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Status: Bibliographieeintrag

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Verfasst von:Otto, Ann-Christin [VerfasserIn]   i
 Gan-Schreier, Hongying [VerfasserIn]   i
 Zhu, Xingya [VerfasserIn]   i
 Tuma-Kellner, Sabine [VerfasserIn]   i
 Staffer, Simone [VerfasserIn]   i
 Ganzha, Alexandra [VerfasserIn]   i
 Liebisch, Gerhard [VerfasserIn]   i
 Chamulitrat, Walee [VerfasserIn]   i
Titel:Group VIA phospholipase A2 deficiency in mice chronically fed with high-fat-diet attenuates hepatic steatosis by correcting a defect of phospholipid remodeling
Verf.angabe:Ann-Christin Otto, Hongying Gan-Schreier, Xingya Zhu, Sabine Tuma-Kellner, Simone Staffer, Alexandra Ganzha, Gerhard Liebisch, Walee Chamulitrat
E-Jahr:2019
Jahr:5 February 2019
Umfang:15 S.
Fussnoten:Gesehen am 20.08.2019
Titel Quelle:Enthalten in: Biochimica et biophysica acta / Molecular and cell biology of lipids
Ort Quelle:Amsterdam : Elsevier, 1998
Jahr Quelle:2019
Band/Heft Quelle:1864(2019), 5, Seite 662-676
ISSN Quelle:1879-2618
Abstract:A defect of hepatic remodeling of phospholipids (PL) is seen in non-alcoholic fatty liver disease and steatohepatitis (NASH) indicating pivotal role of PL metabolism in this disease. The deletion of group VIA calcium-independent phospholipase A2 (iPla2β) protects ob/ob mice from hepatic steatosis (BBAlip 1861, 2016, 440-461), however its role in high-fat diet (HFD)-induced NASH is still elusive. Here, wild-type and iPla2β-null mice were subjected to chronic feeding with HFD for 6 months. We showed that protection was observed in iPla2β-null mice with an attenuation of diet-induced body and liver-weight gains, liver enzymes, serum free fatty acids as well as hepatic TG and steatosis scores. iPla2β deficiency under HFD attenuated the levels of 1-stearoyl lysophosphatidylcholine (LPC), lysophosphatidylethanolamine (LPE), and lysophosphatidylinositol (LPI) as well as elevation of hepatic arachidonate, arachidonate-containing cholesterol esters and prostaglandin E2. More importantly, this deficiency rescued a defect in PL remodeling and attenuated the ratio of saturated and unsaturated PL. The protection by iPla2β deficiency was not observed during short-term HFD feeding of 3 or 5 weeks which showed no PL remodeling defect. In addition to PC/PE, this deficiency reversed the suppression of PC/PI and PE/PI among monounsaturated PL. However, this deficiency did not modulate hepatic PL contents and PL ratios in ER fractions, ER stress, fibrosis, and inflammation markers. Hence, iPla2β inactivation protected mice against hepatic steatosis and obesity during chronic dietary NASH by correcting PL remodeling defect and PI composition relative to PC and PE.
DOI:doi:10.1016/j.bbalip.2019.01.012
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.bbalip.2019.01.012
 Volltext: http://www.sciencedirect.com/science/article/pii/S138819811830221X
 DOI: https://doi.org/10.1016/j.bbalip.2019.01.012
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Fatty acid homeostasis
 High-fat diet
 NASH
 Phospholipid remodeling
 Phospholipidomes
 PLA2G6
K10plus-PPN:1671655915
Verknüpfungen:→ Zeitschrift

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