Department of Emergency Medicine, University of Palermo, Palermo, Italy.
Clin Drug Investig. 2003;23(11):717-24. doi: 10.2165/00044011-200323110-00004.
Angiotensin-converting enzyme (ACE) probably influences the fibrinolytic system at a central point by converting angiotensin I to angiotensin II, which increases plasminogen activator inhibitor-1 (PAI-1) activity. This effect appears to be mediated in humans via the angiotensin II type 1 (AT(1)) receptor. The objective of this study was to evaluate, in patients with mild to moderate hypertension, the change in tissue plasminogen activator (t-PA) and PAI-1 plasma levels after treatment with an AT(1)-receptor blocker (losartan 50 mg/day) or an ACE inhibitor (delapril 60 mg/day).
30 hypertensive patients and 15 controls were enrolled. Essential hypertension was established by a medical history, physical examination and the absence of clinical findings suggestive of a secondary form of hypertension. Preliminary investigations, routine biochemical tests (including clearance of creatinine and oral glucose tolerance test), chest x-ray, standard and 24-hour ECG monitoring, M- and B-mode echocardiography and fundus oculi examinations were performed. No patients had previously received ACE inhibitors or AT(1)-receptor blockers. After a 14-day run-in period with placebo, patients were randomised in a double-blind fashion into two groups: 15 patients were randomised to losartan 50 mg/day (group 1), 15 patients were randomised to delapril 60 mg/day (group 2), and 15 healthy subjects were used as controls (group 3). Plasma PAI-1 and t-PA antigen were determined by enzyme-linked immunosorbent assay and a photometric method at the end of the run-in period and after 6 months of treatment.
There were no significant differences among the three groups regarding age, sex, body mass index and smoking. After 6 months, both groups of patients showed a reduction in blood pressure values. The losartan group did not demonstrate significant changes in PAI-1 levels (96.52 +/- 23.73 and 99.89 +/- 22.18 mug/L, pre- and post-treatment, respectively) or in t-PA antigen levels (26.17 +/- 6.18 and 27.32 +/- 5.91 mug/L, pre- and post-treatment, respectively). The delapril group showed no significant changes in PAI-1 levels (97.73 +/- 25.75 and 86.12 +/- 13.12 mug/L, pre- and post-treatment, respectively), but did show a statistically significant difference (p < 0.005) in t-PA antigen levels (25.71 +/- 6.40 and 32.24 +/- 5.31 mug/L, pre- and post-treatment, respectively). The losartan group demonstrated significantly higher post-treatment PAI-1 values than the delapril group (p = 0.048).
The study showed that losartan does not affect fibrinolytic parameters, while delapril resulted in an insignificant reduction in PAI-1 and a significant increase in t-PA levels. Further studies are clearly required in order to establish whether these different effects on the fibrinolytic system between ACE inhibitors and AT(1)-receptor blockers may have clinical relevance.
血管紧张素转换酶(ACE)可能通过将血管紧张素 I 转化为血管紧张素 II 来影响纤溶系统,从而增加纤溶酶原激活物抑制剂-1(PAI-1)的活性。这种作用似乎是通过人类的血管紧张素 II 型 1(AT(1))受体介导的。本研究的目的是评估在患有轻度至中度高血压的患者中,在使用 AT(1)受体阻滞剂(洛沙坦 50mg/天)或 ACE 抑制剂(赖诺普利 60mg/天)治疗后,组织型纤溶酶原激活物(t-PA)和 PAI-1 血浆水平的变化。
共纳入 30 例高血压患者和 15 名对照者。原发性高血压通过病史、体格检查和无提示继发性高血压的临床发现来确定。初步检查包括清除肌酐和口服葡萄糖耐量试验、胸部 X 线、标准和 24 小时心电图监测、M 型和 B 型超声心动图以及眼底检查。无患者曾接受 ACE 抑制剂或 AT(1)受体阻滞剂治疗。在安慰剂洗脱期 14 天后,患者被随机分为两组:15 例患者随机分为洛沙坦 50mg/天(第 1 组),15 例患者随机分为赖诺普利 60mg/天(第 2 组),15 例健康受试者作为对照组(第 3 组)。在洗脱期结束和治疗 6 个月时,通过酶联免疫吸附试验和分光光度法测定血浆 PAI-1 和 t-PA 抗原。
三组患者在年龄、性别、体重指数和吸烟方面无显著差异。治疗 6 个月后,两组患者的血压值均降低。洛沙坦组 PAI-1 水平无显著变化(分别为 96.52±23.73 和 99.89±22.18μg/L,治疗前后)或 t-PA 抗原水平(分别为 26.17±6.18 和 27.32±5.91μg/L,治疗前后)。赖诺普利组 PAI-1 水平无显著变化(分别为 97.73±25.75 和 86.12±13.12μg/L,治疗前后),但 t-PA 抗原水平有统计学意义差异(p<0.005)(分别为 25.71±6.40 和 32.24±5.31μg/L,治疗前后)。洛沙坦组治疗后 PAI-1 值明显高于赖诺普利组(p=0.048)。
本研究表明,洛沙坦不影响纤溶参数,而赖诺普利则导致 PAI-1 水平降低和 t-PA 水平升高,但无统计学意义。显然需要进一步研究,以确定 ACE 抑制剂和 AT(1)受体阻滞剂对纤溶系统的这些不同影响是否具有临床意义。