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Article: The effect of aquaporin-4 inhibition on cerebrospinal fluid-tissue water exchange in mouse brain detected by magnetization transfer indirect spin labeling MRI

TitleThe effect of aquaporin-4 inhibition on cerebrospinal fluid-tissue water exchange in mouse brain detected by magnetization transfer indirect spin labeling MRI
Authors
KeywordsAQP4
CSF
magnetization transfer
magnetization transfer indirect spin labeling
MRI
water exchange
Issue Date1-Jan-2024
PublisherWiley
Citation
NMR in Biomedicine, 2024, v. 37, n. 7 How to Cite?
AbstractThe fluid transport of cerebrospinal fluid (CSF) and interstitial fluid in surrounding tissues plays an important role in the drainage pathway that facilitates waste clearance from the brain. This pathway is known as the glymphatic or perivascular system, and its functions are dependent on aquaporin-4 (AQP4). Recently, magnetization transfer indirect spin labeling (MISL) magnetic resonance imaging (MRI) has been proposed as a noninvasive and noncontrast-enhanced method for detecting water exchange between CSF and brain tissue. In this study, we first optimized the MISL sequence at preclinical 3 T MRI, and then studied the correlation of MISL in CSF with magnetization transfer (MT) in brain tissue, as well as the altered water exchange under AQP4 inhibition, using C57BL/6 mice. Results showed a strong correlation of MISL signal with MT signal. With the AQP4 inhibitor, we observed a significant decrease in MISL value (P < 0.05), suggesting that the hampered AQP4 activity led to decreased water exchange between CSF and brain tissue or the impairment of the glymphatic function. Overall, our findings demonstrate the potential application of MISL in assessing brain water exchange at 3 T MRI and its potential clinical translation.
Persistent Identifierhttp://hdl.handle.net/10722/348685
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.949

 

DC FieldValueLanguage
dc.contributor.authorChen, Zilin-
dc.contributor.authorLai, Joseph H.C.-
dc.contributor.authorXu, Jiadi-
dc.contributor.authorZhang, Hao-
dc.contributor.authorHuang, Jianpan-
dc.contributor.authorChan, Kannie W.Y.-
dc.date.accessioned2024-10-12T00:30:04Z-
dc.date.available2024-10-12T00:30:04Z-
dc.date.issued2024-01-01-
dc.identifier.citationNMR in Biomedicine, 2024, v. 37, n. 7-
dc.identifier.issn0952-3480-
dc.identifier.urihttp://hdl.handle.net/10722/348685-
dc.description.abstractThe fluid transport of cerebrospinal fluid (CSF) and interstitial fluid in surrounding tissues plays an important role in the drainage pathway that facilitates waste clearance from the brain. This pathway is known as the glymphatic or perivascular system, and its functions are dependent on aquaporin-4 (AQP4). Recently, magnetization transfer indirect spin labeling (MISL) magnetic resonance imaging (MRI) has been proposed as a noninvasive and noncontrast-enhanced method for detecting water exchange between CSF and brain tissue. In this study, we first optimized the MISL sequence at preclinical 3 T MRI, and then studied the correlation of MISL in CSF with magnetization transfer (MT) in brain tissue, as well as the altered water exchange under AQP4 inhibition, using C57BL/6 mice. Results showed a strong correlation of MISL signal with MT signal. With the AQP4 inhibitor, we observed a significant decrease in MISL value (P < 0.05), suggesting that the hampered AQP4 activity led to decreased water exchange between CSF and brain tissue or the impairment of the glymphatic function. Overall, our findings demonstrate the potential application of MISL in assessing brain water exchange at 3 T MRI and its potential clinical translation.-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofNMR in Biomedicine-
dc.subjectAQP4-
dc.subjectCSF-
dc.subjectmagnetization transfer-
dc.subjectmagnetization transfer indirect spin labeling-
dc.subjectMRI-
dc.subjectwater exchange-
dc.titleThe effect of aquaporin-4 inhibition on cerebrospinal fluid-tissue water exchange in mouse brain detected by magnetization transfer indirect spin labeling MRI-
dc.typeArticle-
dc.identifier.doi10.1002/nbm.5093-
dc.identifier.scopuseid_2-s2.0-85180921971-
dc.identifier.volume37-
dc.identifier.issue7-
dc.identifier.eissn1099-1492-
dc.identifier.issnl0952-3480-

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