吡格列酮和二甲双胍对实验模型中腹腔粘连形成的影响

Mehmet Ali Yücesoy, Engin Hatipoğlu, Osman Alperen Balık, Karolin Yanar, Şebnem Batur, Osman Şimşek, Bedii Berat Apaydın
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引用次数: 0

摘要

背景:本研究通过在实验性粘连模型中采用组织病理学、免疫组化和生化分析,评估二甲双胍或吡格列酮在预防或减少术后腹腔内粘连(PIAA)发生方面的作用:方法:50 只 Wistar-Albino 大鼠分为五组:方法:50 只 Wistar-Albino 大鼠分为五组:I 组(对照组)、II 组(假治疗组)、III 组(透明质酸组)、IV 组(二甲双胍组)和 V 组(吡格列酮组)。除假治疗组外,其他实验组均采用刮宫法诱导粘连。10 天后,对大鼠实施安乐死以进行评估。采用奈尔评分法评估大鼠的宏观粘连程度。采用免疫组织化学和酶联免疫吸附试验(ELISA)方法评估血清、腹腔灌洗液和肠组织样本。在血清和腹腔灌洗液样本中测量了果糖胺、白细胞介素-6(IL-6)、转化生长因子-β(TGF-β)和纤维连接蛋白的水平:结果:各组的奈尔评分和 I 型或 III 型胶原染色评分相似(均为 p>0.05)。与对照组相比,吡格列酮可明显降低血清 IL-6 和 TGF-β 水平(分别为 p=0.002 和 p=0.008)。与对照组相比,二甲双胍组和吡格列酮组腹腔灌洗液中的 IL-6 均升高,而与假组相比,吡格列酮组大鼠腹腔灌洗液中的纤连蛋白水平较低(均为 p):在实验大鼠模型中,尽管未观察到组织学影响,但吡格列酮而非二甲双胍对防止 PIAA 的形成有积极的生化影响。要进一步了解吡格列酮对 PIAA 形成的影响,还需要对吡格列酮进行不同剂量/持续时间的实验研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of pioglitazone and metformin on abdominal adhesion formation in an experimental model.

Background: This study evaluated the use of metformin or pioglitazone in preventing or reducing the development of post-operative intra-abdominal adhesion (PIAA) by employing histopathological, immunohistochemical, and biochemical analyses in an experimental adhesion model.

Methods: Fifty Wistar-Albino rats were divided into five groups: Group I (Control), Group II (Sham Treatment), Group III (Hy-aluronic Acid), Group IV (Metformin), and Group V (Pioglitazone). Adhesions were induced in the experimental groups, except for the sham group, using the scraping method. After 10 days, rats were euthanized for evaluation. Macroscopic adhesion degrees were assessed using Nair's scoring system. Immunohistochemical and enzyme-linked immunosorbent assay (ELISA) methods were utilized to assess serum, peritoneal lavage, and intestinal tissue samples. Fructosamine, interleukin-6 (IL-6), transforming growth factor-beta (TGF-β), and fibronectin levels were measured in serum and peritoneal lavage samples.

Results: The groups exhibited similar Nair scores and Type I or Type III Collagen staining scores (all, p>0.05). Pioglitazone significantly reduced serum IL-6 and TGF-β levels compared to controls (p=0.002 and p=0.008, respectively). Both metformin and pioglitazone groups showed elevated IL-6 in peritoneal lavage relative to controls, while fibronectin levels in the lavage were lower in pioglitazone-treated rats compared to the sham group (all, p<0.005).

Conclusion: Pioglitazone, but not metformin, demonstrated a positive biochemical impact on preventing PIAA formation in an experimental rat model, although histological impacts were not observed. Further experimental studies employing different dose/duration regimens of pioglitazone are needed to enhance our understanding of its effect on PIAA formation.

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