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Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation

Smoke from wildland fires has been shown to produce neuroinflammation in preclinical models, characterized by neural infiltrations of neutrophils and monocytes, as well as altered neurovascular endothelial phenotypes. To address the longevity of such outcomes, the present study examined the neuroinf...

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Autores principales: Scieszka, David, Jin, Yan, Noor, Shahani, Barr, Ed, Garcia, Marcus, Begay, Jessica, Herbert, Guy, Hunter, Russell P, Bhaskar, Kiran, Kumar, Rahul, Gullapalli, Rama, Bolt, Alicia, McCormick, Mark A., Bleske, Barry, Gu, Haiwei, Campen, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275049/
https://www.ncbi.nlm.nih.gov/pubmed/37333410
http://dx.doi.org/10.21203/rs.3.rs-3002040/v1
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author Scieszka, David
Jin, Yan
Noor, Shahani
Barr, Ed
Garcia, Marcus
Begay, Jessica
Herbert, Guy
Hunter, Russell P
Bhaskar, Kiran
Kumar, Rahul
Gullapalli, Rama
Bolt, Alicia
McCormick, Mark A.
Bleske, Barry
Gu, Haiwei
Campen, Matthew
author_facet Scieszka, David
Jin, Yan
Noor, Shahani
Barr, Ed
Garcia, Marcus
Begay, Jessica
Herbert, Guy
Hunter, Russell P
Bhaskar, Kiran
Kumar, Rahul
Gullapalli, Rama
Bolt, Alicia
McCormick, Mark A.
Bleske, Barry
Gu, Haiwei
Campen, Matthew
author_sort Scieszka, David
collection PubMed
description Smoke from wildland fires has been shown to produce neuroinflammation in preclinical models, characterized by neural infiltrations of neutrophils and monocytes, as well as altered neurovascular endothelial phenotypes. To address the longevity of such outcomes, the present study examined the neuroinflammatory and metabolomic temporal dynamics after inhalation exposures from biomass-derived smoke. 2-month-old female C57BL/6J mice were exposed to wood smoke every other day for two weeks at an average exposure concentration of 0.5mg/m(3). Subsequent serial euthanasia occurred at 1-, 3-, 7-, 14-, and 28-days post-exposure. Flow cytometry of right hemispheres revealed two endothelial populations of PECAM (CD31), high and medium expressors, with wood smoke inhalation causing an increased proportion of PECAM(Hi). These populations of PECAM(Hi) and PECAM(Med) were associated with an anti-inflammatory and pro-inflammatory response, respectively, and their inflammatory profiles were largely resolved by the 28-day mark. However, activated microglial populations (CD11b(+)/CD45(low)) remained higher in wood smoke-exposed mice than controls at day 28. Infiltrating neutrophil populations decreased to levels below controls by day 28. However, the MHC-II expression of the peripheral immune infiltrate remained high, and the population of neutrophils retained an increased expression of CD45, Ly6C, and MHC-II. Utilizing an unbiased approach examining the metabolomic alterations, we observed notable hippocampal perturbations in neurotransmitter and signaling molecules like glutamate, quinolinic acid, and 5-α-dihydroprogesterone. Utilizing a targeted panel designed to explore the aging-associated NAD(+) metabolic pathway, wood smoke exposure drove fluctuations and compensations across the 28-day time course, ending with decreased hippocampal NAD(+) abundance at day 28. Summarily, these results indicate a highly dynamic neuroinflammatory environment, with potential resolution extending past 28 days, the implications of which may include long-term behavioral changes, systemic and neurological sequalae directly associated wtith wildfire smoke exposure.
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spelling pubmed-102750492023-06-17 Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation Scieszka, David Jin, Yan Noor, Shahani Barr, Ed Garcia, Marcus Begay, Jessica Herbert, Guy Hunter, Russell P Bhaskar, Kiran Kumar, Rahul Gullapalli, Rama Bolt, Alicia McCormick, Mark A. Bleske, Barry Gu, Haiwei Campen, Matthew Res Sq Article Smoke from wildland fires has been shown to produce neuroinflammation in preclinical models, characterized by neural infiltrations of neutrophils and monocytes, as well as altered neurovascular endothelial phenotypes. To address the longevity of such outcomes, the present study examined the neuroinflammatory and metabolomic temporal dynamics after inhalation exposures from biomass-derived smoke. 2-month-old female C57BL/6J mice were exposed to wood smoke every other day for two weeks at an average exposure concentration of 0.5mg/m(3). Subsequent serial euthanasia occurred at 1-, 3-, 7-, 14-, and 28-days post-exposure. Flow cytometry of right hemispheres revealed two endothelial populations of PECAM (CD31), high and medium expressors, with wood smoke inhalation causing an increased proportion of PECAM(Hi). These populations of PECAM(Hi) and PECAM(Med) were associated with an anti-inflammatory and pro-inflammatory response, respectively, and their inflammatory profiles were largely resolved by the 28-day mark. However, activated microglial populations (CD11b(+)/CD45(low)) remained higher in wood smoke-exposed mice than controls at day 28. Infiltrating neutrophil populations decreased to levels below controls by day 28. However, the MHC-II expression of the peripheral immune infiltrate remained high, and the population of neutrophils retained an increased expression of CD45, Ly6C, and MHC-II. Utilizing an unbiased approach examining the metabolomic alterations, we observed notable hippocampal perturbations in neurotransmitter and signaling molecules like glutamate, quinolinic acid, and 5-α-dihydroprogesterone. Utilizing a targeted panel designed to explore the aging-associated NAD(+) metabolic pathway, wood smoke exposure drove fluctuations and compensations across the 28-day time course, ending with decreased hippocampal NAD(+) abundance at day 28. Summarily, these results indicate a highly dynamic neuroinflammatory environment, with potential resolution extending past 28 days, the implications of which may include long-term behavioral changes, systemic and neurological sequalae directly associated wtith wildfire smoke exposure. American Journal Experts 2023-06-05 /pmc/articles/PMC10275049/ /pubmed/37333410 http://dx.doi.org/10.21203/rs.3.rs-3002040/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Scieszka, David
Jin, Yan
Noor, Shahani
Barr, Ed
Garcia, Marcus
Begay, Jessica
Herbert, Guy
Hunter, Russell P
Bhaskar, Kiran
Kumar, Rahul
Gullapalli, Rama
Bolt, Alicia
McCormick, Mark A.
Bleske, Barry
Gu, Haiwei
Campen, Matthew
Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title_full Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title_fullStr Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title_full_unstemmed Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title_short Neuroinflammatory and Metabolomic Temporal Dynamics Following Wood Smoke Inhalation
title_sort neuroinflammatory and metabolomic temporal dynamics following wood smoke inhalation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275049/
https://www.ncbi.nlm.nih.gov/pubmed/37333410
http://dx.doi.org/10.21203/rs.3.rs-3002040/v1
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