Instituto de Ensino e Pesquisa da Santa Casa de Belo Horizonte, Santa Efigênia, Belo Horizonte-MG, Brazil.
Inflamm Res. 2012 Jan;61(1):37-41. doi: 10.1007/s00011-011-0386-6. Epub 2011 Oct 11.
To investigate the effects of rosiglitazone, a peroxisome proliferator-activated receptor-γ agonist, on the secretion of vascular endothelial growth factor (VEGF) by peripheral blood mononuclear cells (PBMCs) and on the generation of reactive oxygen species (ROS) by leukocytes.
PBMCs and leukocytes were obtained from venous blood samples collected from 20 healthy individuals. VEGF secretion was evaluated using a commercial ELISA kit, while ROS production was determined using a luminol-dependent chemiluminescence assay.
Rosiglitazone and calphostin C (a protein kinase C inhibitor) inhibited VEGF secretion by PBMCs by 63.7 and 62.3%, respectively. Both agents reduced ROS production in non-stimulated human leukocytes and down-regulated the enhanced generation of ROS in leukocytes that had been stimulated with the PKC activator phorbol 12,13-dibutyrate.
The results support the involvement of PKC as a direct, and/or NADPH-oxidase as an indirect, target for the action of rosiglitazone on VEGF secretion by PBMCs and ROS production in human leukocytes.
研究过氧化物酶体增殖物激活受体-γ 激动剂罗格列酮对人外周血单个核细胞(PBMC)分泌血管内皮生长因子(VEGF)和白细胞产生活性氧(ROS)的影响。
采用酶联免疫吸附试验(ELISA)试剂盒检测 PBMC 分泌 VEGF 的情况,用化学发光法检测白细胞 ROS 的产生。
罗格列酮和 calphostin C(蛋白激酶 C 抑制剂)分别抑制 PBMC 分泌 VEGF 达 63.7%和 62.3%。两种药物均减少了非刺激状态下人白细胞产生的 ROS,并抑制了 PKC 激活剂佛波醇 12,13-二丁酸酯刺激后白细胞 ROS 生成的增强。
结果提示 PKC 作为直接靶点,以及/或 NADPH 氧化酶作为间接靶点,参与了罗格列酮对 PBMC 分泌 VEGF 和人白细胞产生 ROS 的作用。