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前列腺素E1在勃起功能障碍中的剂量依赖性效应及副作用

Dose-dependent effect and side-effect of prostaglandin E1 in erectile dysfunction.

作者信息

Schramek P, Waldhauser M

机构信息

Department of Urology, University of Vienna, Austria.

出版信息

Br J Clin Pharmacol. 1989 Nov;28(5):567-71. doi: 10.1111/j.1365-2125.1989.tb03543.x.

Abstract
  1. Recent work has demonstrated artificial penile erection after intracavernous injection of prostaglandin E1 (PGE1). A possible dose-response relationship between PGE1 and its erectile action was examined in a double-blind, cross-over designed, placebo-controlled study. 2. Twenty patients aged (mean +/- s.d.) 45 +/- 10.5 years suffering from psychogenic erectile dysfunction were tested on four occasions. Subjects received four intracavernous injections of saline containing either no other substance, preservative, 5 micrograms or 10 micrograms PGE1. 3. Investigations revealed clear dose-dependency of PGE1 in the grade and duration of erection achieved as well as in the latency between injection and achievement of erection (P less than 0.001). Saline and preservative did not induce erection. 4. Some local pain of varying grades did occur in 11/20 patients after 5 micrograms PGE1 and in 14/20 patients after 10 micrograms PGE1 injected intracavernously. This side-effect was caused by PGE1 itself and also showed a clear dose-relation (P = 0.0035). 5. Prostaglandin E1 appears to be a promising substance for diagnostic and therapeutic purposes in erectile dysfunction. Despite the discomfort observed in some patients, PGE1 is very effective even in low doses. PGE1 10 micrograms is suggested as the appropriate initial diagnostic dose for intracavernous injection to differentiate between the normal and pathological cavernous-vascular system.
摘要
  1. 近期研究表明,海绵体内注射前列腺素E1(PGE1)后可实现人工阴茎勃起。在一项双盲、交叉设计、安慰剂对照研究中,对PGE1与其勃起作用之间可能存在的剂量反应关系进行了研究。2. 对20名年龄(均值±标准差)为45±10.5岁、患有心因性勃起功能障碍的患者进行了4次测试。受试者接受了4次海绵体内注射,注射的盐溶液中分别不含其他物质、含防腐剂、含5微克或10微克PGE1。3. 研究发现,PGE1在勃起的程度和持续时间以及注射与勃起之间的潜伏期方面存在明显的剂量依赖性(P<0.001)。盐水和防腐剂未诱发勃起。4. 11/20的患者在海绵体内注射5微克PGE1后出现了不同程度的局部疼痛,14/20的患者在注射10微克PGE1后出现了局部疼痛。这种副作用是由PGE1本身引起的,也呈现出明显的剂量关系(P = 0.0035)。5. 前列腺素E1似乎是用于勃起功能障碍诊断和治疗的一种有前景的物质。尽管在一些患者中观察到了不适,但PGE1即使在低剂量时也非常有效。建议将10微克PGE1作为海绵体内注射的合适初始诊断剂量,以区分正常和病理性海绵体血管系统。

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