key: cord-0070322-szoep785
authors: Zheng, Binbin; Yang, Hongbo; Zhang, Jianan; Wang, Xueli; Sun, Hao; Hu, Fan; Li, Qian; Jiang, Liping; Su, Yue; Peng, Qilin; Tang, Yulin; Liu, Wen-Tao; He, Xueming; Fan, Yixin; Zhu, Xia
title: Lidocaine Alleviates Sepsis-Induced Acute Lung Injury in Mice by Suppressing Tissue Factor and Matrix Metalloproteinase-2/9
date: 2021-11-12
journal: Oxid Med Cell Longev
DOI: 10.1155/2021/3827501
sha: dee6e789541c0bd11a364f6464b52f6f228adcce
doc_id: 70322
cord_uid: szoep785

Acute lung injury (ALI) is one of the fatal symptoms of sepsis. However, there were no effective clinical treatments. TF accumulation-induced fibrin deposit formations and coagulation abnormalities in pulmonary vessels contribute to the lethality of ALI. Suppressor of cytokine signaling 3 (SOCS3) acts as an endogenous negative regulator of the TLR4/TF pathway. We hypothesized that inducing SOCS3 expression using lidocaine to suppress the TLR4/TF pathway may alleviate ALI. Hematoxylin and eosin (H&E), B-mode ultrasound, and flow cytometry were used to measure the pathological damage of mice. Gelatin zymography was used to measure matrix metalloproteinase-2/9 (MMP-2/9) activities. Western blot was used to assay the expression of protein levels. Here, we show that lidocaine could increase the survival rate of ALI mice and ameliorate the lung injury of ALI mice including reducing the edema, neutrophil infiltration, and pulmonary thrombosis formation and increasing blood flow velocity. Moreover, in vitro and in vivo, lidocaine could increase the expression of p-AMPK and SOCS3 and subsequently decrease the expression of p-ASK1, p-p38, TF, and the activity of MMP-2/9. Taken together, our study demonstrated that lidocaine could inhibit the TLR4/ASK1/TF pathway to alleviate ALI via activating AMPK-SOCS3 axis.

Acute lung injury (ALI) caused by sepsis is one of the main causes of death in ICU patients. Unfortunately, therapies to prevent or treat ALI remain elusive. It is urgent to further investigate the pathogenesis of sepsis-induced ALI and find effective strategy.

The pathological characteristics of ALI mainly include coagulation abnormalities, thrombus, hypoxemia, diffuse infiltration of the lungs, and decreased functional lung volume [1] . Tissue factor (TF) is a primary trigger for coagulation and thrombus formation, playing a pivotal role in blood clotting activation [2] . Recent study showed that the expression of tissue factor (TF) was significantly increased in LPS-induced ALI model in mice, leading to a hypercoagulable state in the pulmonary vasculature [3] . TF expressed in the microvasculature acts as a critical initiator of blood coagulation in ALI, while using the neutralizing antibody to inhibit TF before lethal sepsis prevents ALI in baboons [4, 5] . In addition, study found that antithrombin (hirudin) could also have a protective effect on endotoxemia mice by reducing fibrin deposition [6] . These studies indicated that moderate anticoagulation has certain therapeutic effect on sepsis-induced ALI.

Apoptosis signal-regulating kinase (ASK1) is a member of the MAP3K family, which is activated by a number of cellular stressors, such as oxidative stress and inflammatory cytokines [7, 8] . Study found that ASK1 activation could significantly induce the expression of TF [9] , participating in regulation of hemostasis and thrombosis [10] . As the upstream signaling molecule of ASK1, Toll-like receptor 4 (TLR4) plays an important role in the activation of innate immunity, inducing the production of IL-6, TNF-α, and even TF through the p38/ NF-κB signaling [11] [12] [13] . Thus, inhibition of the TLR4/ ASK1 signaling pathway may be beneficial to ALI. Suppressor of cytokine signaling 3 (SOCS3) is an inhibitor of cytokine signaling pathways, which have been found that can negatively regulate the TLR4-mediated signaling pathway [14] , and our previous study also found that inducing the overexpression of SOCS3 can inhibit the activation of the TLR4-p38 pathway [15] . Taken together, upregulating SOCS3 expression to inhibit TLR4-ASK1 axis and decrease TF expression may be an effective strategy to alleviate ALI.

