Molecular Medicine Reports Molecular Medicine Reports 1791-2997 1791-3004 D.A. Spandidos 10.3892/mmr.2021.12390 MMR-0-0-12390 Articles Tumor necrosis factor α-induced protein 8-like 2 contributes to penehyclidine hydrochloride pretreatment against lipopolysaccharide-induced acute lung injury in a mouse model YuanMin 1 * JingGuoqing 2 * KongQian 1 MingTingqian 1 SongXuemin 2 WuXiaojing 1 Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China Department of Anesthesiology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China Correspondence to: Professor Xuemin Song, Department of Anesthesiology, Zhongnan Hospital of Wuhan University, 169 East Lake Road, Wuhan, Hubei 430071, P.R. China, E-mail: xueminsong@whu.edu.cn Professor Xiaojing Wu, Department of Anesthesiology, Renmin Hospital of Wuhan University, 238 Liberation Road, Wuhan, Hubei 430060, P.R. China, E-mail: rm000851@whu.edu.cn

Contributed equally

 11 2021 31 08 2021 24 5 750 12112020 12032021 Copyright © 2021, Spandidos Publications 2021

The aim of the present study was to investigate the effect of penehyclidine hydrochloride (PHC) pretreatment on mice with lipopolysaccharide (LPS)-induced acute lung injury (ALI) and its possible underlying mechanisms. Mice were randomly separated into six groups: i) Sham group; ii) LPS group; iii) LPS + PHC group; iv) tumor necrosis factor a-induced protein 8-like protein 2 (TIPE2) group; v) LPS + TIPE2 group; and vi) LPS + TIPE2 + PHC group. The ALI model was induced using LPS through intratracheal injection. The mice received adenovirus gene to induce the overexpression of TIPE2. After mice were sacrificed, lung injury indices were assessed, and arterial blood, bronchoalveolar lavage fluid and lung tissues were collected for subsequent assays. Expression levels of related proteins were detected by using western blotting. It was found that compared with the sham group, the mice treated with LPS showed increased lung injury and dysfunctions of gas exchange. However, these trends were significantly ameliorated in the LPS + PHC group. Evaluation of protein expression in lung tissues showed that the increased expression of nuclear NF-κB p65 and p-c-Jun N-terminal kinase (JNK) induced by LPS were suppressed in the LPS + PHC group and the expression of TIPE2 was increased. The mice that received adenovirus gene to induce TIPE2 overexpression could also showed protective effects compared with the mice in the LPS group. However, the expression of TIPE2 decreased rather than increased in LPS group. In the mice pretreated with PHC, the expression of TIPE2 increased in mice with LPS-induced ALI. To conclude, PHC pretreatment could inhibit the occurrence of inflammation and apoptosis in LPS-induced ALI. This process may be related to the activation of TIPE2 and the inhibition of NF-κB and JNK signaling pathway in the lungs of mice.

 acute lung injury tumor necrosis factor α-induced protein 8-like protein 2 penehyclidine hydrochloride inflammation NF-κB c-Jun N-terminal kinase National Natural Science Foundation of Chinahttp://dx.doi.org/10.13039/501100001809 81571941 81901952 This study was supported by the National Natural Science Foundation of China (grant nos. 81571941 and 81901952). Introduction

Acute lung injury (ALI) refers to acute hypoxic respiratory dysfunction induced by various direct or interconnecting injury factors, such as pneumonia, pyemia, reperfusion injury and shock (1). In severe cases, it can develop into acute respiratory distress syndrome (ARDS), which is associated with severe symptoms such as disruption of the alveolar epithelial barrier, proteinaceous pulmonary edema, acute inflammation and abnormalities in gas exchange (2). The pathophysiology of ALI is a complex process that includes the recruitment of neutrophils, increased numbers of inflammatory cytokines and the apoptosis of epithelial cells (3,4). In previous years, the morbidity and mortality rates of ALI/ARDS are still high despite improved knowledge on these conditions and treatment methods (5,6). In clinical settings, the occurrence of ALI is often unpredictable, therefore, exploring potential effective pretreatments to reduce the risk of ALI is necessary. Sepsis induced by lipopolysaccharide (LPS) release is one of the most common injury factors in the induction of ALI/ARDS (7,8). The inflammatory responses activated by LPS via binding to Toll-like receptors (TLRs) are the underlying mechanism of lung injury in patients with ALI (9–11). Therefore, finding more effective methods of targeting specific biomarkers are needed to reduce inflammatory responses and alleviate cell apoptosis.

