Englander Institute for Precision Medicine

In vivo T1 mapping for quantifying glymphatic system transport and cervical lymph node drainage.

TitleIn vivo T1 mapping for quantifying glymphatic system transport and cervical lymph node drainage.
Publication TypeJournal Article
Year of Publication2020
AuthorsXue Y, Liu X, Koundal S, Constantinou S, Dai F, Santambrogio L, Lee H, Benveniste H
JournalSci Rep
Volume10
Issue1
Pagination14592
Date Published2020 Sep 03
ISSN2045-2322
KeywordsAnimals, Biological Transport, Brain Mapping, Drainage, Glymphatic System, Heterocyclic Compounds, Lymph Nodes, Magnetic Resonance Imaging, Male, Mice, Mice, Inbred C57BL, Neck, Organometallic Compounds
Abstract

Dynamic contrast-enhanced magnetic resonance imaging (MRI) for tracking glymphatic system transport with paramagnetic contrast such as gadoteric acid (Gd-DOTA) administration into cerebrospinal fluid (CSF) requires pre-contrast data for proper quantification. Here we introduce an alternative approach for glymphatic system quantification in the mouse brain via T1 mapping which also captures drainage of Gd-DOTA to the cervical lymph nodes. The Gd-DOTA injection into CSF was performed on the bench after which the mice underwent T1 mapping using a 3D spoiled gradient echo sequence on a 9.4 T MRI. In Ketamine/Xylazine (KX) anesthetized mice, glymphatic transport and drainage of Gd-DOTA to submandibular and deep cervical lymph nodes was demonstrated as 25-50% T1 reductions in comparison to control mice receiving CSF saline. To further validate the T1 mapping approach we also verified increased glymphatic transport of Gd-DOTA transport in mice anesthetized with KX in comparison with ISO. The novel T1 mapping method allows for quantification of glymphatic transport as well as drainage to the deep and superficial cervical lymph nodes. The ability to measure glymphatic transport and cervical lymph node drainage in the same animal longitudinally is advantageous and time efficient and the coupling between the two systems can be studied and translated to human studies.

DOI10.1038/s41598-020-71582-x
Alternate JournalSci Rep
PubMed ID32884041
PubMed Central IDPMC7471332
Grant ListRF1 AG057705 / AG / NIA NIH HHS / United States
UL1 TR001863 / TR / NCATS NIH HHS / United States
R01AG057705 / GF / NIH HHS / United States

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