de Assis Adriano M, Rieger Débora K, Longoni Aline, Battu Cintia, Raymundi Suzeli, da Rocha Ricardo F, Andreazza Ana C, Farina Marcelo, Rotta Liane N, Gottfried Carmen, Gonçalves Carlos A, Moreira José Cláudio, Perry Marcos L S
Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, 90035-003, Porto Alegre, RS, Brazil
Exp Biol Med (Maywood). 2009 Nov;234(11):1296-304. doi: 10.3181/0904-RM-126.
Many studies have demonstrated that DNA damage may be associated with type 2 diabetes mellitus (T2DM) and its complications. The goal of this study was to evaluate the effects of the potential relationship between fat (thermolyzed) intake, glucose dyshomeostasis and DNA injury in rats. Biochemical parameters related to glucose metabolism (i.e., blood glucose levels, insulin tolerance tests, glucose tolerance tests and fat cell glucose oxidation) and general health parameters (i.e., body weight, retroperitoneal and epididymal adipose tissue) were evaluated in rats after a 12-month treatment with either a high fat or a high thermolyzed fat diet. The high fat diet (HFD) and high fat thermolyzed diet (HFTD) showed increased body weight and impaired insulin sensitivity at the studied time-points in insulin tolerance test (ITT) and glucose tolerance test (GTT). Interestingly, only animals subjected to the HFTD diet showed decreased epididymal fat cell glucose oxidation. We show which high fat diets have the capacity to reduce glycogen synthesis by direct and indirect pathways. HFTD promoted an increase in lipid peroxidation in the liver, demonstrating significant damage in lipids in relation to other groups. Blood and hippocampus DNA damage was significantly higher in animals subjected to HFDs, and the highest damage was observed in animals from the HFTD group. Striatum DNA damage was significantly higher in animals subjected to HFDs, compared with the control group. These results show a positive correlation between high fat diet, glucose dyshomeostasis, oxidative stress and DNA damage.
许多研究表明,DNA损伤可能与2型糖尿病(T2DM)及其并发症有关。本研究的目的是评估大鼠脂肪(热解)摄入、葡萄糖稳态失衡与DNA损伤之间潜在关系的影响。在用高脂肪或高热解脂肪饮食治疗12个月后,对大鼠与葡萄糖代谢相关的生化参数(即血糖水平、胰岛素耐量试验、葡萄糖耐量试验和脂肪细胞葡萄糖氧化)和一般健康参数(即体重、腹膜后和附睾脂肪组织)进行了评估。在胰岛素耐量试验(ITT)和葡萄糖耐量试验(GTT)的研究时间点,高脂肪饮食(HFD)和高热解脂肪饮食(HFTD)显示体重增加且胰岛素敏感性受损。有趣的是,只有接受HFTD饮食的动物附睾脂肪细胞葡萄糖氧化减少。我们表明,高脂肪饮食有能力通过直接和间接途径减少糖原合成。HFTD促进了肝脏脂质过氧化的增加,表明与其他组相比脂质有显著损伤。接受HFDs的动物血液和海马体DNA损伤明显更高,并且在HFTD组动物中观察到最高的损伤。与对照组相比,接受HFDs的动物纹状体DNA损伤明显更高。这些结果表明高脂肪饮食、葡萄糖稳态失衡、氧化应激与DNA损伤之间存在正相关。