期刊文献+

增龄对雄性大鼠阴茎海绵体平滑肌中P47^(phox)表达的影响

Effect of aging on the expression of P47^(phox) in rat penile corporal cavernosum smooth muscle
原文传递
导出
摘要 目的探讨增龄对雄性SD大鼠阴茎海绵体平滑肌中P47^(phox)表达的影响。方法 4月、8月和12月龄3组SD大鼠各20只,取阴茎海绵体平滑肌,应用Real-time RT-PCR和Western印迹法检测各组阴茎海绵体平滑肌组织中P47^(phox)的基因和蛋白表达的变化。结果荧光定量RT-PCR显示P47^(phox) mRNA的表达随年龄增长逐渐增高,8月龄大鼠阴茎海绵体平滑肌P47^(phox) mRNA的表达是4月龄大鼠的1.28倍,12月龄大鼠阴茎海绵体平滑肌P47^(phox) mRNA的表达是4月龄大鼠的8.57倍。Western印迹法显示,P47^(phox)蛋白在大鼠阴茎海绵体平滑肌组织中的表达随年龄增长逐渐增高。结论随着月龄的增加,P47^(phox) mRNA和蛋白质水平在大鼠阴茎海绵体平滑肌中逐渐增高,P47^(phox)可能在增龄诱导阴茎勃起功能障碍过程中发挥重要作用。 Objective To investigate the effect of aging on the expression of P47phoxin rat penile corporal cavernosum smooth muscle. Methods Sixty male Sprague-Dawley rats were divided into 3 groups based on age (4, 8, 12 months old respectively, 20 rats in each'group). The penile corpora cavernosa smooth muscles of rats were collected for detecting the gene expression and protein levels of P47phox Results Aging led to an increase in P47phox mRNA and protein levels in male Sprague-Dawley rats. The P47phox mRNA level in 8-month old group was 1.28 fold higher than that in 4-month old group. The P47phox mRNA levels in 12-month old group were 8.57 fold higher than that in 4-month old group. Conclusion All the results suggest that aged rats with high levels of P47phox gene and protein expression might contribute to age-related erectile dysfunction.
出处 《中国男科学杂志》 CAS CSCD 2010年第3期17-20,共4页 Chinese Journal of Andrology
关键词 阴茎 衰老 大鼠 P47phox penis aging rats P47phox
  • 相关文献

参考文献16

  • 1张庆江,朱积川,许清泉,姜辉.三城市2226例男性勃起功能流行病学调查[J].中国男科学杂志,2003,17(3):191-193. 被引量:161
  • 2饶可,刘继红.氧化应激与男性勃起功能障碍[J].中国男科学杂志,2009,23(3):66-68. 被引量:5
  • 3饶可,刘继红.NADPH氧化酶与男性勃起功能障碍[J].中华男科学杂志,2009,15(5):455-458. 被引量:7
  • 4Selvin E, Burnett AL, Platz EA. Prevalence and risk factors for erectile dysfunction in the US. Am J Med 2007; 120(2): 151-157.
  • 5Bivalacqua TJ, Armstrong JS, Biggerstaff J, et al. Gene transfer of extracellular SOD to the penis reduces O2^-* and improves erectile function in aged rats. Am J Physiol Heart Circ Physiol 2003; 284(4): H1408-1421.
  • 6Ferrini MG, Davila HH, Valente EG, et al. Aging-related induction of inducible nitric oxide synthase is vasculoprotective to the arterial media. Cardiovasc Res 2004; 61 (4): 796-805.
  • 7Agarwal A, Nandipati KC, Sharma RK, et al. Role of oxidative stress in the pathophysiological mechanism of erectile dysfunction. JAndrol 2006;27(3): 335-347.
  • 8Jeremy JY, Angelini GD, Khan M, et al. Platelets, oxidant stress and erectile dysfunction: an hypothesis. Cardiovasc Res 2000; 46(1): 50-54.
  • 9Schreibelt G, Kooij G, Reijerkerk A, et al. Reactive oxygen species alter brain endothelial tight junction dynamics via RhoA, PI3 kinase, and PKB signaling.FASEB J 2007; 21(13): 3666-3676.
  • 10Chitaley K, Wingard CJ, Clinton Webb R, et al. Antagonism of Rho-kinase stimulates rat penile erection via a nitric oxide-independent pathway. Nat Med 2001; 7(1): 119-122.

二级参考文献54

  • 1饶可,杜广辉,杨为民.血脂异常与男性勃起功能的相关性研究[J].中华男科学杂志,2005,11(2):112-115. 被引量:6
  • 2卫焘,薄庭亮.阳萎症的病因分析:附410例资料分析[J].中华泌尿外科杂志,1989,10(3):136-138. 被引量:9
  • 3陈媛,周枚主编.自由基-炎症与衰老性疾病.北京:科学出版社,2007:1-27
  • 4Thannickal VJ, Fanburg BL. Am J Physiol Lung Cell Mol Physiol 2000; 279(6): L1005-L1028
  • 5Khan MA, Thompson CS, Mumtaz FH, et al. World J Urol 2001;19(3): 220-224
  • 6Aqarwal A, Nandipati KC, Sharma RK, et al. J Androl 2006; 27(3): 335-347
  • 7Schreibelt G, Kooij G, Reijerkerk A, et al. FASEB J 2007; 21(13): 3666-3676
  • 8Chitaley K, Wingard C J, Clinton Webb R, et al. Nat Med 2001; 7(1): 119-122
  • 9Kim SC, Kim IK, Seo KK, et al. Urol Res 1997; 25(5): 341-346
  • 10Ahn TY, Gomez-Coronado D, Martinez V, et al. Int J Impot Res 1999; 11:9-14

共引文献170

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