Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states

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Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states. / Eftekhari, Sajedeh; Westgate, Connar Stanley James; Johansen, Katrine Printz; Bruun, Signe Rath; Jensen, Rigmor H.

In: Fluids and Barriers of the CNS, Vol. 17, No. 1, 39, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Eftekhari, S, Westgate, CSJ, Johansen, KP, Bruun, SR & Jensen, RH 2020, 'Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states', Fluids and Barriers of the CNS, vol. 17, no. 1, 39. https://doi.org/10.1186/s12987-020-00199-z

APA

Eftekhari, S., Westgate, C. S. J., Johansen, K. P., Bruun, S. R., & Jensen, R. H. (2020). Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states. Fluids and Barriers of the CNS, 17(1), [39]. https://doi.org/10.1186/s12987-020-00199-z

Vancouver

Eftekhari S, Westgate CSJ, Johansen KP, Bruun SR, Jensen RH. Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states. Fluids and Barriers of the CNS. 2020;17(1). 39. https://doi.org/10.1186/s12987-020-00199-z

Author

Eftekhari, Sajedeh ; Westgate, Connar Stanley James ; Johansen, Katrine Printz ; Bruun, Signe Rath ; Jensen, Rigmor H. / Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states. In: Fluids and Barriers of the CNS. 2020 ; Vol. 17, No. 1.

Bibtex

@article{9422d25aade94f84802561173a3b1509,
title = "Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states",
abstract = "Background: Elevated intracranial pressure (ICP) is observed in association with a range of brain disorders. There is limited insight into the regulatory mechanisms of ICP under physiological conditions, and consequently also under pathological conditions. Thereby, to understand the mechanisms underlying ICP dynamics, precise, valid and long-term ICP recordings are of importance in the preclinical setting. Herein, we used a novel telemetric system for ICP recordings which allowed for long-term recordings in freely-moving rats. The aim was to investigate ICP dynamics under different physiological states and investigate how factors such as surgery/recovery, body position, light-dark, co-housing, weight and anesthesia may influence ICP and its waveforms. Methods: A telemetric device was implanted epidurally in rats and signals were recorded continuously for up to 50 days (n = 14). Recording was divided into three experimental periods: a surgical recovery period (RP), a physiological period (PP) and an experimental period (EP). Histology was performed to study the morphology of implanted rats and non-implanted rats (n = 17). Results: For the first time, we can demonstrate continuous ICP recordings in freely-moving and co-housed rats for up to 50 days with a high degree of stability. The mean ICP in the recording periods were; RP: 3.2 ± 0.6 mmHg, PP: 5.0 ± 0.6 mmHg and EP: 4.7 ± 0.6 mmHg. In the RP, the ICP was significantly lower compared to the PP (P = 0.0034). Significant light-dark difference in ICP with 21% increase in respiratory slow-wave amplitude was observed in the co-housed animals but not in single-housed animals. The ICP signal was raised during the dark period relative to the light (Δ0.3 ± 0.07 mmHg, P = 0.0043). Administration of anesthesia gave a short-term increase in ICP followed by a significant decrease in ICP. No signs of tissue damage or inflammation were found in the implanted brains. Conclusions: ICP dynamics were influenced by several factors such as, use of anesthesia, light-dark difference and housing conditions. Our study demonstrates the importance of performing ICP physiological measurements in freely-moving animals. This has significant implications for moving the preclinical research field forward in order to properly study ICP physiology during disease development and to explore drug targets for alleviating increased ICP. ",
keywords = "Anesthesia, Cerebrospinal fluid, Choroid plexus, Freely-moving, GFAP, Intracranial pressure, Neurophysiology, Telemetry system, Waveforms",
author = "Sajedeh Eftekhari and Westgate, {Connar Stanley James} and Johansen, {Katrine Printz} and Bruun, {Signe Rath} and Jensen, {Rigmor H.}",
year = "2020",
doi = "10.1186/s12987-020-00199-z",
language = "English",
volume = "17",
journal = "Fluids and Barriers of the CNS",
issn = "2045-8118",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Long-term monitoring of intracranial pressure in freely-moving rats; Impact of different physiological states

AU - Eftekhari, Sajedeh

AU - Westgate, Connar Stanley James

AU - Johansen, Katrine Printz

AU - Bruun, Signe Rath

AU - Jensen, Rigmor H.

