Department of Anesthesiology, Third Affiliated Hospital, Guangzhou Medical University, Guangzhou 510150, China.
Mediators Inflamm. 2013;2013:627831. doi: 10.1155/2013/627831. Epub 2013 Jun 11.
Dexmedetomidine (DEX) is an α 2-adrenergic agonist. It decreases the levels of norepinephrine release, resulting in a reduction of postsynaptic adrenergic activity. In the present study, the effects of DEX on postpartum bleeding-induced multiple organ dysfunction syndrome (BMODS) were studied in rats in which BMODS was induced by the combination of hypotension and clamping of the superior mesenteric artery. We evaluated the role of dexmedetomidine (DEX) in cytokine release during postpartum BMODS in rats. In summary, the present study demonstrated that DEX administration reduced IFN-r and IL-4 release and decreased lung injury during postpartum BMODS. It is possible that DEX administration decreased inflammatory cytokine production in BMODS by inhibiting inflammation and free radical release by leukocytes independent of the DEX dose.
右美托咪定(DEX)是一种α2-肾上腺素能激动剂。它可降低去甲肾上腺素的释放水平,从而减少突触后肾上腺素能活性。在本研究中,通过低血压和肠系膜上动脉夹闭相结合的方法诱导大鼠发生产后多器官功能障碍综合征(BMODS),研究了 DEX 对其的影响。我们评估了右美托咪定(DEX)在大鼠产后 BMODS 时细胞因子释放中的作用。总之,本研究表明,DEX 给药可减少 IFN-r 和 IL-4 的释放,并减轻产后 BMODS 时的肺损伤。DEX 给药可能通过抑制白细胞的炎症和自由基释放来减少 BMODS 中的炎症细胞因子产生,且这一作用与 DEX 剂量无关。