Trihydroxycholanoyl-taurine in brains of rodents with hepatic encephalopathy.


Journal

Journal of mass spectrometry : JMS
ISSN: 1096-9888
Titre abrégé: J Mass Spectrom
Pays: England
ID NLM: 9504818

Informations de publication

Date de publication:
Jun 2021
Historique:
revised: 22 03 2021
received: 14 01 2021
accepted: 01 04 2021
entrez: 4 5 2021
pubmed: 5 5 2021
medline: 16 11 2021
Statut: ppublish

Résumé

Hepatic encephalopathy (HE), a neurological disease resulting from liver failure, is difficult to manage and its causes are unclear. Bile acids have been postulated to be involved in the provenance and progression of various diseases including HE. Hence, the characterization of bile acid profiles in the brains of subjects with and without liver failure can provide important clues for the potential treatment of HE. Nanoflow ultra-performance liquid chromatography electrospray ionization ion mobility mass spectrometry (UPLC-ESI-IM-MS) is a highly sensitive method for detection of specific molecules, such as bile acids in brain samples, at biologically relevant concentrations. We used UPLC-ESI-IM-MS to characterize bile acid profiles in brain samples from seven "healthy" control rodents and 22 "diseased" rodents with liver failure (i.e., induced HE). An isomer of trihydroxycholanoyl-taurine was detected in brain tissue samples from both rats and mice with induced HE; however, this isomer was not detected in the brains of healthy rats and mice. Our findings were confirmed by comparing IM arrival times (AT), exact mass measurements (m/z), and mass spectral fragmentation patterns of the experimentally observed suspected species to standards of trihydroxycholanoyl-taurine isomers. Moreover, In Silico Fractionation was employed to provide an additional analytical dimension to verify bile acid identifications.

Identifiants

pubmed: 33942437
doi: 10.1002/jms.4729
doi:

Substances chimiques

Bile Acids and Salts 0
Taurine 1EQV5MLY3D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e4729

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK112803
Pays : United States
Organisme : United States Department of Veterans Affairs Biomedical Laboratory Research and Development Service
ID : BX002638
Organisme : United States Department of Veterans Affairs Biomedical Laboratory Research and Development Service
ID : DK082435

Informations de copyright

© 2021 John Wiley & Sons Ltd. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

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Auteurs

Amy N W Schnelle (ANW)

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.

Luke T Richardson (LT)

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.

Michael E Pettit (ME)

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.
BioTherapeutics Analytical Development, Janssen Research and Development, LLC, 200 Great Valley Parkway, Malvern, Pennsylvania, 19355, USA.

Sharon DeMorrow (S)

Research Services, Central Texas Veterans Health Care System, Temple, Texas, 76504, USA.
Pharmacology and Toxicology Division, College of Pharmacy, University of Texas at Austin, Austin, Texas, 78712, USA.
Department of Internal Medicine, Dell Medical School, University of Texas at Austin, Austin, Texas, 78712, USA.

Touradj Solouki (T)

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.

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