全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
药学学报  2013 

成纤维细胞生长因子21对胰岛素抵抗所致高血压的治疗作用

, PP. 1409-1414

Keywords: 成纤维细胞生长因子21,胰岛素抵抗,高血压,果糖

Full-Text   Cite this paper   Add to My Lib

Abstract:

本文研究考察成纤维细胞生长因子21(fgf21)对果糖诱导的胰岛素抵抗高血压模型的治疗作用及其机制。10%果糖诱导sd大鼠4周建立胰岛素抵抗高血压模型,成模后随机分为4组:模型对照组及fgf210.25、0.1和0.05μmol·kg-1·d-1剂量组,5只相同周龄的正常sd大鼠作为正常对照组。每天注射1次,治疗4周,给药期间每周监测大鼠体重,采用尾套法检测收缩压变化;口服葡萄糖耐量试验(ogtt)及胰岛素稳态评价模型检测胰岛素抵抗情况;给药结束时留取血清样本分别测定血清胰岛素、血脂、血糖水平。结果显示,治疗4周后,不同剂量fgf21治疗组大鼠收缩压均下降至正常水平[(122.2±3.5)mmhg,p<0.01],而注射生理盐水的模型对照组大鼠的收缩压在治疗期间一直维持在较高水平[(142.5±4.5)mmhg]。24h观察各组大鼠血压发现,fgf21治疗组大鼠24h血压基本维持在(130±4.5)mmhg,各时间段血压均显著低于模型对照组[(130±4.5)vs(143±5.5)mmhg,p<0.01]。fgf21治疗组大鼠血脂改善明显,总胆固醇与甘油三酯含量均显著下降至正常水平。fgf21各治疗组大鼠血清no含量均显著高于模型对照组[(7.32±0.11),(7.24±0.13),(6.94±0.08)vs(6.56±0.19)μmol·l-1,p<0.01],且其改善程度呈现明显的剂量依赖性,表明fgf21可明显升高果糖诱导高血压模型大鼠血清no含量,改善内皮释放no功能。ogtt及homa-ir结果显示,经fgf21治疗4周后胰岛素抵抗亦明显得到改善,且呈现剂量依赖性。因此本研究揭示了fgf21通过改善胰岛素抵抗,显著降低sd大鼠由于胰岛素抵抗所引起的高血压。这一发现为临床应用fgf21治疗原发性高血压奠定了理论基础。

References

[1]  huangx,yuc,jinc,etal.forcedexpressionofhepatocyte-specificfibroblastgrowthfactor21delaysinitiationofchemicallyinducedhepatocarcinogenesis[j].molcarcinog,2006,45:934-942.
[2]  liuq,liym,liuhl.effectsofl-arginineonbloodpressureandinsulin-resistanceinfructose-fedrats[j].medjchinpapf(武警医学),2006,17:261-263.
[3]  weil,wangxx.clinicalobservationofglucosemetabolisminelderlyhypertensivepatients[j].clinmedchina(中国综合临床),2004,20:113-114.
[4]  zhaocx,wangph,lihw,etal.mechanismsofhypertensionandinsulinresistanceinfructose-inducedhypertensiveratmodelandtherapeuticeffectsofhumantissuekallikreingeneonthem[j].chinjcardiol(中华心血管病杂志),2003,10:756-761.
[5]  kharitonenkova,wroblewskivj,koestera,etal.themetabolicstateofdiabeticmonkeysisregulatedbyfibroblastgrowthfactor-21[j].endocrinology,148:774-781.
[6]  coskunt,binaha,schneiderma,etal.fibroblastgrowthfactor21correctsobesityinmice[j].endocrinology,2008,149:6018-6027.
[7]  sembard,crastoc,straitj,etal.elevatedserumfibroblastgrowthfactor21isassociatedwithhypertensionincommunity-dwellingadults[j].jhumhypertens,2013,27:397-399.
[8]  xux,zhaocx,wangl,etal.increasedcyp2j3expressionreducesinsulinresistanceinfructose-treatedratsanddb/dbmice[j].diabetes,2010,59:997-1005.
[9]  xuj,lloyddj,halec,etal.fibroblastgrowthfactor21reverseshepaticsteatosis,increasesenergyexpenditure,andimprovesinsulinsensitivityindiet-inducedobesemice[j].diabetes,2009,58:250-259.
[10]  nishimurat,nakatakey,konishim,etal.identificationofanovelfgf,fgf-21,preferentiallyexpressedintheliver[j].biochimbiophysacta,2000,1492:203-206.
[11]  bellds.hypertensionandantihypertensivetherapyasriskfactorsfortype2diabetesmellitus[j].nengljmed,2000,343:580.
[12]  kharitonenkova,shiyanovatl,lids,etal.fgf-21asanovelmetabolicregulator[j].jclininvest,2005,115:1627-1635.
[13]  sungp,yexl,rengp,etal.fibroblastgrowthfactor-21mediateshepaticglucosemetabolismoftype1diabetesmodelanditsmechanism[j].progbiochembiophys,2011,38:953-960.
[14]  xux,tul,wangl,etal.cyp2j3genedeliveryreducesinsulinresistanceviaupregulationofenosinfructose-treatedrats[j].cardiovascdiabetol,2011,10:114.
[15]  zhangxq,albrahimioa,olsensk,etal.receptorspecificityofthefibroblastgrowthfactorfamily.thecompletemammalianfgffamily[j].jbiolchem,2006,281:15694-15700.
[16]  congln,chenh,liy,etal.physiologicalroleofaktininsulin-stimulatedtranslocationofglut4intransfectedratadiposecells[j].molendocrinol,1997,11:1881-1890.
[17]  sasaokat,ishikim,sawat,etal.comparisonoftheinsulinandinsulin-likegrowthfactor1mitogenicintracellularsignalingpathways[j].endocrinology,1996,137:4427-4434.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133