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二十二碳六烯酸补充对幼鼠早期产后 PM2.5 暴露引起的认知功能障碍和海马突触可塑性损伤的保护作用。

Protective effects of docosahexaenoic acid supplementation on cognitive dysfunction and hippocampal synaptic plasticity impairment induced by early postnatal PM2.5 exposure in young rats.

机构信息

Department of Neurology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Neurodevelopment and Cognitive Disorders, No. 136, Zhongshan Er Road, Yuzhong District, Chongqing, 400014, China.

Department of Pediatrics, Shenzhen Baoan Women's and Children's Hospital, Jinan University, Shenzhen, 518101, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6563-6575. doi: 10.1007/s00210-024-03028-4. Epub 2024 Mar 9.

Abstract

PM2.5 exposure is a challenging environmental issue that is closely related to cognitive development impairment; however, currently, relevant means for prevention and treatment remain lacking. Herein, we determined the preventive effect of docosahexaenoic acid (DHA) supplementation on the neurodevelopmental toxicity induced by PM2.5 exposure. Neonatal rats were divided randomly into three groups: control, PM2.5, and DHA + PM2.5 groups. DHA could ameliorate PM2.5-induced learning and memory dysfunction, as well as reverse the impairment of hippocampal synaptic plasticity, evidenced by enhanced long-term potentiation, recovered synaptic ultrastructure, and increased expression of synaptic proteins. Moreover, DHA increased CREB phosphorylation and BDNF levels and attenuated neuroinflammation and oxidative stress, reflected by lower levels of IBA-1, IL-1β, and IL-6 and increased levels of SOD1 and Nrf2. In summary, our findings demonstrated that supplementation of DHA effectively mitigated the cognitive dysfunction and synaptic plasticity impairment induced by early postnatal exposure to PM2.5. These beneficial effects may be attributed to the upregulation of the CREB/BDNF signaling pathway, as well as the reduction of neuroinflammation and oxidative stress.

摘要

PM2.5 暴露是一个具有挑战性的环境问题,与认知发育损伤密切相关;然而,目前仍然缺乏相关的预防和治疗手段。在此,我们确定了二十二碳六烯酸(DHA)补充对 PM2.5 暴露诱导的神经发育毒性的预防作用。新生大鼠随机分为三组:对照组、PM2.5 组和 DHA+PM2.5 组。DHA 可以改善 PM2.5 引起的学习和记忆功能障碍,并逆转海马突触可塑性的损伤,表现在长时程增强增强、突触超微结构恢复以及突触蛋白表达增加。此外,DHA 增加了 CREB 磷酸化和 BDNF 水平,并减轻了神经炎症和氧化应激,表现为 IBA-1、IL-1β 和 IL-6 水平降低,SOD1 和 Nrf2 水平升高。总之,我们的研究结果表明,DHA 的补充有效地减轻了早期产后 PM2.5 暴露引起的认知功能障碍和突触可塑性损伤。这些有益的效果可能归因于 CREB/BDNF 信号通路的上调,以及神经炎症和氧化应激的减少。

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