Pinto Bruno Araújo Serra, Melo Thamys Marinho, Flister Karla Frida Torres, França Lucas Martins, Moreira Vanessa Ribeiro, Kajihara Daniela, Mendes Nelmar Oliveira, Pereira Silma Regina, Laurindo Francisco Rafael Martins, Paes Antonio Marcus Andrade
Laboratory of Experimental Physiology, Department of Physiological Sciences, Federal University of Maranhão, Av. dos Portugueses 1966, Bacanga, São Luís 65080-805, MA, Brazil.
Laboratory of Genetics and Molecular Biology, Department of Biology, Federal University of Maranhão, Av. dos Portugueses 1966, Bacanga, São Luís 65080-805, MA, Brazil.
Antioxidants (Basel). 2022 Jul 19;11(7):1395. doi: 10.3390/antiox11071395.
Metabolic dysfunctions, such as hyperglycemia and insulin resistance, have been associated to cognitive impairment and dementia regardless of advanced age, although the underlying mechanisms are still elusive. Thus, this study investigates the deleterious effects of metabolic syndrome (MetS) induced by long-term exposure to a high-sucrose diet on motor and cognitive functions of male adult rats and its relationship with hippocampal endoplasmic reticulum (ER) stress. Weaned Wistar male rats were fed a high-sucrose diet until adulthood (HSD; 6 months old) and compared to both age-matched (CTR; 6 months old) and middle-aged chow-fed rats (OLD; 20 months old). MetS development, serum redox profile, behavioral, motor, and cognitive functions, and hippocampal gene/protein expressions for ER stress pro-adaptive and pro-apoptotic pathways, as well as senescence markers were assessed. Prolonged exposure to HSD induced MetS hallmarked by body weight gain associated to central obesity, hypertriglyceridemia, insulin resistance, and oxidative stress. Furthermore, HSD rats showed motor and cognitive decline similar to that in OLD animals. Noteworthy, HSD rats presented marked hippocampal ER stress characterized by failure of pro-adaptive signaling and increased expression of Chop, p21, and Parp-1 cleavage, markers of cell death and aging. This panorama resembles that found in OLD rats. In toto, our data showed that early and sustained exposure to a high-sucrose diet induced MetS, which subsequently led to hippocampus homeostasis disruption and premature impairment of motor and cognitive functions in adult rats.
代谢功能障碍,如高血糖和胰岛素抵抗,无论年龄大小,都与认知障碍和痴呆有关,尽管其潜在机制仍不清楚。因此,本研究调查长期高糖饮食诱导的代谢综合征(MetS)对成年雄性大鼠运动和认知功能的有害影响及其与海马内质网(ER)应激的关系。将断奶的Wistar雄性大鼠喂以高糖饮食直至成年(HSD组;6个月大),并与年龄匹配的(CTR组;6个月大)和中年正常饮食喂养的大鼠(OLD组;20个月大)进行比较。评估了MetS的发展、血清氧化还原谱、行为、运动和认知功能,以及海马中ER应激促适应和促凋亡途径的基因/蛋白表达以及衰老标志物。长期暴露于高糖饮食会诱导MetS,其特征是与中心性肥胖相关的体重增加、高甘油三酯血症、胰岛素抵抗和氧化应激。此外,HSD组大鼠表现出与OLD组动物相似的运动和认知能力下降。值得注意的是,HSD组大鼠表现出明显的海马ER应激,其特征是促适应信号传导失败以及细胞死亡和衰老标志物Chop、p21和Parp-1裂解的表达增加。这种情况与OLD组大鼠相似。总体而言,我们的数据表明,早期和持续暴露于高糖饮食会诱导MetS,随后导致成年大鼠海马内环境稳态破坏以及运动和认知功能过早受损。