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Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging

Cerebral blood flow is an important parameter in many diseases and functional studies that can be accurately measured in humans using arterial spin labelling (ASL) MRI. However, although rat models are frequently used for preclinical studies of both human disease and brain function, rat CBF measurem...

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Autores principales: Larkin, James R, Simard, Manon A, Khrapitchev, Alexandre A, Meakin, James A, Okell, Thomas W, Craig, Martin, Ray, Kevin J, Jezzard, Peter, Chappell, Michael A, Sibson, Nicola R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681434/
https://www.ncbi.nlm.nih.gov/pubmed/29498562
http://dx.doi.org/10.1177/0271678X18756218
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author Larkin, James R
Simard, Manon A
Khrapitchev, Alexandre A
Meakin, James A
Okell, Thomas W
Craig, Martin
Ray, Kevin J
Jezzard, Peter
Chappell, Michael A
Sibson, Nicola R
author_facet Larkin, James R
Simard, Manon A
Khrapitchev, Alexandre A
Meakin, James A
Okell, Thomas W
Craig, Martin
Ray, Kevin J
Jezzard, Peter
Chappell, Michael A
Sibson, Nicola R
author_sort Larkin, James R
collection PubMed
description Cerebral blood flow is an important parameter in many diseases and functional studies that can be accurately measured in humans using arterial spin labelling (ASL) MRI. However, although rat models are frequently used for preclinical studies of both human disease and brain function, rat CBF measurements show poor consistency between studies. This lack of reproducibility is due, partly, to the smaller size and differing head geometry of rats compared to humans, as well as the differing analysis methodologies employed and higher field strengths used for preclinical MRI. To address these issues, we have implemented, optimised and validated a multiphase pseudo-continuous ASL technique, which overcomes many of the limitations of rat CBF measurement. Three rat strains (Wistar, Sprague Dawley and Berlin Druckrey IX) were used, and CBF values validated against gold-standard autoradiography measurements. Label positioning was found to be optimal at 45°, while post-label delay was optimised to 0.55 s. Whole brain CBF measures were 109 ± 22, 111 ± 18 and 100 ± 15 mL/100 g/min by multiphase pCASL, and 108 ± 12, 116 ± 14 and 122 ± 16 mL/100 g/min by autoradiography in Wistar, SD and BDIX cohorts, respectively. Tumour model analysis shows that the developed methods also apply in disease states. Thus, optimised multiphase pCASL provides robust, reproducible and non-invasive measurement of CBF in rats.
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spelling pubmed-66814342019-09-16 Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging Larkin, James R Simard, Manon A Khrapitchev, Alexandre A Meakin, James A Okell, Thomas W Craig, Martin Ray, Kevin J Jezzard, Peter Chappell, Michael A Sibson, Nicola R J Cereb Blood Flow Metab Original Articles Cerebral blood flow is an important parameter in many diseases and functional studies that can be accurately measured in humans using arterial spin labelling (ASL) MRI. However, although rat models are frequently used for preclinical studies of both human disease and brain function, rat CBF measurements show poor consistency between studies. This lack of reproducibility is due, partly, to the smaller size and differing head geometry of rats compared to humans, as well as the differing analysis methodologies employed and higher field strengths used for preclinical MRI. To address these issues, we have implemented, optimised and validated a multiphase pseudo-continuous ASL technique, which overcomes many of the limitations of rat CBF measurement. Three rat strains (Wistar, Sprague Dawley and Berlin Druckrey IX) were used, and CBF values validated against gold-standard autoradiography measurements. Label positioning was found to be optimal at 45°, while post-label delay was optimised to 0.55 s. Whole brain CBF measures were 109 ± 22, 111 ± 18 and 100 ± 15 mL/100 g/min by multiphase pCASL, and 108 ± 12, 116 ± 14 and 122 ± 16 mL/100 g/min by autoradiography in Wistar, SD and BDIX cohorts, respectively. Tumour model analysis shows that the developed methods also apply in disease states. Thus, optimised multiphase pCASL provides robust, reproducible and non-invasive measurement of CBF in rats. SAGE Publications 2018-03-02 2019-08 /pmc/articles/PMC6681434/ /pubmed/29498562 http://dx.doi.org/10.1177/0271678X18756218 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Larkin, James R
Simard, Manon A
Khrapitchev, Alexandre A
Meakin, James A
Okell, Thomas W
Craig, Martin
Ray, Kevin J
Jezzard, Peter
Chappell, Michael A
Sibson, Nicola R
Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title_full Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title_fullStr Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title_full_unstemmed Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title_short Quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
title_sort quantitative blood flow measurement in rat brain with multiphase arterial spin labelling magnetic resonance imaging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681434/
https://www.ncbi.nlm.nih.gov/pubmed/29498562
http://dx.doi.org/10.1177/0271678X18756218
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