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Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid

Vujic, N; Korbelius, M; Leopold, C; Duta-Mare, M; Rainer, S; Schlager, S; Goeritzer, M; Kolb, D; Eichmann, TO; Diwoky, C; Zimmer, A; Zimmermann, R; Lass, A; Radovic, B; Kratky, D.
Monoglyceride lipase deficiency affects hepatic cholesterol metabolism and lipid-dependent gut transit in ApoE-/- mice.
Oncotarget. 2017; 8(20):33122-33136 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG


Autor/innen der Med Uni Graz:
Duta-Mare Madalina-Cristina
Göritzer Madeleine
Kolb-Lenz Dagmar
Korbelius Melanie
Kratky Dagmar
Leopold Christina
Radovic Branislav
Rainer Silvia
Schlager Stefanie
Vujic Nemanja

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Plum Analytics:
Number of Figures: 6
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Monoglyceride lipase (MGL) hydrolyzes monoglycerides (MGs) to glycerol and fatty acids. Among various MG species MGL also degrades 2-arachidonoylglycerol (2-AG), the most abundant endocannabinoid and potent activator of cannabinoid receptors (CBR) 1 and 2. MGL-knockout (-/-) mice exhibit pronounced 2-AG accumulation, but lack central cannabimimetic effects due to CB1R desensitization. We have previously shown that MGL affects plaque stability in apolipoprotein E (ApoE)-/- mice, an established animal model for dyslipidemia and atherosclerosis. In the current study, we investigated functional consequences of MGL deficiency on lipid and energy metabolism in ApoE/MGL double knockout (DKO) mice. MGL deficiency affected hepatic cholesterol metabolism by causing increased cholesterol elimination via the biliary pathway. Moreover, DKO mice exhibit lipid-triggered delay in gastric emptying without major effects on overall triglyceride and cholesterol absorption. The observed phenotype of DKO mice is likely not a consequence of potentiated CB1R signaling but rather dependent on the activation of alternative signaling pathways. We conclude that MGL deficiency causes complex metabolic changes including cholesterol metabolism and regulation of gut transit independent of the endocannabinoid system.
Find related publications in this database (using NLM MeSH Indexing)
Alcohol Oxidoreductases - metabolism
Animals -
Apolipoproteins E - genetics
Arachidonic Acids - metabolism
Asialoglycoproteins - deficiency
Asialoglycoproteins - genetics
Atherosclerosis - metabolism
Cholesterol - metabolism
Disease Models, Animal -
Dyslipidemias - metabolism
Endocannabinoids - metabolism
Gene Knockout Techniques -
Glycerides - metabolism
Intestinal Mucosa - metabolism
Lectins, C-Type - deficiency
Lectins, C-Type - genetics
Liver - metabolism
Male -
Membrane Proteins - deficiency
Membrane Proteins - genetics
Mice -

Find related publications in this database (Keywords)
cannabinoid receptor
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