Chronic infusion of sterile peritoneal dialysis solution abrogates enhanced peritoneal gene expression responses to chronic peritoneal catheter presence.

El Rasheid Zakaria, Paul J Matheson, Ryan T Hurt, Richard N Garrison
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Abstract

Chronic exposure to sterile peritoneal dialysis (PD) solutions is associated with microvascular and interstitial changes within the blood-peritoneal barrier (peritoneum). These changes are commonly linked to loss of peritoneal function over time, presumably because of angiogenesis-related increased vascular area. However, the effects on peritoneal microvascular function of chronic peritoneal exposure to PD solutions are unknown. The present study examined peritoneal microvascular function after chronic exposure to sterile PD solution. Six rats underwent permanent catheter insertion under anesthesia. Three rats were treated with approximately 16 mL conventional PD solution daily for 6 weeks; catheter insertion controls received 1 mL saline daily. At 6 weeks, visceral peritoneal microvascular function was assessed in vivo using intravital microscopy. Endothelial cell functions were assessed using messenger RNA (mRNA) gene microarray analysis. In both groups, significant angiogenesis was seen, predominantly in the base of the mesentery. Sensitivity and reactivity of the intestinal visceral peritoneal pre-capillary arterioles (A3 arterioles, 8 - 15 microm in diameter) were decreased in the catheter controls, but not in the chronic PD infusion rats. Chronic catheter presence increased the expression of 18 genes in the controls as compared with 12 genes in the chronic infusion rats. In both groups, expression of fibronectin, integrin-beta, integrin-alpha5, collagen type XVIII-alpha1, and matrix metalloproteinase was enhanced. Endothelial expression of proinflammatory genes (interleukin-1beta, tissue pathway inhibitor, chemokine ligand 2) was enhanced by chronic catheter insertion, but not after chronic PD fluid infusion. Increased expression of genes encoding proteins involved in inflammation and tissue remodeling results from peritoneal catheter-related endothelial cell activation. Chronic exposure of the nonuremic peritoneum to sterile PD solutions overrides the catheter-related endothelial cell proinflammatory phenotype to restore peritoneal microvascular function.

长期输注无菌腹膜透析液消除了腹膜基因表达对慢性腹膜导管存在的增强反应。
慢性暴露于无菌腹膜透析(PD)溶液与血液-腹膜屏障(腹膜)内微血管和间质改变有关。随着时间的推移,这些变化通常与腹膜功能丧失有关,可能是因为血管生成相关的血管面积增加。然而,慢性腹膜暴露于PD溶液对腹膜微血管功能的影响尚不清楚。本研究检测了慢性暴露于无菌PD溶液后的腹膜微血管功能。6只大鼠在麻醉状态下进行永久性导管插入。3只大鼠每日注射约16 mL常规PD溶液,连续6周;插入导管的对照组每日给予生理盐水1ml。6周时,使用活体显微镜评估内脏腹膜微血管功能。采用信使RNA (mRNA)基因微阵列分析评估内皮细胞功能。两组均可见明显的血管新生,主要在肠系膜底部。慢性PD输注大鼠肠道内脏腹膜毛细血管前小动脉(直径8 ~ 15微米的A3小动脉)的敏感性和反应性在导管对照组中下降,但在慢性PD输注大鼠中没有下降。与慢性输注大鼠的12个基因相比,慢性输注大鼠的18个基因表达增加。两组纤维连接蛋白、整合素- β、整合素- α 5、xviii - α 1型胶原蛋白和基质金属蛋白酶的表达均增强。内皮促炎基因(白细胞介素-1 β、组织通路抑制剂、趋化因子配体2)的表达在慢性导管插入后增强,但在慢性PD液输注后没有增强。腹膜导管相关内皮细胞活化导致炎症和组织重塑相关蛋白编码基因表达增加。非尿毒症腹膜长期暴露于无菌PD溶液中,会破坏导管相关内皮细胞的促炎表型,从而恢复腹膜微血管功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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