Key result
Endocannabinoid receptor blockade increases hepatocyte growth factor and reduces insulin in obese women with PCOS.
Why the study?
Activation of the endocannabinoid system via CB-1 receptor is associated with liver injury and fatty liver metabolism, and CB1 receptor antagonism may ameliorate NAFLD.
Does endocannabinoid receptor blockade alter hepatocyte growth factor and insulin levels in obese women with polycystic ovary syndrome?
Does endocannabinoid receptor blockade alter hepatocyte growth factor and insulin levels in obese women with polycystic ovary syndrome?
Endocannabinoid receptor blockade may modulate hepatocyte growth factor and insulin levels in obese women with polycystic ovary syndrome, potentially impacting fatty liver metabolism.
Answers are grounded in this paper and cite their sources.
CB1 blockade may improve metabolic markers in PCOS; leaves open any role in NAFLD pending randomized data.
There is evidence from animal and in-vitro studies that activation of the endocannabinoid system (EC) through cannabinoid receptor 1 (CB-1) is associated with liver injury, inflammation and hepatocellular carcinoma.1 Data suggests endogenous cannabinoids (EC) are related to fatty liver metabolism with a role in non-alcoholic fatty liver disease (NAFLD) through modulating lipid metabolism that may be ameliorated by CB1 receptor antagonism with rimonabant.2 This is of particular importance as NAFLD is the most common cause of chronic liver disease with liver dysfunction leading liver cirrhosis. The diagnosis of NAFLD can only be confirmed by a liver biopsy, as liver enzymes such as alanine aminotransferase (ALT) used, as a serum marker may not be elevated.
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Sathyapalan et al. (2016) studied Polycystic ovary syndrome and obesity. Endocannabinoid receptor blockade was evaluated on Hepatocyte growth factor and insulin levels. Endocannabinoid receptor blockade increases hepatocyte growth factor and reduces insulin levels in obese women with polycystic ovary syndrome.
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