Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Department of Clinical Biochemistry, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Mol Biol Rep. 2023 Jun;50(6):4781-4789. doi: 10.1007/s11033-023-08412-6. Epub 2023 Apr 7.
In this study, a comparison between centrally and systemically administered erythropoietin (EPO) was performed on nephroprotection during hemorrhagic shock (HS) in male rats.
Male rats were allocated into four experimental groups. (1) Sham; a guide cannula was inserted into the left lateral ventricle and other cannulas were placed into the left femoral artery and vein. (2) HS; stereotaxic surgery was done to insert a cannula in the left lateral ventricle and after a 7-day recovery; hemorrhagic shock and resuscitation were performed. (3) EPO-systemic; the procedure was the same as the HS group except that animals received 300 IU/kg erythropoietin into the femoral vein immediately before resuscitation. (4) EPO-central; animals was treated with erythropoietin (2 IU/rat) into the left lateral ventricle before resuscitation. Arterial oxygen saturation (SaO) was measured during experiments. Urine and renal tissue samples were stored for ex-vivo indices assessments.
Erythropoietin (systemically/centrally administered) significantly improved SaO renal functional and oxidative stress parameters and decreased renal inflammatory (TNF-α and IL-6) mRNA expression compared to the HS group. EPO-treated groups showed a decrease in active form of caspase-3 protein level and an increase in autophagy activity in comparison with the HS group.
Considering the fact that the effective dose of systemic EPO (300 IU/kg) was roughly 50 times higher than that of central administration (2 IU/rat), centrally administered EPO was accompanied by more advantageous consequences than systemic way. EPO is likely to act as a neuro-modulator or neuro-mediator in the central protection of organs including the kidneys.
在这项研究中,比较了中枢和系统给予红细胞生成素(EPO)对雄性大鼠失血性休克(HS)期间肾脏保护的作用。
雄性大鼠被分为四组。(1)假手术组:将引导套管插入左侧侧脑室,其他套管插入左侧股动脉和静脉。(2)HS 组:进行立体定向手术将套管插入左侧侧脑室,7 天后进行失血性休克和复苏。(3)EPO-系统组:操作与 HS 组相同,但动物在复苏前立即通过股静脉给予 300 IU/kg 的红细胞生成素。(4)EPO-中枢组:动物在复苏前用红细胞生成素(2 IU/只)注入左侧侧脑室。实验过程中测量动脉血氧饱和度(SaO)。收集尿液和肾组织样本,用于体外指标评估。
与 HS 组相比,EPO(系统/中枢给予)显著改善了 SaO、肾功能和氧化应激参数,并降低了肾炎症(TNF-α 和 IL-6)mRNA 表达。与 HS 组相比,EPO 治疗组的活性形式 caspase-3 蛋白水平降低,自噬活性增加。
考虑到系统给予 EPO(300 IU/kg)的有效剂量大约是中枢给予(2 IU/rat)的 50 倍,中枢给予 EPO 比系统给予具有更有利的效果。EPO 可能在包括肾脏在内的器官的中枢保护中作为神经调节剂或神经递质发挥作用。