Department of Anaesthesiology, University of Hong Kong, Queen Mary Hospital, Pokfulam Road, Hong Kong.
Br J Anaesth. 2012 Oct;109(4):529-39. doi: 10.1093/bja/aes209. Epub 2012 Jun 28.
Opioids have been shown to attenuate ischaemia-reperfusion injury (IRI) in a number of organs. We evaluated the effect of morphine pretreatment on IRI in both normal and cirrhotic rat liver.
Morphine was administered either i.v. or intrathecally (i.t.) 10 min before initiating 1 h of ischaemia followed by 6 h reperfusion in normal rat liver. Hepatic injury was assessed histologically using Suzuki's criteria. These manoeuvres were repeated using the optimal dose of morphine after administration of naloxone methiodide and wortmannin. Serum levels of transaminases were measured, and expression of phosphorylated Akt, Jak2, and STAT3 were assessed by immunoblotting. Similar procedures were repeated on rats with carbon tetrachloride-induced liver cirrhosis, and the levels of phosphorylated protein kinase C (PKC), haem oxygenase-1 (HO-1), and inducible nitric oxide synthase (iNOS) were also evaluated, as these proteins have beneficial effects during IRI.
Morphine pretreatment at 100 µg kg(-1) (i.v.) or 10 µg (i.t.) reduced necrosis, apoptosis, and serum transaminase levels, and increased phosphorylated Akt and STAT3 but not JAK2 expression in normal liver. These changes were reversed by prior administration of naloxone methiodide and wortmannin. Although morphine preconditioning was also protective in cirrhotic liver, STAT3 and JAK2 phosphorylation status was unchanged. There was, however, increased expression of phosphorylated PKC and HO-1, and a reduction in iNOS.
Morphine preconditioning protects against IRI in both normal and cirrhotic rat liver. This involves opioid receptors, phosphatidylinositol-3-kinase, and Akt. The downstream pathways involved are different for cirrhotic liver, with preliminary evidence suggesting involvement of HO-1.
阿片类药物已被证明可减轻许多器官的缺血再灌注损伤(IRI)。我们评估了吗啡预处理对正常和肝硬化大鼠肝脏IRI 的影响。
在正常大鼠肝脏中,于缺血前 10 分钟静脉内(iv.)或鞘内(i.t.)给予吗啡,随后进行 1 小时缺血和 6 小时再灌注。使用 Suzuki 标准通过组织学评估肝损伤。在用纳洛酮甲碘化物和wortmannin 给予吗啡的最佳剂量后,重复这些操作。测量血清转氨酶水平,并通过免疫印迹评估磷酸化 Akt、Jak2 和 STAT3 的表达。在四氯化碳诱导的肝硬化大鼠中重复类似的程序,并评估磷酸化蛋白激酶 C(PKC)、血红素加氧酶-1(HO-1)和诱导型一氧化氮合酶(iNOS)的水平,因为这些蛋白质在 IRI 期间具有有益作用。
在正常肝脏中,100μg/kg(iv.)或 10μg(i.t.)吗啡预处理可减少坏死、凋亡和血清转氨酶水平,并增加磷酸化 Akt 和 STAT3 但不增加 JAK2 表达。这些变化被纳洛酮甲碘化物和 wortmannin 预先给药逆转。尽管吗啡预处理在肝硬化肝脏中也是保护性的,但 STAT3 和 JAK2 磷酸化状态没有改变。然而,磷酸化 PKC 和 HO-1 的表达增加,iNOS 减少。
吗啡预处理可保护正常和肝硬化大鼠肝脏免受 IRI。这涉及阿片受体、磷脂酰肌醇-3-激酶和 Akt。涉及的下游途径在肝硬化肝脏中不同,初步证据表明涉及 HO-1。