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细胞外信号调节激酶和蛋白激酶B在糖尿病大鼠阴茎海绵体的表达 被引量:1

Expressions of ERK1/2 and PKB/Akt in the corpus cavernosum of diabetic rats
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摘要 目的 研究细胞外信号调节激酶(ERK1/2)和蛋白激酶B(PKB/Akt)在糖尿病大鼠阴茎海绵体中的表达,探讨糖尿病大鼠勃起功能障碍(ED)可能存在的发病机制.方法 20只8周龄雄性Wistar大鼠随机分成对照组(A组)和实验组(B组).实验组采用1%链脲佐菌素(STZ)腹腔注射建立I型糖尿病大鼠模型,对照组给予等量生理盐水腹腔注射,4周后采用免疫组化及RT-PCR技术检测ERK1/2和PKB/Akt在大鼠阴茎海绵体中的表达.结果 ERK1、ERK2的mRNA和ERK1/2蛋白的表达量在B组(0.7343±0.0820、0.7962±0.0730、0.1574±0.0350)较A组(0.3943±0.0900、0.4156±0.0590、0.1205±0.0360)显著升高,差异具统计学意义(P〈0.05);PKB/Akt的mRNA和PKB/Akt蛋白的表达量在B组(0.9884±0.0460、0.1822±0.0470)与A组(0.9417±0.0540、0.1586±0.0220)差异无统计学意义(P〉0.05).结论 ERK1/2和PKB/Akt在糖尿病大鼠阴茎海绵体中均有表达,糖尿病大鼠阴茎海绵体ERK1/2表达增强可能与糖尿病大鼠ED的发生有关. Objective To analyze the expressions of ERK1/2 and PKB/Akt in corpus cavemosums of diabetic rats and explore the possible mechanism of erectile dysfimction(ED) of diabetic rats. Methods Twenty Wistar rats with 8 weeks age were randomly devided into group A( the control group) and group B (the experimental group group). Rats in group B were given peritoneal injection with 1% streptozocm and rats in group A were injected with equal volume 0.9% normal saline. Four weeks later, the expressions of ERK1/2 and PKB/Akt in corpus cavemosum of rats were detected by immunohistochemistry staining and RT-PCR. Results The mRNA expression of ERK1 and ERK2, as well as the protein expression of ERK1/2 in corpus cavemosum of rats in group B(0.7343±0.0820, 0.7962±0.0730 and 0.1574±0.0350) was significantly higher than that in group A(0.3943±0.0900, 0.4156±0.0590 and 0.1205±0.0360)(P〈0.05). No significant difference was found in the mRNA and protein expression of PKB/Akt between in group B (0.9884±0.0460 and 0.1822±0.0470) and m group A(0.9417±0.0540 and 0.1586±0.0220)(P〉0.05). Conclusion The expressions of ERK1/2 and PKB/Akt were all detected in penile tissue of diabetic rots. Whereas, high expression of ERK1/2 in corpus cavemosum might be associated with development of ED of diabetic rats.
出处 《中国男科学杂志》 CAS CSCD 2011年第1期3-7,10,共6页 Chinese Journal of Andrology
基金 四川省科技厅基金(060045)
关键词 细胞外信号调节MAP激酶类 蛋白激酶类 糖尿病 阴茎海绵体 勃起功能障碍 大鼠 extracellular signal-regulated MAP kinases protein kinases diabetes mellitus corpus cavernosum erectile dysfunction rats
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参考文献12

  • 1EL-Sakka AI,Tayeb KA.Erectile dysfunction risk factors in noninsulin dependent diabetic Saudi patients.J Urol 2003,169(3):1043-1047.
  • 2Sommer F,Klotz T,Steinritz D,et al.MAP kinase 1/2 (Erk 1/2) and serine/threonine specific protein kinase Akt/PKB expression and activity in the human corpus cavernosum.Int J Impot Res 2002,14(4):217-225.
  • 3Cduliano F.New horizons in erectile and endothelial dysfunction research and therapies.Int J Impot Res 2008,20 Suppl 2:S2-8.
  • 4Musicki B,Kramer MF,Becket RE,et al.Inactivation of phosphorylated endothelial nitric oxide synthasc (Ser 1177) by O-GIcNAc in diabetes-associated erectile dysfunction.Proc Natl Acad Sci USA 2005,102(33):11870-11875.
  • 5Bernier SG,Haldar S,Michel T.Bradykinin-regulated interactions of the mitogen-activated protein kinase pathway with the endothelial nitric-oxide synthase.J Biol Chem 2000,275(39):30707-30715.
  • 6Dimmeler S,Fleming I,Fisslthaler B,et al.Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation.Nature 1999;399(6736):601-605.
  • 7Carneiro FS,Giachini FR,Lima VV,et al.DOCA-salt treatment enhances responses to endothein-1 in murine corpus cavernosum.Can J Physiol Pharmacol 2008,86 (6):320-328.
  • 8Hurt KJ,Musicki B,Palese MA,et al.Akt-dependent phosphorylation of endothelial nitric-oxide synthase mediates penile erection.Proc Nail Acad Sci USA 2002,99(6):4061-4066.
  • 9Lee MY,Sorensen GL,Holmskov U,et al.The presence and activity of SP-D in porcine coronary endothelial cells depend on Akt/PI(3)K,Erk and nitric oxide and decrease after multiple passaging.Mol Immunol 2009,46(6):1050-1057.
  • 10Landau D,Eshet R,Troib A,et al.Incrcased renal Akt/m TOR and MAPK signaling in type I diabetes in the absence of IGF type 1 receptor activation.Endocrine 2009,36(1):126-134.

同被引文献25

  • 1Staal SP. Proc Natl Acad Sci USA 1987; 84(14): 5034-5037.
  • 2Nicholson KM,Anderson NG. Cell Signal 2002; 14(5): 381-395.
  • 3Woodgett JR. Curr Opin Cell Bio12005; 17(2): 150-157.
  • 4Wang X, MeCullough KD, Franke TF, et al. JBiol Chem 2000; 275(19): 14624-14631.
  • 5Rommel C, Camps M, Jill. Nat Rev Immunol 2007: 7 (3): 191-201.
  • 6Manning BD, Cantley LC. Cell 2007; 129(7): 1261-1274.
  • 7Tong Z, Fan Y, Zhang W, et al. CellRes 2009; 19(6): 710-719.
  • 8Zhang M, Fang X, Liu H, et al. Cancer Lett 2007: 252 (2): 244-258.
  • 9Ichiki T, Jougasaki M, Setoguchi M, et al. Am JPhysiol Heart Circ Physiol 2008; 294(2): H750-H763.
  • 10Maira SM, Galetic I, Brazil DP, et al. Science 2001: 294(5541): 374-380.

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