Lidocaine is a common amide-type local anesthetic. Recent study indicated that local anesthetics using lidocaine could inhibit LPS-induced tissue factor messenger RNA (TF mRNA) level in endothelial and monocytes, but the underlying mechanism is unclear [16] . Our previous study has shown that lidocaine could upregulate the expression of SOCS3 and inhibit the activation of TLR4 signal, as well as suppress neuroinflammation [17] . Given the above discussion, we hypothesized lidocaine could induce SOCS3 production in the lungs, decreasing TF expression and alleviating LPS-induced ALI.

Hubei Tianyao Pharmaceutical Co. Ltd. LPS (catalog no. L2630) and compound C (catalog no. P5499) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Antibody for SOCS3 (catalog no. ab16030), HIF-1α (catalog no. ab1), and TF (catalog no. ab189483) was purchased from Abcam (Cambridge, MA, USA). Antibody for phosphorylated AMPactivated protein kinase (p-AMPK) (Thr172; catalog no. 2531), phosphorylated ASK1 (catalog no. 3762S), and phosphorylated p38 mitogen-activated protein kinase (p38; Tyr180/Tyr182; catalog no. 9211) was purchased from Cell Signaling Technology (Beverly, MA, USA). Antibody for β-actin (catalog no. A1978) was purchased from Sigma-Aldrich. Fetal bovine serum (FBS) was purchased from Gibco, and other cell culture media and supplements were purchased from KenGen (KenGen Biotech, China). All other reagents were from Sigma-Aldrich (St. Louis, MO, USA).

Adult male CD-1 mice (18-22 g) were purchased from the Experimental Animal Center at Nanjing Medical University, Nanjing, China. Animals were housed five to six per cage under pathogen-free conditions with soft bedding under controlled temperature (22 ± 2°C) and a 12 h light/dark cycle (lights on at 8 : 00 a.m.). Animals were allowed to acclimate to these conditions for at least 3 days before inclusion in experiments. For each group of experiments, the animals were matched by age and body weight. All procedures were conducted in accordance with the guidelines and regulations of the National Institutes of Health (NIH) and were approved by the Ethics Committee of Nanjing Medical University (No. IACUC-1902012) .

The model of sepsis-induced ALI was induced by a single intraperitoneal (i.p.) injection of 12.5 mg/kg of LPS in mice as previously described [18, 19] . Mice were randomly divided into 6 groups (n = 12) according to treatment, including control group (Con), LPS group, lidocaine (2 mg/kg)+LPS group, lidocaine (4 mg/kg)+LPS group, lidocaine (8 mg/kg)+LPS group, and lidocaine (8 mg/kg) group. For the survival rate and body weight experiments, different concentrations of lidocaine (2, 4, and 8 mg/kg) were intravenous (i.v.) injection into mice through the tail vein every 12 h for 3 consecutive days. For the other experiments, lidocaine (2, 4, and 8 mg/kg) was i.v. injection into mice through the tail vein 30 min before LPS injection.

Measurement. The methods to collect BALF were described previously [20] . After LPS injection for 12 h, the mice were anesthetized by 1% sodium amobarbital, and then, the thorax was opened. 500 μL of PBS was injected, retrieved the liquid from the trachea, and repeated three times. The samples were centrifuged at 5000 rpm for 10 min, and the supernatants were collected. The total protein level in BALF was measured by the BCA kit (Thermo Scientific, MA, USA) according to the manufacturer's protocol.

