Natural Products Research Division, Department of Biological and Biomedical Sciences, Aga Khan University Medical College, Karachi 74800, Pakistan.
Lipids Health Dis. 2013 Mar 28;12:44. doi: 10.1186/1476-511X-12-44.
The metabolic syndrome (MS) is a combination of metabolic abnormalities that lead to an increased risk of cardiovascular diseases. Due to its rising incidence and demanding life-long use of multiple drugs, there is a growing interest in testing and developing new allopathic, complementary and alternative therapies for controlling or curing disorders of MS. The discovery of new therapeutic modalities requires animal models of disease and currently available models have limitations. Developing an appropriate animal model for MS to achieve various therapeutic targets remains a challenge and this study aims to develop a rat model which closely depicts MS in humans.
Rat model of MS was developed by replacing 60% of diet with fructose. Four groups of Sprague-Dawley rats were either given whole wheat or refined flour with and without fructose for 8 weeks. Data were analyzed on SPSS and Graphpad Prism using ANOVA with Tukey's and Bonferonni tests for multiple group comparison. A p-value of less than 0.05 was considered significant for differences between groups.
Replacing whole wheat with refined wheat flour in rat chow in 60% fructose-fed Sprague-Dawley rats resulted in hypertension (p 0.01), hyper-insulinemia (p < 0.001), hyperglycemia (p 0.03) and a reduction in HDL levels (p 0.002) at 4 weeks while hyper-triglyceridemia (p 0.001) with endothelial dysfunction was observed at 8 weeks.
It is concluded that the refined wheat flour with 60% fructose in diet hastens the development of metabolic syndrome in 4 weeks and replacing whole wheat flour with refined flour in diet induces a more effective abnormality including a low HDL. Further studies may be directed to assess the associated pathological changes, which can be used to study the effect of different therapeutic modalities on an animal model of MS with low HDL.
代谢综合征(MS)是一组代谢异常的组合,会增加心血管疾病的风险。由于其发病率不断上升,且需要长期使用多种药物,因此人们越来越感兴趣地测试和开发新的对抗疗法、补充和替代疗法来控制或治愈 MS 相关疾病。发现新的治疗方法需要疾病的动物模型,而目前可用的模型存在局限性。开发一种与人类 MS 密切相关的合适的动物模型来实现各种治疗目标仍然是一个挑战,本研究旨在开发一种大鼠模型来实现这一目标。
通过用果糖替代 60%的饮食来建立 MS 大鼠模型。将四组 Sprague-Dawley 大鼠分别给予全麦或精制面粉,并在有无果糖的情况下喂养 8 周。使用 SPSS 和 Graphpad Prism 软件对数据进行分析,采用 ANOVA 进行多组比较,并使用 Tukey 和 Bonferroni 检验进行多重比较。组间差异有统计学意义的 p 值设定为<0.05。
在 60%果糖喂养的 Sprague-Dawley 大鼠的饲料中用精制面粉替代全麦面粉,导致大鼠在 4 周时出现高血压(p<0.01)、高胰岛素血症(p<0.001)、高血糖(p<0.03)和高密度脂蛋白(HDL)水平降低(p<0.002),而在 8 周时出现高甘油三酯血症(p<0.001)和内皮功能障碍。
用饮食中的 60%果糖替代精制面粉可在 4 周内加速代谢综合征的发展,而用饮食中的精制面粉替代全麦面粉可引起更有效的异常,包括低 HDL。进一步的研究可能旨在评估相关的病理变化,这些变化可用于研究不同治疗方法对 HDL 水平低的 MS 动物模型的影响。