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通过减少血管内皮生长因子的产生,奥曲肽改善了高渗腹膜透析液引起的腹膜血管改变。

By reducing production of vascular endothelial growth factor octreotide improves the peritoneal vascular alterations induced by hypertonic peritoneal dialysis solution.

作者信息

Günal Ali Ihsan, Celiker Hüseyin, Akpolat Nusret, Ustündag Bilal, Duman Soner, Akcicek Fehmi

机构信息

Departments of Nephrology, Firat University School of Medicine, Elazig, Turkey.

出版信息

Perit Dial Int. 2002 May-Jun;22(3):301-6.

Abstract

OBJECTIVE

Chronic peritoneal dialysis (PD) may eventually result in vascular alterations of varying degree, which lead to progressive reduction in dialytic efficacy. Although the pathogenesis has not been elucidated yet, vascular endothelial growth factor (VEGF) has been proposed to play a central role in the process leading to vascular alterations.

DESIGN

Rats were allocated to three groups: no treatment, intraperitoneal introduction of hypertonic PD solution alone, and intraperitoneal introduction of hypertonic PD solution plus octreotide. After 4 weeks, a 1-hour peritoneal equilibration test (PET) was performed. Dialysate-to-plasma urea ratio (D/P urea), glucose reabsorption (D1/D0 glucose), ultrafiltration volume (UF), and levels of dialysate protein and VEGF were determined. Peritoneal membrane histology was evaluated by light microscopy.

RESULTS

Compared with the control group, rats treated with hypertonic PD solution showed dramatically deranged peritoneal function tests (UF: 5.8 +/- 0.9 mL vs 1.3 +/- 0.6 mL; D/P urea: 0.49 +/- 0.1 vs 0.74 +/- 0.04; D1/D0 glucose: 0.55 +/- 0.05 vs 0.34 +/- 0.06) and morphology (thickness: 4.6 +/- 0.4 mu vs 62 +/- 12 mu; neovascularisation: 0.1 +/- 0.3 vessels per field vs 2.2 +/- 0.3 vessels per field). Similarly, a higher level of VEGF was found in the rats treated with hypertonic PD solution. In rats treated with hypertonic solution plus octreotide, peritoneal thickness was not completely reduced (25 +/- 5 mu), but peritoneal functions were protected (UF: 4.0 +/- 0.5 mL; D/P urea: 0.58 +/- 0.02; D1/D0 glucose: 0.51 +/- 0.02). Moreover, VEGF level and neoangiogenesis were significantly less in the octreotide group than in the group treated with hypertonic dextrose alone.

CONCLUSION

Our data document that, by increasing the production of VEGF, a high glucose concentration can cause vascular alterations within the peritoneal membrane. Octreotide can protect against the vascular alterations and preserve peritoneal function by inhibiting overexpression of VEGF and regulating the inflammatory response in the peritoneum.

摘要

目的

慢性腹膜透析(PD)最终可能导致不同程度的血管改变,进而导致透析疗效逐渐降低。尽管其发病机制尚未阐明,但血管内皮生长因子(VEGF)被认为在导致血管改变的过程中起核心作用。

设计

将大鼠分为三组:未治疗组、单纯腹腔内注入高渗腹膜透析液组和腹腔内注入高渗腹膜透析液加奥曲肽组。4周后,进行1小时的腹膜平衡试验(PET)。测定透析液与血浆尿素比值(D/P尿素)、葡萄糖重吸收(D1/D0葡萄糖)、超滤量(UF)以及透析液蛋白和VEGF水平。通过光学显微镜评估腹膜组织学。

结果

与对照组相比,接受高渗腹膜透析液治疗的大鼠腹膜功能试验显著紊乱(超滤量:5.8±0.9 mL对1.3±0.6 mL;D/P尿素:0.49±0.1对0.74±0.04;D1/D0葡萄糖:0.55±0.05对0.34±0.06),形态学也有改变(厚度:4.6±0.4μm对62±12μm;新生血管形成:每视野0.1±0.3条血管对每视野2.2±0.3条血管)。同样,接受高渗腹膜透析液治疗的大鼠VEGF水平更高。在接受高渗溶液加奥曲肽治疗的大鼠中,腹膜厚度未完全恢复正常(25±5μm),但腹膜功能得到了保护(超滤量:4.0±0.5 mL;D/P尿素:0.58±0.02;D1/D0葡萄糖:0.51±0.02)。此外,奥曲肽组的VEGF水平和新生血管形成明显低于单纯高渗葡萄糖治疗组。

结论

我们的数据表明,高糖浓度可通过增加VEGF的产生导致腹膜内血管改变。奥曲肽可通过抑制VEGF的过度表达和调节腹膜内的炎症反应来预防血管改变并维持腹膜功能。

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