Şimşek Tamer, Ersoy Ömer Faik, Özsoy Zeki, Yenidoğan Erdinç, Kayaoğlu Hüseyin Ayhan, Özkan Namık, Şahin Mustafa
Department of General Surgery, Gaziosmanpaşa University School of Medicine, Tokat, Turkey.
Turk J Surg. 2018 Jul 1;34(2):111-116. doi: 10.5152/turkjsurg.2018.3771. eCollection 2018.
We aimed to investigate the effect of 10 mg/kg sildenafil on the structure and function of the liver in a rat model of obstructive jaundice.
Sixty-two male Wistar albino rats were distributed into six different groups. Obstructive jaundice was performed by legating the common bile duct. 10 mg/kg sildenafil citrate in drinking water was delivered orally after the operation before sacrificing them. Rats were sacrificed either after 10 or 28 days according to the study design. The blood and tissue samples from the liver were obtained to perform a biochemical and histopathological analysis to study functional and structural changes in the liver.
At the 10th day, there was no difference between the sildenafil-treated and control groups with regard to the aspartate aminotransferase and alanine aminotransferase levels (p=0.423, p=0.661). The alkaline phosphatase total bilirubin levels among the groups were statistically different (p<0.001). At the 28th day, liver function tests except alanine aminotransferase showed significant differences among the groups (p<0.001). Liver function tests did not changed significantly between the 10th and 28th day in sildenafil-treated rats (p>0.05). Significant differences were observed among the groups with regard to cholestasis, fibrosis, inflammation, and necrosis (p<0.001). However, edema increased in the sildenafil-treated group (p<0.001). On the 28th day, the severity of structural changes in the liver after obstructive jaundice, except edema, reduced significantly (p<0.001). The sildenafil-treated groups at different time points didn't show any statistical difference in histopathological changes (p>0.05).
Oral administration of 10 mg/kg sildenafil citrate dramatically reverses the biochemical and histopathological liver changes induced by obstructive jaundice in rats.
我们旨在研究10mg/kg西地那非对梗阻性黄疸大鼠模型肝脏结构和功能的影响。
62只雄性Wistar白化大鼠被分为六个不同的组。通过结扎胆总管制造梗阻性黄疸。术后在处死大鼠前,经口给予饮用水中含10mg/kg枸橼酸西地那非。根据研究设计,在术后10天或28天处死大鼠。采集肝脏的血液和组织样本进行生化和组织病理学分析,以研究肝脏的功能和结构变化。
在第10天,西地那非治疗组和对照组之间的天冬氨酸转氨酶和丙氨酸转氨酶水平无差异(p=0.423,p=0.661)。各组间碱性磷酸酶和总胆红素水平有统计学差异(p<0.001)。在第28天,除丙氨酸转氨酶外,肝功能检查在各组间显示出显著差异(p<0.001)。西地那非治疗的大鼠在第10天和第28天之间肝功能检查无显著变化(p>0.05)。在胆汁淤积、纤维化、炎症和坏死方面,各组间观察到显著差异(p<0.001)。然而,西地那非治疗组的水肿增加(p<0.001)。在第28天,梗阻性黄疸后肝脏结构变化的严重程度,除水肿外,显著减轻(p<0.001)。不同时间点的西地那非治疗组在组织病理学变化上未显示出任何统计学差异(p>0.05)。
口服10mg/kg枸橼酸西地那非可显著逆转大鼠梗阻性黄疸诱导的肝脏生化和组织病理学变化。