PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats
Type C hepatic encephalopathy (HE) is a complex neuropsychiatric disorder occurring as a consequence of chronic liver disease. Alterations in energy metabolism have been suggested in type C HE, but in vivo studies on this matter remain sparse and have reported conflicting results. Here, we propose a...
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Veröffentlicht in: | Analytical biochemistry 2022-06, Vol.647, p.114606-114606, Article 114606 |
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creator | Mosso, Jessie Yin, Ting Poitry-Yamate, Carole Simicic, Dunja Lepore, Mario McLin, Valérie A. Braissant, Olivier Cudalbu, Cristina Lanz, Bernard |
description | Type C hepatic encephalopathy (HE) is a complex neuropsychiatric disorder occurring as a consequence of chronic liver disease. Alterations in energy metabolism have been suggested in type C HE, but in vivo studies on this matter remain sparse and have reported conflicting results. Here, we propose a novel preclinical 18F-FDG PET methodology to compute quantitative 3D maps of the regional cerebral metabolic rate of glucose (CMRglc) from a labelling steady-state PET image of the brain and an image-derived input function. This quantitative approach shows its strength when comparing groups of animals with divergent physiology, such as HE animals. PET CMRglc maps were registered to an atlas and the mean CMRglc from the hippocampus and the cerebellum were associated to the corresponding localized 1H MR spectroscopy acquisitions. This study provides for the first time local and quantitative information on both brain glucose uptake and neurometabolic profile alterations in a rat model of type C HE. A 2-fold lower brain glucose uptake, concomitant with an increase in brain glutamine and a decrease in the main osmolytes, was observed in the hippocampus and in the cerebellum. These novel findings are an important step towards new insights into energy metabolism in the pathophysiology of HE.
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[Display omitted]</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2022.114606</identifier><language>eng</language><publisher>Elsevier Inc</publisher><subject>18F-FDG PET ; 1H MRS ; animal models ; Bile duct ligation ; cerebellum ; Cerebral metabolic rate of glucose ; encephalopathy ; energy metabolism ; glucose ; glutamine ; hippocampus ; liver diseases ; pathophysiology ; quantitative analysis ; Rat brain ; spectroscopy ; Type C hepatic encephalopathy</subject><ispartof>Analytical biochemistry, 2022-06, Vol.647, p.114606-114606, Article 114606</ispartof><rights>2022 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2476-c0690b581dd4e393c449011c2b56fccb24ceca19246d3fc3ef08ddffc3db72e73</citedby><cites>FETCH-LOGICAL-c2476-c0690b581dd4e393c449011c2b56fccb24ceca19246d3fc3ef08ddffc3db72e73</cites><orcidid>0000-0002-6600-2696 ; 0000-0001-5136-075X ; 0000-0002-3084-4277 ; 0000-0001-6318-9507 ; 0000-0003-4582-2465 ; 0000-0002-8068-3344</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003269722000628$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Mosso, Jessie</creatorcontrib><creatorcontrib>Yin, Ting</creatorcontrib><creatorcontrib>Poitry-Yamate, Carole</creatorcontrib><creatorcontrib>Simicic, Dunja</creatorcontrib><creatorcontrib>Lepore, Mario</creatorcontrib><creatorcontrib>McLin, Valérie A.</creatorcontrib><creatorcontrib>Braissant, Olivier</creatorcontrib><creatorcontrib>Cudalbu, Cristina</creatorcontrib><creatorcontrib>Lanz, Bernard</creatorcontrib><title>PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats</title><title>Analytical biochemistry</title><description>Type C hepatic encephalopathy (HE) is a complex neuropsychiatric disorder occurring as a consequence of chronic liver disease. Alterations in energy metabolism have been suggested in type C HE, but in vivo studies on this matter remain sparse and have reported conflicting results. Here, we propose a novel preclinical 18F-FDG PET methodology to compute quantitative 3D maps of the regional cerebral metabolic rate of glucose (CMRglc) from a labelling steady-state PET image of the brain and an image-derived input function. This quantitative approach shows its strength when comparing groups of animals with divergent physiology, such as HE animals. PET CMRglc maps were registered to an atlas and the mean CMRglc from the hippocampus and the cerebellum were associated to the corresponding localized 1H MR spectroscopy acquisitions. This study provides for the first time local and quantitative information on both brain glucose uptake and neurometabolic profile alterations in a rat model of type C HE. A 2-fold lower brain glucose uptake, concomitant with an increase in brain glutamine and a decrease in the main osmolytes, was observed in the hippocampus and in the cerebellum. These novel findings are an important step towards new insights into energy metabolism in the pathophysiology of HE.