Tumor necrosis factor (TNF) α-induced protein 8-like protein 2 (TNFAIP8/TIPE2) are a family of proteins that play essential roles as negative regulators of inflammation and immune homeostasis (12). As a member of the TNFAIP8 family, TIPE2 can also play an anti-inflammatory role by negatively regulating T cell receptor (TCR) and TLR signaling (13). Previous reports have stated that TIPE2 can negatively regulate TCR and TLR signaling via binding to caspase-8 and inhibiting the activation of protein-1 (AP-1) and NF-κB (14,15). Furthermore, the depletion of TIPE2 can cause significantly increased levels of inflammatory mediators and severe inflammatory disease (16,17). Furthermore, binding of LPS to TLR4 has been found to lead to the excessive release of pro-inflammatory cytokines through promoting the activation of NF-κB and c-Jun N-terminal kinase (JNK) (18), the release of these inflammatory mediators can eventually cause serve lung injury in ALI (19). In our previous experiments, we observed the expression of TIPE2 in lung epithelial cells and macrophages. Immunohistochemical staining of TIPE2 protein expression in the lung showed that the expression of TIPE2 protein was significantly increased in the alveolar epithelium after adeno-associated virus-TIPE2 administration and adeno-associated virus-mediated TIPE2 overexpression remarkably inhibited inflammation and cell apoptosis induced by LPS (20). Thus, this evidence suggests that TIPE2 may have therapeutic implications in LPS-induced ALI.

Penehyclidine hydrochloride (PHC) is a common drug used in surgery that plays a significant role in inhibiting the secretion of salivary and airway glands through intravenous infusion prior to anesthesia (21). Several previous studies have confirmed that PHC exerts protective effects in the treatment of ALI. Treatment with PHC has been found to relieve LPS-induced pulmonary impairment and block LPS-mediated lung apoptosis (22), furthermore, it has been observed that ARDS rats administrated with PHC showed reduced inflammatory factor production and lipid peroxidation (23). Additionally, PHC also been shown to exert a notable effect on inhibiting the TLR4 signaling pathway in traumatic lung injury (24). In a previous study, we found that pulmonary microvascular endothelial apoptosis and lung damage induced by LPS could be inhibited through blocking the JNK and NF-κB signaling pathway (25,26), whereas TIPE2 and PHC could both be used to block p38 MAPK and NF-κB pathways in microglia (15,24,27). Therefore, we speculated that there is an association and underlying mechanism that exists between TIPE2 and PHC treatment in the prevention and treatment of ALI. Thus, the present study investigated the potential effect of TIPE2 in the treatment of ALI with PHC by measuring the degree of lung injury and related protein expression.

 Materials and methods <sec> <title>Animal preparation

All animals received humane care in compliance with the Principles of Laboratory Animal Care (28). The experimental protocol was approved by the Animal Care and Use Committee of the Medical Ethics Committee of Renmin Hospital of Wuhan University (Wuhan, China).

Adult male BALB/c mice (age, 6–8 weeks old; weight, ~20±5 g) were housed in conditions with a controlled temperature (20–24°C) and humidity (40–60%), with a 12-h light/dark cycle and access to food and water ad libitum. A total of 60 mice were randomly divided into the following six groups: i) Sham group; ii) LPS group (group LPS), the mice received an intraperitoneal injection with LPS to establish the ALI model at a dose of 5 mg/kg (9); iii) LPS + PHC group (group P+LPS), the mice received intraperitoneal injection with PHC at a dose of 2 mg/kg (24) before the ALI model was established; iv) TIPE2 group (group TIPE2), the mice received adenovirus gene to induce the overexpression of pulmonary TIPE2; v) LPS + TIPE2 group (group T+LPS); and vi) LPS + TIPE2 + PHC group (group T+LPS+P). LPS was purchased from Sigma-Aldrich (Merck KGaA) and PHC was from Chengdu List Pharmaceutical Co., Ltd.

