Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain

The involvement of the primary motor cortex (M1) in chronic low back pain (LBP) is a relatively new concept. Decreased M1 excitability and an analgesic effect after M1 stimulation have been recently reported. However, the neurochemical changes underlying these functional M1 changes are unknown. The...

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Main Authors: Anda E. Popescu, Linda VanDillen, Patrick Gorman, Carmen M. Cirstea, Byron J. Gajewski, Steven Z. George, Kenneth E. McCarson, Neena K. Sharma, William M. Brooks
Format: Article
Language:English
Published: MDPI AG 2012-08-01
Series:Brain Sciences
Subjects:
Online Access:http://www.mdpi.com/2076-3425/2/3/319
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spelling doaj-453cae09b2f240f790686287a710dd6f2020-11-24T22:10:33ZengMDPI AGBrain Sciences2076-34252012-08-012331933110.3390/brainsci2030319Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back PainAnda E. PopescuLinda VanDillenPatrick GormanCarmen M. CirsteaByron J. GajewskiSteven Z. GeorgeKenneth E. McCarsonNeena K. SharmaWilliam M. BrooksThe involvement of the primary motor cortex (M1) in chronic low back pain (LBP) is a relatively new concept. Decreased M1 excitability and an analgesic effect after M1 stimulation have been recently reported. However, the neurochemical changes underlying these functional M1 changes are unknown. The current study investigated whether neurochemicals specific to neurons and glial cells in both right and left M1 are altered. N-Acetylaspartate (NAA) and myo-inositol (mI) were measured with proton magnetic resonance spectroscopy in 19 subjects with chronic LBP and 14 healthy controls. We also examined correlations among neurochemicals within and between M1 and relationships between neurochemical concentrations and clinical features of pain. Right M1 NAA was lower in subjects with LBP compared to controls (p = 0.008). Left M1 NAA and mI were not significantly different between LBP and control groups. Correlations between neurochemical concentrations across M1s were different between groups (p = 0.008). There were no significant correlations between M1 neurochemicals and pain characteristics. These findings provide preliminary evidence of neuronal depression and altered neuronal-glial interactions across M1 in chronic LBP. http://www.mdpi.com/2076-3425/2/3/319chronic low back painprimary motor cortexmagnetic resonance spectroscopyN-acetylaspartatemyo-inositol
collection DOAJ
language English
format Article
sources DOAJ
author Anda E. Popescu
Linda VanDillen
Patrick Gorman
Carmen M. Cirstea
Byron J. Gajewski
Steven Z. George
Kenneth E. McCarson
Neena K. Sharma
William M. Brooks
spellingShingle Anda E. Popescu
Linda VanDillen
Patrick Gorman
Carmen M. Cirstea
Byron J. Gajewski
Steven Z. George
Kenneth E. McCarson
Neena K. Sharma
William M. Brooks
Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
Brain Sciences
chronic low back pain
primary motor cortex
magnetic resonance spectroscopy
N-acetylaspartate
myo-inositol
author_facet Anda E. Popescu
Linda VanDillen
Patrick Gorman
Carmen M. Cirstea
Byron J. Gajewski
Steven Z. George
Kenneth E. McCarson
Neena K. Sharma
William M. Brooks
author_sort Anda E. Popescu
title Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
title_short Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
title_full Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
title_fullStr Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
title_full_unstemmed Neurochemical Analysis of Primary Motor Cortex in Chronic Low Back Pain
title_sort neurochemical analysis of primary motor cortex in chronic low back pain
publisher MDPI AG
series Brain Sciences
issn 2076-3425
publishDate 2012-08-01
description The involvement of the primary motor cortex (M1) in chronic low back pain (LBP) is a relatively new concept. Decreased M1 excitability and an analgesic effect after M1 stimulation have been recently reported. However, the neurochemical changes underlying these functional M1 changes are unknown. The current study investigated whether neurochemicals specific to neurons and glial cells in both right and left M1 are altered. N-Acetylaspartate (NAA) and myo-inositol (mI) were measured with proton magnetic resonance spectroscopy in 19 subjects with chronic LBP and 14 healthy controls. We also examined correlations among neurochemicals within and between M1 and relationships between neurochemical concentrations and clinical features of pain. Right M1 NAA was lower in subjects with LBP compared to controls (p = 0.008). Left M1 NAA and mI were not significantly different between LBP and control groups. Correlations between neurochemical concentrations across M1s were different between groups (p = 0.008). There were no significant correlations between M1 neurochemicals and pain characteristics. These findings provide preliminary evidence of neuronal depression and altered neuronal-glial interactions across M1 in chronic LBP.
topic chronic low back pain
primary motor cortex
magnetic resonance spectroscopy
N-acetylaspartate
myo-inositol
url http://www.mdpi.com/2076-3425/2/3/319
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