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DOI 10.1016/j.cbi.2016.03.026

Медицинская библиотека · Chemico-biological interactions · 2016

Evaluation of hypocholesterolemic effect of oleuropein in cholesterol-fed rats.

Hadrich Fatma, Mahmoudi Asma, Bouallagui Zouhaier, Feki Ines, Isoda Hiroko, Feve Bruno, Sayadi Sami

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Аннотация

Oleuropein, which is the major compound of olive leaves, has been reported to exert several pharmacological properties, including anti-cancer, antidiabetic and anti-atherosclerotic activities. The objective of this study was to evaluate the effect of oleuropein on adiponectin level in high cholesterol diet (HCD) induced obesity in rat and the molecular mechanism underlying its activation. Our results showed that orally administered oleuropein (50 mg/kg) by gavage for 8 weeks decreased the body weight, adipose tissue mass and triglyceride and attenuated steatosis in liver. Moreover, the effect of oleuropein on adiponectin, an important hormone with fatty-acid oxidation properties, was evaluated and our data illustrated that oleuropein supplementation increased serum adiponectin concentration. The effects of oleuropein on protein expression related to lipogenic genes were investigated and our results showed that its administration significantly inhibited peroxisome proliferator-activated receptor γ (PPARγ), sterol regulatory element-binding protein-1c (SREBP-1c) and fatty-acid synthase (FAS). In addition, oleuropein stimulated the HCD-induced inhibition of AMP-activated protein kinase (AMPK) in epididymal adipose tissues. These results suggest that oleuropein exerts anti-obesity effects in HCD rats by activating AMPK and suppressing PPAR γ (Peroxisome proliferator-activated receptor γ) expression in adipose tissues. These data provide that oleuropein has important implications for preventing obesity.

Для цитирования: Hadrich Fatma, Mahmoudi Asma, Bouallagui Zouhaier, Feki Ines, Isoda Hiroko, Feve Bruno, Sayadi Sami. Evaluation of hypocholesterolemic effect of oleuropein in cholesterol-fed rats.. Chemico-biological interactions. 2016. DOI: 10.1016/j.cbi.2016.03.026.

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