File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/mrm.23121
- Scopus: eid_2-s2.0-80053040009
- PMID: 21928357
- WOS: WOS:000295356500004
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Diffusion-weighted magnetic resonance spectroscopy: A novel approach to investigate intramyocellular lipids
Title | Diffusion-weighted magnetic resonance spectroscopy: A novel approach to investigate intramyocellular lipids | ||||
---|---|---|---|---|---|
Authors | |||||
Keywords | diffusion extramyocellular lipids IMCL intramyocellular lipids MRS skeletal muscle | ||||
Issue Date | 2011 | ||||
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0740-3194/ | ||||
Citation | Magnetic Resonance In Medicine, 2011, v. 66 n. 4, p. 937-944 How to Cite? | ||||
Abstract | Motivated by the potential difference between intramyocellular lipid (IMCL) and extramyocellular lipid (EMCL) in their microscopically restricted diffusion environments, proton diffusion properties in IMCL and EMCL were characterized by diffusion-weighted magnetic resonance spectroscopy. Ex vivo experiments were conducted on fresh pig lower hindlimb muscle samples. In vivo experiments were performed on the lower hindlimbs of normal adult Sprague-Dawley rats. Ex vivo apparent diffusion coefficients at 20°C were found to be in the ranges of (10.8 ± 0.5) × 10 -6 to (15.8 ± 0.8) × 10 -6 mm 2/s for EMCL and (1.6 ± 0.6) × 10 -6 to (2.4 ± 0.7) × 10 -6 mm 2/s for IMCL depending on the diffusion weighting direction relative to muscle fiber orientation. In vivo apparent diffusion coefficients of EMCL and IMCL were measured as (13.8 ± 0.9) × 10 -6 and (4.6 ± 0.7) × 10 -6 mm 2/s, respectively, along the direction perpendicular to muscle fiber orientation. Our results demonstrated that the apparent diffusion coefficient of EMCL was substantially higher than that of IMCL. Therefore, EMCL could be effectively suppressed by proper diffusion weighting to achieve reliable detection of IMCL despite unknown or/and multiple muscle fiber orientations. Such lipid proton diffusion approach can be used for robust IMCL separation and identification. Furthermore, it may provide new biophysical insights in the investigation of lipid metabolism in obesity and diabetes. © 2011 Wiley-Liss, Inc. | ||||
Persistent Identifier | http://hdl.handle.net/10722/155658 | ||||
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 1.343 | ||||
ISI Accession Number ID |
Funding Information: Grant sponsor: Hong Kong Research Grant Council; Grant number: HKU7826/10M. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Xiao, L | en_US |
dc.contributor.author | Wu, EX | en_US |
dc.date.accessioned | 2012-08-08T08:34:42Z | - |
dc.date.available | 2012-08-08T08:34:42Z | - |
dc.date.issued | 2011 | en_US |
dc.identifier.citation | Magnetic Resonance In Medicine, 2011, v. 66 n. 4, p. 937-944 | en_US |
dc.identifier.issn | 0740-3194 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/155658 | - |
dc.description.abstract | Motivated by the potential difference between intramyocellular lipid (IMCL) and extramyocellular lipid (EMCL) in their microscopically restricted diffusion environments, proton diffusion properties in IMCL and EMCL were characterized by diffusion-weighted magnetic resonance spectroscopy. Ex vivo experiments were conducted on fresh pig lower hindlimb muscle samples. In vivo experiments were performed on the lower hindlimbs of normal adult Sprague-Dawley rats. Ex vivo apparent diffusion coefficients at 20°C were found to be in the ranges of (10.8 ± 0.5) × 10 -6 to (15.8 ± 0.8) × 10 -6 mm 2/s for EMCL and (1.6 ± 0.6) × 10 -6 to (2.4 ± 0.7) × 10 -6 mm 2/s for IMCL depending on the diffusion weighting direction relative to muscle fiber orientation. In vivo apparent diffusion coefficients of EMCL and IMCL were measured as (13.8 ± 0.9) × 10 -6 and (4.6 ± 0.7) × 10 -6 mm 2/s, respectively, along the direction perpendicular to muscle fiber orientation. Our results demonstrated that the apparent diffusion coefficient of EMCL was substantially higher than that of IMCL. Therefore, EMCL could be effectively suppressed by proper diffusion weighting to achieve reliable detection of IMCL despite unknown or/and multiple muscle fiber orientations. Such lipid proton diffusion approach can be used for robust IMCL separation and identification. Furthermore, it may provide new biophysical insights in the investigation of lipid metabolism in obesity and diabetes. © 2011 Wiley-Liss, Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.interscience.wiley.com/jpages/0740-3194/ | en_US |
dc.relation.ispartof | Magnetic Resonance in Medicine | en_US |
dc.subject | diffusion | - |
dc.subject | extramyocellular lipids | - |
dc.subject | IMCL | - |
dc.subject | intramyocellular lipids | - |
dc.subject | MRS | - |
dc.subject | skeletal muscle | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Diabetes Mellitus - Metabolism | en_US |
dc.subject.mesh | Diffusion | en_US |
dc.subject.mesh | Extracellular Space - Physiology | en_US |
dc.subject.mesh | Hindlimb | en_US |
dc.subject.mesh | Intracellular Fluid - Physiology | en_US |
dc.subject.mesh | Lipid Metabolism | en_US |
dc.subject.mesh | Lipids - Analysis | en_US |
dc.subject.mesh | Magnetic Resonance Spectroscopy - Methods | en_US |
dc.subject.mesh | Muscle, Skeletal - Metabolism | en_US |
dc.subject.mesh | Obesity - Metabolism | en_US |
dc.subject.mesh | Phantoms, Imaging | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Swine | en_US |
dc.title | Diffusion-weighted magnetic resonance spectroscopy: A novel approach to investigate intramyocellular lipids | en_US |
dc.type | Article | en_US |
dc.identifier.email | Wu, EX:ewu1@hkucc.hku.hk | en_US |
dc.identifier.authority | Wu, EX=rp00193 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/mrm.23121 | en_US |
dc.identifier.pmid | 21928357 | - |
dc.identifier.scopus | eid_2-s2.0-80053040009 | en_US |
dc.identifier.hkuros | 206794 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-80053040009&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 66 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 937 | en_US |
dc.identifier.epage | 944 | en_US |
dc.identifier.eissn | 1522-2594 | - |
dc.identifier.isi | WOS:000295356500004 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Xiao, L=53064880500 | en_US |
dc.identifier.scopusauthorid | Wu, EX=7202128034 | en_US |
dc.identifier.issnl | 0740-3194 | - |