Ohnishi A, Mihara M, Yasuda S, Tomono Y, Hasegawa J, Tanaka T
Department of Internal Medicine Daisan Hospital, Jikei University School of Medicine, Tokyo, Japan.
J Pharmacol Exp Ther. 1994 Jul;270(1):342-7.
Dynorphin-A is an endogenously released hormone that is now recognized as a kappa-opioid receptor agonist. Because kappa-agonists have been reported to induce water diuresis through negative modulation of antidiuretic hormone release and/or action, in the present study we investigated the aquaretic effects and safety of E2078, a metabolically stable dynorphin-A analog, in 21 healthy subjects after single (1.0, 2.0, 3.0, 5.0, 7.5 and 10.0 mg, i.m.) and repeated (5.0 mg t.i.d. for 4 and 1/3 days) administration. E2078 dose-dependently increased the 0 to 4-hr urine volume, which plateaued between 1032.4 +/- 130.1 and 1286.2 +/- 113.0 ml/4 hr (mean +/- S.E.M.) at doses of between 5.0 and 10.0 mg. The drug decreased urine osmolality (Uosm) markedly, by 17 to 27%, and the free-water clearance (CH2O) became positive, changing from -1.8 +/- 0.2 (placebo) to 0.8 +/- 0.3-2.8 +/- 0.4 ml/min after a single E2078 administration (P < .01). In the repeated-dose study, the first dose of E2078 increased the 0 to 5-hr urine output (1256 +/- 164.9 ml/5 h), lowered Uosm (151.8 +/- 13.3 mOsm/kg) and brought about a positive CH2O (1.9 +/- 0.2 ml/min). These values were similar to those seen after the single dose, but after the subsequent doses these aquaretic effects were attenuated, although the ranges of these same parameters were still significantly greater (P < .01-0.05) (441.4 +/- 102.4-585.3 +/- 131.9 ml/5 hr, 322.8 +/- 21.9-378.2 +/- 47.7 mOsm/kg and -0.2 +/- 0.2-(-)0.6 +/- 0.2 ml/min, respectively) than the day -1 base line (164.1 +/- 41.3 ml/5 hr, 992.0 +/- 80.6 mOsm/kg and -1.2 +/- 0.2 ml/min, respectively). Urinary excretion of electrolytes (Na, K and Cl) was not altered during either study period. A single E2078 administration reduced plasma antidiuretic hormone dose-dependently. On repeated dosing, the plasma concentration had rebounded to approximately 3 pg/ml by the time of the first dose on days 3 and 5, which lowered it again. The present results suggest that E2078 is a safe and effective aquaretic and could be a useful therapeutic tool for patients with water-retaining diseases.
强啡肽A是一种内源性释放的激素,现已被确认为κ-阿片受体激动剂。由于据报道κ-激动剂可通过对抗利尿激素释放和/或作用的负调节来诱导水利尿,因此在本研究中,我们调查了代谢稳定的强啡肽A类似物E2078在21名健康受试者单次(1.0、2.0、3.0、5.0、7.5和10.0毫克,肌肉注射)和重复(5.0毫克,每日三次,共4又1/3天)给药后的利水作用和安全性。E2078剂量依赖性地增加了0至4小时的尿量,在5.0至10.0毫克剂量时,尿量在1032.4±130.1至1286.2±113.0毫升/4小时(平均值±标准误)之间达到平稳状态。该药物显著降低了尿渗透压(Uosm),降低了17%至27%,自由水清除率(CH2O)变为正值,单次注射E2078后从-1.8±0.2(安慰剂)变为0.8±0.3至2.8±0.4毫升/分钟(P<.01)。在重复给药研究中,E2078的第一剂增加了0至5小时的尿量(1256±164.9毫升/5小时),降低了Uosm(151.8±13.3毫摩尔/千克)并产生了正值的CH2O(1.9±0.2毫升/分钟)。这些值与单次给药后观察到的值相似,但在随后的剂量后,这些利水作用减弱,尽管这些相同参数的范围仍显著大于(P<.01至0.05)第-1天基线值(分别为164.1±41.3毫升/5小时、992.0±80.6毫摩尔/千克和-1.2±0.2毫升/分钟)(分别为441.4±102.4至585.3±131.9毫升/5小时、322.8±21.9至378.2±47.7毫摩尔/千克和-0.2±0.2至-0.6±0.2毫升/分钟)。在两个研究期间,电解质(钠、钾和氯)的尿排泄均未改变。单次注射E2078可剂量依赖性地降低血浆抗利尿激素。在重复给药时,到第3天和第5天首次给药时,血浆浓度已反弹至约3皮克/毫升,随后又降低。目前的结果表明,E2078是一种安全有效的利水药物,可能是治疗水潴留性疾病患者的有用治疗工具。