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药理靶点与腹膜重塑

Pharmacologic targets and peritoneal membrane remodeling.

作者信息

Farhat Karima, Stavenuiter Andrea W D, Beelen Rob H J, Ter Wee Piet M

机构信息

Department of Nephrology,1 VU University Medical Center, and Department of Molecular Cell Biology and Immunology,2 VU University, Amsterdam, Netherlands.

出版信息

Perit Dial Int. 2014 Jan-Feb;34(1):114-23. doi: 10.3747/pdi.2011.00332.

DOI:10.3747/pdi.2011.00332
PMID:24525599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3923701/
Abstract

Peritoneal dialysis (PD) is associated with functional and structural changes of the peritoneal membrane, also known as peritoneal remodeling. The peritoneal membrane is affected by many endogenous and exogenous factors such as cytokines, PD fluids, and therapeutic interventions. Here, we present an overview of various studies that have investigated pharmacologic interventions aimed at regression of peritoneal damage and prolongation of PD treatment.

摘要

腹膜透析(PD)与腹膜的功能和结构变化相关,也称为腹膜重塑。腹膜受到许多内源性和外源性因素的影响,如细胞因子、腹膜透析液和治疗干预措施。在此,我们概述了各项研究,这些研究调查了旨在逆转腹膜损伤和延长腹膜透析治疗时间的药物干预措施。

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Pharmacologic targets and peritoneal membrane remodeling.药理靶点与腹膜重塑
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2
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STAT3/HIF-1α signaling activation mediates peritoneal fibrosis induced by high glucose.STAT3/HIF-1α 信号通路激活介导高糖诱导的腹膜纤维化。
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Is there such a thing as biocompatible peritoneal dialysis fluid?是否存在生物相容的腹膜透析液?
Pediatr Nephrol. 2017 Oct;32(10):1835-1843. doi: 10.1007/s00467-016-3461-y. Epub 2016 Oct 8.
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Inhibition of EGF Receptor Blocks the Development and Progression of Peritoneal Fibrosis.表皮生长因子受体的抑制作用可阻断腹膜纤维化的发展与进程。
J Am Soc Nephrol. 2016 Sep;27(9):2631-44. doi: 10.1681/ASN.2015030299. Epub 2015 Dec 17.

本文引用的文献

1
Changes in peritoneal membrane permeability and proteinuria in patients on peritoneal dialysis after treatment with paricalcitol − a preliminary study.帕立骨化醇治疗后腹膜透析患者腹膜通透性和蛋白尿的变化——一项初步研究
Clin Nephrol. 2012 Aug;78(2):93-9. doi: 10.5414/CN107570.
2
Effects of biocompatible versus standard fluid on peritoneal dialysis outcomes.生物相容性与标准液对腹膜透析结果的影响。
J Am Soc Nephrol. 2012 Jun;23(6):1097-107. doi: 10.1681/ASN.2011121201. Epub 2012 Mar 22.
3
Twelve weeks of pioglitazone therapy significantly attenuates dysmetabolism and reduces inflammation in continuous ambulatory peritoneal dialysis patients--a randomized crossover trial.吡格列酮治疗 12 周可显著改善持续性不卧床腹膜透析患者的代谢紊乱和减轻炎症——一项随机交叉试验。
Perit Dial Int. 2012 Sep-Oct;32(5):507-15. doi: 10.3747/pdi.2011.00116. Epub 2012 Mar 1.
4
The effect of vitamin D derivatives on vascular calcification associated with inflammation.维生素D衍生物对与炎症相关的血管钙化的影响。
Nephrol Dial Transplant. 2012 Jun;27(6):2206-12. doi: 10.1093/ndt/gfr555. Epub 2011 Oct 24.
5
Pharmacological modulation of peritoneal injury induced by dialysis fluids: is it an option?透析液诱导的腹膜损伤的药理学调节:这是一种选择吗?
Nephrol Dial Transplant. 2012 Feb;27(2):478-81. doi: 10.1093/ndt/gfr543. Epub 2011 Sep 29.
6
Angiogenesis in peritoneal dialysis.腹膜透析中的血管生成。
Kidney Blood Press Res. 2011;34(4):245-52. doi: 10.1159/000326953. Epub 2011 Jun 21.
7
L-carnitine is an osmotic agent suitable for peritoneal dialysis.左旋肉碱是一种适合腹膜透析的渗透剂。
Kidney Int. 2011 Sep;80(6):645-54. doi: 10.1038/ki.2011.117. Epub 2011 Apr 27.
8
Benfotiamine protects against peritoneal and kidney damage in peritoneal dialysis.苯磷汀可预防腹膜透析中腹膜和肾脏损伤。
J Am Soc Nephrol. 2011 May;22(5):914-26. doi: 10.1681/ASN.2010070750. Epub 2011 Apr 21.
9
Difference in the expression of hormone receptors and fibrotic markers in the human peritoneum--implications for therapeutic targets to prevent encapsulating peritoneal sclerosis.人类腹膜中激素受体和纤维生成标志物表达的差异——预防包裹性腹膜硬化症治疗靶点的启示。
Perit Dial Int. 2011 May-Jun;31(3):291-300. doi: 10.3747/pdi.2010.00118. Epub 2011 Mar 31.
10
The biocompatibility of neutral pH, low-GDP peritoneal dialysis solutions: benefit at bench, bedside, or both?中性 pH 值、低 GDP 腹膜透析液的生物相容性:是仅在实验室有益,还是在病床和实验室均有益?
Kidney Int. 2011 Apr;79(8):814-24. doi: 10.1038/ki.2010.515. Epub 2011 Jan 19.