VX2兔继发性肝肿瘤模型血浆中谷胱甘肽种类和眼药浓度的变化。

R Abbas, R S Kombu, R A Ibarra, K K Goyal, H Brunengraber, J R Sanabria
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引用次数: 16

摘要

目的:现有肿瘤标志物对肝脏肿瘤的诊断敏感性/特异性较低。本研究旨在评估肝脏的氧化还原状态,作为肿瘤生存和生长的替代物。方法:测定兔(n = 6) VX2肝癌植入后健康状态和肿瘤生长状态血浆谷胱甘肽(GSH:GSSG)、眼酸盐(OA)浓度及其周转量。当兔子被处死时,肿瘤被允许生长14天。取肝,测定肝组织中半胱氨酸浓度。结果:100%的兔均有肿瘤生长。实验动物肿瘤植入前后和假动物GSH/GSSG的浓度和标记相似。肿瘤植入后实验动物OA浓度与肿瘤植入前实验动物及假手术动物相比均显著升高(P < 0.05)。半胱氨酸(谷胱甘肽的前体)浓度在肿瘤附近的肝组织中显著降低(P < 0.05)。结论:肝脏氧化还原状态的紊乱可能是早期肿瘤生长的替代指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The dynamics of glutathione species and ophthalmate concentrations in plasma from the VX2 rabbit model of secondary liver tumors.

The dynamics of glutathione species and ophthalmate concentrations in plasma from the VX2 rabbit model of secondary liver tumors.

The dynamics of glutathione species and ophthalmate concentrations in plasma from the VX2 rabbit model of secondary liver tumors.

The dynamics of glutathione species and ophthalmate concentrations in plasma from the VX2 rabbit model of secondary liver tumors.

Purpose: Available tumor markers have low sensitivity/specificity for the diagnosis of liver tumors. The present study was designed to evaluate the oxidoreductive status of the liver as surrogates of tumor subsistence and growth.

Methods: Glutathione species (GSH:GSSG), ophthalmate (OA) concentrations, and their turnover were measured in plasma of rabbits (n = 6) in their healthy state and in the state of tumor growth after implantation of the VX2 carcinoma in their liver. Tumors were allowed to grow for a period of 14 days when rabbits were sacrificed. Livers were removed and cysteine concentration was measured in liver tissue.

Results: Tumor growth was found in 100% of the rabbits. Concentration and labeling of GSH/GSSG were similar in experimental animals before and after tumor implantation and to sham animals. In contrast, OA concentration increased significantly in experimental animals after tumor implantation when compared to same animals prior to tumor implantation and to sham animals (P < .05). The concentration of cysteine, a precursor of GSH, was found to be significantly lower in the liver tissue adjacent to the tumor (P < .05).

Conclusion: Disturbances in the oxidoreductive state of livers appear to be a surrogate of early tumor growth.

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