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Future strategies for treating erectile dysfunction.治疗勃起功能障碍的未来策略。
Rev Urol. 2002;4 Suppl 3(Suppl 3):S48-53.
2
Sildenafil: a review of its use in erectile dysfunction.西地那非:对其在勃起功能障碍治疗中应用的综述。
Drugs. 1999 Jun;57(6):967-89. doi: 10.2165/00003495-199957060-00015.
3
[Efficacy and safety of sildenafil in men with type 2 diabetes mellitus and erectile dysfunction].西地那非对2型糖尿病合并勃起功能障碍男性患者的疗效与安全性
Med Clin (Barc). 2002 Jun 29;119(4):121-4. doi: 10.1016/s0025-7753(02)73339-3.
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Inhibition of Cyclic GMP Export by Multidrug Resistance Protein 4: A New Strategy to Treat Erectile Dysfunction?多药耐药蛋白4对环磷酸鸟苷输出的抑制作用:治疗勃起功能障碍的新策略?
J Sex Med. 2017 Apr;14(4):502-509. doi: 10.1016/j.jsxm.2017.02.005. Epub 2017 Mar 1.
5
Efficacy and safety of sildenafil citrate in the treatment of erectile dysfunction in patients with ischemic heart disease.枸橼酸西地那非治疗缺血性心脏病患者勃起功能障碍的疗效与安全性。
Am J Cardiol. 1999 Mar 4;83(5A):29C-34C. doi: 10.1016/s0002-9149(99)00045-4.
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Efficacy and Safety of Sildenafil by Age in Men With Erectile Dysfunction.西地那非对不同年龄勃起功能障碍男性的疗效与安全性
J Sex Med. 2016 May;13(5):852-9. doi: 10.1016/j.jsxm.2016.02.166.
7
The role of nitric oxide in erectile dysfunction: implications for medical therapy.一氧化氮在勃起功能障碍中的作用:对药物治疗的启示。
J Clin Hypertens (Greenwich). 2006 Dec;8(12 Suppl 4):53-62. doi: 10.1111/j.1524-6175.2006.06026.x.
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Separate or combined treatments with daily sildenafil, molsidomine, or muscle-derived stem cells prevent erectile dysfunction in a rat model of cavernosal nerve damage.每日使用西地那非、吗多明或肌肉源性干细胞单独或联合治疗可预防海绵体神经损伤大鼠模型的勃起功能障碍。
J Sex Med. 2012 Nov;9(11):2814-26. doi: 10.1111/j.1743-6109.2012.02913.x. Epub 2012 Sep 13.
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Gene transfer of prepro-calcitonin gene-related peptide restores erectile function in the aged rat.前降钙素基因相关肽的基因转移可恢复老年大鼠的勃起功能。
Biol Reprod. 2001 Nov;65(5):1371-7. doi: 10.1095/biolreprod65.5.1371.
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TNF-alpha knockout mice have increased corpora cavernosa relaxation.肿瘤坏死因子-α基因敲除小鼠的海绵体舒张增强。
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Evolution of penile prosthetic devices.阴茎假体装置的演变
Korean J Urol. 2015 Mar;56(3):179-86. doi: 10.4111/kju.2015.56.3.179. Epub 2015 Mar 3.

