Quantitative assessment of cerebral venous blood T2 in mouse at 11.7T: Implementation, optimization, and age effect

Research output: Contribution to journalArticle

Abstract

Purpose: To develop a non-contrast-agent MRI technique to quantify cerebral venous T2 in mice. Methods: We implemented and optimized a T2-relaxation-under-spin-tagging (TRUST) sequence on an 11.7 Tesla animal imaging system. A flow-sensitive-alternating-inversion-recovery (FAIR) module was used to generate control and label images, pair-wise subtraction of which yielded blood signals. Then, a T2-preparation module was applied to produce T2-weighted images, from which blood T2 was quantified. We conducted a series of technical studies to optimize the imaging slice position, inversion slab thickness, post-labeling delay (PLD), and repetition time. We also performed three physiological studies to examine the venous T2 dependence on hyperoxia (N=4), anesthesia (N=3), and brain aging (N=5). Results: Our technical studies suggested that, for efficient data acquisition with minimal bias in estimated T2, a preferred TRUST protocol was to place the imaging slice at the confluence of sagittal sinuses with an inversion-slab thickness of 2.5-mm, a PLD of 1000 ms and a repetition time of 3.5 s. Venous T2 values under normoxia and hyperoxia (inhaling pure oxygen) were 26.9±1.7 and 32.3±2.2 ms, respectively. Moreover, standard isoflurane anesthesia resulted in a higher venous T2 compared with dexmedetomidine anesthesia (N=3; P=0.01) which is more commonly used in animal functional MRI studies to preserve brain function. Venous T2 exhibited a decrease with age (N=5; P<0.001). Conclusion: We have developed and optimized a noninvasive method to quantify cerebral venous blood T2 in mouse at 11.7T. This method may prove useful in studies of brain physiology and pathophysiology in animal models.

Original languageEnglish (US)
JournalMagnetic Resonance in Medicine
DOIs
StateAccepted/In press - Jan 1 2017

Fingerprint

Hyperoxia
Anesthesia
Brain
Dexmedetomidine
Isoflurane
Inhalation
Animal Models
Magnetic Resonance Imaging
Oxygen

Keywords

  • Aging effect
  • Anesthesia effect
  • Blood oxygenation
  • Cerebral venous T
  • Hyperoxia
  • Mouse
  • MRI
  • TRUST

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Cite this

@article{57b5723a20214c5ab8bffe98842c52b9,
title = "Quantitative assessment of cerebral venous blood T2 in mouse at 11.7T: Implementation, optimization, and age effect",
abstract = "Purpose: To develop a non-contrast-agent MRI technique to quantify cerebral venous T2 in mice. Methods: We implemented and optimized a T2-relaxation-under-spin-tagging (TRUST) sequence on an 11.7 Tesla animal imaging system. A flow-sensitive-alternating-inversion-recovery (FAIR) module was used to generate control and label images, pair-wise subtraction of which yielded blood signals. Then, a T2-preparation module was applied to produce T2-weighted images, from which blood T2 was quantified. We conducted a series of technical studies to optimize the imaging slice position, inversion slab thickness, post-labeling delay (PLD), and repetition time. We also performed three physiological studies to examine the venous T2 dependence on hyperoxia (N=4), anesthesia (N=3), and brain aging (N=5). Results: Our technical studies suggested that, for efficient data acquisition with minimal bias in estimated T2, a preferred TRUST protocol was to place the imaging slice at the confluence of sagittal sinuses with an inversion-slab thickness of 2.5-mm, a PLD of 1000 ms and a repetition time of 3.5 s. Venous T2 values under normoxia and hyperoxia (inhaling pure oxygen) were 26.9±1.7 and 32.3±2.2 ms, respectively. Moreover, standard isoflurane anesthesia resulted in a higher venous T2 compared with dexmedetomidine anesthesia (N=3; P=0.01) which is more commonly used in animal functional MRI studies to preserve brain function. Venous T2 exhibited a decrease with age (N=5; P<0.001). Conclusion: We have developed and optimized a noninvasive method to quantify cerebral venous blood T2 in mouse at 11.7T. This method may prove useful in studies of brain physiology and pathophysiology in animal models.",
keywords = "Aging effect, Anesthesia effect, Blood oxygenation, Cerebral venous T, Hyperoxia, Mouse, MRI, TRUST",
author = "Zhiliang Wei and Jiadi Xu and Peiying Liu and Lin Chen and Wenbo Li and {Van Zijl}, {Peter C} and Hanzhang Lu",
year = "2017",
month = "1",
day = "1",
doi = "10.1002/mrm.27046",
language = "English (US)",
journal = "Magnetic Resonance in Medicine",
issn = "0740-3194",
publisher = "John Wiley and Sons Inc.",

