Effect of Leucine Administration on Creatine Kinase Activity in Rat Brain
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Aksenov, M., AksenovaM., Butterfield, A.D., and Markesbery, W.R. (2000). Oxidative modification of creatine kinase BB in Alzheimer's disease brain. J. Neurochem. 74:2520-2527.
Aksenov, M.Y., Aksenova, M.V., Payne, R.M., Smith, C.D., Markesbery, W.R., and Carney, J.M. (1997). The expression of creatine kinase isoenzymes in neocortex of patients with neurodegenerative disorders: Alzheimer's and Pick's disease. Experim. Neurol. 146:458-465.
Aksenov, M., Aksenova, M., Payne, R.M., Trojanovski, J.Q., Schmidt, K.L., Carney, J.M., Butterfield, D.A., and Markesbery, W.R. (1999). Oxidation of cytosolic proteins and expression of creatine kinase BB in frontal lobes of neurodegenerative disorders. Dement. Geriatr. Cogn. Disord. 10:158-165.
Araujo, P., Wasserman, G.F., Tallini, K., Furlanetto, V., Vargas, C.R., Wannmacher, C.M., Dutra-Filho, C.S., Wyse, A.T.S., and Wajner, M. (2001). Reduction of large neutral amino acids levels in plasma and brain of hyperleucinemic rats. Neurochem. Int. 38:529-537.
Brustovetsky, N., Brustovetsky, T., and Dubinsky, J.M. (2001). On the mechanisms of neuroprotection by creatine and phosphocreatine. J. Neurochem. 76:425-434.
Chuang, D.T., and Shih, V.E. (2001). Maple syrup urine disease (branched-chain ketoaciduria). In (C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle, eds.), The Metabolic & Molecular Bases of Inherited Diseases, 8th edn., McGraw-Hill, New York, pp. 1667-1724.
Coitinho, A.S., de Mello, C.F., Lima, T.T., de Bastiani, J., Fighera, M.R., and Wajner, M. (2001). Pharmacological evidence that alpha-keto isovaleric acid induces convulsions through GABAergic and glutamatergic mechanisms in rats. Brain Res. 894:68-73.
Dancis, J., Hutzler, J., and Levitz, M. (1960). Metabolism of the white blood cells in maple syrup urine disease. Biochim. Biophys. Acta 43:342-347.
David, S.S., Shoemaker, M., and Haley, B.E. (1998). Abnormal properties of creatine kinase in Alzheimer's disease brain: Correlation of reduced enzyme activity and active site photolabelling with aberrant cytosol-membrane partitioning. Mol. Brain Res. 54:276-287.
Fontella, F.U., Gassen, E., Pulrolnik, V., Wannmacher, C.M.D., Klein, A.B., Wajner, M., and Dutra-Filho, C.S. (2002). Stimulation of lipid peroxidation in vitro in rat brain by the metabolites accumulating in maple syrup urine disease. Metab. Brain Dis. 17:47-54.
Hensley, K., Hall, N., Subramaniam, R., Cole, P., Harris, M., Aksenova, M.V., Aksenov, M.Y., Gabbita, S.P., Carney, J.M., Lowell, M., Markesbery, W.R., and Butterfield, D.A. (1995). Brain regional correspondence between Alzheimer's disease histopathology biomarkers of protein oxidation. J. Neurochem. 65:2146-2156.
Hughes, B.P. (1962). A method for estimation of serum creatine kinase and its use in comparing creatine kinase and aldolase activity in normal and pathological sera. Clin. Chim. Acta 7:597-603.
Jouvet, P., Rustin, P., Taylor, D.L., Pocock, J.M., Felderhoff-Mueser, U., Mazarakis, N.D., Sarraf, C., Joashi, U., Kozma, M., Greenwood, K., Edwards, A.D., and Mehemet, A. (2000). Branched chain amino acids induce apoptosis in neural cells without mitochondrial membrane depolarization or cytochrome c release: Implications for neurological impairment associated with maple syrup urine disease. Mol. Biol. Cell. 11:1919-1932.
Kamei, A., Takashima, S., Ctlan, F., and Becker, L.E. (1992). Abnormal dentritic development in maple syrup urine disease. Pediatr. Neurol. 8:145-147.
Kiil, R., and Rokkones, T. (1964). Late manifesting variant of branched-chain ketoaciduria (maple syrup urine disease). Acta. Paediatr. 53:356-361.
Lowry, O.H., Rosebrough, N.J., Farr, A.L., and Randal, R.J. (1951). Protein measurement with a Folin phenol reagent. J. Biol. Chem. 193:265-275.
