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新型磷酸二酯酶4(PDE4)抑制剂罗氟司特的体外抗炎和免疫调节潜力

Anti-inflammatory and immunomodulatory potential of the novel PDE4 inhibitor roflumilast in vitro.

作者信息

Hatzelmann A, Schudt C

机构信息

Byk Gulden, Department of Biochemistry, P.O. Box 100301, 48403 Konstanz, Germany.

出版信息

J Pharmacol Exp Ther. 2001 Apr;297(1):267-79.

Abstract

From a series of benzamide derivatives, roflumilast (3-cyclo-propylmethoxy-4-difluoromethoxy-N-[3,5-di-chloropyrid-4-yl]-benzamide) was identified as a potent and selective PDE4 inhibitor. It inhibits PDE4 activity from human neutrophils with an IC(50) of 0.8 nM without affecting PDE1 (bovine brain), PDE2 (rat heart), and PDE3 and PDE5 (human platelets) even at 10,000-fold higher concentrations. Roflumilast is almost equipotent to its major metabolite formed in vivo (roflumilast N-oxide) and piclamilast (RP 73401), however, more than 100-fold more potent than rolipram and Ariflo (cilomilast; SB 207499). The anti-inflammatory and immunomodulatory potential of roflumilast and the reference compounds was investigated in various human leukocytes using cell-specific responses: neutrophils [N-formyl-methyl-leucyl-phenylalanine (fMLP)-induced formation of LTB(4) and reactive oxygen species (ROS)], eosinophils (fMLP- and C5a-induced ROS formation), monocytes, monocyte-derived macrophages, and dendritic cells (lipopolysaccharide-induced tumor necrosis factor-alpha synthesis), and CD4+ T cells (anti-CD3/anti-CD28 monoclonal antibody-stimulated proliferation, IL-2, IL-4, IL-5, and interferon-gamma release). Independent of the cell type and the response investigated, the corresponding IC values (for half-maximum inhibition) of roflumilast were within a narrow range (2-21 nM), very similar to roflumilast N-oxide (3-40 nM) and piclamilast (2-13 nM). In contrast, cilomilast (40-3000 nM) and rolipram (10-600 nM) showed greater differences with the highest potency for neutrophils. Compared with neutrophils and eosinophils, representing the terminal inflammatory effector cells, the relative potency of roflumilast and its N-oxide for monocytes, CD4+ T cells, and dendritic cells is substantially higher compared with cilomilast and rolipram, probably reflecting an improved immunomodulatory potential. The efficacy of roflumilast in vitro and in vivo (see accompanying article in this issue) suggests that roflumilast will be useful in the treatment of chronic inflammatory disorders such as asthma and chronic obstructive pulmonary disease.

摘要

从一系列苯甲酰胺衍生物中,罗氟司特(3-环丙基甲氧基-4-二氟甲氧基-N-[3,5-二氯吡啶-4-基]-苯甲酰胺)被鉴定为一种强效且选择性的磷酸二酯酶4(PDE4)抑制剂。它抑制人中性粒细胞的PDE4活性,半数抑制浓度(IC50)为0.8 nM,即使在浓度高出10000倍时,也不影响PDE1(牛脑)、PDE2(大鼠心脏)以及PDE3和PDE5(人血小板)。罗氟司特与其体内形成的主要代谢产物(罗氟司特N-氧化物)和吡拉米司特(RP 73401)几乎具有同等效力,然而,其效力比咯利普兰和阿瑞吡坦(西洛司特;SB 207499)高出100多倍。利用细胞特异性反应,在多种人类白细胞中研究了罗氟司特及对照化合物的抗炎和免疫调节潜力:中性粒细胞[N-甲酰基-甲基-亮氨酰-苯丙氨酸(fMLP)诱导的白三烯B4(LTB4)形成和活性氧(ROS)]、嗜酸性粒细胞(fMLP和C5a诱导的ROS形成)、单核细胞、单核细胞衍生的巨噬细胞以及树突状细胞(脂多糖诱导的肿瘤坏死因子-α合成),还有CD4 + T细胞(抗CD3/抗CD28单克隆抗体刺激的增殖、白细胞介素-2、白细胞介素-4、白细胞介素-5和干扰素-γ释放)。无论所研究的细胞类型和反应如何,罗氟司特的相应半数抑制浓度(IC值)都在一个狭窄范围内(2 - 21 nM),与罗氟司特N-氧化物(3 - 40 nM)和吡拉米司特(2 - 13 nM)非常相似。相比之下,西洛司特(40 - 3000 nM)和咯利普兰(10 - 600 nM)表现出更大差异,对中性粒细胞的效力最高。与代表终末炎症效应细胞的中性粒细胞和嗜酸性粒细胞相比,罗氟司特及其N-氧化物对单核细胞、CD4 + T细胞和树突状细胞的相对效力,与西洛司特和咯利普兰相比显著更高,这可能反映出其免疫调节潜力有所改善。罗氟司特在体外和体内的疗效(见本期随附文章)表明,罗氟司特将有助于治疗慢性炎症性疾病,如哮喘和慢性阻塞性肺疾病。

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