与成年大鼠相比,青春期前大鼠对缺血性肾损伤的抵抗力更强,恢复速度更快。

M Fernández, A Medina, E Carbajo, F Santos, A Cobo, J Alvarez, J Rodríguez, P Fernández
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引用次数: 4

摘要

采用双侧夹持肾蒂60,75或90min来描述青春期前大鼠缺血性急性肾功能衰竭(ARF)的演变。为了验证ARF进化中存在年龄条件差异,成年大鼠暴露于40,60或75分钟的夹紧。7天后,相同夹紧次数下,幼鼠的存活率明显高于成年大鼠(60分钟89比35%,75分钟69比35%)。幼龄大鼠大多在缺血后24小时内死亡,而成年大鼠的死亡风险延长至缺血后第4天。血清尿素氮和肌酐分别在缺血后第1天和第3天达到峰值。在幼鼠中,这些肾脏功能标记物在第5天和第6天恢复正常,而在成年动物中,它们在研究结束时仍保持升高。幼龄大鼠的生长曲线与假手术动物的生长曲线相似,而成年大鼠在研究结束时甚至没有达到初始体重。对夹持后7天获得的肾脏的分析显示,成年大鼠的组织病理学病变更严重,增殖活性更高(假手术动物的10-40倍,而年轻大鼠的2-4倍)。我们的研究结果表明,幼龄大鼠的肾脏对缺血的抵抗力更强,并且从缺血损伤中恢复得更快。因此,青年大鼠和成年大鼠缺血性ARF的实验模型明显不同。
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Prepubertal rats are more resistant to ischemic renal injury and recover more rapidly than adult rats.

Bilateral clamping of renal pedicles during 60, 75 or 90 min was used to characterize the evolution of ischemic acute renal failure (ARF) in prepubertal rats. To verify the existence of age-conditioned differences in the evolution of ARF, adult rats were exposed to 40, 60 or 75 min of clamping. After 7 days, survival rate was significantly better in young than adult rats for identical times of clamping (89 vs. 35% for 60 min and 69 vs. 35% for 75 min). Young rats largely died within the first 24 h following ischemia while the risk of death extended until the 4th day after ischemia in adult rats. Peak values of serum urea nitrogen and creatinine were observed on the 1st and 3rd day after ischemia in young and adult rats, respectively. In young rats, these markers of renal function returned to normal on days 5 and 6 whereas they remained elevated at the end of the study in adult animals. Growth curves of young rats paralleled those of sham-operated animals from the 3rd day of clamping whereas adult rats did not even reach the initial weight at the end of the study. Analysis of kidneys obtained 7 days after clamping revealed more severe histopathological lesions in adult rats as well as a higher proliferative activity (10-40 times the value of sham-operated animals versus 2-4 times the control value in young rats). Our findings indicate that kidneys from young rats are more resistant to ischemia and recover more quickly from the ischemic insult. Therefore, the experimental model of ischemic ARF is clearly different in young and adult rats.

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