For the histological analysis, the mice were anesthetized by 1% sodium amobarbital and sacrificed and then quickly collected the lung tissues from mice. The samples were fixed in 10% formalin for 24 h and then dehydrated in a series of graded ethanol and finally embedded in paraffin. Then, microtome sections (4 μm) were cut and stained with hematoxylin and eosin (H&E). Images were taken under a light microscope (Leica, Germany) by two investigators blinded to a group assignment. Six random fields of each lung section were examined.

Wet-to-Dry Ratio Assay. Lung wet-to-dry ratio was used as an index of lung edema. After LPS injection for 12 h, mice were sacrificed, and the lung tissues (both lobes) were immediately weighed after collection and recorded as wet weight. The lung tissues were then placed into an oven at 60°C for 72 h and weighed as dry weight. Lung wet-to-dry ratio was calculated by dividing the wet by the dry weights.

2.6. Ultrasonic Testing. The mice were anesthetized by 1% sodium amobarbital, and ultrasonic testing was performed by the US GE E9 ultrasonic machine and 11L ultrasonic 2

Oxidative Medicine and Cellular Longevity probe. The test method was referred to Lichtenstein DA double blue dot + PLAPS point detection which checks the distribution of the B line and assesses the distribution area of the B line in the scanning area for semiquantitative analysis. In order to correct the measurement bias, a doubleblind design was used during the ultrasonic detection. Neither the investigators nor the sonographers were aware of the type of the mouse group. Each mouse underwent ultrasonic detection for three times, and the detection was repeated by two sonographers with more than 3 years' experience. The average values of the two measurements were statistically analyzed. 

Mice were anaesthetized deeply with 1% sodium amobarbital and then collected blood samples, and the red blood cell lysis buffer (Sigma-Aldrich, MO, USA) was added into the blood for 20 min, after centrifugation (1000 r/min, 5 min) and collected the cells, then added the 1% BSA into the cells, and centrifugation (1000 r/min) again for 5 min, and then the cells were collected and stained with monoclonal anti-mouse antibodies: CD45-PE, CD11b-APE, and Ly6G. Cells were stained for 40 min on ice before being washed and analyzed on a FACSVerse flow cytometer (BD, NJ, USA) using FlowJo V10.0.7 (Tree Star, Ashland, USA). CD45 + CD11b + Ly6G + -positive cells were considered neutrophils.

2.11. Statistical Analyses. GraphPad Prism 6 software (GraphPad Software, San Diego, CA) was used to conduct all the statistical analyses. Kaplan-Meier survival analysis was completed using the log rank (Mantel-Cox) test. Data were statistically evaluated by one-way or two-way analysis of variance (ANOVA) followed by the Bonferroni post hoc tests. Results were represented as the mean ± SEM of three independent experiments. Results described as significant were based on a criterion of P < 0:05.

As shown in Figure 1 (a), mice administered with LPS (12.5 mg/ kg, i.p.) showed decreased survival (20%) on the 7 th day as compared to the control group (100%), whereas preadministration of lidocaine (8 mg/kg, i.v.) could significantly increase LPS-treated mouse survival rate. Besides, compared with the LPS group, preadministration of lidocaine (8 mg/kg, i.v.) could also increase the weight of mice from 24:4 ± 0:52 g to 26:43 ± 1:11 g (Figure 1 (b)). Moreover, it was found that LPS stimulation for 12 h significantly increased the ratio of wet-to-dry weight of mouse lung tissues from 4:52 ± 0:06 to 6:52 ± 0:76 ( Figure 1 (c)), and the B-mode ultrasound imaging also indicated that LPS significantly induce pulmonary edema in mice ( Figure 1 (d)), whereas these effects could be reversed by lidocaine (Figures 1(c) and 1(d)). Further study has found that in i.v. injection of 8 mg/kg of lidocaine into mice for 12 h, the plasma drug concentration reached the lung tissue of 370:3 ± 94:3 ng/mL ( Figure S1 and Table S1 ). In addition, through total protein quantification and flow cytometry detection, it was found that the total protein content in BALF and the number of neutrophils in the blood of LPS-treated mice were significantly increased, and these effects could be reversed by lidocaine (Figures 1(e) and 1(g)), indicating that lidocaine could alleviate LPS-induced severe alveolar leakage. These data suggested that lidocaine could significantly alleviate sepsis-induced ALI.

