Rizos Evangelos C, Spyrou Athanasia, Liberopoulos Evangelos N, Papavasiliou Eleni C, Saougos Vasilis, Tselepis Alexandros D, Elisaf Moses
Department of Internal Medicine, Medical School, University of Ioannina, 45110 Ioannina, Greece.
Open Cardiovasc Med J. 2007;1:22-6. doi: 10.2174/1874192400701010022. Epub 2007 Nov 14.
The effect of the anti-hypertensive drug eprosartan on metabolic parameters is currently not extensively documented. We evaluated the effect of eprosartan on parameters involved in atherogenesis, oxidative stress and clotting activity. This open-label unblinded intervention study included 40 adult patients with essential hypertension taking eprosartan. Eprosartan significantly reduced by 8% (p<0.001) the systolic and by 13% (p<.001) the diastolic blood pressure, and in-creased by 24% the time needed to produce oxidative by-products (p=0.001), a marker of oxidative stress. In contrast, ep-rosartan did not alter 8-isoprostane (8-epiPGF2a) levels, another marker of oxidative stress. Additionally, eprosartan re-duced by 14% aspartate aminotransferase and by 21% then alanine aminotransferase activity, while it had a neutral effect on the lipid profile and apolipoprotein levels and did not influence glucose homeostasis, creatinine and uric acid levels. Eprosartan did not affect the clotting/fibrinolytic status (estimated by plasminogen activator inhibitor 1, tissue plasmino-gen activator and a2 antiplasmin levels), or the enzymatic activity of the lipoprotein associated phospholipase A2 (Lp-PLA2) and paraoxonase 1 (PON1). In conclusion, eprosartan should be mainly considered as an anti-hypertensive agent with neutral effects on most of the metabolic parameters in hypertensive patients.
抗高血压药物依普罗沙坦对代谢参数的影响目前尚无广泛记录。我们评估了依普罗沙坦对动脉粥样硬化、氧化应激和凝血活性相关参数的影响。这项开放标签、非盲法干预研究纳入了40名服用依普罗沙坦的成年原发性高血压患者。依普罗沙坦使收缩压显著降低8%(p<0.001),舒张压显著降低13%(p<0.001),并使产生氧化副产物所需时间增加24%(p=0.001),氧化副产物是氧化应激的一个标志物。相比之下,依普罗沙坦并未改变另一个氧化应激标志物8-异前列腺素(8-epiPGF2a)的水平。此外,依普罗沙坦使天冬氨酸转氨酶活性降低14%,丙氨酸转氨酶活性降低21%,而对血脂谱和载脂蛋白水平具有中性作用,且不影响葡萄糖稳态、肌酐和尿酸水平。依普罗沙坦不影响凝血/纤维蛋白溶解状态(通过纤溶酶原激活物抑制剂1、组织纤溶酶原激活物和α2抗纤溶酶水平评估),也不影响脂蛋白相关磷脂酶A2(Lp-PLA2)和对氧磷酶1(PON1)的酶活性。总之,依普罗沙坦应主要被视为一种对高血压患者大多数代谢参数具有中性作用的抗高血压药物。