Zhu Shuang, Park Soyoung, Lim Yeseo, Shin Sunhye, Han Sung Nim
Department of Food and Nutrition, College of Human Ecology, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea.
Department of Food and Nutrition, College of Human Ecology, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea.; Research Institute of Human Ecology, Seoul National University, Seoul 08826, Korea.
Nutr Res Pract. 2016 Oct;10(5):477-486. doi: 10.4162/nrp.2016.10.5.477. Epub 2016 Jun 16.
BACKGROUND/OBJECTIVES: Consumption of pine nut oil (PNO) was shown to reduce weight gain and attenuate hepatic steatosis in mice fed a high-fat diet (HFD). The aim of this study was to examine the effects of PNO on both intestinal and hepatic lipid metabolism in mice fed control or HFD.
MATERIALS/METHODS: Five-week-old C57BL/6 mice were fed control diets containing 10% energy fat from either Soybean Oil (SBO) or PNO, or HFD containing 15% energy fat from lard and 30% energy fat from SBO or PNO for 12 weeks. Expression of genes related to intestinal fatty acid (FA) uptake and channeling (, , , ), intestinal chylomicron synthesis (, , ), hepatic lipid uptake and channeling (, , , ), hepatic triacylglycerol (TAG) lipolysis and FA oxidation (, , , , ), as well as very low-density lipoprotein (VLDL) assembly () were determined by real-time PCR.
In intestine, significantly lower mRNA expression ( < 0.05) and a tendency of lower mRNA levels ( = 0.07) was observed in PNO-fed mice, indicating that PNO consumption may decrease intestinal FA uptake and chylomicron assembly. PNO consumption tended to result in higher hepatic mRNA levels of ( = 0.08) and ( = 0.05). Significantly higher hepatic mRNA levels of and were detected in mice fed PNO diet ( < 0.05). These results suggest that PNO could increase hepatic TAG metabolism; mitochondrial fatty acid oxidation and VLDL assembly.
PNO replacement in the diet might function in prevention of excessive lipid uptake by intestine and improve hepatic lipid metabolism in both control diet and HFD fed mice.
背景/目的:食用松子油(PNO)可减少高脂饮食(HFD)喂养小鼠的体重增加并减轻肝脏脂肪变性。本研究旨在探讨PNO对正常饮食或HFD喂养小鼠肠道和肝脏脂质代谢的影响。
材料/方法:将5周龄的C57BL/6小鼠分别喂食含10%能量脂肪的大豆油(SBO)或PNO的对照饮食,或含15%能量脂肪的猪油和30%能量脂肪的SBO或PNO的HFD,持续12周。通过实时PCR测定与肠道脂肪酸(FA)摄取和转运(、、、)、肠道乳糜微粒合成(、、)、肝脏脂质摄取和转运(、、、)、肝脏三酰甘油(TAG)脂解和FA氧化(、、、、)以及极低密度脂蛋白(VLDL)组装()相关基因的表达。
在肠道中,喂食PNO的小鼠中mRNA表达显著降低(<0.05),mRNA水平有降低趋势(=0.07),表明食用PNO可能会减少肠道FA摄取和乳糜微粒组装。食用PNO往往会导致肝脏mRNA水平升高(=0.08)和(=0.05)。喂食PNO饮食的小鼠肝脏中mRNA水平显著升高(<0.05)。这些结果表明,PNO可增加肝脏TAG代谢、线粒体脂肪酸氧化和VLDL组装。
在正常饮食和HFD喂养的小鼠中,饮食中用PNO替代可能有助于预防肠道过度摄取脂质并改善肝脏脂质代谢。