Coagulopathy. Many clinical studies showed that virtually most of septic patients had coagulation abnormalities. Therefore, in this study, we intend to investigate the effect of lidocaine on pulmonary coagulation function induced by LPS in mice. As shown in Figure 2 (Figure 2(c) ). Altogether, these results suggested that lidocaine could ameliorate LPS-induced pulmonary coagulation disorders.

Activity Induced by LPS in Plasma. Previous studies have found that the circulating blood in patients with sepsis presents a hypercoagulable state [21] , and Shaver et al. have also found that the severity of LPS-induced ALI is positively correlated with the level of TF in the circulating blood in mice [22] . In this study, we detected TF expression and MMP-2/9 activity in the plasma of LPS-treated mice. As shown in Figures 3(a) and 3(b) , compared with the control group, LPS (12.5 mg/kg, i.p.) significantly increased the expression level of TF, up to 6.6-fold, and the activities of MMP-2/9 in plasma were increased up to 2.92fold and 3.33-fold, respectively, whereas preadministration of lidocaine (4 and 8 mg/kg, i.p.) could reverse the LPS-induced upregulation of TF and MMP-2/9 in mice (Figures 3(a) and  3(b) ). In addition, lidocaine (8 mg/kg) could also significantly reduce the activity of MMP-2/9 in BALF of LPS-treated mice from 19.97-fold to 3.37-fold and from 13.76-fold to 5.87-fold, respectively (Figures 3(c) and 3(d) ).

Expression and MMP-2/9 Activity in the Lungs. We further investigated the signaling pathway of the LPS-induced high level of TF and MMP-2/9 in mice. It has been reported that ASK1 is crucial for the formation of thrombus [10] , and ASK1 activation may also increase the transcription level of TF mRNA through the MAPK signaling [3] . Compared with the LPS group, LPS could significantly induce the upregulation of p-ASK1 and p-p38 in the lungs of mice up to 2.45-fold and 2.87-fold, respectively, while lidocaine (4 and 8 mg/kg, i.p.) significantly inhibited the activation of ASK1 and p38 (Figures 4(a) and 4(b) ). In addition, LPS could also induce the expression of TF, HIF-1α, and MMP-2/9 in the lungs, whereas preadministration with 4 or 8 mg/kg of lidocaine could significantly inhibit these effects (Figures 4(c) and 4(f)). These data suggested that lidocaine could decrease the expression of TF, HIF-1α, and MMP-2/9 by inhibiting the ASK1-p38 signaling pathway. were collected 12 h after LPS given. Significant difference was revealed following one-way ANOVA ( * P < 0:05, * * P < 0:01, and * * * P < 0:001 vs. control; # P < 0:05 and ## P < 0:01 vs. LPS-treated group; Bonferroni post hoc tests). 6 Oxidative Medicine and Cellular Longevity 3.5. Lidocaine Significantly Increased the Expression of p-AMPK and SOCS3 In Vitro and In Vivo. Our previous studies showed that lidocaine could induce the expression of SOCS3 and inhibit neuroinflammation in an AMPKdependent manner [17] . Therefore, we also investigated whether lidocaine could activate AMPK and induce the production of SOCS3 in lung tissues of mice in vivo. Different concentrations of lidocaine (2, 4, and 8 mg/kg) were administrated to mice; data showed that lidocaine (4 and 8 mg/kg) significantly activated AMPK and induced SOCS3 expression in vivo (Figures 5(a) and 5(b) ). Moreover, we also performed corresponding experiments on THP1 cells in vitro. of each group) were collected 12 h after LPS given. Significant difference was revealed following one-way or two-way ANOVA ( * P < 0:05, * * P < 0:01, and * * * P < 0:001 vs. control; # P < 0:05 and ## P < 0:01 vs. LPS-treated group; Bonferroni post hoc tests). 7 Oxidative Medicine and Cellular Longevity the control group, the expression level of TF induced by LPS (100 ng/mL) was increased approximately 2-fold, and the activities of MMP-2/9 were increased nearly 15.7-fold and 5.6-fold, respectively. Moreover, THP1 cell pretreatment with lidocaine (50 μM) for 6 h could increase the expression level of p-AMPK and SOCS3 in vitro (Figures 6(c) and 6(d)), whereas preadministration of AMPK inhibitor (compound C, 10 μM) 30 min before LPS stimulation could significantly reduce the expression level of p-AMPK and SOCS3 from 2:01 ± 0:08 -fold to 1:35 ± 0:11-fold and from 2:01 ± 0:14-fold to 1:20 ± 0:18-fold, respectively (Figures 6(c) and 6(d)). Besides, lidocaine also effectively decreased the expression of p-ASK1, p-p38, and TF and the activity of MMP-2/9, while pretreatment with compound C (10 μM) could abolish the inhibition of lidocaine on these proteins (Figures 6(e)-6(i)).

