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Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease

Response to inflammation is a key determinant in many diseases and their outcomes. Diseases that commonly affect older people are frequently associated with altered inflammatory processes. Neuroinflammation has been described in Parkinson's disease (PD) brain. PD is characterized by the loss of...

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Autores principales: Ingram, Thomas L., Shephard, Freya, Sarmad, Sarir, Ortori, Catherine A., Barrett, David A., Chakrabarti, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521528/
https://www.ncbi.nlm.nih.gov/pubmed/32855358
http://dx.doi.org/10.18632/aging.103937
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author Ingram, Thomas L.
Shephard, Freya
Sarmad, Sarir
Ortori, Catherine A.
Barrett, David A.
Chakrabarti, Lisa
author_facet Ingram, Thomas L.
Shephard, Freya
Sarmad, Sarir
Ortori, Catherine A.
Barrett, David A.
Chakrabarti, Lisa
author_sort Ingram, Thomas L.
collection PubMed
description Response to inflammation is a key determinant in many diseases and their outcomes. Diseases that commonly affect older people are frequently associated with altered inflammatory processes. Neuroinflammation has been described in Parkinson's disease (PD) brain. PD is characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta and at the sub-cellular level, mitochondrial dysfunction is a key feature. However, there is evidence that a different region of the brain, the cerebellum, is involved in the pathophysiology of PD. We report relative levels of 40 pro- and anti-inflammatory cytokines measured in PD and control cerebellar mitochondria. These data were obtained by screening cytokine antibody arrays. In parallel, we present concentrations of 29 oxylipins and 4 endocannabinoids measured in mitochondrial fractions isolated from post-mortem PD cerebellum with age and sex matched controls. Our oxylipin and endocannabinoid data were acquired via quantitation by LC-ESI—MS/MS. The separate sample sets both show there are clearly different inflammatory profiles between the sexes in control samples. Sex specific profiles were not maintained in cerebellar mitochondria isolated from PD brains.
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spelling pubmed-75215282020-10-02 Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease Ingram, Thomas L. Shephard, Freya Sarmad, Sarir Ortori, Catherine A. Barrett, David A. Chakrabarti, Lisa Aging (Albany NY) Research Paper Response to inflammation is a key determinant in many diseases and their outcomes. Diseases that commonly affect older people are frequently associated with altered inflammatory processes. Neuroinflammation has been described in Parkinson's disease (PD) brain. PD is characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta and at the sub-cellular level, mitochondrial dysfunction is a key feature. However, there is evidence that a different region of the brain, the cerebellum, is involved in the pathophysiology of PD. We report relative levels of 40 pro- and anti-inflammatory cytokines measured in PD and control cerebellar mitochondria. These data were obtained by screening cytokine antibody arrays. In parallel, we present concentrations of 29 oxylipins and 4 endocannabinoids measured in mitochondrial fractions isolated from post-mortem PD cerebellum with age and sex matched controls. Our oxylipin and endocannabinoid data were acquired via quantitation by LC-ESI—MS/MS. The separate sample sets both show there are clearly different inflammatory profiles between the sexes in control samples. Sex specific profiles were not maintained in cerebellar mitochondria isolated from PD brains. Impact Journals 2020-08-27 /pmc/articles/PMC7521528/ /pubmed/32855358 http://dx.doi.org/10.18632/aging.103937 Text en Copyright: © 2020 Ingram et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ingram, Thomas L.
Shephard, Freya
Sarmad, Sarir
Ortori, Catherine A.
Barrett, David A.
Chakrabarti, Lisa
Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title_full Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title_fullStr Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title_full_unstemmed Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title_short Sex specific inflammatory profiles of cerebellar mitochondria are attenuated in Parkinson’s disease
title_sort sex specific inflammatory profiles of cerebellar mitochondria are attenuated in parkinson’s disease
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521528/
https://www.ncbi.nlm.nih.gov/pubmed/32855358
http://dx.doi.org/10.18632/aging.103937
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