期刊文献+

紫甘薯花青素对高脂饮食导致小鼠脑部炎症反应的保护作用 被引量:8

Protective Effect of Purple Sweet Potato Color On the Neuroinflammation Induced by High Fat Diet in T2DM Mice
下载PDF
导出
摘要 目的本研究利用HFD(high fat diet)建立肥胖小鼠神经炎症模型,探讨紫甘薯花青素(purple sweet potato color,PSPC)对HFD诱导的肥胖小鼠脑部神经炎症损伤的影响及分子机制。方法 ICR(institute of cancer research)雄性小鼠100只,按随机数字表法随机分为4组,每组25只,分别为:正常对照组、HFD组、HFD+PSPC组、PSPC组。HFD+PSPC组、PSPC组灌喂PSPC 700mg/(kg·d),正常对照组、HFD组灌喂同等体积的0.9%的生理盐水,连续喂养灌喂20周,每周两次称量小鼠空腹体重。于第20周进行行为学检测,行为学检测之后立即断颈处死,取脑,分别检测海马与前脑皮质中的COX-2(cyclo-oxygenase-2)在不同处理组的小鼠脑组织中的蛋白表达水平。结果 HFD处理的小鼠体重有显著的升高,而PSPC能够有效改善上述症状,显著改善HFD诱导的小鼠自发活动能力和学习记忆能力的下降,显著抑制HFD诱导的小鼠海马和前脑皮质COX-2的蛋白表达水平增加。结论研究表明,紫甘薯花青素具有神经保护作用,可能的机制是抑制炎症相关蛋白的表达,从而起到抗炎作用。 Objective To investigate the effect of PSPC on the neuroflammation in HFD-induced mouse brain and discuss the mechanism of the protective effect.Methods Male ICR mice were randomly divided into 4 groups,termed as group control,group HFD,group HFD + PSPC,and group PSPC.Mice in group PSPC and group HFD + PSPC were lavaged with purple sweet potato color in 0.9% saline containing 0.1% Tween 80 at a dose of 700mg/(kg · d) for 20 weeks,at the same time,mice in group control and group HFD severed as control group were given saline (0.9%) orally at the same dose.The mice weight was recorded twice a week.In 20th week,the mice were used to behavior tests and protein assays.Results Mice in HFD group had significant increase in the body weight and glucose level,compared with the control group.PSPC could significantly reverse the impairment of motor and exploration behavior induced by HFD in the open field tasks,and also improve learning and memory ability in step-through tests,could markedly decrease the high level expression of COX-2 in hippocampus and frontal cortex of brain that treated with HFD.Conclusion The results above showed that PSPC had anti-inflammatory property.The possible mechanism is that PSPC decreases the expression of inflammatory protein COX-2.
出处 《医学研究杂志》 2014年第4期118-121,共4页 Journal of Medical Research
关键词 紫甘薯花青素 HFD 行为学检测 COX-2 PSPC HFD Behavior test COX-2
  • 相关文献

参考文献12

  • 1Meissburger B,Ukropec J,Roeder E,et al.Adipogenesis and insulin sensitivity in obesity are regulated by retinoid-related orphan receptor gamma[J].EMBO Mol Med,2011,3(11):637-651.
  • 2赵铁耘,李秀钧.糖尿病诊治研究新理念[J].中国实用内科杂志,2005,25(4):302-304. 被引量:46
  • 3Gerrits A J,Gitz E,Koekman CA,et al.Induction of insulin resistance by the adipokines resistin,leptin,plasminogen activator inhibitor-1 and retinol binding protein 4 in human megakaryocytes[J].Haematologica,2012,97(8):1149-1157.
  • 4Guri A J,Hontecillas R.Dietary abscisic acid ameliorates glucose tolerance and obesity-related inflammation in db/db mice fed high-fat diets[J].Clinical Nutrition,2007,26(1):107-116.
  • 5贺炜,王征.紫甘薯花青素提取物抗氧化能力的稳定性[J].现代生物进展,2009,9(7):1268-1271.
  • 6Shih PH,Yeh CT,Yen GC.Effects of anthocyanidin on the inhibition of proliferation and induction of apoptosis in human gastric adenocarcinoma cells[J].Food Chem Toxicol,2005,43 (10):1557-1566.
  • 7Wang YJ,Zheng YL,Lu J,et al.Purple sweet potato color suppresses lipopolysaccharide-induced acute inflammatory response in mouse brain.[J].Neurochemistry International,2010,56:424-430.
  • 8Frye CA,Alicia A.Progesterone enhances performance of aged mice in cortical or hippocampal tasks[J].Neurosci Lett,2008,437 (2):116-120.
  • 9Cai W,Zhu Y,Furuya K,et al.Two different molecular mechanisms underlying progesterone neuroprotection against ischemic brain damage[J].Neuropharmacology,2008,55(2):127-138.
  • 10Wong C,Wang Z.Prevalence of type 2 diabetes mellitus of Chinese populations in China's Mainland,Hong Kong,and Taiwan[J].Diabetes Research and Clinical Practice,2006,73(2):126-134.

二级参考文献9

  • 1李军,李秀钧,张杰,罗梅,周桥,赵桂芝.糖耐量受损大鼠胰岛α细胞胰高血糖素及神经肽Y的表达[J].中华内分泌代谢杂志,2004,20(3):185-189. 被引量:31
  • 2Knowler WC, Barrett-Connor E, Fowler SE, et al. Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin.N Engl J Med,2002,346(6) :393-403.
  • 3Chiasson JL, Josse RG, Gomis R, et al. Acarbose treatment and the risk of cardiovascular disease and hypertension in patients with impaired glucose tolerance: the STOP-NIDDM trial. JAMA,2003,290(4) :486-494.
  • 4Hanefeld M, Koehler C, Henkel E, et al. Post-challenge hyperglycemia relates more strongly than fasting hyperglycemia with carotid intimae-media thickness: the RIAD study. Diabet Med, 2000, 17(12) :212-218.
  • 5DECOOE Study Group. The European Diabetes Epidemiology Group. Glucose tolerance and cardiovascular mortality:comparison of fasting and 2-hour diagnostic criteria. Arch Intern Med,2001,161( 3 ) :397-405.
  • 6Pimenta W, Korytkowski M, Mitrakou A, et al. Pancreatic beta-cell dysfunction as the primary genetic lesion in NIDDM. Evidence from studies in normal glucose tolerant individuals with a first-degree NIDDM relative. JAMA, 1995,273 (23): 1855-1861.
  • 7Luo M, Xiujun L, Li J, et al. Study on insulin receptor content and distribution of islet α-cell in diabetic rats-prelimary insight into the mechanism of pancreasticd-cell insulin resistance. Diabetes, 2004,53 (suppl 2) :A313.
  • 8Broenlee M. The pathobiology of diabetic complication:a unifying mechanism. Diabetes,2004,53 (suppl 2) :6.
  • 9The expert committee on the diagnosis and classification of diabetes mellitus:follow-up report on the diagnosis of diabetes mellitus. Diabetes Care,2003,26( 11 ) :3160-3167.

共引文献45

同被引文献130

引证文献8

二级引证文献76

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