메뉴 건너뛰기




Volumn 220, Issue 2, 2009, Pages 219-223

Oxidative stress sensitivity in ALS muscle cells

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENIN; ANTIOXIDANT; COPPER ZINC SUPEROXIDE DISMUTASE; DYNACTIN; MITOCHONDRIAL DNA; PARAQUAT; PROTEIN NOGO A; RNA BINDING PROTEIN; SYNAPTOBREVIN; TAR DNA BINDING PROTEIN;

EID: 71549164101     PISSN: 00144886     EISSN: 10902430     Source Type: Journal    
DOI: 10.1016/j.expneurol.2009.08.023     Document Type: Note
Times cited : (8)

References (57)
  • 1
    • 0013911740 scopus 로고
    • Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis
    • Afifi A.K., Aleu F.P., Goodgold J., and MacKay B. Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology 16 (1966) 475-481
    • (1966) Neurology , vol.16 , pp. 475-481
    • Afifi, A.K.1    Aleu, F.P.2    Goodgold, J.3    MacKay, B.4
  • 2
    • 33646452761 scopus 로고    scopus 로고
    • Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis models
    • Bergemalm D., Jonsson P.A., Graffmo K.S., Andersen P.M., Brannstrom T., Rehnmark A., and Marklund S.L. Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis models. J. Neurosci. 26 (2006) 4147-4154
    • (2006) J. Neurosci. , vol.26 , pp. 4147-4154
    • Bergemalm, D.1    Jonsson, P.A.2    Graffmo, K.S.3    Andersen, P.M.4    Brannstrom, T.5    Rehnmark, A.6    Marklund, S.L.7
  • 3
    • 33749056809 scopus 로고    scopus 로고
    • ALS: a disease of motor neurons and their nonneuronal neighbors
    • Boillee S., Vande Velde C., and Cleveland D.W. ALS: a disease of motor neurons and their nonneuronal neighbors. Neuron 52 (2006) 39-59
    • (2006) Neuron , vol.52 , pp. 39-59
    • Boillee, S.1    Vande Velde, C.2    Cleveland, D.W.3
  • 6
    • 67349115326 scopus 로고    scopus 로고
    • Increased sensitivity of myoblasts to oxidative stress in amyotrophic lateral sclerosis peripheral tissues
    • Bradley L.J., Taanman J.W., Kallis C., and Orrell R.W. Increased sensitivity of myoblasts to oxidative stress in amyotrophic lateral sclerosis peripheral tissues. Exp. Neurol. 218 (2009) 92-97
    • (2009) Exp. Neurol. , vol.218 , pp. 92-97
    • Bradley, L.J.1    Taanman, J.W.2    Kallis, C.3    Orrell, R.W.4
  • 11
    • 0029809528 scopus 로고    scopus 로고
    • Amyotrophic lateral sclerosis: oxidative energy metabolism and calcium homeostasis in peripheral blood lymphocytes
    • Curti D., Malaspina A., Facchetti G., Camana C., Mazzini L., Tosca P., Zerbi F., and Ceroni M. Amyotrophic lateral sclerosis: oxidative energy metabolism and calcium homeostasis in peripheral blood lymphocytes. Neurology 47 (1996) 1060-1064
    • (1996) Neurology , vol.47 , pp. 1060-1064
    • Curti, D.1    Malaspina, A.2    Facchetti, G.3    Camana, C.4    Mazzini, L.5    Tosca, P.6    Zerbi, F.7    Ceroni, M.8
  • 13
    • 34147131311 scopus 로고    scopus 로고
    • Inhibition of p38 mitogen activated protein kinase activation and mutant SOD1(G93A)-induced motor neuron death
    • Dewil M., dela Cruz V.F., Van Den Bosch L., and Robberecht W. Inhibition of p38 mitogen activated protein kinase activation and mutant SOD1(G93A)-induced motor neuron death. Neurobiol. Dis. 26 (2007) 332-341
    • (2007) Neurobiol. Dis. , vol.26 , pp. 332-341
    • Dewil, M.1    dela Cruz, V.F.2    Van Den Bosch, L.3    Robberecht, W.4
  • 16
    • 65949094823 scopus 로고    scopus 로고
    • Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models
