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Skeletal muscle maximal mitochondrial activity in ambulatory children with cerebral palsy.
- Source :
-
Developmental medicine and child neurology [Dev Med Child Neurol] 2021 Oct; Vol. 63 (10), pp. 1194-1203. Date of Electronic Publication: 2021 Jan 03. - Publication Year :
- 2021
-
Abstract
- Aim: To compare skeletal muscle mitochondrial enzyme activity and mitochondrial content between independently ambulatory children with cerebral palsy (CP) and typically developing children.<br />Method: Gracilis biopsies were obtained from 12 children during surgery (n=6/group, children with CP: one female, five males, mean age 13y 4mo, SD 5y 1mo, 4y 1mo-17y 10mo; typically developing children: three females, three males, mean age 16y 5mo, SD 1y 4mo, 14y 6mo-18y 2mo). Spectrophotometric enzymatic assays were used to evaluate the activity of mitochondrial electron transport chain complexes. Mitochondrial content was evaluated using citrate synthase assay, mitochondrial DNA copy number, and immunoblots for specific respiratory chain proteins.<br />Results: Maximal enzyme activity was significantly (50-80%) lower in children with CP versus typically developing children, for complex I (11nmol/min/mg protein, standard error of the mean [SEM] 1.7 vs 20.7nmol/min/mg protein, SEM 4), complex II (6.9nmol/min/mg protein, SEM 1.2 vs 21nmol/min/mg protein, SEM 2.7), complex III (31.9nmol/min/mg protein, SEM 7.4 vs 72.7nmol/min/mg protein, SEM 7.2), and complex I+III (7.4nmol/min/mg protein, SEM 2.5 vs 31.8nmol/min/mg protein, SEM 9.3). Decreased electron transport chain activity was not the result of lower mitochondrial content.<br />Interpretation: Skeletal muscle mitochondrial electron transport chain enzymatic activity but not mitochondrial content is reduced in independently ambulatory children with CP. Decreased mitochondrial oxidative capacity might explain reported increased energetics of movement and fatigue in ambulatory children with CP. What this paper adds Skeletal muscle mitochondrial electron transport chain enzymatic activity is reduced in independently ambulatory children with cerebral palsy (CP). Mitochondrial content appears to be similar between children with CP and typically developing children.<br /> (Published 2021. This article is a U.S. Government work and is in the public domain in the USA.)
- Subjects :
- Adolescent
Case-Control Studies
Child
Child, Preschool
DNA, Mitochondrial metabolism
Electron Transport Complex I metabolism
Electron Transport Complex II metabolism
Electron Transport Complex III metabolism
Female
Humans
Male
Mitochondria, Muscle enzymology
Spectrophotometry
Cerebral Palsy metabolism
Electron Transport Chain Complex Proteins metabolism
Mitochondria, Muscle metabolism
Muscle, Skeletal metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1469-8749
- Volume :
- 63
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Developmental medicine and child neurology
- Publication Type :
- Academic Journal
- Accession number :
- 33393083
- Full Text :
- https://doi.org/10.1111/dmcn.14785