Askari N, Mahboudi F, Haeri-Rohani A, Kazemi B, Sarrami R, Edalat R, Ahmadiani A
School of Biology, College of Science, University of Tehran, Tehran, Iran.
Scand J Immunol. 2008 Jan;67(1):47-52. doi: 10.1111/j.1365-3083.2007.02043.x.
Antinociceptive potency of opioids is greater against various noxious stimuli in animals with peripheral inflammation. Opioid agonists stimulate activation of G-protein-coupled receptor. Changes in the resting levels of G-protein subtypes could have an effect on intracellular signalling pathways. The present study was designed to investigate the effects of analgesic morphine treatment on the level G-protein subunits mRNA in the presence and absence of inflammation. Our results showed that the carrageenan administration increased G-protein subunits. Administration of analgesic dose of morphine alone and in the presence of inflammation induced different alterations in the levels of G-protein mRNA. Taken together, the results obtained using real time RT-PCR suggested that G-protein genes expression levels following the acute administration of morphine between animals with and without inflammation could influence, at least in part, analgesic responsiveness.
在患有外周炎症的动物中,阿片类药物对各种有害刺激的镇痛效力更强。阿片类激动剂刺激G蛋白偶联受体的激活。G蛋白亚型静息水平的变化可能会影响细胞内信号通路。本研究旨在调查在存在和不存在炎症的情况下,镇痛剂量的吗啡治疗对G蛋白亚基mRNA水平的影响。我们的结果表明,角叉菜胶给药可增加G蛋白亚基。单独给予镇痛剂量的吗啡以及在存在炎症的情况下给予吗啡,会导致G蛋白mRNA水平发生不同的变化。综合来看,使用实时RT-PCR获得的结果表明,急性给予吗啡后,有炎症和无炎症动物的G蛋白基因表达水平可能至少部分影响镇痛反应性。