PY - 2020

Y1 - 2020

N2 - Background: Elevated intracranial pressure (ICP) is observed in association with a range of brain disorders. There is limited insight into the regulatory mechanisms of ICP under physiological conditions, and consequently also under pathological conditions. Thereby, to understand the mechanisms underlying ICP dynamics, precise, valid and long-term ICP recordings are of importance in the preclinical setting. Herein, we used a novel telemetric system for ICP recordings which allowed for long-term recordings in freely-moving rats. The aim was to investigate ICP dynamics under different physiological states and investigate how factors such as surgery/recovery, body position, light-dark, co-housing, weight and anesthesia may influence ICP and its waveforms. Methods: A telemetric device was implanted epidurally in rats and signals were recorded continuously for up to 50 days (n = 14). Recording was divided into three experimental periods: a surgical recovery period (RP), a physiological period (PP) and an experimental period (EP). Histology was performed to study the morphology of implanted rats and non-implanted rats (n = 17). Results: For the first time, we can demonstrate continuous ICP recordings in freely-moving and co-housed rats for up to 50 days with a high degree of stability. The mean ICP in the recording periods were; RP: 3.2 ± 0.6 mmHg, PP: 5.0 ± 0.6 mmHg and EP: 4.7 ± 0.6 mmHg. In the RP, the ICP was significantly lower compared to the PP (P = 0.0034). Significant light-dark difference in ICP with 21% increase in respiratory slow-wave amplitude was observed in the co-housed animals but not in single-housed animals. The ICP signal was raised during the dark period relative to the light (Δ0.3 ± 0.07 mmHg, P = 0.0043). Administration of anesthesia gave a short-term increase in ICP followed by a significant decrease in ICP. No signs of tissue damage or inflammation were found in the implanted brains. Conclusions: ICP dynamics were influenced by several factors such as, use of anesthesia, light-dark difference and housing conditions. Our study demonstrates the importance of performing ICP physiological measurements in freely-moving animals. This has significant implications for moving the preclinical research field forward in order to properly study ICP physiology during disease development and to explore drug targets for alleviating increased ICP.

AB - Background: Elevated intracranial pressure (ICP) is observed in association with a range of brain disorders. There is limited insight into the regulatory mechanisms of ICP under physiological conditions, and consequently also under pathological conditions. Thereby, to understand the mechanisms underlying ICP dynamics, precise, valid and long-term ICP recordings are of importance in the preclinical setting. Herein, we used a novel telemetric system for ICP recordings which allowed for long-term recordings in freely-moving rats. The aim was to investigate ICP dynamics under different physiological states and investigate how factors such as surgery/recovery, body position, light-dark, co-housing, weight and anesthesia may influence ICP and its waveforms. Methods: A telemetric device was implanted epidurally in rats and signals were recorded continuously for up to 50 days (n = 14). Recording was divided into three experimental periods: a surgical recovery period (RP), a physiological period (PP) and an experimental period (EP). Histology was performed to study the morphology of implanted rats and non-implanted rats (n = 17). Results: For the first time, we can demonstrate continuous ICP recordings in freely-moving and co-housed rats for up to 50 days with a high degree of stability. The mean ICP in the recording periods were; RP: 3.2 ± 0.6 mmHg, PP: 5.0 ± 0.6 mmHg and EP: 4.7 ± 0.6 mmHg. In the RP, the ICP was significantly lower compared to the PP (P = 0.0034). Significant light-dark difference in ICP with 21% increase in respiratory slow-wave amplitude was observed in the co-housed animals but not in single-housed animals. The ICP signal was raised during the dark period relative to the light (Δ0.3 ± 0.07 mmHg, P = 0.0043). Administration of anesthesia gave a short-term increase in ICP followed by a significant decrease in ICP. No signs of tissue damage or inflammation were found in the implanted brains. Conclusions: ICP dynamics were influenced by several factors such as, use of anesthesia, light-dark difference and housing conditions. Our study demonstrates the importance of performing ICP physiological measurements in freely-moving animals. This has significant implications for moving the preclinical research field forward in order to properly study ICP physiology during disease development and to explore drug targets for alleviating increased ICP.

KW - Anesthesia

KW - Cerebrospinal fluid

KW - Choroid plexus

KW - Freely-moving

KW - GFAP

KW - Intracranial pressure

KW - Neurophysiology

KW - Telemetry system

KW - Waveforms

U2 - 10.1186/s12987-020-00199-z

DO - 10.1186/s12987-020-00199-z

M3 - Journal article

C2 - 32517699

AN - SCOPUS:85086354825

VL - 17

JO - Fluids and Barriers of the CNS

JF - Fluids and Barriers of the CNS

SN - 2045-8118

IS - 1

M1 - 39

ER -

ID: 253235366