Acute systemic LPS-exposure impairs perivascular CSF distribution in mice

Abstract Background The exchange of cerebrospinal (CSF) and interstitial fluid is believed to be vital for waste clearance in the brain. The sleep-dependent glymphatic system, which is comprised of perivascular flow of CSF and is largely dependent on arterial pulsatility and astrocytic aquaporin-4 (...

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Main Authors: Oscar Manouchehrian, Marta Ramos, Sara Bachiller, Iben Lundgaard, Tomas Deierborg
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Journal of Neuroinflammation
Subjects:
LPS
CSF
Online Access:https://doi.org/10.1186/s12974-021-02082-6
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spelling doaj-feccedfae79b4477a885f299a31201392021-01-31T16:04:59ZengBMCJournal of Neuroinflammation1742-20942021-01-0118111310.1186/s12974-021-02082-6Acute systemic LPS-exposure impairs perivascular CSF distribution in miceOscar Manouchehrian0Marta Ramos1Sara Bachiller2Iben Lundgaard3Tomas Deierborg4Experimental Neuroinflammation Laboratory, Department of Experimental Medical Science, Lund UniversityDepartment of Experimental Medical Science, Lund UniversityExperimental Neuroinflammation Laboratory, Department of Experimental Medical Science, Lund UniversityDepartment of Experimental Medical Science, Lund UniversityExperimental Neuroinflammation Laboratory, Department of Experimental Medical Science, Lund UniversityAbstract Background The exchange of cerebrospinal (CSF) and interstitial fluid is believed to be vital for waste clearance in the brain. The sleep-dependent glymphatic system, which is comprised of perivascular flow of CSF and is largely dependent on arterial pulsatility and astrocytic aquaporin-4 (AQP4) expression, facilitates much of this brain clearance. During the last decade, several observations have indicated that impaired glymphatic function goes hand in hand with neurodegenerative diseases. Since pathologies of the brain carry inflammatory components, we wanted to know how acute inflammation, e.g., with lipopolysaccharide (LPS) injections, would affect the glymphatic system. In this study, we aim to measure the effect of LPS on perivascular CSF distribution as a measure of glymphatic function. Methods Three hours after injection of LPS (1 mg/kg i.p.), C57bl/6 mice were (1) imaged for two CSF tracers, injected into cisterna magna, (2) transcardially perfused with buffer, or (3) used for physiological readouts. Tracer flow was imaged using a low magnification microscope on fixed brains, as well as using vibratome-cut slices for measuring tracer penetration in the brain. Cytokines, glial, and BBB-permeability markers were measured with ELISAs, Western blots, and immunohistochemistry. Cerebral blood flow was approximated using laser Doppler flowmetry, respiration and heart rate with a surgical monitor, and AQP4-polarization was quantified using confocal microscopy of immunolabeled brain sections. Results LPS-injections significantly lowered perivascular CSF tracer flow and penetration into the parenchyma. No differences in AQP4 polarization, cytokines, astroglial and BBB markers, cerebral blood flow, or respiration were detected in LPS-injected mice, although LPS did elevate cortical Iba1+ area and heart rate. Conclusions This study reports another physiological response after acute exposure to the bacterial endotoxin LPS, namely the statistically significant decrease in perivascular distribution of CSF. These observations may benefit our understanding of the role of systemic inflammation in brain clearance.https://doi.org/10.1186/s12974-021-02082-6LPSCSFMicrogliaGlymphatic SystemAQP4Inflammation
collection DOAJ
language English
format Article
sources DOAJ
author Oscar Manouchehrian
Marta Ramos
Sara Bachiller
Iben Lundgaard
Tomas Deierborg
spellingShingle Oscar Manouchehrian
Marta Ramos
Sara Bachiller
Iben Lundgaard
Tomas Deierborg
Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
Journal of Neuroinflammation
LPS
CSF
Microglia
Glymphatic System
AQP4
Inflammation
author_facet Oscar Manouchehrian
Marta Ramos
Sara Bachiller
Iben Lundgaard
Tomas Deierborg
author_sort Oscar Manouchehrian
title Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
title_short Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
title_full Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
title_fullStr Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
title_full_unstemmed Acute systemic LPS-exposure impairs perivascular CSF distribution in mice
title_sort acute systemic lps-exposure impairs perivascular csf distribution in mice
publisher BMC
series Journal of Neuroinflammation
issn 1742-2094
publishDate 2021-01-01
description Abstract Background The exchange of cerebrospinal (CSF) and interstitial fluid is believed to be vital for waste clearance in the brain. The sleep-dependent glymphatic system, which is comprised of perivascular flow of CSF and is largely dependent on arterial pulsatility and astrocytic aquaporin-4 (AQP4) expression, facilitates much of this brain clearance. During the last decade, several observations have indicated that impaired glymphatic function goes hand in hand with neurodegenerative diseases. Since pathologies of the brain carry inflammatory components, we wanted to know how acute inflammation, e.g., with lipopolysaccharide (LPS) injections, would affect the glymphatic system. In this study, we aim to measure the effect of LPS on perivascular CSF distribution as a measure of glymphatic function. Methods Three hours after injection of LPS (1 mg/kg i.p.), C57bl/6 mice were (1) imaged for two CSF tracers, injected into cisterna magna, (2) transcardially perfused with buffer, or (3) used for physiological readouts. Tracer flow was imaged using a low magnification microscope on fixed brains, as well as using vibratome-cut slices for measuring tracer penetration in the brain. Cytokines, glial, and BBB-permeability markers were measured with ELISAs, Western blots, and immunohistochemistry. Cerebral blood flow was approximated using laser Doppler flowmetry, respiration and heart rate with a surgical monitor, and AQP4-polarization was quantified using confocal microscopy of immunolabeled brain sections. Results LPS-injections significantly lowered perivascular CSF tracer flow and penetration into the parenchyma. No differences in AQP4 polarization, cytokines, astroglial and BBB markers, cerebral blood flow, or respiration were detected in LPS-injected mice, although LPS did elevate cortical Iba1+ area and heart rate. Conclusions This study reports another physiological response after acute exposure to the bacterial endotoxin LPS, namely the statistically significant decrease in perivascular distribution of CSF. These observations may benefit our understanding of the role of systemic inflammation in brain clearance.
topic LPS
CSF
Microglia
Glymphatic System
AQP4
Inflammation
url https://doi.org/10.1186/s12974-021-02082-6
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