Impairment of mitochondrial metabolism differentially affects striatal neuronal subtypes

&NA; Electrophysiological and microfluorometric measurements were combined to analyse the responses of rat striatal medium spiny (MS) and large aspiny (LA) interneurons to the mitochondrial uncoupler carbonyl cyanide p‐trifluoromethoxyphenylidrazone (FCCP). FCCP produced a membrane depolarisation coupled to an irreversible increase in intracellular calcium [Ca2+]i in MS. Conversely, LA interneurons hyperpolarised and a moderate [Ca2+]i rise was observed. Cyclosporin A, inhibitor of the mitochondrial membrane transition pore, prevented the FCCP‐induced changes in LA interneurons, whereas only a partial reduction was observed in MS cells. The present results indicate that mitochondrial Ca2+ released into the cytosol may contribute to the selective vulnerability to metabolic impairment in striatal neuronal subtypes.

[1]  Todd B. Sherer,et al.  Chronic systemic pesticide exposure reproduces features of Parkinson's disease , 2000, Nature Neuroscience.

[2]  J. Dubinsky,et al.  Limitations of Cyclosporin A Inhibition of the Permeability Transition in CNS Mitochondria , 2000, The Journal of Neuroscience.

[3]  J. Kordower,et al.  Cyclosporin A protects striatal neurons in vitro and in vivo from 3‐nitropropionic acid toxicity , 2000, The Journal of comparative neurology.

[4]  P. Calabresi,et al.  Involvement of Intracellular Calcium Stores during Oxygen/Glucose Deprivation in Striatal Large Aspiny Interneurons , 2000, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[5]  J. Dubinsky,et al.  Dual Responses of CNS Mitochondria to Elevated Calcium , 2000, The Journal of Neuroscience.

[6]  S. Scheff,et al.  Cyclosporin A significantly ameliorates cortical damage following experimental traumatic brain injury in rodents. , 1999, Journal of neurotrauma.

[7]  M Crompton,et al.  The mitochondrial permeability transition pore and its role in cell death. , 1999, The Biochemical journal.

[8]  P. Calabresi,et al.  Electrophysiological recordings and calcium measurements in striatal large aspiny interneurons in response to combined O2/glucose deprivation. , 1999, Journal of neurophysiology.

[9]  M. Beal,et al.  Mitochondria in Neurodegeneration: Bioenergetic Function in Cell Life and Death , 1999, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[10]  J M Dubinsky,et al.  Calcium‐induced activation of the mitochondrial permeability transition in hippocampal neurons , 1998, Journal of neuroscience research.

[11]  G. Kroemer,et al.  Inhibitors of permeability transition interfere with the disruption of the mitochondrial transmembrane potential during apoptosis , 1996, FEBS letters.

[12]  B. Rosen,et al.  Evidence for irnnairment of energy metabofism in vivo in Huntington's disease using localized 1H NMR spectroscopy , 1993, Neurology.

[13]  D. Choi Calcium-mediated neurotoxicity: relationship to specific channel types and role in ischemic damage , 1988, Trends in Neurosciences.

[14]  Joseph B. Martin,et al.  Sparing of acetylcholinesterase-containing striatal neurons in Huntington's disease , 1987, Brain Research.

[15]  R. Tsien,et al.  A new generation of Ca2+ indicators with greatly improved fluorescence properties. , 1985, The Journal of biological chemistry.