 Surgical procedure and animal treatment

All surgical procedures were performed under anesthesia using an intraperitoneal injection of pentobarbital sodium at a dose of 50 mg/kg (Sigma-Aldrich; Merck KGaA). Following anesthesia, the animals were injected with LPS (intratracheal). The sham group mice were intratracheally administered with sterile phosphate-buffered saline (PBS) as controls. For the last three groups, BALB/c mice were given recombinant adeno-associated virus of pAAV-FLAG-mTIPE2-IRES-ZsGREEN (Han Heng Biotechnology Co., Ltd.) via intratracheal administration to induce TIPE2 overexpression before LPS administration. The adeno-associated virus that expressed no transgene was used as a negative control. Sham group mice were treated with the control adeno-associated virus.

 Histological examination

A total of 24 h after LPS treatment, the mice were euthanized with excessive pentobarbital sodium (100 mg/kg; intraperitoneal injection). Animal death was confirmed by observation of apnea and asystole. After mice were sacrificed, the lung tissues were collected to observe lung histopathology. The whole lung lobes were fixed with 4% (v/v) paraformaldehyde at 4°C for 48 h. Then, the tissues were embedded in paraffin and sectioned into 4-mm thick slices. Hematoxylin and eosin (H&E)-stained slides were prepared with H&E solution (Sigma-Aldrich; Merck KGaA) for 3 min at room temperature. Subsequently, slides were observed under a light microscope (magnification, ×200; BX51; Olympus Corporation) to observe morphological changes in the lung tissues. The degree of lung injury was scored from 0 to 4 according to the levels of inflammation in alveolar and peribronchial lesions (23).

 Lung water content measurement

The right lung tissues were immediately removed after the chests of the mice were opened. The tissues were then blotted to remove any excess blood and weighed for the wet weight. Following dehydration at 65°C in a drying oven for 48 h, tissues were reweighed to obtain the dry weight. The wet/dry ratio was calculated as an index for pulmonary edema.

 Lung neutrophils, protein concentration and proinflammatory cytokines in bronchoalveolar lavage fluid (BALF)

The lungs of mice were washed with ice-cold PBS to obtain the BALF. The BALF samples were centrifuged at 1,000 × g for 15 min at 4°C for subsequent assays. A hemocytometer was used to count the total inflammatory cells in the BALF. To analyze differential cell counting, Wright's Stain solution (Sigma-Aldrich; Merck KGaA) was used to stain the cells for 2 min at room temperature, and the number of polymorphonuclear neutrophils (PMNs) was counted according to the staining results. Myeloperoxidase (MPO) activity was determined using the MPO Activity Assay kit (cat. no. A044-1-1; Nanjing Jiancheng Bioengineering Institute) and the specific value was expressed as unit/mg tissue. The levels of proinflammatory cytokines, such as TNF-α, IL-6 and IL-1β, in the BALF were determined using commercially available enzyme-linked immunosorbent assay kits (IL-1β, cat. no. RLB00; IL-6, cat. no. R6000B; TNF-α, cat. no. RTA00; R&D Systems, Inc.).

 Arterial blood gas analysis

At the end of the surgical procedure, appropriate amounts of blood samples were extracted from the arteries of mice in each group and these samples were injected into an ABL700 Radiometer (Radiometer America) to determine pH values, partial pressure of oxygen (PaO2), PaO2/fraction of inspired oxygen (FiO2) and partial pressure of carbon dioxide (PaCO2). These indicators were used to analyze the gas exchange function in the lungs of mice from different groups.

 Western blotting

Lung tissues stored at −80°C were crushed and mixed with RIPA lysate buffer (Sigma-Aldrich; Merck KGaA) to extract proteins. Equal amounts of proteins (30 µg) were separated via 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and then separated proteins were transferred to polyvinylidene difluoride membranes. Following which, membranes were blocked with 5% skimmed milk for 2 h at room temperature, and then incubated at 4°C overnight with the following primary antibodies: Anti-cleaved caspase 9 (1:1,000; cat. no. 9507; Cell Signaling Technology, Inc.), anti-cleaved caspase 3 (1:1,000; cat. no. 9661; Cell Signaling Technology, Inc.), anti-Bax (1:2,000; cat. no. ab32503; Abcam), anti-Bcl-2 (1:1,000; cat. no. ab196495; Abcam), anti-phosphorylated (p)-JNK (1:1,000; cat. no. 4668; Cell Signaling Technology, Inc.), anti-JNK (1:1,000; cat. no. 9252; Cell Signaling Technology, Inc.), anti-TIPE2 (1:1,000; cat. no. DF3326; Affinity Biosciences), anti-β-actin (1:1,000; cat. no. 8457; Cell Signaling Technology, Inc.), anti-NF-κB p65 (1:1,000; cat. no. ab16502; Abcam) and anti-Lamin A (1:1,000; cat. no. ab26300; Abcam). The next day the membranes were incubated with a horseradish peroxidase-labeled secondary antibody (1:2,000; cat. no. 7074; Cell Signaling Technology, Inc.) for 2 h at room temperature. Subsequently, the protein bands were visualized using an ECL detection kit (Thermo Fisher Scientific, Inc.) in the dark, according to the manufacturer's instructions. The expression levels of relevant proteins were analyzed by Image Lab software (version 5.2.1; Bio-Rad Laboratories, Inc.).