Manos, P., Bryan, G.K., and Edmond, J. (1991). Creatine kinase activity in postnatal rat brain development and in cultured neurons, astrocytes, and oligodendrocytes. J. Neurochem. 56:2101-2107.
Mello, C.F., Feksa, L., Brusque, A.M., Wannmacher, C.M.D., and Wajner, M. (1999). Chronic early leucine administration induces behavioral deficits in rats. Life Sciences 65:747-755.
Menkes, J.H. (1959). Maple syrup urine disease: Isolation and identification of organic acids in the urine. Pediatrics 23:348-353.
Prensky, A.L., and Moser, H.W. (1966). Brain lipids, proteolipids, and free amino acids in maple syrup urine disease. J. Neurochem. 13:863-874.
Reis, M., Farage, M., and Wolosker, H. (2000). Chloride-dependent inhibition of vesicular glutamate uptake by by alpha-keto acids accumulated in maple syrup urine disease. Biochim. Biophys. Acta 1475:114-118.
Riviello, J.J., Jr., Rezvani, L., Digeorge, A.M., and Foley, C.M. (1991). Cerebral edema causing death in children with maple syrup urine disease. J. Pediatr. 119:42-45.
Saks, V.A., Ventura-Clapier, R., and Aliev, M.K. (1996). Metabolic control and metabolic capacity: Two aspects of creatine kinase functioning in the cells. Biochim. Biophys. Acta 1274:81-88.
Tavares, R.G., Santos, C.E., Tasca, C.I., Wajner, M., Souza, D.O., and Dutra-Filho, C.S. (2000). Inhibition of glutamate uptake into synaptic vesicles of rat brain by the metabolites accumulating in maple syrup urine disease. J. Neurol. Sci. 181:44-49.
Tomimoto, H., Yamamoto, K., Homburger, H.A., and Yanagihara, T. (1993). Immunoelectron microscopic investigation of creatine kinase BB-isoenzyme after cerebral ischemia in gerbils. Acta Neuropathol. 86:447-455.
Wallimann, T., Dolder, M., Schlattner, U., Eder, M., Hornemann, T., Kraft, T., and Stolz, M. (1998a). Creatine kinase: An enzyme with a central role in cellular energy metabolism. MAGMA 6:116-119.
Wallimann, T., Dolder, M., Schlattner, U., Eder, M., Hornemann, T., O'Gorman, E., Ruck, E., and Brdiczka, D. (1998b). Some new aspects of creatini kinase (CK): Compartmentation, structure, function and regulation for cellular and mitochondrial bioenergetics and physiology. Biofactors 8:229-234.
Wallimann, T., Wyss, M., Brdiczka, D., and Nicolay, K. (1992). Intracellular compartmentation, structure and function of creatine kinase in tissues with high and fluctuating energy demands: The ‘phosphocreatine circuit’ for cellular energy homeostasis. Biochem. J. 281:21-40.
Wyse, A.T.S., Bolognesi, G., Brusque, A.M., Wajner, M., and Wannmacher, C.M.D. (1995). Na+, K+-ATPase activity in the synaptic plasma membrane from the cerebral cortex of rats subjected to chemically induced phenylketonuria. Med. Sci. Res. 23:261-262.
Wyss, M., Smeitink, J., Wevers, R.A., and Wallimann, T. (1992). Mitochondrial creatine kinase: A key enzyme of aerobic energy metabolism. Biochim. Biophys. Acta 1102:119-166.
Yudkoff, M. (1997). Brain metabolism of branched-chain amino acids. Glia 21:92-98.
Zielke, H.R., Huang, Y., Baab, P.J., Collins, R.M. Jr., Zielke, C.L., and Tildon, J.T. (1997). Effects of alpha-ketoisocaproate and leucine on the in vivo oxidation of glutamate and glutamine in the rat brain. Neurochem. Res. 22:1159-1164.
Zielke, H.R., Huang, Y., and Tildon, J.T. (1996). Elevation of amino acids in the interstitial space of the rat brain following infusion of a large neutral amino acid and keto acids by microdialysis: Alpha-ketocaproate infusion. Dev. Neurosci. 18:420-425.
Zielke, H.R., Zielke, C.L., Baab, P.J., and Collins, R.M. (2002). Large neutral amino acids auto exchange when infused by microdialysis into the rat brain: Implication for maple syrup urine disease and phenylketonuria. Neurochem. Int. 40:347-354.