Mangiafico R A, Malatino L S, Santonocito M, Messina R, Attinà T, Dell'Arte S, Sarnataro F
Institute of Internal Medicine L. Condorelli, University of Catania, Italy.
Int J Clin Pharmacol Ther. 1999 Jul;37(7):347-51.
Endothelin-1 (ET-1) is a vasoconstrictor mitogenic peptide whose plasma concentrations are increased in patients with peripheral arterial occlusive disease (PAOD). The aim of this study was to investigate whether changes in plasma ET-1 concentrations occur after a 4-week treatment with prostaglandin (PG) E1 in patients with intermittent claudication.
PATIENTS, MATERIAL AND METHODS: Twenty-four non-trained outpatients with Fontaine stage II PAOD (20 men and 4 women, mean age 63+/-7 years, age range 48-72 years) were randomized to receive over a 4-week period either PGE1 (60 microg given daily i.v. over 2 hours in 250 ml saline, n = 12) or placebo (250 ml saline, n = 12). Plasma levels of ET-1 were measured by radioimmunoassay at baseline and after treatment period. Before and after treatment pain-free walking distance (PFWD) and maximum walking distance (MWD) were evaluated by treadmill walking test as the target parameters for assessing treatment efficacy.
At week 4, PFWD and MWD significantly increased in comparison to baseline only in PGE1 treatment group (from 136+/-38 m to 246+/-95 m, p = 0.0004, and from 238+/-54 m to 411+/-137 m, p = 0.0001, respectively). At the end of the treatment period with PGE1, ET-1 plasma concentration decreased from 4.50+/-0.8 pmol/l to 3.6+/-1.1 pmol/l (p = 0.002), whereas it remained unchanged in placebo group. A significant correlation between the decrease in ET-1 plasma levels and the increase in the PFWD and MWD (r = -0.92, p < 0.0001; r = -0.78, p = 0.002, respectively) was detected in PGE1 treatment group.
Reduced ET-1 plasma concentrations after PGE1 treatment could be an index of improved endothelial function and/or could contribute to a reduction in vascular resistance and vessel wall growth in PAOD patients. Moreover, plasma ET-1 could be a marker of clinical improvement in these patients.
内皮素 -1(ET -1)是一种血管收缩性促有丝分裂肽,外周动脉闭塞性疾病(PAOD)患者的血浆浓度会升高。本研究的目的是调查间歇性跛行患者接受前列腺素(PG)E1 4周治疗后血浆 ET -1浓度是否发生变化。
患者、材料与方法:24例未经训练的Fontaine II期PAOD门诊患者(20例男性,4例女性,平均年龄63±7岁,年龄范围48 - 72岁)被随机分为两组,在4周内分别接受PGE1(60μg每日静脉滴注2小时,溶于250ml生理盐水中,n = 12)或安慰剂(250ml生理盐水,n = 12)。在基线和治疗期结束后通过放射免疫分析法测量血浆ET -1水平。治疗前后通过跑步机行走试验评估无痛行走距离(PFWD)和最大行走距离(MWD),作为评估治疗效果的目标参数。
在第4周时,仅PGE1治疗组的PFWD和MWD与基线相比显著增加(分别从136±38m增加到246±95m,p = 0.0004;从238±54m增加到411±137m,p = 0.0001)。在PGE1治疗期结束时,ET -1血浆浓度从4.50±0.8pmol/l降至3.6±1.1pmol/l(p = 0.002),而安慰剂组则保持不变。在PGE1治疗组中检测到ET -1血浆水平的降低与PFWD和MWD的增加之间存在显著相关性(分别为r = -0.92,p < 0.0001;r = -0.78,p = 0.002)。
PGE1治疗后血浆ET -1浓度降低可能是内皮功能改善的指标,和/或有助于降低PAOD患者的血管阻力和血管壁生长。此外,血浆ET -1可能是这些患者临床改善的标志物。