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促红细胞生成素对放射性造影剂诱导的肾小管上皮细胞损伤的保护作用。

Protective effect of erythropoietin against radiocontrast-induced renal tubular epithelial cell injury.

作者信息

Kolyada Alexey Y, Liangos Orfeas, Madias Nicolaos E, Jaber Bertrand L

机构信息

Department of Medicine, Division of Nephrology, Kidney and Dialysis Research Laboratory, Caritas St. Elizabeth's Medical Center, Boston, Mass. 02135, USA.

出版信息

Am J Nephrol. 2008;28(2):203-9. doi: 10.1159/000110089. Epub 2007 Oct 24.

Abstract

BACKGROUND/AIMS: Recombinant human erythropoietin (rhEpo) has been shown to reduce tissue injury following ischemia-reperfusion. We examined whether rhEpo protects in vitro renal tubular epithelial cells against radiocontrast media-induced injury.

METHODS

LLC-PK1 renal tubular epithelial cells were exposed to non-ionic radiocontrast agent iohexol (low-osmolar) or iodixanol (iso-osmolar), with or without rhEpo (200 U/ml). Following a 6-hour exposure, cells were incubated for 24 h in radiocontrast-free culture medium. Cell viability was then assessed by the MTT assay. We also assessed cell apoptosis by the TUNEL assay, and activities of caspase-3, caspase-8, and caspase-9 were determined by a luminescence assay.

RESULTS

rhEpo improved viability of iohexol-treated LLC-PK1 cells by 27 +/- 6% (88.1 +/- 1.5 vs. 70.8 +/- 3.3%, p = 0.008). Similarly, rhEpo improved the viability of iodixanol-treated LLC-PK1 cells by 26 +/- 4% (82.5 +/- 2.1vs. 65.7 +/- 1.7%, p = 0.028). rhEpo also decreased apoptosis rates of iohexol-treated LLC-PK1 cells (6.4 +/- 0.9/1,000 cells vs. 14.8 +/- 2.4/1,000 cells, p = 0.028), and iodixanol-treated LLC-PK1 cells (8.0 +/- 1.2/1,000 cells vs. 13.5 +/- 1.9/1,000 cells, p = 0.028). In iohexol-treated LLC-PK1 cells, rhEpo attenuated activation of caspase-3 (p = 0.003), caspase-8 (p = 0.033) and caspase-9 (p = 0.055).

CONCLUSION

rhEpo attenuates in vitro renal tubular epithelial cell injury induced by low- and iso-osmolar radiocontrast media, possibly by reduction of caspases activation and apoptosis rates.

摘要

背景/目的:重组人促红细胞生成素(rhEpo)已被证明可减轻缺血再灌注后的组织损伤。我们研究了rhEpo是否能在体外保护肾小管上皮细胞免受造影剂诱导的损伤。

方法

将LLC-PK1肾小管上皮细胞暴露于非离子型造影剂碘海醇(低渗)或碘克沙醇(等渗),同时或不同时添加rhEpo(200 U/ml)。暴露6小时后,将细胞在无造影剂的培养基中孵育24小时。然后通过MTT法评估细胞活力。我们还通过TUNEL法评估细胞凋亡,并通过发光法测定caspase-3、caspase-8和caspase-9的活性。

结果

rhEpo使碘海醇处理的LLC-PK1细胞活力提高了27±6%(88.1±1.5%对70.8±3.3%,p = 0.008)。同样,rhEpo使碘克沙醇处理的LLC-PK1细胞活力提高了26±4%(82.5±2.1%对65.7±1.7%,p = 0.028)。rhEpo还降低了碘海醇处理的LLC-PK1细胞的凋亡率(6.4±0.9/1000细胞对14.8±2.4/1000细胞,p = 0.028),以及碘克沙醇处理的LLC-PK1细胞的凋亡率(8.0±1.2/1000细胞对13.5±1.9/1000细胞,p = 0.028)。在碘海醇处理的LLC-PK1细胞中,rhEpo减弱了caspase-3(p = 0.003)、caspase-8(p = 0.033)和caspase-9(p = 0.055)的激活。

结论

rhEpo可减轻低渗和等渗造影剂诱导的体外肾小管上皮细胞损伤,可能是通过降低半胱天冬酶激活和凋亡率实现的。

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