In this study, we found that lidocaine could increase the survival rate and weight of LPS-treated mice and reduce the pulmonary edema. We also found that lidocaine could significantly reduce the formation of pulmonary thrombosis in LPS-treated mice, increase blood flow velocity in the subclavian artery, and ameliorate the histopathological damage. Further research show that lidocaine could significantly inhibit the LPS-induced activation of the ASK1-p38-TF/ MMP-2/9 signaling pathway in vivo and in vitro, which depends on AMPK-SOCS3 axis. These results indicated that lidocaine may alleviate sepsis-induced ALI by activating AMPK-SOCS3 axis to inhibit the ASK1-p38-TF/MMP-2/9 signaling pathway.

Acute lung injury (ALI) was first defined in 1967 [23] and characterized as excessive pulmonary inflammation, alveolar-capillary barrier disruption, and pulmonary edema [24] . Numerous studies have demonstrated that in the early stages of infection-induced sepsis ALI, circulating neutrophils infiltrate the lung interstitial and the alveolar cavity to clear microbial pathogens; however, sustained large neutrophil infiltrations could also exacerbate lung damage [25, 26] . There have also been reported that neutrophils have been detected in BALF of acute respiratory distress syndrome (ARDS)/ALI patients, and the number of neutrophils is positively correlated with the severity of lung injury prognosis [27, 28] , and the conditional knockout of neutrophils in LPS-treated mice could significantly reduce pulmonary edema and improve ALI [29] . In this study, we also found that the total protein content in BALF was significantly increased in LPS-treated mice (Figure 1(e) ), and a large number of neutrophils were detected in the blood (Figures 1(f) and 1(g) ). Besides, pathological tissue section results also found that a 9 Oxidative Medicine and Cellular Longevity large number of neutrophils infiltrated into the lung interstitial; interestingly, these effects could be reversed by lidocaine (Figure 2(c) ). Study showed that neutrophils could release a large number of inflammatory cytokines and MMPs [30] . MMPs are one of the endopeptidases that could specifically degrade extracellular matrix and chemical or physical barriers, (h, i) Activity of MMP-2/9 in the supernatants was measured by gelatin zymography, and the densitometry values were normalized. THP1 cells were pretreated with compound C (10 μM) for half an hour before lidocaine treatment, and then, cells were cultured with lidocaine (50 μM) for 6 h, followed by LPS treatment (100 ng/mL) for another 12 h. Then, the cells were collected and analyzed (n = 3 of each group). Significant difference was revealed following one-way or two-way ANOVA ( * P < 0:05, * * P < 0:01, and * * * P < 0:001 vs. control; # P < 0:05, ## P < 0:01, and ### P < 0:001 vs. LPS-treated group; $ P < 0:05 and $$ P < 0:01 vs. lidocaine and LPS-treated group; Bonferroni post hoc tests). Figure 7: Lidocaine-induced inflammation tolerance alleviates LPS-induced acute lung injury. LPS leads to upregulation of tissue factor (TF) and MMP-2/9 via the TLR4-ASK1-p38 signaling pathway and results in endothelial injury, a hypercoagulable state in the blood vessels, and robust inflammatory