本文引用的文献

1
Integrative erectile biology. The effects of age and disease on gap junctions and ion channels and their potential value to the treatment of erectile dysfunction.整合性勃起生物学。年龄和疾病对缝隙连接和离子通道的影响及其对勃起功能障碍治疗的潜在价值。
Urol Clin North Am. 2001 May;28(2):217-31, vii. doi: 10.1016/s0094-0143(05)70133-6.
2
The effect of adeno-associated virus mediated brain derived neurotrophic factor in an animal model of neurogenic impotence.腺相关病毒介导的脑源性神经营养因子在神经源性阳痿动物模型中的作用
J Urol. 2001 Jun;165(6 Pt 1):2103-9. doi: 10.1097/00005392-200106000-00078.
3
Antagonism of Rho-kinase stimulates rat penile erection via a nitric oxide-independent pathway.Rho激酶的拮抗作用通过一条不依赖一氧化氮的途径刺激大鼠阴茎勃起。
Nat Med. 2001 Jan;7(1):119-22. doi: 10.1038/83258.
4
The worldwide prevalence and epidemiology of erectile dysfunction.勃起功能障碍的全球患病率及流行病学
Int J Impot Res. 2000 Oct;12 Suppl 4:S6-S11. doi: 10.1038/sj.ijir.3900567.
5
Erectile dysfunction.勃起功能障碍
N Engl J Med. 2000 Jun 15;342(24):1802-13. doi: 10.1056/NEJM200006153422407.
6
Differential ICP responses elicited by electrical stimulation of medial preoptic area.电刺激内侧视前区引发的颅内压差异反应。
Am J Physiol Heart Circ Physiol. 2000 Mar;278(3):H964-70. doi: 10.1152/ajpheart.2000.278.3.H964.
7
Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter.使用带有神经元特异性启动子的重组腺病毒在神经元中进行高效基因转移和长期表达。
Gene Ther. 1999 Nov;6(11):1884-92. doi: 10.1038/sj.gt.3301008.
8
Future treatment for ED: growth factors and gene therapy.勃起功能障碍的未来治疗:生长因子与基因治疗。
Int J Impot Res. 1999 Sep;11 Suppl 1:S56-7. doi: 10.1038/sj.ijir.3900485.
9
Gene transfer of endothelial nitric oxide synthase to the penis augments erectile responses in the aged rat.将内皮型一氧化氮合酶基因导入阴茎可增强老年大鼠的勃起反应。
Proc Natl Acad Sci U S A. 1999 Sep 28;96(20):11648-52. doi: 10.1073/pnas.96.20.11648.
10
Clinical efficacy of sildenafil citrate based on etiology and response to prior treatment.基于病因及既往治疗反应的枸橼酸西地那非临床疗效
J Urol. 1999 Sep;162(3 Pt 1):722-5. doi: 10.1097/00005392-199909010-00024.

治疗勃起功能障碍的未来策略。

Future strategies for treating erectile dysfunction.

作者信息

Rajfer Jacob, Magee Thomas, Gonzalez-Cadavid Nestor

出版信息

Rev Urol. 2002;4 Suppl 3(Suppl 3):S48-53.

PMID:16986014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1476023/
Abstract

Erectile dysfunction affects over half of all men between 50 and 70 years of age, and by the age of 40, about 40% of men may suffer from some form of erectile dysfunction. Many disease states, such as diabetes, hypertension, depression, and vascular disease, are associated with the condition, which may occur many years prior to the onset of these disorders. The phenomenal success of sildenafil in improving erections in men with erectile dysfunction is due to the fact that the drug, as a phosphodiesterase inhibitor, improves the relaxation of smooth muscle cells, which become dysfunctional with the aging process. However, not everyone responds to this medication, mainly because the efficacy of the drug is directly dependent on the release of nitric oxide from the nerve terminals of the cavernosal nerve, and this may become defective with aging/certain disease states. The goal of gene therapy for organic impotence is to allow the patient to sustain physiologically elicited erections without resorting to pharmacological treatment immediately prior to the sexual act. Experimental efforts in gene therapy for erectile dysfunction are likely to continue intensively in a series of directions, some specific to the nature of the selected gene to be manipulated or the physiology of the corpora cavernosa itself, and others extrapolatable from the advancement of gene therapy in general.

摘要

勃起功能障碍影响着超过半数年龄在50至70岁之间的男性,到40岁时,约40%的男性可能患有某种形式的勃起功能障碍。许多疾病状态,如糖尿病、高血压、抑郁症和血管疾病,都与这种情况相关,而勃起功能障碍可能在这些疾病发病前很多年就已出现。西地那非在改善勃起功能障碍男性勃起方面取得了显著成功,这是因为该药物作为一种磷酸二酯酶抑制剂,可改善平滑肌细胞的舒张功能,而平滑肌细胞会随着衰老过程出现功能障碍。然而,并非每个人对这种药物都有反应,主要是因为药物的疗效直接取决于海绵体神经末梢释放一氧化氮的情况,而这可能会随着衰老/某些疾病状态而出现缺陷。器质性阳痿基因治疗的目标是让患者在性行为前无需借助药物治疗就能维持生理诱导的勃起。勃起功能障碍基因治疗的实验工作可能会在一系列方向上继续深入开展,有些方向特定于所选要操控基因的性质或海绵体自身的生理学,其他方向则可从基因治疗的总体进展中推断出来。