0000000000660237

AUTHOR

Grzegorz Godlewski

showing 2 related works from this author

Hepatic CB1 receptor is required for development of diet-induced steatosis, dyslipidemia, and insulin and leptin resistance in mice

2007

Diet-induced obesity is associated with fatty liver, insulin resistance, leptin resistance, and changes in plasma lipid profile. Endocannabinoids have been implicated in the development of these associated phenotypes, because mice deficient for the cannabinoid receptor CB1 (CB1-/-) do not display these changes in association with diet-induced obesity. The target tissues that mediate these effects, however, remain unknown. We therefore investigated the relative role of hepatic versus extrahepatic CB1 receptors in the metabolic consequences of a high-fat diet, using liver-specific CB1 knockout (LCB1-/-) mice. LCB1(-/-) mice fed a high-fat diet developed a similar degree of obesity as that of …

LeptinMalemedicine.medical_specialtymedicine.medical_treatmentBiologyMiceInsulin resistanceReceptor Cannabinoid CB1Internal medicinemedicineGlucose homeostasisAnimalsInsulinObesityDyslipidemiasMice KnockoutLeptinInsulinmusculoskeletal neural and ocular physiologyFatty liverGeneral Medicinemedicine.diseaseEndocannabinoid systemAnimal FeedFatty LiverMice Inbred C57BLEndocrinologyLivernervous systemFemalelipids (amino acids peptides and proteins)SteatosisInsulin ResistanceDyslipidemiapsychological phenomena and processesResearch Article
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Inhibiting fatty acid amide hydrolase normalizes endotoxin-induced enhanced gastrointestinal motility in mice

2012

Background and purpose Gastrointestinal (GI) motility is regulated in part by fatty acid ethanolamides (FAEs), including the endocannabinoid (EC) anandamide (AEA). The actions of FAEs are terminated by fatty acid amide hydrolase (FAAH). We investigated the actions of the novel FAAH inhibitor AM3506 on normal and enhanced GI motility. Experimental approach We examined the effect of AM3506 on electrically-evoked contractility in vitro and GI transit and colonic faecal output in vivo, in normal and FAAH-deficient mice treated with saline or LPS (100 µg·kg(-1), i.p.), in the presence and absence of cannabinoid (CB) receptor antagonists. mRNA expression was measured by quantitative real time-PCR…

Pharmacologymedicine.medical_specialtyCannabinoid receptormedicine.medical_treatmentdigestive oral and skin physiologyMotilityIleumAnandamideBiologyEndocannabinoid systemchemistry.chemical_compoundEndocrinologymedicine.anatomical_structurenervous systemchemistryFatty acid amide hydrolaseInternal medicinemedicinelipids (amino acids peptides and proteins)CannabinoidReceptorpsychological phenomena and processesBritish Journal of Pharmacology
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