Department of Clinical and Experimental Medicine and Pharmacology, School of Medicine, University of Messina, Via C. Valeria, Gazzi, 98100 Messina, Italy.
Eur J Pharmacol. 2011 Oct 1;668(1-2):305-16. doi: 10.1016/j.ejphar.2011.06.049. Epub 2011 Jul 8.
Adenosine A(2A) receptor agonists may be important regulators of inflammation. The aim of this study was to investigate the effects of CGS 21680 (0.1mg/kgi.p.), an agonist of the adenosine (A(2A)) receptor, in a mouse model of carrageenan-induced pleurisy. Injection of carrageenan into the pleural cavity of mice elicited an acute inflammatory response characterised by: infiltration of neutrophils in lung tissues and subsequent lipid peroxidation, increased production of nitric oxide (NO), cytokines such as tumour necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) and increased expression of intercellular adhesion molecule (ICAM-1) and platelet-adhesion molecule (P-selectin). Furthermore, carrageenan induced the expression of nuclear factor-κB (NF-κB), inducible nitric oxide synthase (iNOS), nitrotyrosine, the activation of poly-ADP-ribosyl polymerase (PARP), as well as induced apoptosis (FAS-ligand expression, Bax and Bcl-2 expression) in the lung tissues. Administration of CGS 21680, 30 min prior to challenge with carrageenan, caused a significant reduction of all the parameters of inflammation measured. In addition, to confirm the anti-inflammatory effect of CGS 21680, we have also evaluated the effects of CGS 21680 post-treatment (30 min after the challenge with carrageenan) and we have demonstrated that also it caused a reduction of neutrophil infiltration and the degree of lung injury. Thus, based on these findings we propose that adenosine A(2A) receptor agonists such as CGS 21680 may be useful in the treatment of various inflammatory diseases.
腺苷 A(2A) 受体激动剂可能是炎症的重要调节因子。本研究旨在探讨 CGS 21680(0.1mg/kg,i.p.),一种腺苷(A(2A))受体激动剂,在卡拉胶诱导的胸膜炎小鼠模型中的作用。向小鼠胸膜腔注射卡拉胶可引发急性炎症反应,其特征为:肺组织中中性粒细胞浸润,随后脂质过氧化,一氧化氮(NO)生成增加,细胞因子如肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)增加,细胞间黏附分子(ICAM-1)和血小板黏附分子(P-选择素)表达增加。此外,卡拉胶诱导核因子-κB(NF-κB)、诱导型一氧化氮合酶(iNOS)、硝基酪氨酸的表达,多聚 ADP-核糖聚合酶(PARP)的激活以及肺组织中细胞凋亡(FAS-配体表达、Bax 和 Bcl-2 表达)。在卡拉胶攻击前 30 分钟给予 CGS 21680 可显著降低所有炎症参数。此外,为了确认 CGS 21680 的抗炎作用,我们还评估了 CGS 21680 治疗后(卡拉胶攻击后 30 分钟)的作用,结果表明它也可减少中性粒细胞浸润和肺损伤程度。因此,基于这些发现,我们提出腺苷 A(2A) 受体激动剂如 CGS 21680 可用于治疗各种炎症性疾病。