-258
    • Thackray, A.M.1    Knight, R.2    Haswell, S.J.3    Bujdoso, R.4    Brown, D.R.5
  • 41
    • 0034797352 scopus 로고    scopus 로고
    • Differential activation of neuronal ERK, JNK/SAPK and p38 in Alzheimer disease: The 'two hit' hypothesis
    • 10.1016/S0047-6374(01)00342-6
    • Zhu X, Castellani RJ, Takeda A, Nunomura A, Atwood CS, Perry G, Smith MA (2001) Differential activation of neuronal ERK, JNK/SAPK and p38 in Alzheimer disease: The 'two hit' hypothesis. Mech Ageing Dev 123:39-46 10.1016/S0047-6374(01)00342-6
    • (2001) Mech. Ageing Dev. , vol.123 , pp. 39-46
    • Zhu, X.1    Castellani, R.J.2    Takeda, A.3    Nunomura, A.4    Atwood, C.S.5    Perry, G.6    Smith, M.A.7
  • 42
    • 1642358352 scopus 로고    scopus 로고
    • Alzheimer's disease: The two-hit hypothesis
    • 10.1016/S1474-4422(04)00707-0
    • Zhu X, Raina AK, Perry G, Smith MA (2004) Alzheimer's disease: The two-hit hypothesis. Lancet Neurol 3:219-226 10.1016/S1474-4422(04)00707-0
    • (2004) Lancet Neurol. , vol.3 , pp. 219-226
    • Zhu, X.1    Raina, A.K.2    Perry, G.3    Smith, M.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.