    • Dupuis L., and Loeffler J.P. Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models. Curr. Opin. Pharmacol. 9 (2009) 341-346
    • (2009) Curr. Opin. Pharmacol. , vol.9 , pp. 341-346
    • Dupuis, L.1    Loeffler, J.P.2
  • 18
    • 0345426778 scopus 로고    scopus 로고
    • Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis
    • Dupuis L., di Scala F., Rene F., de Tapia M., Oudart H., Pradat P.F., Meininger V., and Loeffler J.P. Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis. FASEB J. 17 (2003) 2091-2093
    • (2003) FASEB J. , vol.17 , pp. 2091-2093
    • Dupuis, L.1    di Scala, F.2    Rene, F.3    de Tapia, M.4    Oudart, H.5    Pradat, P.F.6    Meininger, V.7    Loeffler, J.P.8
  • 20
    • 3343020674 scopus 로고    scopus 로고
    • Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model
    • Dupuis L., Oudart H., Rene F., Gonzalez de Aguilar J.L., and Loeffler J.P. Evidence for defective energy homeostasis in amyotrophic lateral sclerosis: benefit of a high-energy diet in a transgenic mouse model. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 11159-11164
    • (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , pp. 11159-11164
    • Dupuis, L.1    Oudart, H.2    Rene, F.3    Gonzalez de Aguilar, J.L.4    Loeffler, J.P.5
  • 23
    • 32644434546 scopus 로고    scopus 로고
    • Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: a temporal study in man
    • Echaniz-Laguna A., Zoll J., Ponsot E., N'Guessan B., Tranchant C., Loeffler J.P., and Lampert E. Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: a temporal study in man. Exp. Neurol. 198 (2006) 25-30
    • (2006) Exp. Neurol. , vol.198 , pp. 25-30
    • Echaniz-Laguna, A.1    Zoll, J.2    Ponsot, E.3    N'Guessan, B.4    Tranchant, C.5    Loeffler, J.P.6    Lampert, E.7
  • 24
    • 63849184477 scopus 로고    scopus 로고
    • Crosstalk signaling between mitochondrial Ca2+ and ROS
    • Feissner R.F., Skalska J., Gaum W.E., and Sheu S.S. Crosstalk signaling between mitochondrial Ca2+ and ROS. Front. Biosci. 14 (2009) 1197-1218
    • (2009) Front. Biosci. , vol.14 , pp. 1197-1218
    • Feissner, R.F.1    Skalska, J.2    Gaum, W.E.3    Sheu, S.S.4
  • 25
    • 0036992290 scopus 로고    scopus 로고
    • Mitochondriopathy as a differential diagnosis of amyotrophic lateral sclerosis
    • Finsterer J. Mitochondriopathy as a differential diagnosis of amyotrophic lateral sclerosis. Amyotroph. Lateral Scler. Other Motor Neuron. Disord. 3 (2002) 219-224
    • (2002) Amyotroph. Lateral Scler. Other Motor Neuron. Disord. , vol.3 , pp. 219-224
    • Finsterer, J.1
  • 26
    • 0037254203 scopus 로고    scopus 로고
    • Mitochondriopathy mimicking amyotrophic lateral sclerosis
    • Finsterer J. Mitochondriopathy mimicking amyotrophic lateral sclerosis. Neurologist 9 (2003) 45-48
    • (2003) Neurologist , vol.9 , pp. 45-48
    • Finsterer, J.1
  • 27
    • 16244363663 scopus 로고    scopus 로고
    • Lactate stress testing in sporadic amyotrophic lateral sclerosis
    • Finsterer J. Lactate stress testing in sporadic amyotrophic lateral sclerosis. Int. J. Neurosci. 115 (2005) 583-591
    • (2005) Int. J. Neurosci. , vol.115 , pp. 583-591
    • Finsterer, J.1
  • 31
    • 33847309054 scopus 로고    scopus 로고
    • A prospective study to evaluate the impact of 31P-MRS to determinate mitochondrial dysfunction in skeletal muscle of ALS patients
