Department of Pharmacy, Changzhou Geriatric Hospital Affiliated to Soochow University, Changzhou No.7 People's Hospital, 288# Yanling East Road, Changzhou, 213000, Jiangsu, China.
Department of Neurosurgery, Suzhou Kowloon Hospital, Shanghai Jiaotong University School of Medicine, #118 Wansheng Street, Suzhou, 215028, Jiangsu, China.
J Neuroinflammation. 2022 Jan 7;19(1):12. doi: 10.1186/s12974-021-02377-8.
Innate immune pre-stimulation can prevent the development of depression-like behaviors in chronically stressed mice; however, whether the same stimulation prevents the development of anxiety-like behaviors in animals remains unclear. We addressed this issue using monophosphoryl lipid A (MPL), a derivative of lipopolysaccharide (LPS) that lacks undesirable properties of LPS but still keeps immune-enhancing activities.
The experimental mice were pre-injected intraperitoneally with MPL before stress exposure. Depression was induced through chronic social defeat stress (CSDS). Behavioral tests were conducted to identify anxiety-like behaviors. Real-time polymerase chain reaction (PCR) and biochemical assays were employed to examine the gene and protein expression levels of pro-inflammatory markers.
A single MPL injection at the dose of 400 and 800 μg/kg 1 day before stress exposure prevented CSDS-induced anxiety-like behaviors, and a single MPL injection (400 μg/kg) five but not 10 days before stress exposure produced similar effect. The preventive effect of MPL on anxiety-like behaviors was also observed in CSDS mice who received a second MPL injection 10 days after the first MPL injection or a 4 × MPL injection 10 days before stress exposure. MPL pre-injection also prevented the production of pro-inflammatory cytokines in the hippocampus and medial prefrontal cortex in CSDS mice, and inhibiting the central immune response by minocycline pretreatment abrogated the preventive effect of MPL on CSDS-induced anxiety-like behaviors and pro-inflammatory cytokine productions in the brain.
Pre-stimulation of the innate immune system by MPL can prevent chronic stress-induced anxiety-like behaviors and neuroinflammatory responses in the brain in mice.
先天免疫预刺激可以预防慢性应激小鼠出现抑郁样行为;然而,同样的刺激是否可以预防动物出现焦虑样行为尚不清楚。我们使用单磷酰脂质 A(MPL)解决了这个问题,MPL 是脂多糖(LPS)的衍生物,缺乏 LPS 的不良特性,但仍具有增强免疫的活性。
实验小鼠在暴露于应激前经腹腔注射 MPL。通过慢性社会挫败应激(CSDS)诱导抑郁。进行行为测试以鉴定焦虑样行为。采用实时聚合酶链反应(PCR)和生化测定法检测促炎标志物的基因和蛋白表达水平。
在应激暴露前 1 天,以 400 和 800μg/kg 的剂量单次注射 MPL 可预防 CSDS 诱导的焦虑样行为,而在应激暴露前 5 天但不是 10 天单次注射 MPL 可产生类似效果。在 CSDS 小鼠中,在第一次 MPL 注射后 10 天接受第二次 MPL 注射或在应激暴露前 10 天接受 4×MPL 注射也观察到 MPL 对焦虑样行为的预防作用。MPL 预处理还可预防 CSDS 小鼠海马体和内侧前额叶皮质中促炎细胞因子的产生,而米诺环素预处理抑制中枢免疫反应则消除了 MPL 对 CSDS 诱导的焦虑样行为和大脑中促炎细胞因子产生的预防作用。
MPL 对先天免疫系统的预刺激可预防慢性应激诱导的小鼠焦虑样行为和大脑中的神经炎症反应。