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作 者:陈洪德[1] 叶雪挺[1] 张奕荣[1] 翁志梁[1] 李澄棣[1]
机构地区:[1]温州医学院附属第一医院泌尿外科,325000
出 处:《中华老年医学杂志》2012年第6期500-502,共3页Chinese Journal of Geriatrics
摘 要:目的观察持续口服小剂量西地那非对良性前列腺增生(BPH)患者前列腺组织中内皮素-1(ET-1)及其受体A、BETAR/ETBR基因表达的影响。方法32例BPH患者随机归入治疗组及对照组,每组各16例。治疗组每日口服西地那非25mg,为期12周。对照组未服用药物。应用免疫组化、酶联免疫吸附法及RT—PCR方法检测并比较两组前列腺组织FT一1及其ETAR的表达。结果ET—1、ETARmRNA及ETBRmRNA在前列腺组织中的表达治疗组明显低于对照组[(53.31±18.56)ng/kg比(83.34±31.38)ng/kg、0.356±0.056比0.624±0.083、0.721±0.083比0.933±0.905,t=-3.295、10.715、6.937,均P〈0.001]。结论持续口服小剂量西地那非能降低BPH组织中ET1及其受体ETA/B基因的表达量。Objective To observe the mRNA expressions of endothelin(ET-1) and endothelin A/B receptors (ETA/B) in tissue of benign prostatic hyperplasia treated by daily low-dose sildenafil. Methods A total of 32 patients with benign prostatic hyperplasia were randomly divided into two groups: treatment(25 mg sildenafi for 12 weeks, n=16) and control (no drug, n=16) groups. Immunohistochemical staining, ELISA and RT-PCR were used to detect the expression levels of ET-1 protein and ET A/B mRNA, respectively. Results The expressions of ET-1 protein and ET A/B mRNA in prostatic tissue were significantly lower in treatment group than in control group[(53.31± 18.56) ng/kgvs. (83.34±31.38) ng/kg, 0. 356 ±0. 056 vs. 0.624±0.083, 0. 721± 0. 083 vs. 0.933±0.905, t=-3.295,10.715, 6. 937, all P〈0. 001]. Conclusions Daily low-dose sildenafil can reduce the expressions of ET-1 and ET A/B receptors mRNA in benign prostatic hyperplasia.
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