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Skeletal muscle maximal mitochondrial activity in ambulatory children with cerebral palsy.

Authors :
Dayanidhi S
Buckner EH
Redmond RS
Chambers HG
Schenk S
Lieber RL
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.)

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