[Display omitted]</description><subject>18F-FDG PET</subject><subject>1H MRS</subject><subject>animal models</subject><subject>Bile duct ligation</subject><subject>cerebellum</subject><subject>Cerebral metabolic rate of glucose</subject><subject>encephalopathy</subject><subject>energy metabolism</subject><subject>glucose</subject><subject>glutamine</subject><subject>hippocampus</subject><subject>liver diseases</subject><subject>pathophysiology</subject><subject>quantitative analysis</subject><subject>Rat brain</subject><subject>spectroscopy</subject><subject>Type C hepatic encephalopathy</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNkL1PwzAQxS0EEqWwM3pkSTk7idOwQSkfUhEIymw550txSZNgJyD-ewJlRWK6N_ze07vH2LGAiQChTtcTU0wkSDkRIlGgdthIQK4iiCHfZSMAiCOp8myfHYSwBhioVI2YeZgv-ezucVUh35i2dfWKm9pycRPdPT7x8NJ8cFN15MnyVdVjE4j3bWde6QerqffNhjpTNJVD3vqmdBUF7mp-cbng3nThkO2Vpgp09HvH7PlqvpzdRIv769vZ-SJCmWQqQlA5FOlUWJtQnMeYJPlQEmWRqhKxkAkSGpHLRNm4xJhKmFpbDsoWmaQsHrOTbe5Q4q2n0OmNC0hVZWpq-qClytJUiSH0H2isRCKnGQwobFH0TQieSt16tzH-UwvQ38PrtTaF_h5eb4cfLGdbCw3fvjvyOqCjGsk6T9hp27i_zV9sxIj3</recordid><startdate>20220615</startdate><enddate>20220615</enddate><creator>Mosso, Jessie</creator><creator>Yin, Ting</creator><creator>Poitry-Yamate, Carole</creator><creator>Simicic, Dunja</creator><creator>Lepore, Mario</creator><creator>McLin, Valérie A.</creator><creator>Braissant, Olivier</creator><creator>Cudalbu, Cristina</creator><creator>Lanz, Bernard</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-6600-2696</orcidid><orcidid>https://orcid.org/0000-0001-5136-075X</orcidid><orcidid>https://orcid.org/0000-0002-3084-4277</orcidid><orcidid>https://orcid.org/0000-0001-6318-9507</orcidid><orcidid>https://orcid.org/0000-0003-4582-2465</orcidid><orcidid>https://orcid.org/0000-0002-8068-3344</orcidid></search><sort><creationdate>20220615</creationdate><title>PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats</title><author>Mosso, Jessie ; Yin, Ting ; Poitry-Yamate, Carole ; Simicic, Dunja ; Lepore, Mario ; McLin, Valérie A. ; Braissant, Olivier ; Cudalbu, Cristina ; Lanz, Bernard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2476-c0690b581dd4e393c449011c2b56fccb24ceca19246d3fc3ef08ddffc3db72e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>18F-FDG PET</topic><topic>1H MRS</topic><topic>animal models</topic><topic>Bile duct ligation</topic><topic>cerebellum</topic><topic>Cerebral metabolic rate of glucose</topic><topic>encephalopathy</topic><topic>energy metabolism</topic><topic>glucose</topic><topic>glutamine</topic><topic>hippocampus</topic><topic>liver diseases</topic><topic>pathophysiology</topic><topic>quantitative analysis</topic><topic>Rat brain</topic><topic>spectroscopy</topic><topic>Type C hepatic encephalopathy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mosso, Jessie</creatorcontrib><creatorcontrib>Yin, Ting</creatorcontrib><creatorcontrib>Poitry-Yamate, Carole</creatorcontrib><creatorcontrib>Simicic, Dunja</creatorcontrib><creatorcontrib>Lepore, Mario</creatorcontrib><creatorcontrib>McLin, Valérie A.</creatorcontrib><creatorcontrib>Braissant, Olivier</creatorcontrib><creatorcontrib>Cudalbu, Cristina</creatorcontrib><creatorcontrib>Lanz, Bernard</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mosso, Jessie</au><au>Yin, Ting</au><au>Poitry-Yamate, Carole</au><au>Simicic, Dunja</au><au>Lepore, Mario</au><au>McLin, Valérie A.</au><au>Braissant, Olivier</au><au>Cudalbu, Cristina</au><au>Lanz, Bernard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats</atitle><jtitle>Analytical biochemistry</jtitle><date>2022-06-15</date><risdate>2022</risdate><volume>647</volume><spage>114606</spage><epage>114606</epage><pages>114606-114606</pages><artnum>114606</artnum><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>Type C hepatic encephalopathy (HE) is a complex neuropsychiatric disorder occurring as a consequence of chronic liver disease. Alterations in energy metabolism have been suggested in type C HE, but in vivo studies on this matter remain sparse and have reported conflicting results. Here, we propose a novel preclinical 18F-FDG PET methodology to compute quantitative 3D maps of the regional cerebral metabolic rate of glucose (CMRglc) from a labelling steady-state PET image of the brain and an image-derived input function. This quantitative approach shows its strength when comparing groups of animals with divergent physiology, such as HE animals. PET CMRglc maps were registered to an atlas and the mean CMRglc from the hippocampus and the cerebellum were associated to the corresponding localized 1H MR spectroscopy acquisitions. This study provides for the first time local and quantitative information on both brain glucose uptake and neurometabolic profile alterations in a rat model of type C HE. A 2-fold lower brain glucose uptake, concomitant with an increase in brain glutamine and a decrease in the main osmolytes, was observed in the hippocampus and in the cerebellum. These novel findings are an important step towards new insights into energy metabolism in the pathophysiology of HE.
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subjects | 18F-FDG PET 1H MRS animal models Bile duct ligation cerebellum Cerebral metabolic rate of glucose encephalopathy energy metabolism glucose glutamine hippocampus liver diseases pathophysiology quantitative analysis Rat brain spectroscopy Type C hepatic encephalopathy |
title | PET CMRglc mapping and 1H-MRS show altered glucose uptake and neurometabolic profiles in BDL rats |
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