Department of Anatomy, College of Medicine, Qassim University, Meleda, Buraydah, Saudi Arabia.
Department of Anatomy and Embryology, Faculty of Medicine, Kasr Al-Ainy, Cairo University, Cairo, Egypt.
Sci Rep. 2020 Jun 1;10(1):8840. doi: 10.1038/s41598-020-64050-z.
Aging causes morphological and functional changes in the cerebellum. This work aimed to demonstrate the implication of JAK1/STAT3/SOCS3 on aging-induced changes of rat cerebellum. Thirty male rats were divided into: adult (12 months), early senile (24 months) and late senile (32 months) groups. Immunohistochemical reaction of the cerebellum to GFAP and caspase-3 was assessed and the expression of JAK1, STAT3, SOCS3 proteins was also evaluated. TNFα as well as the activities of malondialdehyde (MDA) and reduced glutathione (GSH) in cerebellar tissue were also measured. The cerebellum of late senile rats revealed more degenerative changes than early senile rats in the form of increase in GFAP and caspase-3 immunoreaction. Additionally, there was decrease in JAK1and STAT3 expression in early and late senile rats and increase in SOCS3 when compare early and late senile groups with adult one. Enhancement of TNFα was noticed with aging as well as significant decrease in GSH and increase in MDA in early senile group. Moreover, late senile group revealed significant decrease in GSH and increase in MDA. It could be concluded that aging resulting in variable changes of the cerebellum as detected by morphological changes, immunohistochemical reactions of caspase-3 and GFAP and expression of JAK1/STAT3/SOCS3 proteins. Additionally, inflammatory marker TNFα and the activity of oxidative/antioxidative stress markers; malondialdehyde (MDA) and reduced glutathione (GSH) were also affected with aging.
衰老是小脑形态和功能改变的原因。本研究旨在探讨 JAK1/STAT3/SOCS3 在衰老诱导的大鼠小脑变化中的作用。将 30 只雄性大鼠分为成年(12 个月)、早期衰老(24 个月)和晚期衰老(32 个月)组。评估小脑 GFAP 和 caspase-3 的免疫组织化学反应,并评估 JAK1、STAT3、SOCS3 蛋白的表达。还测量了小脑组织中 TNFα 以及丙二醛(MDA)和还原型谷胱甘肽(GSH)的活性。与早期衰老大鼠相比,晚期衰老大鼠的小脑显示出更多的退行性变化,表现为 GFAP 和 caspase-3 免疫反应增加。此外,早期和晚期衰老大鼠的 JAK1 和 STAT3 表达减少,早期和晚期衰老组与成年组相比 SOCS3 表达增加。随着衰老,TNFα 增加,早期衰老组 GSH 显著减少,MDA 增加。此外,晚期衰老组 GSH 明显减少,MDA 增加。可以得出结论,衰老导致小脑形态学变化、caspase-3 和 GFAP 的免疫组织化学反应以及 JAK1/STAT3/SOCS3 蛋白表达的变化。此外,炎症标志物 TNFα 和氧化/抗氧化应激标志物丙二醛(MDA)和还原型谷胱甘肽(GSH)的活性也受到衰老的影响。