期刊文献+

3-磷酸甘油醛脱氢酶活性检测方法的改良及应用 被引量:2

Amendment and application of determination method of glyceraldehyde-3-phosphate dehydrogenase activity
下载PDF
导出
摘要 目的改良3-磷酸甘油醛脱氢酶(GAPDH)活性检测方法,并探讨该方法的应用。方法在经典血清GAPDH检测方法基础上,根据该酶的组织分布特点,将血清样本改为全血样本,并对样本及检测条件作了进一步的改良。在方法学研究的基础上,运用改良后的方法分别检测正常鹌鹑、高嘌呤饮食诱导的模型鹌鹑、正常大鼠及高果糖饮食诱导的模型大鼠全血GAPDH的活性。结果全血与血清GAPDH酶促反应时间曲线类似,变异系数均小于10%。方法学应用结果显示,与正常鹌鹑比,高嘌呤饮食诱导的模型鹌鹑在高尿酸血症及其合并脂、糖代谢紊乱状态下(60~140d)全血GAPDH活性显著降低;与正常大鼠比,高果糖饮食诱导的模型大鼠在高三酰甘油血症及其并发尿酸、糖代谢紊乱下(7~28d),全血GAPDH活性显著降低。结论改良方法血样容易采集,样品用量少,操作简便、重复性较好,经济实用,易于推广应用。 Objective To improve the determination method of glyceraldehyde-3-phosphate dehydrogenase(GAPDH) activity and explore its application.Methods The traditional determination method of GADPH activity was amended by changing serum sample as whole blood sample and reforming the related determination condition,according to GAPDH distribution in the tissue.And then GAPDH activity was detected by newly constructed method on quail and rat models.Results The time curve of whole blood GAPDH activity was similar to serum curve,and coefficient of variation of the tow methods were both less than 10%.The activity of GAPDH was decreased in quails model group,induced by high purine diet,with hyperuricemia and combined with metabolic disturbance of blood fat and glucose(60-140 d),and was also decreased in rats model group,induced by high fructose diet,with hypertriacylglycerolemia and combined with metabolic disturbance of blood uric acid and glucose(7-28 d).Conclusion This newly constructed method could have several advantages as easy collection of sample,less usage amount of sample,good reproducibility and economics.
机构地区 北京中医药大学
出处 《国际检验医学杂志》 CAS 2012年第2期160-161,165,共3页 International Journal of Laboratory Medicine
基金 国家自然科学基金资助项目(81073068 30472282) 北京市自然科学基金资助项目(7052036) 国家重点基础研究发展计划(973计划)(2007CB512605)
关键词 磷酸甘油醛脱氢酶 检测方法 全血 代谢性疾病 phospho glycerate dehydrogenase detection method whole blood metabolic disease
  • 相关文献

参考文献10

  • 1司国爱,欧松,郑希明,韦立任,韦义拢,卢桂荣,韦克波,杨家信,韦丽荣,黄理金.膳食结构对居民健康的影响调查[J].应用预防医学,2006,12(3):149-151. 被引量:8
  • 2Larissa S, Kerri L, Batra, et al. Medical implications of hyperurice- mia[J]. Med Health/Rhode Island, 2009,92 (11) : 353-355.
  • 3张冰,刘小青,胡京红,洪庆涛,张浩军,刘春梅,孔悦.鹌鹑高血尿酸高甘油三酯血症模型塑造[J].中国病理生理杂志,2003,19(8):1148-1150. 被引量:11
  • 4王坤,瞿韬,左砚琴.3一磷酸甘油醛脱氢酶[M].重庆:科学技术文献出版社重庆分社,1989:240—244.
  • 5Burke JR, Enghild J J, Martin ME, et al. Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH [J]. Nat Med, 1996,2 : a47-a50.
  • 6Kish SJ,Lopes Cendes I, Guttman M, et al. Brain glyceraldehyde- 3-phosphate dehydrogenase activity in human trinucleotide repeat disorders[J]. Arch Neurol, 1998,55 ~ 1299-1304.
  • 7Tabrizi SJ, Cleeter MWJ, Xuereb J, et al. Biochemical abnormali ties and excitotoxicity in Huntingtonts disease brain[J]. Ann Neu- rol, 1999,45 : 25-32.
  • 8Epner DE. There are multiple forms of glyceraldehyde-3-phos- phate dehydrogenase in prostate cancer cells and normal prostate cells[J]. Prostate, 1996,28 : 372-378.
  • 9Ripple MO, Wilding G. Alteration of glyceraldehyde-3-phosphate dehydrogenase activity and messenger RNA content by androgen in human prostate carcinoma cells[J]. Cancer Res, 1995,55 : 4234- 4236.
  • 10Meyer-Siegler K, Mansur NR, Wurzer JC, et al. Proliferation-de- pendent regulation of the glyceraldehyde-3-phosphate dehydro- genase/uracil DNA glycosylase gene in human cells[J] Carcino genesis, 1992,13 : 2127-2132.

