Ababneh Suha Khayri, Siyam Ali Abu, Alqaraleh Moath, Al-Rawashde Futoon Abedrabbu, Abbas Muna M, Ababneh Sokiyna, Al-Othman Nihad, Ababneh Islam Khayri, Alkhatib Ahed J
Department of Allied Medical Sciences, Zarqa University College, Al-Balqa Applied University, Zarqa, Jordan.
Department of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Jadara University, Irbid, Jordan.
Mater Sociomed. 2024;36(4):250-256. doi: 10.5455/msm.2024.36.250-256.
Diabetes is not a single disease but rather, it is one aspect of metabolic syndrome. The pathologic aspects of diabetes involve cellular changes that need to be understood.
The main objective of this study was to explore the role of Ki67 in the liver of diabetic rats.
The study methodology involved the induction of diabetes in rats using Alloxan (120 mg/kg). A total of 20 albino rats were randomly assigned into two groups control group (N=10) and diabetes group (n=10). Diabetic group received the dose of alloxan, while the control group received similar dose of normal saline. Glucose level was monitored daily. After the end of the experiment (one -month period), all animals were terminated. Blood samples were taken to measure biochemical investigations including glucose, cholesterol, and triglycerides. Liver tissue was excised and washed with normal saline and fixed in buffered formalin (10%). Liver tissue was processed and stained by hematoxylin and eosin for routine histological examination and also stained by immunohistochemistry for Ki67 biomarker.
The results revealed the efficacy of the diabetic model. All biochemical investigations were significantly higher in the diabetic group compared with that of control group (p<0.001). Histological studies showed the existence of morphological alterations in cells and fatty changes in the diabetic group compared with the control group. The expression of Ki67 was significantly higher in the diabetic group compared with that in the control group (p=0.011).
Taken together, diabetes has adverse effects on the spleen from a histological point of view, and from the expression of Ki67.
糖尿病并非单一疾病,而是代谢综合征的一个方面。糖尿病的病理方面涉及需要了解的细胞变化。
本研究的主要目的是探讨Ki67在糖尿病大鼠肝脏中的作用。
研究方法包括用四氧嘧啶(120mg/kg)诱导大鼠患糖尿病。总共20只白化大鼠被随机分为两组,对照组(N = 10)和糖尿病组(n = 10)。糖尿病组接受四氧嘧啶剂量,而对照组接受相似剂量的生理盐水。每天监测血糖水平。实验结束后(一个月期间),所有动物均被处死。采集血样以测量生化指标,包括葡萄糖、胆固醇和甘油三酯。切除肝脏组织,用生理盐水冲洗,然后固定在10%的缓冲福尔马林中。对肝脏组织进行处理,用苏木精和伊红染色进行常规组织学检查,并用免疫组织化学法对Ki67生物标志物进行染色。
结果显示糖尿病模型有效。糖尿病组所有生化指标均显著高于对照组(p<0.001)。组织学研究表明,与对照组相比,糖尿病组细胞存在形态学改变和脂肪变化。糖尿病组Ki67的表达显著高于对照组(p = 0.011)。
综上所述,从组织学角度以及Ki67的表达来看,糖尿病对脾脏有不良影响。