Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model
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Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model. / Aidt, Frederik Heurlin; Nielsen, Signe Marie Borch; Kanters, Jørgen; Pesta, Dominik; Nielsen, Troels Tolstrup; Nørremølle, Anne; Hasholt, Lis; Christiansen, Michael; Hagen, Christian Munch.
I: PLoS Currents, Bind 5, 2013.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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T1 - Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model
AU - Aidt, Frederik Heurlin
AU - Nielsen, Signe Marie Borch
AU - Kanters, Jørgen
AU - Pesta, Dominik
AU - Nielsen, Troels Tolstrup
AU - Nørremølle, Anne
AU - Hasholt, Lis
AU - Christiansen, Michael
AU - Hagen, Christian Munch
PY - 2013
Y1 - 2013
N2 - Metabolic dysfunction and mitochondrial involvement are recognised as part of the pathology in Huntington's Disease (HD). Post-mortem examinations of the striatum from end-stage HD patients have shown a decrease in the in vitro activity of complexes II, III and IV of the electron transport system (ETS). In different models of HD, evidence of enzyme defects have been reported in complex II and complex IV using enzyme assays. However, such assays are highly variable and results have been inconsistent. We investigated the integrated ETS function ex vivo using a sensitive high-resolution respirometric (HRR) method. The O2 flux in a whole-cell sample combined with the addition of mitochondrial substrates, uncouplers and inhibitors enabled us to accurately quantitate the function of individual mitochondrial complexes in intact mitochondria, while retaining mitochondrial regulation and compensatory mechanisms. We used HRR to examine the mitochondrial function in striata from 12-week old R6/2 mice expressing exon 1 of human HTT with 130 CAG repeats. A significant reduction in complex II and complex IV flux control ratios was found in the R6/2 mouse striatum at 12 weeks of age compared to controls, confirming previous findings obtained with spectrophotometric enzyme assays.
AB - Metabolic dysfunction and mitochondrial involvement are recognised as part of the pathology in Huntington's Disease (HD). Post-mortem examinations of the striatum from end-stage HD patients have shown a decrease in the in vitro activity of complexes II, III and IV of the electron transport system (ETS). In different models of HD, evidence of enzyme defects have been reported in complex II and complex IV using enzyme assays. However, such assays are highly variable and results have been inconsistent. We investigated the integrated ETS function ex vivo using a sensitive high-resolution respirometric (HRR) method. The O2 flux in a whole-cell sample combined with the addition of mitochondrial substrates, uncouplers and inhibitors enabled us to accurately quantitate the function of individual mitochondrial complexes in intact mitochondria, while retaining mitochondrial regulation and compensatory mechanisms. We used HRR to examine the mitochondrial function in striata from 12-week old R6/2 mice expressing exon 1 of human HTT with 130 CAG repeats. A significant reduction in complex II and complex IV flux control ratios was found in the R6/2 mouse striatum at 12 weeks of age compared to controls, confirming previous findings obtained with spectrophotometric enzyme assays.
U2 - 10.1371/currents.hd.d8917b4862929772c5a2f2a34ef1c201
DO - 10.1371/currents.hd.d8917b4862929772c5a2f2a34ef1c201
M3 - Journal article
C2 - 23568011
VL - 5
JO - P L o S Currents
JF - P L o S Currents
SN - 2157-3999
ER -
ID: 47681646