Radosinska Dominika, Gaal Kovalcikova Alexandra, Gardlik Roman, Chomova Maria, Snurikova Denisa, Radosinska Jana, Vrbjar Norbert
Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University in Bratislava, Sasinkova 4, 811 08 Bratislava, Slovakia.
Department of Pediatrics, National Institute of Children's Diseases, Faculty of Medicine, Comenius University in Bratislava, 833 40 Bratislava, Slovakia.
Biology (Basel). 2024 Sep 25;13(10):759. doi: 10.3390/biology13100759.
Type 2 diabetes mellitus has been referred to as being closely related to oxidative stress, which may affect brain functions and brain glucose metabolism due to its high metabolic activity and lipid-rich content. Na,K-ATPase is an essential enzyme maintaining intracellular homeostasis, with properties that can sensitively mirror various pathophysiological conditions such as diabetes. The goal of this study was to determine oxidative stress markers as well as Na,K-ATPase activities in the cerebellum of Zucker diabetic fatty (ZDF) rats depending on diabetes severity. The following groups of male rats were used: Wistar, ZDF Lean (fa/+), and ZDF (fa/fa) rats, arbitrarily divided according to glycemia into ZDF obese (ZO, less severe diabetes) and ZDF diabetic (ZOD, advanced diabetes) groups. In addition to basic biometry and biochemistry, oxidative stress markers were assessed in plasma and cerebellar tissues. The Na, K-ATPase enzyme activity was measured at varying ATP substrate concentrations. The results indicate significant differences in basic biometric and biochemical parameters within all the studied groups. Furthermore, oxidative damage was greater in the cerebellum of both ZDF (fa/fa) groups compared with the controls. Interestingly, Na,K-ATPase enzyme activity was highest to lowest in the following order: ZOD > ZO > Wistar > ZDF lean rats. In conclusion, an increase in systemic oxidative stress resulting from diabetic conditions has a significant impact on the cerebellar tissue independently of diabetes severity. The increased cerebellar Na,K-ATPase activity may reflect compensatory mechanisms in aged ZDF (fa/fa) animals, rather than indicating cerebellar neurodegeneration: a phenomenon that warrants further investigation.
2型糖尿病被认为与氧化应激密切相关,由于其高代谢活性和富含脂质的成分,氧化应激可能会影响脑功能和脑葡萄糖代谢。钠钾ATP酶是维持细胞内稳态的一种关键酶,其特性能够灵敏地反映各种病理生理状况,如糖尿病。本研究的目的是根据糖尿病严重程度,确定Zucker糖尿病肥胖(ZDF)大鼠小脑的氧化应激标志物以及钠钾ATP酶活性。使用了以下几组雄性大鼠:Wistar大鼠、ZDF瘦型(fa/+)大鼠和ZDF(fa/fa)大鼠,并根据血糖水平将ZDF大鼠任意分为ZDF肥胖组(ZO,糖尿病较轻)和ZDF糖尿病组(ZOD,糖尿病晚期)。除了基本的生物测量和生物化学检测外,还评估了血浆和小脑组织中的氧化应激标志物。在不同的ATP底物浓度下测量钠钾ATP酶的活性。结果表明,所有研究组在基本生物测量和生化参数方面存在显著差异。此外,与对照组相比,两个ZDF(fa/fa)组的小脑氧化损伤更大。有趣的是,钠钾ATP酶活性从高到低的顺序为:ZOD>ZO>Wistar>ZDF瘦型大鼠。总之,糖尿病状态导致的全身氧化应激增加对小脑组织有显著影响,且与糖尿病严重程度无关。小脑钠钾ATP酶活性增加可能反映了老年ZDF(fa/fa)动物的代偿机制,而非表明小脑神经退行性变:这一现象值得进一步研究。