二级参考文献8

  • 1陈兴乐,唐振柱,韩彦彬,黄兆勇,黄林,杨娟,阮青,陈钦艳,方志锋,李玉英.广西居民膳食营养状况调查[J].中国公共卫生,2005,21(12):1476-1478. 被引量:21
  • 2吴晓生 李龙官.比色法测定黄嘌呤氧化酶[J].生物化学与生物物理进展,1986,5(1):65-67.
  • 3汪谦主编.动物模型的设计原则和注意事项[A]..现代医学实验方法学:第1版[C].北京:人民卫生出版社,1998.1067—1070.
  • 4[2]教育部体卫艺司.儿童青少年身高标准体重筛查标准[M].北京:中国轻工业出版社,2002.414-431.
  • 5Iris H Hall, John P Scofille, David J, et al. Substituted cyclic imides as potential anti- agents[J]. Life Sci, 1990,46(26) : 1923 - 1927.
  • 6金沈锐,郑军,刘绍唐.小鼠高尿酸血症模型初探[J].成都中医药大学学报,1999,22(1):49-50. 被引量:62
  • 7何立群,聂永红,邹士林.新型尿酸性肾病动物模型的建立[J].上海实验动物科学,2001,21(1):22-25. 被引量:31
  • 8刘小青,张冰,刘春梅,洪庆涛,张浩军,孔悦,唐一鹏.鹌鹑高尿酸血症模型建立初探[J].中国病理生理杂志,2001,17(10):1038-1040. 被引量:36

共引文献15

同被引文献26

  • 1白雪,刘学源.3-磷酸甘油醛脱氢酶和神经系统疾病研究进展[J].神经病学与神经康复学杂志,2010,7(1):60-64. 被引量:1
  • 2Ferdinando G, Michael B. Oxidative Stress and Diabetic Com- plications. Circulation Research 2010, 107z1058-1070.
  • 3Anabela PR,Carlos MP. Diabetes and mltochondrial function: Role of hyperglycemia and oxidative stress. Toxicology and Applied Pharmacology, 2006, 212 :167-178.
  • 4Javle M, Curtin NJ. The role of PARP in DNA repair and its therapeutic exploitation. British Journal of Cancer, 2011, 105 1114-1122.
  • 5Shevalye H, Maksimchyk Y, Watcho P, et al. Poly (ADP-ri- bose) polymerase-1 (PARP-1) gene deficiency alleviates dia- betic kidney disease. Bioehim Biophys Aeta, 2010, 1802 : 1020- 1027.
  • 6Kanwar M, Kowluru RA. Role of glyceraldehyde 3-phosphate dehydrogenase in the development and progression of diabetic retinopathy. Diabetes, 2009, 58.-227-234.
  • 7Khan S, Raghuram GV, Bhargava A, et al. Role and clinical significance of lymphocyte mitochondrial dysfunction in type 2 diabetes mellitus. Transl Res, 2011, 158.. 344-359.
  • 8李天艺.糖尿病微血管病变经葛根素治疗前后3磷酸甘油醛脱氢酶活性变化.郑州大学,2007.
  • 9Wu CC, Yen CC, Lee KI, et al. Involvement of oxidative stress-induced ERK/JNK activation in the Cu(2+)/pyrrolidine dithiocarbamate complex-triggered mitochondria-regulated ap- optosis in pancreatic cell Toxicol Lett, 2012, 208:275-285.
  • 10Wentzel P, Ejdesj6 A, Eriksson UJ. Maternal diabetes in vivo and high glueose in vitro diminish GAPDH activity in rat em- bryos. Diabetes, 2003, 52..1222-1228.

引证文献2

二级引证文献6

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