期刊文献+

松仁油对小鼠脂肪组织中脂代谢相关基因表达的影响 被引量:1

EFFECT OF PINE-SEED OIL ON LIPID METABOLISM-RELATED GENE EXPRESSION IN ADIPOSE TISSUE OF MICE
原文传递
导出
摘要 目的探讨松仁油对脂代谢相关基因表达的影响。方法分别以基础饲料、高脂饲料(20%猪油和80%基础饲料HF)及高脂饲料加松仁油(20%松仁油和80%高脂饲料SHF)饲喂小鼠,记录体重调整饲喂量,于45d和90d时取睾周脂肪,以RT-PCR法测定酰基CoA合成酶(ACS)、脂肪酸转运蛋白(FATP)、激素敏感脂肪酶(HSL)、过氧化物酶体增殖剂激活受体-γ(PPAR-γ)mRNA的表达水平。结果45d时,SHF组与基础组比,ACSmRNA、FATPmRNA、HSLmRNA和PPAR-γmRNA的表达水平分别增加了24.2%、8.8%、10.9%、21.6%。90d时,SHF组与基础组比,ACSmRNA、FATPmRNA、HSLmRNA和PPAR-γmRNA的表达水平分别增加了19.6%、25.7%、60.1%、13.1%;HF组与基础组比ACSmRNA、FATPmRNA、HSLmRNA和PPAR-γmRNA的表达水平分别增加了27.9%、41.7%、51.1%、23.9%。结论松仁油在调节脂质代谢方面具有积极的意义。 Objective To study the influence of pine-seed oil on lipid metabolism-related gene expression. Method The mice were fed by basic food,high fat food (80% basic food added 20% lard, HF) and HF added pine-seed oil (80% high fat food added 20% pine-seed oil, SHF). At 45 d and 90 d, the ACS mRNA, FATP mRNA, HSL mRNA and PPAR mRNA of adipose tissue were measured respectively by RT-PCR. Results At 45 d, compared with the basic group, ACS mRNA, FATP mRNA, HSL mRNA and PPAR-γ mRNA expression level in SHF group increased by 24.2%, 8.8%, 10.9%, 21.6% respectively,and at 90 d,increased by 19.6%, 25.7%, 60.1%, 13.1% respectirely. Compared with the basic group,ACS mRNA, FATP mRNA, HSL mRNA and PPAR-γ mRNA expression level in HF group increased by 27.9%, 41.7%, 51.1%, 23.9% respectively. Conclusion Pine-seed oil is significantly effective in regulation of lipid metabolism.
出处 《营养学报》 CAS CSCD 北大核心 2009年第6期552-555,共4页 Acta Nutrimenta Sinica
基金 哈尔滨市科技创新人才研究专项基金(No2007RFQXN010)
关键词 松仁油 脂代谢 基因表达 pine-seed oil lipid metabolism gene expression
  • 相关文献

参考文献7

二级参考文献45

共引文献185

同被引文献11

  • 1Kim YW, Scarpaee PJ. Repeated fasting/refeeding eJevates plasma leptin without increasing fat in rats [J]. Physiol Behav, 2003, 78: 459-464.
  • 2FanW, BostonBA, KestersonRA, et al. Role of melanocor tinergic neurons in feeding and the agouti obesity syndrome [J]. Nature, 1997, 385: 165-168.
  • 3Halaas JL, Gajiwala KS, Maffei Met al. Weight reducing effects of the plasma protein encoded by the obese gene [J]. Science, 1995, 269: 543-546.
  • 4Meister B. Control of food intake via leptin receptors in the hypothalamus [J]. Vitam Horm, 2000, 59: 265-304.
  • 5Brailoiu GC, Dun SL, Brailoiu E, et al. Nesfatin -1: distribution and interaction with a G protein-coupled receptor in the rat brain [J]. Endocrinology, 2007,148:5088-5094.
  • 6Jen KC, Lu H, Savona L, etal. Long-term weight cycling reduces body weight and fat free mass, but not fat mass in femaleWistar rats [J]. ObesReiat MetabDisord 1995,19: 699-708.
  • 7Kochan Z, KarbowskaJ, Swierczynski J. Unusual increase of lipogenesis in rat white adipose tissue after multiple cycles of starvation-refeeding [J].Metabolism.1997, 46: 10-17.
  • 8Swart I, Jahng JW, Overton JM. Hypothalamic NPY, AGRP, and POMC mRNA responses to leptin and refeeding in mice [J]. Physicol RegulIntegrCompPhysiol, 2002, 283: 1020-1026.
  • 9Park ES, Seong JK, Yi SJ, etal. Changes in orexin A and neuropeptide Y expression in the hypothalamus of the Fasted and high-fat diet fed rats [J]. J Vet Med Sci,2004, 5: 295-302.
  • 10Foo KS, Brismar H, Broberger neuropeptide coexistence of nucleobindin-2 mRNA/ nesfatin-like immunoreactivity in the rat CNS[J]. Neuroscience. 2008, 156: 563-579.

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部