Institute of Fisheries Sciences, Pukyong National University, Busan 46041, Korea.
Department of Marine Bio-Materials & Aquaculture, Pukyong National University, Busan 48513, Korea.
Nutrients. 2020 Mar 20;12(3):837. doi: 10.3390/nu12030837.
Aging-induced cognitive dysfunction can be regulated by probiotics through bidirectional communication with the brain. This study aimed to investigate whether glycoproteins (Cf-hGP) enhanced probiotic-induced improvement of memory in aged rats and the underlying mechanism in the dorsal hippocampus. Cf-hGP were isolated using lectin resin. Cf-hGP (15 mg/kg/day) and/or () (10 CFU/rat/day) were orally administered once a day for 4 weeks. Co-treatment with Cf-hGP and synergistically improved spatial memory in aged rats, which was overturned by functional blocks of brain-derived neurotrophic factor (BDNF) signaling. Increases in BDNF expression and nuclear factor erythroid 2-related factor 2 (Nrf2) phosphorylation were accompanied by mono- and/or co-administration in the dorsal hippocampus, while c-Jun N-terminal kinase (JNK) phosphorylation and glucose-regulated protein 78 expression were decreased. These synergistic effects were downregulated by blocks of BDNF/Nrf2-mediated signaling. In particular, co-treatment, not mono-treatment, reduced phosphorylation of eukaryotic elongation factor 2 (eEF2) regulated by eEF2 kinase and protein phosphatase 2A. Additionally, co-treatment downregulated the interaction between eEF2 kinase and JNK. These data demonstrated that cognitive impairment in aged rats was synergistically diminished by co-treatment with Cf-hGP and through BDNF-mediated regulation of Nrf2 and eEF2 signaling pathways in the dorsal hippocampus.
衰老引起的认知功能障碍可以通过与大脑的双向交流来调节益生菌。本研究旨在探讨糖蛋白(Cf-hGP)是否通过增强益生菌诱导的老年大鼠记忆改善及其在背海马中的潜在机制。使用凝集素树脂分离 Cf-hGP。Cf-hGP(15mg/kg/天)和/或(10 CFU/大鼠/天)每天口服一次,持续 4 周。Cf-hGP 与的协同作用协同改善了老年大鼠的空间记忆,而阻断脑源性神经营养因子(BDNF)信号则逆转了这种作用。在背海马中,BDNF 表达和核因子红细胞 2 相关因子 2(Nrf2)磷酸化的增加伴随着单药和/或联合给药而增加,而 c-Jun N-末端激酶(JNK)磷酸化和葡萄糖调节蛋白 78 表达减少。这些协同作用被 BDNF/Nrf2 介导的信号转导的阻断所下调。特别是,联合治疗而不是单药治疗可降低受真核延伸因子 2 激酶和蛋白磷酸酶 2A 调节的真核延伸因子 2(eEF2)的磷酸化。此外,联合治疗下调了 eEF2 激酶与 JNK 之间的相互作用。这些数据表明,Cf-hGP 和 联合治疗通过 BDNF 介导的背海马中 Nrf2 和 eEF2 信号通路的调节,协同减轻了老年大鼠的认知障碍。