...
首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Gene expression of the renal endothelin system in renal transplant recipients on cyclosporine A based immunosuppression.
【24h】

Gene expression of the renal endothelin system in renal transplant recipients on cyclosporine A based immunosuppression.

机译:基于环孢霉素A的免疫抑制在肾移植受体中肾内皮素系统的基因表达。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

BACKGROUND: Immunosuppressive therapy based on cyclosporine A (CsA) is potentially nephrotoxic, and each dose of CsA is followed by a transient increase in plasma endothelin (ET)-1. The aim of this study was to investigate the effect of CsA based immunosuppressive therapy on renal gene expression of the ET(A) and ET(B) receptor subtypes and preproET-1 in human transplant needle biopsies. METHODS: Twelve living donor renal transplant recipients, median age 51.5 years (range 24-63 years) were included in the study. Immunosuppressive therapy consisted of CsA, azathioprine, and prednisolone. Baseline renal cortical needle biopsies from the living donor kidneys were obtained just before nephrectomy. Follow-up biopsies were obtained from the same transplanted kidneys after 2-6 weeks of immunosuppressive therapy. We used a quantitative, competitive reverse transcriptase polymerase chain reaction assay to measure renal ET(A) and ET(B) receptor subtype mRNAs as well as preproET-1 mRNA levels in each of the biopsies. RESULTS: The renal ET system was not significantly altered by CsA-based immunosuppressive therapy. Median ET(A) mRNA level was 185 (range 35-244) at baseline, and 120 (11-189) amol/microg total RNA after CsA based immunosuppressive therapy (P=0.11). ET(B) mRNA level was 506 (209-1411) at baseline, and 463 (267-1609) amol/microg total RNA at follow-up (P=0.44) and preproET-1 mRNA level was 160 (112-392) before and 221 (187-361) amol/microg total RNA after immunosuppressive therapy based on CsA (P=0.58). CONCLUSION: This study indicates that 2-6 weeks of CsA-based immunosuppression neither significantly influences renal gene expression of the ET(A) or ET(B) receptor subtypes nor preproET-1 in living donor renal transplant kidneys.
机译:背景:基于环孢菌素A(CsA)的免疫抑制疗法具有潜在的肾毒性,每次服用CsA都会导致血浆血浆内皮素(ET)-1短暂升高。这项研究的目的是研究基于CsA的免疫抑制疗法对人类移植针穿刺活检中ET(A)和ET(B)受体亚型以及preproET-1的肾脏基因表达的影响。方法:本研究包括十二位活体供体肾移植受者,中位年龄为51.5岁(范围24-63岁)。免疫抑制疗法包括CsA,硫唑嘌呤和泼尼松龙。肾切除术前从活体供体肾脏获得了基线肾皮质穿刺活检。在2-6周的免疫抑制治疗后,从相同的移植肾脏获得了随访活检。我们使用定量,竞争性逆转录酶聚合酶链反应测定法来测量每个活检中的肾ET(A)和ET(B)受体亚型mRNA和preproET-1 mRNA水平。结果:基于CsA的免疫抑制疗法未明显改变肾脏ET系统​​。基线时,中位ET(A)mRNA水平为185(35-244范围),基于CsA的免疫抑制治疗后总RNA为120(11-189)amol / microg(P = 0.11)。基线时ET(B)mRNA水平为506(209-1411),随访时463(267-1609)amol / microg总RNA(P = 0.44),preproET-1 mRNA水平为160(112-392)基于CsA的免疫抑制治疗之前和之后的总RNA为221(187-361)amol / microg(P = 0.58)。结论:这项研究表明,在活体供体肾移植肾脏中,基于CsA的2-6周的免疫抑制既不会显着影响ET(A)或ET(B)受体亚型的肾基因表达,也不会显着影响preproET-1。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号