infiltration in the lung. Lidocaine pretreatment activates AMPK/SOCS3 axis, which induces inflammatory tolerance and alleviates acute lung injury in mice. 10 Oxidative Medicine and Cellular Longevity such as blood-brain barrier and vascular nerve barrier. Our previous study found that paraquat could significantly increase the activity of MMP-9 in the lung tissue of mice [29] , and evidences have also shown that MMP-9 could in turn exacerbate lung damage [31] . In this study, we also found that the activity of MMP-2/9 was increased in the plasma, BALF, and lung tissue of LPS-treated mice (Figures 3(b) , 3(c), and 3(d) and 4(e) and 4(f)), which may be the cause of alveolar capillary barrier disruption and pulmonary edema. Lidocaine that was administrated half an hour earlier could significantly reduce the activity of MMP-2/9 and alleviate pulmonary edema. In addition, it was also found that LPS could significantly increase the activity of MMP-2/9 in THP1 cells in vitro (Figure 6 (b)), and these effects could be reversed by lidocaine (Figures 6(h) and 6(i)). Previous study has indicated that coagulopathy appeared in the circulation of patients with sepsis [32, 33] , and clinical autopsy reports have also reported fibrin microthrombus in the alveoli and pulmonary vessels of patients with ARDS [34] . Inflammatory stimuli can induce a hypercoagulable state by inducing TF in monocytes and endothelial cells [35] . TF is responsible for triggering the clotting cascade in a variety of thrombotic disorders, thus using anticoagulants, such as tissue factor pathway inhibitor (TFPI) or antithrombin that may be useful in the treatment of ALI and ARDS. TFPI, as an endogenous inhibitor of TF, could directly inhibit activated factor X and, in a factor-dependent manner, produce feedback inhibition of the factor VIIa/TF complex. Evidences also indicated that the lower levels of TFPI are strongly correlated with organ dysfunction as well as worse outcome of severe sepsis [36] . However, activated MMP-9 can degrade TFPI, resulting in the imbalance between TF and TFPI [37] . In addition, the formation of thrombus in the microvascular circulation could also induce the increase of HIF-1α expression [38] [39] [40] , and studies have found that HIF-1α can also mediate the expression of MMP-9 [41] . These would further aggravate sepsisinduced ALI by forming a vicious cycle. In this study, our results showed that LPS could induce the formation of pulmonary thrombosis in LPS-treated mice and reduce blood flow velocity in the subclavian artery, whereas this effect could be abolished by lidocaine (Figures 2(a)-2(c) ). Besides, LPS could also significantly increase the expression of TF in the plasma and lung tissues of mice in the model group (Figures 3(a) and 4(c)), and this was also confirmed in THP1 cells in vitro (Figures 6(a) and 6(g)). However, preadministration of lidocaine significantly reduced the LPS-induced increasing of TF in plasma and lung tissue (Figures 3(a) and 4(c) ) and inhibited the expression of HIF-1α in lung tissue (Figure 4(d) ). Altogether, these data show that lidocaine could significantly inhibit the expression of TF and MMP-2/9 induced by LPS and reduce the formation of pulmonary thrombosis.

