Campia Umberto, Matuskey Linda A, Tesauro Manfredi, Cardillo Carmine, Panza Julio A
MedStar Cardiovascular Research Network, MedStar Heart Institute, 110 Irving Street NW, Room NA-1041, Washington, DC 20010, USA.
MedStar Cardiovascular Research Network, MedStar Heart Institute, 110 Irving Street NW, Room NA-1041, Washington, DC 20010, USA.
Atherosclerosis. 2014 Jun;234(2):436-40. doi: 10.1016/j.atherosclerosis.2014.03.035. Epub 2014 Apr 5.
This study tested the hypothesis that pioglitazone reduces endothelin-1 activity in the forearm vasculature in non-diabetic patients with hypertension or hypercholesterolemia and variable degrees of insulin resistance.
We conducted a single center, randomized, double-blind, placebo controlled, cross-over trial in 80 patients with either hypertension or hypercholesterolemia and further classified as insulin-sensitive or insulin-resistant based on a published insulin sensitivity index. Participants received pioglitazone 45 mg daily or matching placebo for eight weeks. The main endpoint was the change in forearm vascular endothelin-1 activity, as assessed by intra-arterial infusion of the endothelin type A receptor blocker BQ-123, measured at the end of each 8-week treatment period.
Pioglitazone lowered plasma insulin (P < 0.001), improved insulin sensitivity (P < 0.001), increased HDL (P < 0.001), and reduced triglycerides (P = 0.003), free fatty acids (P = 0.005), and C-reactive protein (P = 0.001). However, pioglitazone did not affect the vasodilator response to BQ-123 in the whole group (P = 0.618) and in the diagnosis or insulin sensitivity subgroups. Hence, in non-diabetic patients with hypertension or hypercholesterolemia, PPARγ activation with pioglitazone does not affect endothelin-1 activity, despite enhancing insulin sensitivity and reducing plasma insulin and C-reactive protein levels.
In non-diabetic patients with hypertension or hypercholesterolemia, pioglitazone improves insulin sensitivity, lipid profile, and inflammation but does not affect endothelin activity. Our data suggest that the determinants of endothelin-1 vascular activity in vivo may differ and/or be more complex than those suggested by the results of previous in vitro studies.
本研究检验了以下假设,即吡格列酮可降低高血压或高胆固醇血症且伴有不同程度胰岛素抵抗的非糖尿病患者前臂血管中的内皮素 -1 活性。
我们在 80 例高血压或高胆固醇血症患者中进行了一项单中心、随机、双盲、安慰剂对照的交叉试验,并根据已发表的胰岛素敏感性指数进一步分为胰岛素敏感或胰岛素抵抗组。参与者每天接受 45 毫克吡格列酮或匹配的安慰剂,为期 8 周。主要终点是前臂血管内皮素 -1 活性的变化,通过在每个 8 周治疗期结束时动脉内输注 A 型内皮素受体阻滞剂 BQ -123 进行评估。
吡格列酮降低了血浆胰岛素水平(P < 0.001),改善了胰岛素敏感性(P < 0.001),升高了高密度脂蛋白(P < 0.001),并降低了甘油三酯(P = 0.003)、游离脂肪酸(P = 0.005)和 C 反应蛋白(P = 0.001)。然而,吡格列酮在整个组(P = 0.618)以及诊断或胰岛素敏感性亚组中均未影响对 BQ -123 的血管舒张反应。因此,在高血压或高胆固醇血症的非糖尿病患者中,尽管吡格列酮可增强胰岛素敏感性并降低血浆胰岛素和 C 反应蛋白水平,但通过激活过氧化物酶体增殖物激活受体γ(PPARγ)并不会影响内皮素 -1 活性。
在高血压或高胆固醇血症的非糖尿病患者中,吡格列酮可改善胰岛素敏感性、血脂谱和炎症,但不影响内皮素活性。我们的数据表明,体内内皮素 -1 血管活性的决定因素可能与先前体外研究结果所提示的不同和/或更为复杂。