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The effects of dexamethasone and chlorpromazine on tumour necrosis factor-alpha, interleukin-1 beta, interleukin-1 receptor antagonist and interleukin-10 in human volunteers.地塞米松和氯丙嗪对人类志愿者肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-1受体拮抗剂及白细胞介素-10的影响
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IL-6 and APPs: anti-inflammatory and immunosuppressive mediators.白细胞介素-6与急性时相蛋白:抗炎和免疫抑制介质。
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Valsartan. A review of its pharmacology and therapeutic use in essential hypertension.缬沙坦。其药理学及在原发性高血压治疗应用的综述。
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Interleukin 1 beta, tumour necrosis factor-alpha and interleukin 1 receptor antagonist in newly diagnosed insulin-dependent diabetes mellitus: comparison to long-standing diabetes and healthy individuals.新诊断的胰岛素依赖型糖尿病患者中白细胞介素1β、肿瘤坏死因子-α及白细胞介素1受体拮抗剂:与长期糖尿病患者及健康个体的比较
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Increased serum levels of interleukin-1beta in the systemic circulation of patients with essential hypertension: additional risk factor for atherogenesis in hypertensive patients?原发性高血压患者体循环中白细胞介素-1β血清水平升高:高血压患者动脉粥样硬化形成的额外危险因素?
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Elevated interleukin-1 beta in the circulation of patients with essential hypertension before any drug therapy: a pilot study.原发性高血压患者在任何药物治疗前循环中白细胞介素-1β升高:一项初步研究。
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Oral aspirin and ibuprofen increase cytokine-induced synthesis of IL-1 beta and of tumour necrosis factor-alpha ex vivo.口服阿司匹林和布洛芬会在体外增加细胞因子诱导的白细胞介素-1β和肿瘤坏死因子-α的合成。
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Biologic basis for interleukin-1 in disease.疾病中白细胞介素-1的生物学基础。
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Endurance run increases circulating IL-6 and IL-1ra but downregulates ex vivo TNF-alpha and IL-1 beta production.耐力跑会增加循环中的白细胞介素-6和白细胞介素-1受体拮抗剂,但会下调体外肿瘤坏死因子-α和白细胞介素-1β的产生。
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Angiotensin-converting-enzyme inhibitors suppress synthesis of tumour necrosis factor and interleukin 1 by human peripheral blood mononuclear cells.血管紧张素转换酶抑制剂可抑制人外周血单核细胞合成肿瘤坏死因子和白细胞介素1。
Cytokine. 1995 Aug;7(6):526-33. doi: 10.1006/cyto.1995.0071.

肾素-血管紧张素系统抑制剂对促炎和抗炎细胞因子产生的影响。

The effect of renin-angiotensin system inhibitors on pro- and anti-inflammatory cytokine production.

作者信息

Peeters A C, Netea M G, Kullberg B J, Thien T, van der Meer J W

机构信息

Department of Medicine, University Hospital Nijmegen, The Netherlands.

出版信息

Immunology. 1998 Jul;94(3):376-9. doi: 10.1046/j.1365-2567.1998.00524.x.

DOI:10.1046/j.1365-2567.1998.00524.x
PMID:9767420
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1364256/
Abstract

The balance between pro- and anti-inflammatory cytokines has been implicated in the pathogenesis of infectious and auto-immune diseases, and its modulation has been proposed as a potential therapeutic target. The results reported in the present study show that modulators of the renin-angiotensin system, such as the angiotensin-converting enzyme (ACE)-inhibitor captopril and the angiotensin II receptor type I antagonist valsartan, have potent inhibitory effects on the lipopolysaccharide (LPS)-stimulated production of pro-inflammatory cytokines tumour necrosis factor (TNF) and interleukin-1 (IL-1) in vitro. The anti-inflammatory cytokine IL-1Ra is increased by captopril, whereas IL-6 production is decreased by valsartan. These effects are exerted mainly at high concentrations of the drugs. Administration of one dose of captopril or valsartan in therapeutic dosages to patients with essential hypertension did not influence LPS-stimulated production of cytokines by whole blood. In conclusion, despite inhibitory effects on pro-inflammatory cytokine production in vitro, it is unlikely that captopril or valsartan could be used in anticytokine therapeutic strategies in vivo.

摘要

促炎细胞因子和抗炎细胞因子之间的平衡与感染性疾病和自身免疫性疾病的发病机制有关,调节这种平衡已被提议作为一个潜在的治疗靶点。本研究报告的结果表明,肾素-血管紧张素系统的调节剂,如血管紧张素转换酶(ACE)抑制剂卡托普利和血管紧张素II 1型受体拮抗剂缬沙坦,在体外对脂多糖(LPS)刺激的促炎细胞因子肿瘤坏死因子(TNF)和白细胞介素-1(IL-1)的产生具有强大的抑制作用。卡托普利可增加抗炎细胞因子IL-1Ra,而缬沙坦可降低IL-6的产生。这些作用主要在高浓度药物时发挥。对原发性高血压患者给予一剂治疗剂量的卡托普利或缬沙坦,并不影响LPS刺激全血产生细胞因子。总之,尽管卡托普利或缬沙坦在体外对促炎细胞因子的产生有抑制作用,但它们不太可能用于体内抗细胞因子治疗策略。