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阿托伐他汀通过抑制 NF-κB 通路和 NLRP3 炎性小体激活,部分减轻了手术引起的老年小鼠血脑屏障破坏和认知障碍。

Atorvastatin attenuates surgery-induced BBB disruption and cognitive impairment partly by suppressing NF-κB pathway and NLRP3 inflammasome activation in aged mice.

机构信息

Department of Anesthesiology, Beijing Shijitan Hospital, Capital Medical University, Beijing 100038, China.

Department of Operational Medicine, Tianjin Institute of Environmental & Operational Medicine, Tianjin 300050, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2021 Apr 15;53(5):528-537. doi: 10.1093/abbs/gmab022.

DOI:10.1093/abbs/gmab022
PMID:33674828
Abstract

In clinic, perioperative neurocognitive disorder is becoming a common complication of surgery in old patients. Neuroinflammation and blood-brain barrier (BBB) disruption are important contributors for cognitive impairment. Atorvastatin, as a strong HMG-CoA reductase inhibitor, has been widely used in clinic. However, it remains unclear whether atorvastatin could prevent anesthesia and surgery-induced BBB disruption and cognitive injury by its anti-inflammatory property. In this study, aged C57BL/6J mice were used to address this question. Initially, the mice were subject to atorvastatin treatment for 7 days (10 mg/kg). After a simple laparotomy under 1.5% isoflurane anesthesia, Morris water maze was performed to assess spatial learning and memory. Western blot analysis, immunohistochemistry, and enzyme-linked immunosorbent assay were used to examine the inflammatory response, BBB integrity, and cell apoptosis. Terminal-deoxynucleotidyl transferase mediated nick end labeling assay was used to assess cell apoptosis. The fluorescein sodium and transmission electron microscopy were used to detect the permeability and structure of BBB. The results showed that anesthesia and surgery significantly injured hippocampal-dependent learning and memory, which was ameliorated by atorvastatin. Atorvastatin could also reverse the surgery-induced increase of systemic and hippocampal cytokines, including IL-1β, TNF-α, and IL-6, accompanied by inhibiting the nuclear factor kappa-B (NF-κB) pathway and Nucleotide-Binding Oligomerization Domain, or Leucine Rich Repeat and Pyrin Domain Containing 3 (NLRP3) inflammasome activation, as well as hippocampal neuronal apoptosis. In addition, surgery triggered an increase of BBB permeability, paralleled by a decrease of the ZO-1, occludin, and Claudin 5 proteins in the hippocampus. However, atorvastatin treatment could protect the BBB integrity from the impact of surgery, by up-regulating the expressions of ZO-1, occludin, and Claudin 5. These findings suggest that atorvastatin exhibits neuroprotective effects on cognition in aged mice undergoing surgery.

摘要

在临床实践中,围手术期神经认知障碍正成为老年患者手术的常见并发症。神经炎症和血脑屏障(BBB)破坏是认知障碍的重要因素。阿托伐他汀作为一种强效的 HMG-CoA 还原酶抑制剂,已广泛应用于临床。然而,其抗炎特性是否能预防麻醉和手术引起的 BBB 破坏和认知损伤仍不清楚。在这项研究中,使用老龄 C57BL/6J 小鼠来解决这个问题。首先,小鼠接受阿托伐他汀治疗 7 天(10mg/kg)。在 1.5%异氟烷麻醉下进行简单的剖腹手术后,进行 Morris 水迷宫实验以评估空间学习和记忆。采用 Western blot 分析、免疫组织化学和酶联免疫吸附试验检测炎症反应、BBB 完整性和细胞凋亡。末端脱氧核苷酸转移酶介导的缺口末端标记法检测细胞凋亡。荧光素钠和透射电子显微镜检测 BBB 的通透性和结构。结果表明,麻醉和手术显著损伤了海马依赖性学习和记忆,而阿托伐他汀可改善这种损伤。阿托伐他汀还可以逆转手术引起的全身和海马细胞因子的增加,包括白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6),同时抑制核因子-κB(NF-κB)通路和核苷酸结合寡聚结构域、富含亮氨酸重复和吡咯烷结构域 3(NLRP3)炎症小体的激活,以及海马神经元凋亡。此外,手术引发 BBB 通透性增加,同时海马组织中 ZO-1、occludin 和 Claudin 5 蛋白减少。然而,阿托伐他汀治疗可以通过上调 ZO-1、occludin 和 Claudin 5 的表达来保护 BBB 完整性免受手术的影响。这些发现表明,阿托伐他汀对接受手术的老年小鼠的认知具有神经保护作用。

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