期刊文献+

次黄嘌呤对营养性肥胖小鼠的抗肥胖作用 被引量:1

Anti-Obesity Effect of Hypoxanthine on Nutritionally Obese Mice
下载PDF
导出
摘要 目的:研究次黄嘌呤(hypoxanthine,Hx)对营养性肥胖小鼠抗肥胖作用的影响。方法:将ICR(Institute of Cancer Research)小鼠随机分成6组:空白组、模型组、阳性对照组(左旋肉碱100 mg/kg)和Hx干预组(30、60、90 mg/kg),采用高脂饲料饲喂建立肥胖小鼠模型。口服给药4周后,处死小鼠,收集血液,离心。检测各组小鼠血清甘油三酯、总胆固醇、瘦素和脂联素的含量。制作脂肪组织石蜡切片,经苏木精-伊红(HE)染色颜色观察脂肪细胞的变化。取附睾脂肪经实时荧光定量聚合酶链式反应(real-time quantitative polymerase chain reaction,q RT-PCR),观察小鼠体内肥胖基因(瘦素和脂联素基因)m RNA表达变化。结果:Hx干预组小鼠的脂肪质量显著低于模型组(P<0.05);总胆固醇含量水平均显著低于模型组(P<0.05、P<0.01);Hx中、低剂量组和对照组的瘦素和脂联素m RNA表达量显著低于模型组(P<0.05)。结论:Hx中、低剂量组有较好的抗肥胖作用,其中低剂量组的抗肥胖效果最好。小鼠脂肪细胞切片中脂肪组织形态学为小鼠肥胖造模提供进一步的研究依据。 Objective: To explore the anti-obesity effect of hypoxanthine (Hx) on nutritionally obese mice. Methods:An obese mouse model was established successfully by feeding high-fat diet. The ICR mice were randomly dividedinto six groups, namely, normal control, model control, positive control (L-carnitine, 100 mg/kg) and hypoxanthinetreatment groups (30, 60, and 90 mg/kg). After 4 weeks of oral administration, blood samples were collected andcentrifuged and then the mice were sacrificed. The contents of triglyceride, total cholesterol, leptin and adiponectinin mouse serum were detected. The adipose tissues were made into paraffin section to observe the changes of adiposecells by HE staining. The gene expression levels of leptin and adiponectin in mouse epididymal adipose tissuewere measured by real-time quantitative polymerase chain reaction (qRT-PCR). Results: The body weight of theHx treatment groups were significantly lower than that of the model group (P 〈 0.05); TC levels were significantlylower than those of the model group (P 〈 0.05, P 〈 0.01). The gene expression levels of leptin and adiponectin inthe middle- and low-dose Hx groups and normal control were significantly different from those of the model group(P 〈 0.05). Conclusion: The middle- and low-dose Hx groups had good anti-obesity effect, and the best effect was achievedat the low dose.
出处 《食品科学》 EI CAS CSCD 北大核心 2016年第15期253-258,共6页 Food Science
基金 吉林省科技发展计划项目(20120246) 吉林省教育厅"十二五"科学技术研究项目(2014628)
关键词 肥胖 次黄嘌呤 切片 实时荧光定量聚合酶链式反应(q RT-PCR) obesity hypoxanthine slice real-time quantitative polymerase chain reaction (qRT-PCR)
  • 相关文献

参考文献4

二级参考文献21

  • 1Dube M G,Peptides,2000年,21卷,793页
  • 2Wei Wanghuo,Proc Nat Acad Sci USA,1999年,96卷,10373页
  • 3Cone R D,Recent Prog Horm Res,1996年,51卷,287页
  • 4Elion GB Symposium on immunosuppressive drugs. Biochemistry and pharmacology of purine analogues[ J]. Fed Proc, 1967, 26 : 898-904.
  • 5Weber G. Biochemical strategy of cancer cells and the design of chem- otherapy: G. H. A. Clowes Memorial Lecture[J]. Cancer Res,1983, 43 : 3466-92.
  • 6Sahasranaman S, Howard D, Roy S. Clinical pharmacology and phar- macogenetics of thiopurines[ J]. Eur J Clin Pharmacol, 2008,64(8) : 753-767.
  • 7Leese HJ. Profiles of hypoxanthine guanine phosphoribosyl transferase and adenine phosphoribosyl transferase activities measured in single preimplantation human Embryos by high-performance liquid chromatog- raphy[ J]. Repord Fert, 1991,91 : 197-202.
  • 8Van Asseldonk DP. Limited intra-individual variability in hypoxan- thine-guanine phosphoribosyl transferase, thiopurine s-methyl transfer- ase,and xanthine oxidase activity in inflammatory bowel disease pa- tients during 6-thioguanine therapy [ J ]. Nucleosides, Nucleotides and Nucleic Acids, 2010,29:284-290.
  • 9Someren H, Heneguuwen HB. Rapid detection of hypoxanthine- gua- nine phosphoribosyhransferase on cellogel [ J 1. Httmangenetik, 1974, 22, 75-80.
  • 10Krenitsky TA, Papaioannou R, Elion GB. Human hypoxanthine phos- ph-oribosyltransferase. I Purification, properties and specificity [ J . J Biol Chem, 1969, 244 : 1263-1270.

共引文献58

同被引文献7

引证文献1

二级引证文献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