Effects of Nonsteroidal Anti-Inflammatory Drugs on Interleukin-1 Receptor Antagonist Production in Cultured Human Peripheral Blood Mononuclear Cells

Hidenobu Kusuhara, Hirofumi Matsuyuki, Takeki Okumoto
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引用次数: 11

Abstract

The effects of nonsteroidal anti-inflammatory drugs (NSAIDs), mofezolac, indomethacin, sodium diclofenac, and zaltoprofen, on the production of interleukin-1 receptor antagonist (IL-1ra) were examined in cultured human peripheral blood mononuclear cells (PBMC). Among the NSAIDs tested, mofezolac and sodium diclofenac were found to stimulate the mRNA expression for IL-1ra without affecting the mRNA expression for IL-1β. These two drugs also stimulated the secretion of IL-1ra by PBMC in the absence of bacterial lipopolysaccharide (LPS), however, the stimulatory effect of sodium diclofenac diminished in the presence of LPS. Mofezolac suppressed the mRNA expression for IL-1β in PBMC stimulated with exogenous IL-1β, indicating the secreted IL-1ra in the presence of mofezolac to be biologically active. Since IL-1ra suppresses the function of IL-1, a pro-inflammatory cytokine, the stimulatory effect of such NSAIDs as mofezolac on IL-1ra production could also be one of the mechanisms involved in its anti-inflammatory and antinociceptive actions.

非甾体抗炎药对培养的人外周血单个核细胞白细胞介素-1受体拮抗剂产生的影响
在培养的人外周血单个核细胞(PBMC)中,研究了非甾体抗炎药(NSAIDs)、莫非唑酸、吲哚美辛、双氯芬酸钠和扎尔托洛芬对白细胞介素-1受体拮抗剂(IL-1ra)产生的影响。在所检测的非甾体抗炎药中,莫非唑酸和双氯芬酸钠可以刺激IL-1ra mRNA的表达,而不影响IL-1β mRNA的表达。在不存在细菌脂多糖(LPS)的情况下,这两种药物也能刺激PBMC分泌IL-1ra,而在存在LPS的情况下,双氯芬酸钠的刺激作用减弱。Mofezolac抑制外源性IL-1β刺激的PBMC中IL-1β mRNA的表达,表明Mofezolac存在下分泌的IL-1ra具有生物活性。由于IL-1ra抑制促炎细胞因子IL-1的功能,mofezolac等非甾体抗炎药对IL-1ra产生的刺激作用也可能是其抗炎和抗伤害作用的机制之一。
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