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内皮素抑制剂对环孢素A微血管效应的改善作用。

Amelioration of cyclosporin A effect on microvasculature by endothelin inhibitor.

作者信息

Wilasrusmee Chumpon, Ondocin Phil, Bruch David, Shah Gaurang, Kittur Smita, Wilasrusmee Skuntala, Kittur Dilip S

机构信息

Department of Surgery, SUNY Upstate Medical University, Syracuse, NY 13210, USA.

出版信息

Surgery. 2003 Aug;134(2):384-9. doi: 10.1067/msy.2003.233.

Abstract

BACKGROUND

We have previously shown that endothelial injury by cyclosporin A (CyA) is associated with an increased endothelin-1 (ET-1) release. We now sought to determine, in an animal model of angiogenesis, if inhibiting the effect of ET-1 on endothelial cells (ECs) would reverse the CyA-mediated endothelial injury in an animal model of angiogenesis.

METHODS

An angiogenic mixture of Matrigel (0.5 ml), fibroblast growth factor (1 ng/ml), vascular endothelial growth factor (100 ng/ml), and heparin (64 unit/ml) was injected as a subcutaneous plug in the flank of C3H mice (n = 5). In experimental groups CyA (20 mg/ml), CyA, and BQ 123 (ET-A receptor antagonist), CyA and PD 142893 (ET-A and ET-B receptor antagonist), or CyA and ET-1 antibody were added to the angiogenic mixture. Angiogenesis in the mixture was quantified by modified planimetric point counting method in skin/Matrigel cross-sections stained with factor VIII to highlight endothelial neocapillaries. Mean +/- SD of angiogenic area was analyzed with analysis of variance and Bonferroni test. The survival curves obtained by Kaplan-Meier analysis were compared between the groups, and the statistical significance of survival and mortality rates was computed by log rank's and Fisher's exact test, respectively.

RESULTS

The mean +/- SD of angiogenic area in control animals (without CyA in the angiogenic mixture) was 56.76 +/- 4.2. CyA inhibited angiogenesis in the subcutaneous angiogenic plug. Adding CyA to the angiogenic mixture significantly reduced angiogenic area (5.33 +/- 1.4, P <.001) while vehicle for CyA had no such effect (56.33 +/- 3.8, P =.10). Polyclonal ET-1 antibody or PD 142893 ameliorated the effect of CyA, whereas BQ 123 did not. The mean angiogenic areas in animals with ET-1 antibody, PD 142893, or BQ 123 in the angiogenic mixture were 57.20 +/- 7.5 (P =.06), 46.00 +/- 11.5 (P = 1.0), 8.60 +/- 2.9 (P <.001), respectively.

CONCLUSIONS

Our data show that blocking ET-B receptors specifically ameliorates the microvascular injury to the neocapillaries in angiogenesis caused by CyA. Antiendothelin-1 antibody and ETR antagonist (PD 142893) could, therefore, reduce the ill effects of CyA on microvascular endothelium.

摘要

背景

我们之前已经表明,环孢素A(CyA)所致的内皮损伤与内皮素-1(ET-1)释放增加有关。我们现在试图在血管生成动物模型中确定,抑制ET-1对内皮细胞(ECs)的作用是否会逆转CyA介导的血管生成动物模型中的内皮损伤。

方法

将基质胶(0.5 ml)、成纤维细胞生长因子(1 ng/ml)、血管内皮生长因子(100 ng/ml)和肝素(64单位/ml)的血管生成混合物作为皮下栓子注射到C3H小鼠(n = 5)的侧腹。在实验组中,将CyA(20 mg/ml)、CyA与BQ 123(ET-A受体拮抗剂)、CyA与PD 142893(ET-A和ET-B受体拮抗剂)或CyA与ET-1抗体添加到血管生成混合物中。通过改良的平面计点法对用因子VIII染色的皮肤/基质胶横截面中的血管生成进行定量,以突出内皮新毛细血管。用方差分析和Bonferroni检验分析血管生成面积的均值±标准差。通过Kaplan-Meier分析获得的生存曲线在组间进行比较,生存率和死亡率的统计学显著性分别通过对数秩检验和Fisher精确检验计算。

结果

对照动物(血管生成混合物中无CyA)的血管生成面积均值±标准差为56.76±4.2。CyA抑制皮下血管生成栓中的血管生成。向血管生成混合物中添加CyA可显著降低血管生成面积(5.33±1.4,P <.001),而CyA的溶剂则无此作用(56.33±3.8,P =.10)。多克隆ET-1抗体或PD 142893可改善CyA的作用,而BQ 123则不能。血管生成混合物中含有ET-1抗体、PD 142893或BQ 123的动物的平均血管生成面积分别为57.20±7.5(P =.06)、46.00±11.5(P = 1.0)、8.60±2.9(P <.001)。

结论

我们的数据表明,特异性阻断ET-B受体可改善CyA在血管生成中对新毛细血管的微血管损伤。因此,抗内皮素-1抗体和ETR拮抗剂(PD 142893)可减轻CyA对微血管内皮的不良影响。

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