Department of General Surgery, Istanbul University-Cerrahpaşa, Istanbul-Türkiye.
Department of Biochemistry, Istanbul University-Cerrahpaşa, Istanbul, Turkiye.
Ulus Travma Acil Cerrahi Derg. 2024 Jun;30(6):406-414. doi: 10.14744/tjtes.2024.61732.
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.
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.
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).
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.
本研究通过组织病理学、免疫组织化学和生化分析,在实验性粘连模型中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)形成中的作用。
将 50 只 Wistar-Albino 大鼠分为五组:I 组(对照组)、II 组(假手术组)、III 组(透明质酸组)、IV 组(二甲双胍组)和 V 组(吡格列酮组)。实验组除假手术组外,采用刮除法诱导粘连。10 天后处死大鼠进行评估。采用 Nair 评分系统评估大体粘连程度。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。测量血清和腹腔灌洗液样本中的果糖胺、白细胞介素-6(IL-6)、转化生长因子-β(TGF-β)和纤维连接蛋白水平。
各组的 Nair 评分和 I 型或 III 型胶原染色评分相似(均,p>0.05)。与对照组相比,吡格列酮组血清 IL-6 和 TGF-β水平显著降低(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的腹腔灌洗液中 IL-6 水平升高,而吡格列酮组的灌洗液中纤维连接蛋白水平低于假手术组(均,p<0.005)。
在实验性大鼠模型中,吡格列酮而非二甲双胍在预防 PIAA 形成方面具有积极的生化作用,尽管未观察到组织学影响。需要进行进一步的实验研究,采用不同的吡格列酮剂量/持续时间方案,以增强我们对其预防 PIAA 形成作用的理解。