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Anti-CD163-dexamethasone protects against apoptosis after ischemia/reperfusion injuries in the rat liver

机译:抗CD163-地塞米松在大鼠肝脏缺血/再灌注损伤后免受细胞凋亡

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Aim The Pringle maneuver is a way to reduce blood loss during liver surgery. However, this may result in ischemia/reperfusion injury in the development of which Kupffer cells play a central role. Corticosteroids are known to have anti-inflammatory effects. Our aim was to investigate whether a conjugate of dexamethasone and antibody against the CD163 macrophage cell surface receptor could reduce ischemia/reperfusion injury in the rat liver. Methods Thirty-six male Wistar rats were used for the experiments. Animals were randomly divided into four groups of eight receiving anti-CD163-dexamethasone, high dose dexamethasone, low dose dexamethasone or placebo intravenously 18?h before laparotomy with subsequent 60?min of liver ischemia. After reperfusion for 24?h the animals had their liver removed. Bloods were drawn 30?min and 24?h post ischemia induction. Liver cell apoptosis and necrosis were analyzed by stereological quantification. Results After 24?h' reperfusion, the fraction of cell in non-necrotic tissues exhibiting apoptotic profiles was significantly lower in the high dose dexamethasone (p?=?0.03) and anti-CD163-dex (p?=?0.03) groups compared with the low dose dexamethasone and placebo groups. There was no difference in necrotic cell volume between groups. After 30?min of reperfusion, levels of haptoglobin were significantly higher in the anti-CD163-dex and high dose dexamethasone groups. Alanine aminotransferase and alkaline phosphatase were significantly higher in the high dose dexamethasone group compared to controls after 24?h' reperfusion. Conclusions We show that pharmacological preconditioning with anti-CD163-dex and high dose dexamethasone reduces the number of apoptotic cells following ischemia/reperfusion injury. Highlights ? We investigated the effect of pharmacologic preconditioning with HDD, LDD and anti-CD163-dex on ischemia/reperfusion injury. ? Liver cell apoptosis and necrosis were analyzed by stereological quantification. ? Anti-CD163-dex and high dose dexamethasone reduces the number of apoptotic cells following ischemia/reperfusion injury.
机译:瞄准Pringle Sereuver是一种减少肝脏手术中失血的方法。然而,这可能导致缺血/再灌注损伤在开发中,Kupffer细胞发挥着中心作用。已知皮质类固醇具有抗炎作用。我们的目的是研究地塞米松和抗体对CD163巨噬细胞表面受体的缀合物是否可以降低大鼠肝脏中的缺血/再灌注损伤。方法使用三十六种雄性Wistar大鼠进行实验。将动物随机分为四组八组接受抗CD163-地塞米松,高剂量的地塞米松,低剂量的地塞米松或安慰剂,在腹腔切开术前,随后的60?肝缺血。再灌注24℃后,动物的肝脏被移除。血液吸血30?min和24次缺血诱导后。通过立体定量分析肝细胞凋亡和坏死。结果在24℃'再灌注后,高剂量地塞米松(P≤0.03)和抗CD163-DEX(P?= 0.03)组中,表现出凋亡组织中表现出凋亡谱的非坏死组织中的细胞的级别显着降低用低剂量的地塞米松和安慰剂组。组之间的坏死细胞体积没有差异。再灌注30次,抗CD163-DEX和高剂量地塞米松基团的抗oglobin水平显着高。与24μl再灌注后的对照相比,高剂量地塞米松组中丙氨酸氨基转移酶和碱性磷酸酶显着较高。结论我们表明,用抗CD163-DEX和高剂量地塞米松的药理学预处理降低了缺血/再灌注损伤后的凋亡细胞数。强调 ?我们调查了药物预处理对HDD,LDD和抗CD163-DEX对缺血/再灌注损伤的影响。 ?通过立体定量分析肝细胞凋亡和坏死。 ?抗CD163-DEX和高剂量地塞米松降低缺血/再灌注损伤后凋亡细胞的数量。

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