Abstract

ObjectiveDimethyl fumarate (DMF) has been reported to exert a protective role against diverse lung diseases and cognitive impairment-related diseases. Thus this study aimed to investigate its role on acute lung injury (ALI) and related cognitive impairment in animal model.MethodsC57BL/6 mice were divided into four groups: control group, DMF group, ALI group, and ALI + DMF group. For ALI group, the ALI mice model was created by airway injection of LPS (50 μL, 1 μg/μL); for ALI + DMF group, DMF (dissolved in 0.08% methylcellulose) was treated twice a day for 2 days, and on the third day, mice were injected with LPS for ALI modeling. Mice pre-administered with methylcellulose or DMF without LPS injection (PBS instead) were used as the control group and DMF group, respectively. Morris water maze test was performed before any treatment (0 h) and 6 h after LPS-induction (54 h) to evaluate the cognitive impairment of mice. Next, the brain edema and blood brain barrier (BBB) permeability of ALI mice were assessed by brain water content, Evans blue extravasation and FITC-Dextran uptake assays. In addition, the effect of DMF on the numbers of total cells and neutrophils, protein content in BALF were quantified; the inflammatory factors in BALF, serum, and brain tissues were examined by ELISA, qRT-PCR, and Western blot assays. The effect of DMF on the cognitive impairment-related factor HIF-1α level in lung and brain tissues was also examined by Western blot.ResultsDMF reduced the numbers of total cells, neutrophils and protein content in BALF of ALI mice, inhibited the levels of IL-6, TNF-α and IL-1β in BALF, serum and brain tissues of ALI mice. The protein expressions of p-NF-κB/NF-κB and p-IKBα/IKBα was also suppressed by DMF in ALI mice. Morris water maze test showed that DMF alleviated the cognitive impairment in ALI mice by reducing the escape latency and path length. Moreover, DMF lessened the BBB permeability by decreasing cerebral water content, Evans blue extravasation and FITC-Dextran uptake in ALI mice. The HIF-1α levels in lung and brain tissues of ALI mice were also lessened by DMF.ConclusionIn conclusion, DME had the ability to alleviate the lung injury and cerebral cognitive impairment in ALI model mice. This protective effect partly associated with the suppression of inflammation by DMF.

Highlights

  • Acute lung injury (ALI) and its more serious form of respiratory distress syndrome (ARDS) is reported with a widely variable incidence while can lead to death in ALI patients [1]

  • Dimethyl fumarate (DMF) alleviated ALI‐associated lung injury As shown in Fig. 2A, B, DMF pretreatment alone did not obviously change the numbers of total cells and neutrophils in broncho-alveolar lavage fluid (BALF) compared to the control group, while LPSinduced ALI led to a sharp increase (P < 0.01)

  • DMF administration caused a decrease of total cells and neutrophils in BALF (Fig. 2A, B, P < 0.01)

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Summary

Introduction

Acute lung injury (ALI) and its more serious form of respiratory distress syndrome (ARDS) is reported with a widely variable incidence while can lead to death in ALI patients [1]. Srious pneumonia, trauma, shock, sepsis, cardiothoracic surgery and other related factors are contributed to the occurrence of ALI. In perioperative period of cardiothoracic surgery, the surgeon needs to maintain a suspicion for the risk of ALI, for which is correlated with the surgical prognosis and the causes of operative death [4, 5]. Studies have confirmed that patients with ALI/ARDS have neurocognitive impairment, which seriously affects the patient’s life quality [8, 9]. The current recognizing of the nosogenesis and elements affecting the prognosis of patients has improved, there is still a lack of effective drugs for the treatment of ALI/ARDS [11]. It is necessary to find new drugs with high efficiency and low toxicity, which is of great significance for the treatment of ALI

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