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TY - JOUR

T1 - Quantitative assessment of cerebral venous blood T2 in mouse at 11.7T

T2 - Implementation, optimization, and age effect

AU - Wei, Zhiliang

AU - Xu, Jiadi

AU - Liu, Peiying

AU - Chen, Lin

AU - Li, Wenbo

AU - Van Zijl, Peter C

AU - Lu, Hanzhang

PY - 2017/1/1

Y1 - 2017/1/1

N2 - Purpose: To develop a non-contrast-agent MRI technique to quantify cerebral venous T2 in mice. Methods: We implemented and optimized a T2-relaxation-under-spin-tagging (TRUST) sequence on an 11.7 Tesla animal imaging system. A flow-sensitive-alternating-inversion-recovery (FAIR) module was used to generate control and label images, pair-wise subtraction of which yielded blood signals. Then, a T2-preparation module was applied to produce T2-weighted images, from which blood T2 was quantified. We conducted a series of technical studies to optimize the imaging slice position, inversion slab thickness, post-labeling delay (PLD), and repetition time. We also performed three physiological studies to examine the venous T2 dependence on hyperoxia (N=4), anesthesia (N=3), and brain aging (N=5). Results: Our technical studies suggested that, for efficient data acquisition with minimal bias in estimated T2, a preferred TRUST protocol was to place the imaging slice at the confluence of sagittal sinuses with an inversion-slab thickness of 2.5-mm, a PLD of 1000 ms and a repetition time of 3.5 s. Venous T2 values under normoxia and hyperoxia (inhaling pure oxygen) were 26.9±1.7 and 32.3±2.2 ms, respectively. Moreover, standard isoflurane anesthesia resulted in a higher venous T2 compared with dexmedetomidine anesthesia (N=3; P=0.01) which is more commonly used in animal functional MRI studies to preserve brain function. Venous T2 exhibited a decrease with age (N=5; P<0.001). Conclusion: We have developed and optimized a noninvasive method to quantify cerebral venous blood T2 in mouse at 11.7T. This method may prove useful in studies of brain physiology and pathophysiology in animal models.

AB - Purpose: To develop a non-contrast-agent MRI technique to quantify cerebral venous T2 in mice. Methods: We implemented and optimized a T2-relaxation-under-spin-tagging (TRUST) sequence on an 11.7 Tesla animal imaging system. A flow-sensitive-alternating-inversion-recovery (FAIR) module was used to generate control and label images, pair-wise subtraction of which yielded blood signals. Then, a T2-preparation module was applied to produce T2-weighted images, from which blood T2 was quantified. We conducted a series of technical studies to optimize the imaging slice position, inversion slab thickness, post-labeling delay (PLD), and repetition time. We also performed three physiological studies to examine the venous T2 dependence on hyperoxia (N=4), anesthesia (N=3), and brain aging (N=5). Results: Our technical studies suggested that, for efficient data acquisition with minimal bias in estimated T2, a preferred TRUST protocol was to place the imaging slice at the confluence of sagittal sinuses with an inversion-slab thickness of 2.5-mm, a PLD of 1000 ms and a repetition time of 3.5 s. Venous T2 values under normoxia and hyperoxia (inhaling pure oxygen) were 26.9±1.7 and 32.3±2.2 ms, respectively. Moreover, standard isoflurane anesthesia resulted in a higher venous T2 compared with dexmedetomidine anesthesia (N=3; P=0.01) which is more commonly used in animal functional MRI studies to preserve brain function. Venous T2 exhibited a decrease with age (N=5; P<0.001). Conclusion: We have developed and optimized a noninvasive method to quantify cerebral venous blood T2 in mouse at 11.7T. This method may prove useful in studies of brain physiology and pathophysiology in animal models.

KW - Aging effect

KW - Anesthesia effect

KW - Blood oxygenation

KW - Cerebral venous T

KW - Hyperoxia

KW - Mouse

KW - MRI

KW - TRUST

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