We further investigated the way how lidocaine exerted anti-inflammatory and anticoagulant effects to reduce ALI caused by sepsis. Previous studies have found that ASK1 is essential for the formation of thrombus, and conditional knockout of ASK1 or the use of pharmacologic inhibitors of ASK1 can significantly prolong the bleeding time of mice [10] . In addition, LPS can also induce the increase of TF expression by mediating the activation of the ASK1-p38 signaling pathway [3] . In this study, we also found that LPS significantly induce the expression of p-ASK1, p-p38, and TF in lung tissue, and preadministration of lidocaine at different concentrations (4 and 8 mg/kg) could inhibit these effects (Figures 4(a)-4(c) ). As an important negative regulator of cytokine signaling pathways, SOCS3 plays a vital role in a variety of inflammatory diseases, such as multiple sclerosis [42] , experimental autoimmune encephalomyelitis [43] , pain [15] , and airway inflammation [44] . Moreover, several studies have found that overexpression of SOCS3 could simultaneously inhibit a variety of inflammatory signals, including TLR4, TNF-R, IL-1R, and IL-6R [45, 46] . Additionally, our previous research also indicated that lidocaine could induce the upregulation of SOCS3, and using SOCS3 small interfering RNA to knockdown SOCS3 sufficiently abolished anti-inflammatory effects of lidocaine; besides, we also found that lidocaine induced upregulation of SOCS3 expression in an AMPK-dependent manner [17] , and recent studies have also attempted to use the anti-inflammatory cytokines, such as IL-4, IL-10, and IL-13, to inhibit TF expression in monocytes and protect against ALI [47] . In this study, we further investigated whether lidocaine can mediate AMPK activation and SOCS3 expression in LPS-induced acute lung injury model and whether lidocaine can alleviate LPS-mediated pulmonary edema, coagulation dysfunction, and inflammatory response. Our results show that lidocaine could significantly reduce the level of IL-1β, TNF-α, and IL-6 in the serum and lung tissue of LPS-treated mice ( Figure S2 ). Moreover, lidocaine could also significantly induce the expression of p-AMPK and SOCS3 in vitro and in vivo ( Taken together, these results indicate that lidocaine may promote the expression of SOCS3 in an AMPK-dependent manner, inhibiting the activation of the ASK1-p38-TF/MMP-2/9 signaling pathway to decrease the formation of thrombus and to alleviate sepsis-induced ALI (Figure 7) .

In conclusion, we provided the experimental evidence that lidocaine could alleviate sepsis-induced ALI via activating AMPK/SOCS3 axis to inhibit the ASK1-p38-TF/MMP-2/9 signaling pathway. Our findings further enriched the pathogenesis of ALI and provide a potential treatment for ALI.

The data used to support the findings of this study are available from the corresponding authors with reasonable request.

The authors declare no conflict of interest.

Coagulation abnormalities in acute lung injury and sepsis

SENP3 in monocytes/macrophages up-regulates tissue factor and mediates lipopolysaccharide-induced acute lung injury by enhancing JNK phosphorylation

Apoptosis signalregulating kinase 1-mediated signaling pathway regulates lipopolysaccharide-induced tissue factor expression in pulmonary microvasculature

Blockade of tissue factor: treatment for organ injury in established sepsis

Yesassociated protein (YAP) signaling regulates lipopolysaccharide-induced tissue factor expression in human endothelial cells

Inhibition of intravascular thrombosis in murine endotoxemia by targeted expression of hirudin and tissue factor pathway inhibitor analogs to activated endothelium

Physiological roles of ASK1-mediated signal transduction in oxidative stress-and endoplasmic reticulum stressinduced apoptosis: advanced findings from ASK1 knockout mice

Roles of MAPKKK ASK1 in stress-induced cell death

The lipid peroxidation product 4-hydroxy-2-nonenal induces tissue factor decryption via ROS generation and the thioredoxin system

Ask1 regulates murine platelet granule secretion, thromboxane A2 generation, and thrombus formation

Resveratrol inhibits LPSinduced inflammation through suppressing the signaling cascades of TLR4-NF-κB/MAPKs/IRF3

Ginsenoside Rb1 exerts antiinflammatory effects in vitro and in vivo by modulating Tolllike receptor 4 dimerization and NF-kB/MAPKs signaling pathways

4-O-Carboxymethylascochlorin inhibits expression levels of on inflammation-related cytokines and matrix metalloproteinase-9 through NF-kappaB/ MAPK/TLR4 signaling pathway in LPS-activated RAW264.7 cells

Suppressors of cytokine signaling and immunity

Induction of suppressor of cytokine signaling 3 via HSF-1-HSP70-TLR4 axis attenuates neuroinflammation and ameliorates postoperative pain

