维生素 B9 膳食补充剂可使高胆固醇饮食小鼠模型中的脂质代谢调节基因表达正常化

A. E. Burova, A. P. Reykh, A. V. Gorlova, E. P. Svirin, K. N. Zabegalov, K. D. Chaprov, A. E. Umrukhin, T. V. Strekalova
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摘要

西方饮食(WD)是一种以摄入过多胆固醇、饱和脂肪酸和糖为特征的营养方式;这种营养模式可导致 2 型糖尿病、代谢综合征和其他疾病,尤其是在老龄化时期。寻找有效的方法来控制由 WD 引起的代谢综合征似乎是一项相关的研究任务。遗憾的是,这一问题在目前的文献中还没有引起足够的重视。在这项研究中,我们利用小鼠 WD 模型来研究一种基于琥珀酸二氯麟(DS)和叶酸(维生素 B9)的食物补充剂的潜在效果,这两种物质都是线粒体功能的激活剂。我们研究了葡萄糖耐量、海马依赖性学习参数以及在使用 WD 的老龄小鼠大脑和肝脏中 WD 负作用分子标记的 RT-PCR 相对基因表达。小鼠C57BL/6为12个月大,在WD上饲养3周;一些组通过水接受В9(5毫克/千克/天)或DS(150毫克/千克/天)或它们的组合。我们进行了食物置换和恐惧条件学习测试,然后对肝脏和大脑中的几个基因进行了RT-PCR检测。我们发现,在恐惧条件反射测试中,葡萄糖耐量降低,颗粒移位速度加快,冻结时间缩短。这可能表明饲养在 WD 上的小鼠存在认知缺陷和冲动性。施用 DS 和 B 可减轻大部分这些变化。此外,肝脏中 FASN 的表达增加也表明了 WD 在衰老过程中产生负面影响的新机制。以 B9 和 DS 为基础的食物补充剂可使 FASN 的表达和行为正常化,并改善 WD饲养小鼠的葡萄糖耐量。我们的研究结果为进一步研究食品补充剂对衰老过程中代谢参数调节的治疗和预防作用开辟了新的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Vitamin B9-based Dietary Supplement Normalizes the Expression of Lipid Metabolism Regulatory Genes in a Mouse Model of a High-cholesterol Diet
The Western Diet (WD) is a nutritional style characterized by excessive intake of cholesterol, saturated fatty acids and sugars; this nutritional pattern can cause type 2 diabetes, metabolic syndrome and other disorders, particularly during ageing. The search for effective approaches to managing the metabolic syndrome caused by WD seems to be a relevant research task. Unfortunately, this issue has attracted insufficient attention in the current literature. In this work, we use a mouse model of WD to study potential effects of a food supplement based on dicholine succinate (DS) and folic acid (vitamin B9), which are activators of mitochondrial functions. We study glucose tolerance, parameters of hippocampus-dependent learning and relative gene expression in RT-PCR of molecular markers of negative WD effects in the brain and liver of aging mice housed on WD. Mice C57BL/6 were 12 months old and housed on WD for 3 weeks; some groups received В9 (5 mg/kg/day) or DS (150 mg/kg/day), or their combination, via water. We carried out food displacement and fear conditioning learning tests followed by RT-PCR of several genes in the liver and brain. We found a decreased glucose tolerance, an elevated speed of pellet displacement and a reduction of freezing time in the fear conditioning test. This may suggest cognitive deficits and impulsivity of mice housed on WD. The administration of DS and B diminished most of these changes. In addition, the increased expression of FASN in the liver points to new mechanisms of negative WD effects during aging. The food supplement based on B9 and DS normalizes FASN expression and behavior, as well as glucose tolerance in WD-housed mice. Our results open new perspectives for further studies of therapeutic and preventive effects of food supplements on the regulation of metabolic parameters during ageing.
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