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非诺贝特激活过氧化物酶体增殖物激活受体-α作用并不抑制内毒素血症诱导的炎症反应。

Peroxisome Proliferator-Activated Receptor-α Agonism With Fenofibrate Does Not Suppress Inflammatory Responses to Evoked Endotoxemia.

机构信息

Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA (C.K.M., J.F.F., J.T.-M., S.K., R.Y.S., P.N.P., M.H.U.U., N.N.M., M.P.R.).

出版信息

J Am Heart Assoc. 2012 Aug;1(4):e002923. doi: 10.1161/JAHA.112.002923. Epub 2012 Aug 24.

Abstract

BACKGROUND

Data conflict with regard to whether peroxisome proliferator-activated receptor-α agonism suppresses inflammation in humans. We hypothesized that in healthy adults peroxisome proliferator-activated receptor-α agonism with fenofibrate would blunt the induced immune responses to endotoxin (lipopolysaccharide [LPS]), an in vivo model for the study of cardiometabolic inflammation.

METHODS AND RESULTS

In the Fenofibrate and omega-3 Fatty Acid Modulation of Endotoxemia (FFAME) trial, 36 healthy volunteers (mean age 26±7 years, mean body mass index 24±3 kg/m(2), 44% female, 72% white) were randomized to fenofibrate 145 mg or placebo daily. After 6 to 8 weeks of treatment, subjects underwent a low-dose LPS challenge. Clinical and blood measurements were collected at randomization, before LPS administration, and serially for 24 hours after LPS administration. We examined area under the curve for evoked responses by treatment group. Compared to placebo, but before LPS challenge, fenofibrate reduced total cholesterol and tended to decrease triglycerides, consistent with achieved therapeutic plasma levels of fenofibric acid. In the placebo group, LPS induced a modest inflammatory response with increased cytokines and chemokines (2- to 4-hour post-LPS 8-fold increase in tumor necrosis factor-α, 9-fold increase in interleukin-6, 9-fold increase in interleukin-10, and 10-fold increase in monocyte chemotactic protein-1; all P<0.001) and acute-phase reactants (24-hour post-LPS 15-fold increase in serum amyloid A and 9-fold increase in C-reactive protein; both P<0.001). Compared to placebo, however, fenofibrate did not significantly attenuate LPS-induced levels of plasma cytokines, chemokines, or acute-phase proteins.

CONCLUSIONS

These data suggest a lack of systemic antiinflammatory properties of fenofibrate at clinically relevant dosing in humans.

CLINICAL TRIAL REGISTRATION

URL: http://clinicaltrials.gov/ct2/show/NCT01048502. Unique identifier: NCT01048502. (J Am Heart Assoc. 2012;1:e002923 doi: 10.1161/JAHA.112.002923.).

摘要

背景

关于过氧化物酶体增殖物激活受体-α激动剂是否能抑制人类炎症,数据存在冲突。我们假设,在健康成年人中,用非诺贝特进行过氧化物酶体增殖物激活受体-α激动治疗,会减弱内毒素(脂多糖[LPS])诱导的免疫反应,LPS 是研究心脏代谢炎症的体内模型。

方法和结果

在非诺贝特和 ω-3 脂肪酸对内毒素血症的调制(FFAME)试验中,36 名健康志愿者(平均年龄 26±7 岁,平均体重指数 24±3kg/m2,44%为女性,72%为白人)被随机分配到非诺贝特 145mg 或安慰剂每日治疗。经过 6-8 周的治疗后,受试者接受了低剂量 LPS 挑战。在随机分组、给予 LPS 前以及 LPS 给予后 24 小时连续进行临床和血液测量。我们通过治疗组来检查诱发反应的曲线下面积。与安慰剂相比,但在 LPS 挑战之前,非诺贝特降低了总胆固醇,且倾向于降低甘油三酯,与实现的非诺贝特酸治疗血浆水平一致。在安慰剂组,LPS 诱导了适度的炎症反应,增加了细胞因子和趋化因子(LPS 后 2-4 小时肿瘤坏死因子-α增加 8 倍,白细胞介素-6 增加 9 倍,白细胞介素-10 增加 9 倍,单核细胞趋化蛋白-1 增加 10 倍;所有 P<0.001)和急性相反应物(LPS 后 24 小时血清淀粉样蛋白 A 增加 15 倍,C 反应蛋白增加 9 倍;所有 P<0.001)。然而,与安慰剂相比,非诺贝特并没有显著减弱 LPS 诱导的血浆细胞因子、趋化因子或急性相蛋白水平。

结论

这些数据表明,在人类中,用临床相关剂量的非诺贝特治疗,并没有表现出系统的抗炎特性。

临床试验注册

网址:http://clinicaltrials.gov/ct2/show/NCT01048502。独特标识符:NCT01048502。(J Am Heart Assoc. 2012;1:e002923 doi: 10.1161/JAHA.112.002923.)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f90/3487364/425490ab3640/jah3-1-e002923-g1.jpg

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