Protective effects of pumpkin (Cucurbita pepo L.) seed oil on rat liver damage induced by chronic alcohol consumption

被引:5
作者
Radic, Ivan [1 ]
Miric, Mirjana [1 ]
Mijovic, Milica [2 ]
Tatalovic, Nikola [3 ]
Mitic, Milos [4 ]
Nestorovic, Vojkan [5 ]
Adzic, Miroslav [4 ]
Blagojevic, Dusko P. [3 ]
Popovic, Ljiljana [1 ]
Hudomal, Snezana Janicijevic [6 ]
机构
[1] Univ Pristina, Fac Med Sci, Inst Pathol Physiol, Kosovska Mitrovica 38220, Serbia
[2] Univ Pristina, Fac Med Sci, Inst Pathol, Kosovska Mitrovica 38220, Serbia
[3] Univ Belgrade, Natl Inst Republ Serbia, Inst Biol Res Sinifa Stankovir, Dept Physiol, Bulevar Despota Stefana 142, Belgrade 11060, Serbia
[4] Univ Belgrade, Natl Inst Republ Serbia, VINCA Inst Nucl Sci, Dept Mol Biol & Endocrinol, Mike Petrovica Alasa 12-14, Belgrade 11351, Serbia
[5] Univ Pristina, Fac Med Sci, Inst Physiol, Kosovska Mitrovica 38220, Serbia
[6] Univ Pristina, Fac Med Sci, Inst Pharmacol & Toxicol, Kosovska Mitrovica 38220, Serbia
关键词
chronic alcohol consumption; alcoholic liver disease; pumpkin seed oil; antioxidant enzymes; NF-kappa B; TUMOR-NECROSIS-FACTOR; KAPPA-B ACTIVATION; KUPFFER CELLS; LIPID PROFILE; FATTY-ACIDS; GLUTATHIONE; ZINC; PARAMETERS; TOCOPHEROL; DISEASE;
D O I
10.2298/ABS201205008R
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pumpkin seed oil (PSO) possesses a protective potential against liver injury due to the presence of biologically active ingredients. Adult male albino rats were administrated PSO (per os, 2 mL/kg b.w./day) and a 12% ethanol solution in water, ad libitum, with an average intake of 8.14 g of ethanol/kg bw/day for 6 weeks. Congestion, hepatic central vein dilation, portal vein branch dilation, Kupffer cell hyperplasia, fatty liver changes, hepatocyte focal necrosis were observed after daily alcohol intake. All observed changes were reduced when PSO was ingested with ethanol. PSO intake itself induced discrete cellular edema, congestion and slight dilatation of the central and portal vain branches. Chronic ethanol intake elevated catalase (CAT) activity and glutathione reductase (GR) protein expression; concomitant PSO intake had no effect on CAT activity or GR protein expression. PSO intake decreased the activities of GR, glutathione-S-transferase (GST) and xanthine oxidase (XOD) in the liver, probably due to the ingestion of antioxidants. Intake of PSO and ethanol significantly decreased cytosolic superoxide dismutase (SOD1) and increased NF-kappa B protein expression compared to ethanol intake, suggesting that the protective effects of PSO were mediated by the NF-kappa B signaling pathway. Our results reveal a therapeutic potential of PSO in alcoholic liver disease.
引用
收藏
页码:123 / 133
页数:11
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