    • Grehl T., Fischer S., Muller K., Malin J.P., and Zange J. A prospective study to evaluate the impact of 31P-MRS to determinate mitochondrial dysfunction in skeletal muscle of ALS patients. Amyotroph. Lateral Scler. 8 (2007) 4-8
    • (2007) Amyotroph. Lateral Scler. , vol.8 , pp. 4-8
    • Grehl, T.1    Fischer, S.2    Muller, K.3    Malin, J.P.4    Zange, J.5
  • 33
    • 62149094382 scopus 로고    scopus 로고
    • Cu/Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of mitochondria and perturbs Ca2+ homeostasis in SOD1G93A mice
    • Jaiswal M.K., and Keller B.U. Cu/Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of mitochondria and perturbs Ca2+ homeostasis in SOD1G93A mice. Mol. Pharmacol. 75 (2009) 478-489
    • (2009) Mol. Pharmacol. , vol.75 , pp. 478-489
    • Jaiswal, M.K.1    Keller, B.U.2
  • 35
    • 18244390714 scopus 로고    scopus 로고
    • Synergy of insulin-like growth factor-1 and exercise in amyotrophic lateral sclerosis
    • Kaspar B.K., Frost L.M., Christian L., Umapathi P., and Gage F.H. Synergy of insulin-like growth factor-1 and exercise in amyotrophic lateral sclerosis. Ann. Neurol. 57 (2005) 649-655
    • (2005) Ann. Neurol. , vol.57 , pp. 649-655
    • Kaspar, B.K.1    Frost, L.M.2    Christian, L.3    Umapathi, P.4    Gage, F.H.5
  • 36
    • 0038103806 scopus 로고    scopus 로고
    • Regular exercise is beneficial to a mouse model of amyotrophic lateral sclerosis
    • Kirkinezos I.G., Hernandez D., Bradley W.G., and Moraes C.T. Regular exercise is beneficial to a mouse model of amyotrophic lateral sclerosis. Ann. Neurol. 53 (2003) 804-807
    • (2003) Ann. Neurol. , vol.53 , pp. 804-807
    • Kirkinezos, I.G.1    Hernandez, D.2    Bradley, W.G.3    Moraes, C.T.4
  • 40
    • 0029793872 scopus 로고    scopus 로고
    • Quantitative immunocytochemical analysis of the spinal cord in G86R superoxide dismutase transgenic mice: neurochemical correlates of selective vulnerability
    • Morrison B.M., Gordon J.W., Ripps M.E., and Morrison J.H. Quantitative immunocytochemical analysis of the spinal cord in G86R superoxide dismutase transgenic mice: neurochemical correlates of selective vulnerability. J. Comp. Neurol. 373 (1996) 619-631
    • (1996) J. Comp. Neurol. , vol.373 , pp. 619-631
    • Morrison, B.M.1    Gordon, J.W.2    Ripps, M.E.3    Morrison, J.H.4
  • 41
    • 60549090787 scopus 로고    scopus 로고
    • The Psi(m) depolarization that accompanies mitochondrial Ca2+ uptake is greater in mutant SOD1 than in wild-type mouse motor terminals
    • Nguyen K.T., Garcia-Chacon L.E., Barrett J.N., Barrett E.F., and David G. The Psi(m) depolarization that accompanies mitochondrial Ca2+ uptake is greater in mutant SOD1 than in wild-type mouse motor terminals. Proc. Natl. Acad. Sci. U. S. A. 106 (2009) 2007-2011
    • (2009) Proc. Natl. Acad. Sci. U. S. A. , vol.106 , pp. 2007-2011
    • Nguyen, K.T.1    Garcia-Chacon, L.E.2    Barrett, J.N.3    Barrett, E.F.4    David, G.5
  • 42
    • 57649178442 scopus 로고    scopus 로고
    • Oxidative stress and energy crises in neuronal dysfunction
    • Nicholls D.G. Oxidative stress and energy crises in neuronal dysfunction. Ann. N.Y. Acad. Sci. 1147 (2008) 53-60
    • (2008) Ann. N.Y. Acad. Sci. , vol.1147 , pp. 53-60
    • Nicholls, D.G.1
  • 43
    • 48249103957 scopus 로고    scopus 로고
    • A systematic review of antioxidant treatment for amyotrophic lateral sclerosis/motor neuron disease
    • Orrell R.W., Lane R.J., and Ross M. A systematic review of antioxidant treatment for amyotrophic lateral sclerosis/motor neuron disease. Amyotroph. Lateral Scler. 9 (2008) 195-211
