Anesthesia and Operation Center, Chinese PLA General Hospital, Beijing 100853, China.
Department of Anesthesiology, The General Hospital of the PLA Rocket Force, Beijing, China.
Int Immunopharmacol. 2018 Dec;65:438-447. doi: 10.1016/j.intimp.2018.10.020. Epub 2018 Oct 30.
Neuroinflammation is believed to be one of the primary causes of cognitive impairment. Previous studies showed that the antioxidant vitamin C (Vit C) performs many beneficial functions such as immunostimulant and anti-inflammatory actions, but its role in inflammatory cognitive impairment is unclear. In the current study, we investigated the effect and possible mechanism of action of Vit C in lipopolysaccharide (LPS)-induced cognitive impairment. Intracerebroventricular LPS-induced memory impairment was used as the model for neuroinflammatory cognitive dysfunction. Vit C was administered by intracerebroventricular microinjection 30 min prior to LPS exposure. It was found that Vit C significantly protected animals from LPS-induced memory impairment as evidenced by improved performance in the Morris water maze and novel object recognition tests without changes in spontaneous locomotor activity. Vit C pretreatment inhibited the activation of microglia and the production of pro-inflammatory cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). Furthermore, Vit C pretreatment markedly decreased the malondialdehyde (MDA) level, increased superoxide dismutase (SOD) activity, and modulated the Bax/Bcl-2 ratio and p-p38 MAPK activation in the hippocampus of LPS-treated mice. Together, these results suggest that vitamin C pretreatment could protect mice from LPS-induced cognitive impairment, possibly through the modulation of oxidative stress and inflammatory responses.
神经炎症被认为是认知障碍的主要原因之一。先前的研究表明,抗氧化维生素 C(Vit C)具有许多有益的功能,如免疫刺激和抗炎作用,但它在炎症性认知障碍中的作用尚不清楚。在本研究中,我们研究了 Vit C 在脂多糖(LPS)诱导的认知障碍中的作用及其可能的作用机制。侧脑室注射 LPS 诱导的记忆损伤被用作神经炎症性认知功能障碍的模型。Vit C 通过侧脑室微注射在 LPS 暴露前 30 分钟给予。结果发现,Vit C 显著保护动物免受 LPS 诱导的记忆损伤,表现在 Morris 水迷宫和新物体识别测试中的表现得到改善,而自发运动活动没有变化。Vit C 预处理抑制小胶质细胞的激活和促炎细胞因子的产生,包括肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)。此外,Vit C 预处理显著降低了丙二醛(MDA)水平,增加了超氧化物歧化酶(SOD)活性,并调节了 LPS 处理小鼠海马中的 Bax/Bcl-2 比值和 p-p38 MAPK 激活。综上所述,这些结果表明,Vit C 预处理可以保护小鼠免受 LPS 诱导的认知障碍,可能通过调节氧化应激和炎症反应。