Local anesthetics inhibit tissue factor expression in activated monocytes via inhibition of tissue factor mRNA synthesis

Lidocaine alleviates morphine tolerance via AMPK-SOCS3-dependent neuroinflammation suppression in the spinal cord

Suppression of NLRP3 inflammasome by erythropoietin via the EPOR/JAK2/STAT3 pathway contributes to attenuation of acute lung injury in mice

Therapeutic Effect of the Tuber of Alisma orientale on Lipopolysaccharide-Induced Acute Lung Injury

Inhibitory functions of maslinic acid on particulate matter-induced lung injury through TLR4-mTOR-autophagy pathways

Coagulation and sepsis

Regulation of alveolar procoagulant activity and permeability in direct acute lung injury by lung epithelial tissue factor

Acute respiratory distress in adults

Acute respiratory distress syndrome

15-Epi-LXA4 and 17-epi-RvD1 restore TLR9-mediated impaired neutrophil phagocytosis and accelerate resolution of lung inflammation

Neutrophil adaptations upon recruitment to the lung: new concepts and implications for homeostasis and disease

Bronchoalveolar fluid and plasma inflammatory biomarkers in contemporary ARDS patients

Contribution of neutrophils to acute lung injury

Doxycycline alleviates paraquat-induced acute lung injury by inhibiting neutrophilderived matrix metalloproteinase 9

Neutrophils in the initiation and resolution of acute pulmonary inflammation: understanding biological function and therapeutic potential

Hirsutanol A attenuates lipopolysaccharide-mediated matrix metalloproteinase 9 expression and cytokines production and improves endotoxemia-induced acute sickness behavior and acute lung injury

The coagulopathy of acute sepsis

Effect of a recombinant human soluble thrombomodulin on mortality in patients with sepsis-associated coagulopathy: the SCARLET randomized clinical trial

Intravascular coagulation associated with the adult respiratory distress syndrome

Diagnostic and prognostic utility of tissue factor for severe sepsis and sepsis-induced acute lung injury

Sepsis-induced coagulation in the baboon lung is associated with decreased tissue factor pathway inhibitor

Matrix Metalloproteinases Cleave Tissue Factor Pathway Inhibitor

Overexpression of matrix metalloproteinase-9 promotes intravascular thrombus formation in porcine coronary arteries in vivo

Vascular responses to hypoxia and ischemia

Hypoxia-inducible factor-1 in arterial disease: a putative therapeutic target

Overexpression of MMP-9 and HIF-1α in breast cancer cells under hypoxic conditions

Signal transducer and activator of transcription-3/suppressor of cytokine signaling-3 (STAT3/SOCS3) axis in myeloid cells regulates neuroinflammation

Preferential recruitment of neutrophils into the cerebellum and brainstem contributes to the atypical experimental autoimmune encephalomyelitis phenotype

Resident alveolar macrophage-derived vesicular SOCS3 dampens allergic airway inflammation

SOCS3 negatively regulates IL-6 signaling in vivo

Suppressor of cytokine signaling-3 inhibits interleukin-1 signaling by targeting the TRAF-6/TAK1 complex

Inhibition of IL-1 induced tissue factor (TF) synthesis and procoagulant activity (PCA) in purified human monocytes by IL-4, IL-10 and IL-13

The authors would like to thank Dr. Xue 

The supplementary material for this article can be found online. Figure S1 : the plasma drug concentration of lidocaine at various time points. Figure S2 : lidocaine significantly suppressed LPS-induced inflammatory response in mice. Figure  S3 : lidocaine alleviated sepsis-induced acute lung injury via activating AMPK/SOCS3 axis to inhibit the ASK1-p38-TF/ MMP-2/9 signaling pathway in MLE-12 cells in vitro. Table  S1 : pharmacokinetic variables of lidocaine following i.v. administration of 8 mg/kg of lidocaine for 12 h to mice (mean ± SD, n = 3). (Supplementary Materials)