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阿利吉仑渗透到脂肪和骨骼肌组织中,并降低肥胖高血压患者的肾素-血管紧张素系统活性。

Aliskiren penetrates adipose and skeletal muscle tissue and reduces renin-angiotensin system activity in obese hypertensive patients.

机构信息

Franz Volhard Clinical Research Center, Charité, Berlin, Germany.

出版信息

J Hypertens. 2012 Mar;30(3):561-6. doi: 10.1097/HJH.0b013e32834f6b43.

Abstract

OBJECTIVE

In animals, the direct renin inhibitor aliskiren showed extensive tissue binding in the kidney and long-lasting renal effects. Aliskiren provides prolonged blood pressure-lowering effects following treatment discontinuation in patients. Therefore, we investigated whether aliskiren attains tissue concentrations sufficient to inhibit local renin-angiotensin system (RAS) activity in patients.

METHODS

We included 10 hypertensive patients with abdominal adiposity in an open-label study. Following 1-2 weeks washout, patients received 2 weeks placebo, then 4 weeks aliskiren 300 mg once daily, followed by 4 weeks washout, and then 4 weeks amlodipine 5 mg once daily. Drug concentrations and RAS biomarkers were measured in interstitial fluid using microdialysis and in biopsies from abdominal subcutaneous adipose and skeletal muscle.

RESULTS

We detected aliskiren in all compartments. After 4 weeks of treatment, microdialysate aliskiren concentrations (ng/ml) were 2.4 ± 2.1 (adipose) and 7.1 ± 4.2 (skeletal muscle), similar to plasma concentrations (8.4 ± 4.4); tissue concentrations (ng/g) were 29.0 ± 16.7 (adipose) and 107.3 ± 68.6 (skeletal muscle). Eight weeks after discontinuation, aliskiren was measurable in tissue biopsies but not in plasma or in interstitial fluid. Pooled microdialysate samples from two sets of four patients suggested reduction in tissue angiotensin II with aliskiren but not with amlodipine.

CONCLUSION

In obese hypertensive patients, aliskiren penetrates adipose and skeletal muscle tissue at levels that are apparently sufficient to reduce tissue RAS activity. Furthermore, tissue binding may contribute to aliskiren's prolonged blood pressure-lowering effect following discontinuation.

摘要

目的

在动物体内,直接肾素抑制剂阿利吉仑在肾脏中具有广泛的组织结合,并具有持久的肾脏作用。阿利吉仑在停药后仍能持续降低血压。因此,我们研究了阿利吉仑是否能达到足以抑制患者局部肾素-血管紧张素系统(RAS)活性的组织浓度。

方法

我们纳入了 10 名患有腹部肥胖的高血压患者,进行了一项开放标签研究。在洗脱期 1-2 周后,患者先接受 2 周安慰剂治疗,然后接受 4 周阿利吉仑 300mg 每日一次治疗,随后进行 4 周洗脱期,然后再接受 4 周氨氯地平 5mg 每日一次治疗。使用微透析法测量间质液中的药物浓度和 RAS 生物标志物,并测量腹部皮下脂肪和骨骼肌活检组织中的 RAS 生物标志物。

结果

我们在所有部位都检测到了阿利吉仑。治疗 4 周后,微透析液中阿利吉仑浓度(ng/ml)分别为 2.4±2.1(脂肪组织)和 7.1±4.2(骨骼肌),与血浆浓度(8.4±4.4)相似;组织浓度(ng/g)分别为 29.0±16.7(脂肪组织)和 107.3±68.6(骨骼肌)。停药 8 周后,组织活检仍可检测到阿利吉仑,但血浆和间质液中不可检测到。来自两组各 4 名患者的合并微透析样本表明,阿利吉仑降低了组织血管紧张素 II,但氨氯地平没有。

结论

在肥胖的高血压患者中,阿利吉仑渗透到脂肪组织和骨骼肌组织中,水平显然足以降低组织 RAS 活性。此外,组织结合可能有助于阿利吉仑停药后血压持续降低。

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