Nejad Khojasteh Hoseiny, Gharib-Naseri Mohammad Kazem, Sarkaki Alireza, Dianat Mahin, Badavi Mohammad, Farbood Yaghoub
Abadan Arvand International Division, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Physiology Research Center and Department of Physiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Iran J Basic Med Sci. 2017 Jan;20(1):75-82. doi: 10.22038/ijbms.2017.8098.
Global cerebral ischemia-reperfusion (GCIR) causes disturbances in brain functions as well as other organs such as kidney. Our aim was to evaluate the protective effects of ellagic acid (EA) on certain renal disfunction after GCIR.
Adult male Wistar rats (n=32, 250-300 g) were used. GCIR was induced by bilateral vertebral and common carotid arteries occlusion (4-VO). Animal groups were: 1) received DMSO/saline (10%) as solvent of EA, 2) solvent + GCIR, 3) EA + GCIR, and 4) EA. Under anesthesia with ketamine/xylazine, GCIR was induced (20 and 30 min respectively) in related groups. EA (100 mg/kg, dissolved in DMSO/saline (10%) or solvent was administered (1.5 ml/kg) orally for 10 consecutive days to the related groups. EEG was recorded from NTS in GCIR treated groups.
Our data showed that: a) EEG in GCIR treated groups was flattened. b) GCIR reduced GFR (<0.01) and pretreatment with EA attenuated this reduction. c) BUN was increased by GCIR (<0.001) and pretreatment with EA improved the BUN to normal level. d) Serum creatinine concentration was elevated by GCIR but not significantly, however, in EA+GCIR group serum creatinine was reduced (<0.05). e) GCIR induced proteinuria (<0.05) but, EA was unable to reduced proteinuria.
Results indicate that GCIR impairs certain renal functions and EA as an antioxidant can improve these functions. Our results suggest the possible usefulness of ellagic acid in patients with brain stroke.
全脑缺血再灌注(GCIR)会导致脑功能以及肾脏等其他器官出现紊乱。我们的目的是评估鞣花酸(EA)对GCIR后某些肾功能障碍的保护作用。
使用成年雄性Wistar大鼠(n = 32,体重250 - 300克)。通过双侧椎动脉和颈总动脉闭塞(4 - VO)诱导GCIR。动物分组如下:1)接受二甲基亚砜/盐水(10%)作为EA的溶剂;2)溶剂 + GCIR;3)EA + GCIR;4)EA。在氯胺酮/赛拉嗪麻醉下,对相关组分别诱导GCIR(20分钟和30分钟)。相关组连续10天口服给予EA(100毫克/千克,溶于二甲基亚砜/盐水(10%)或溶剂,剂量为1.5毫升/千克)。在接受GCIR治疗的组中,从孤束核记录脑电图。
我们的数据显示:a)接受GCIR治疗的组脑电图变平。b)GCIR降低了肾小球滤过率(<0.01),而EA预处理减弱了这种降低。c)GCIR使血尿素氮升高(<0.001),EA预处理使血尿素氮恢复到正常水平。d)GCIR使血清肌酐浓度升高,但不显著,然而,在EA + GCIR组中血清肌酐降低(<0.05)。e)GCIR诱导蛋白尿(<0.05),但EA未能降低蛋白尿。
结果表明GCIR损害某些肾功能,而EA作为抗氧化剂可改善这些功能。我们的结果提示鞣花酸对脑卒中患者可能有用。