    • (2008) Amyotroph. Lateral Scler. , vol.9 , pp. 195-211
    • Orrell, R.W.1    Lane, R.J.2    Ross, M.3
  • 44
    • 0030970281 scopus 로고    scopus 로고
    • Oxidative stress mediates impairment of muscle function in transgenic mice with elevated level of wild-type Cu/Zn superoxide dismutase
    • Peled-Kamar M., Lotem J., Wirguin I., Weiner L., Hermalin A., and Groner Y. Oxidative stress mediates impairment of muscle function in transgenic mice with elevated level of wild-type Cu/Zn superoxide dismutase. Proc. Natl. Acad. Sci. U. S. A. 94 (1997) 3883-3887
    • (1997) Proc. Natl. Acad. Sci. U. S. A. , vol.94 , pp. 3883-3887
    • Peled-Kamar, M.1    Lotem, J.2    Wirguin, I.3    Weiner, L.4    Hermalin, A.5    Groner, Y.6
  • 46
    • 0028888945 scopus 로고
    • Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis
    • Ripps M.E., Huntley G.W., Hof P.R., Morrison J.H., and Gordon J.W. Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 689-693
    • (1995) Proc. Natl. Acad. Sci. U. S. A. , vol.92 , pp. 689-693
    • Ripps, M.E.1    Huntley, G.W.2    Hof, P.R.3    Morrison, J.H.4    Gordon, J.W.5
  • 47
    • 0344012223 scopus 로고    scopus 로고
    • Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: a hospital-based case-control study
    • Ro L.S., Lai S.L., Chen C.M., and Chen S.T. Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: a hospital-based case-control study. Muscle Nerve 28 (2003) 737-743
    • (2003) Muscle Nerve , vol.28 , pp. 737-743
    • Ro, L.S.1    Lai, S.L.2    Chen, C.M.3    Chen, S.T.4
  • 48
    • 34250612194 scopus 로고    scopus 로고
    • Sodium valproate exerts neuroprotective effects in vivo through CREB-binding protein-dependent mechanisms but does not improve survival in an amyotrophic lateral sclerosis mouse model
    • Rouaux C., Panteleeva I., Rene F., Gonzalez de Aguilar J.L., Echaniz-Laguna A., Dupuis L., Menger Y., Boutillier A.L., and Loeffler J.P. Sodium valproate exerts neuroprotective effects in vivo through CREB-binding protein-dependent mechanisms but does not improve survival in an amyotrophic lateral sclerosis mouse model. J. Neurosci. 27 (2007) 5535-5545
    • (2007) J. Neurosci. , vol.27 , pp. 5535-5545
    • Rouaux, C.1    Panteleeva, I.2    Rene, F.3    Gonzalez de Aguilar, J.L.4    Echaniz-Laguna, A.5    Dupuis, L.6    Menger, Y.7    Boutillier, A.L.8    Loeffler, J.P.9
  • 49
    • 33846087291 scopus 로고    scopus 로고
    • Mitochondrial alterations in the spinal cord of patients with sporadic amyotrophic lateral sclerosis
    • Sasaki S., and Iwata M. Mitochondrial alterations in the spinal cord of patients with sporadic amyotrophic lateral sclerosis. J. Neuropathol. Exp. Neurol. 66 (2007) 10-16
    • (2007) J. Neuropathol. Exp. Neurol. , vol.66 , pp. 10-16
    • Sasaki, S.1    Iwata, M.2
  • 56
    • 0029053881 scopus 로고
    • An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
    • Wong P.C., Pardo C.A., Borchelt D.R., Lee M.K., Copeland N.G., Jenkins N.A., Sisodia S.S., Cleveland D.W., and Price D.L. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 14 (1995) 1105-1116
    • (1995) Neuron , vol.14 , pp. 1105-1116
    • Wong, P.C.1    Pardo, C.A.2    Borchelt, D.R.3    Lee, M.K.4    Copeland, N.G.5    Jenkins, N.A.6    Sisodia, S.S.7    Cleveland, D.W.8    Price, D.L.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.