Musicki Biljana, Champion Hunter C, Becker Robyn E, Kramer Melissa F, Liu Tongyun, Sezen Sena F, Burnett Arthur L
Department of Urology and Division of Cardiology, The Johns Hopkins Hospital, Baltimore, Maryland 21287, USA.
J Urol. 2005 Oct;174(4 Pt 1):1493-6. doi: 10.1097/01.ju.0000173006.47623.2c.
Conflicting information exists regarding the long-term efficacy of phosphodiesterase-5 (PDE5) inhibitor therapy for erectile dysfunction, particularly in regard to whether therapeutic resistance occurs. We investigated the erectile response, and cavernous PDE5 expression and activity after continuous long-term administration of sildenafil at verified therapeutic plasma concentrations, applying an in vivo rat model of age related erectile dysfunction.
Male Fisher 344 young (4 months old) and aged (19 months old) rats (National Institute of Aging, Bethesda, Maryland) were injected with sildenafil mesylate (20 mg/kg) or saline subcutaneously every 8 hours for 3 weeks. After a 10 to 18-hour washout period electrical stimulation of the cavernous nerve was performed to assess penile erection. Penes were excised to measure PDE5 protein expression and activity, and blood was collected for sildenafil measurement. Responses were compared with those determined 30 minutes after a single sildenafil injection.
Chronic sildenafil treatment increased the detumescence phase in young and aged rats (p <0.05), although aged rats showed a greater increase than young rats. Baseline cavernous PDE5 expression and activity were greater in aged vs young rats (p <0.05). After chronic sildenafil treatment cavernous PDE5 expression was increased in young (p <0.05) but not in aged rats. Chronic and acute sildenafil treatment similarly inhibited PDE5 activity in the penis of young and aged rats (p <0.05), coincident with its free plasma concentrations equivalent to clinically therapeutic ranges.
Pharmacological PDE5 inhibitor therapy with sildenafil chronically does not result in treatment resistance. Rather, therapeutic efficacy is maintained and apparently more pronounced with erectile impairment than with normal erectile ability.
关于磷酸二酯酶-5(PDE5)抑制剂治疗勃起功能障碍的长期疗效存在相互矛盾的信息,尤其是关于是否会出现治疗抵抗。我们使用年龄相关性勃起功能障碍的体内大鼠模型,研究了在已证实的治疗性血浆浓度下持续长期给予西地那非后勃起反应以及海绵体PDE5的表达和活性。
雄性Fisher 344幼龄(4个月大)和老龄(19个月大)大鼠(美国国立衰老研究所,马里兰州贝塞斯达)每8小时皮下注射甲磺酸西地那非(20 mg/kg)或生理盐水,持续3周。在10至18小时的洗脱期后,进行海绵体神经电刺激以评估阴茎勃起。切除阴茎以测量PDE5蛋白表达和活性,并采集血液用于西地那非测定。将反应与单次注射西地那非30分钟后测定的反应进行比较。
慢性西地那非治疗增加了幼龄和老龄大鼠的消肿期(p<0.05),尽管老龄大鼠的增加幅度大于幼龄大鼠。老龄大鼠的基线海绵体PDE5表达和活性高于幼龄大鼠(p<0.05)。慢性西地那非治疗后,幼龄大鼠海绵体PDE5表达增加(p<0.05),而老龄大鼠未增加。慢性和急性西地那非治疗同样抑制了幼龄和老龄大鼠阴茎中的PDE5活性(p<0.05),同时其游离血浆浓度相当于临床治疗范围。
长期使用西地那非进行药理学PDE5抑制剂治疗不会导致治疗抵抗。相反,治疗效果得以维持,并且在勃起功能受损时比正常勃起能力时更为明显。