 Statistical analysis

All experiments were repeated in triplicate. The data are presented as the mean ± standard deviation. Data analysis was performed using SPSS 17.0 software (SPSS, Inc.) with one-way ANOVA followed by the Tukey-Kramer post hoc test. P<0.05 was considered to indicate a statistically significant difference.

 Results <sec> <title>PHC pretreatment and TIPE2 overexpression ameliorates lung injury in mice with ALI

The pathological changes in lung tissues, degree of pulmonary inflammation and the survival rate of mice in different groups were compared to evaluate the degree of lung injury. Pathological changes of lung tissues were examined by H&E staining. In the sham and TIPE2 groups, the structure of pulmonary alveoli was complete and the alveolar wall was smooth without obvious exudation of pulmonary stroma. Whereas, in the LPS group, there was an increased number of infiltrated neutrophils, the septum was wider and thicker, and alveolar wall edema was observed; however, alveolar wall edema and neutrophil infiltration were notably alleviated in the P+LPS and T+LPS groups (Fig. 1A). Overall, lung injury score in these groups were significantly decreased compared with the LPS group (P<0.05; Fig. 1B). In the T+LPS+P group, treatment with PHC and TIPE2 overexpression at the same time led to an increased protective effect compared with PHC or TIPE2 alone (P+LPS group vs. T+LPS+P group, P<0.05; T+LPS group vs. T+LPS+P group, P<0.05; Fig. 1A and B).

The ratio of PMNs to total cells in the BALF, BALF protein content, MPO activity and lung wet/dry ratio were analyzed at 24 h after LPS injection. Results of data analysis indicated that all these values were significantly increased in the LPS group compared with the sham group (P<0.05), but this trend was partially inhibited in the T+LPS, P+LPS and T+LPS+P groups (P<0.05; Fig. 1C-F).

 PHC pretreatment and TIPE2 overexpression improves gas exchange in the lungs of LPS-induced mice

Gas analysis of arterial blood showed a significant decrease in PaO2 and an increase in PaCO2 in the LPS group (P<0.05; Fig. 2B and C). Similarly, the pH and PaO2/FiO2 ratio in arterial blood were decreased in the LPS group compared with the sham group (P<0.05; Fig. 2A and D). In the T+LPS, P+LPS and T+LPS+P groups, the dysfunction of gas exchange induced by LPS stimulation was partially reversed (P<0.05; Fig. 2A-D).

 PHC pretreatment and TIPE2 overexpression attenuates the expression of pro-inflammatory cytokines

As one of the most important cytokines in the induction of ALI, TNF-α has a synergistic effect with IL-6 and IL-1β in ALI development. According to the present study, it was found that the expression levels of these cytokines were significantly increased in the LPS group. Furthermore, compared with the mice in the LPS group, the expression levels of these cytokines were significantly downregulated in the T+LPS, P+LPS and T+LPS+P groups (P<0.05; Fig. 3A-C).

 Effects of PHC pretreatment and TIPE2 overexpression on the expression of different proteins in the lung tissues of mice

Mice were humanely sacrificed and the expression levels of related proteins were determined via western blotting (Fig. 4A). As shown in Fig. 4, the expression levels of pro-apoptotic proteins, such as Bax, cleaved caspase 3 and cleaved caspase 9, in mice lung tissue increased in the LPS group compared with the sham group (P<0.05; Fig. 4B, E and F), whereas the expression levels of anti-apoptotic Bcl-2 decreased compared with the sham group (P<0.05; Fig. 4C). In addition, the ratio of Bax/Bcl-2 increased in the LPS group compared with the sham group (P<0.05; Fig. 4I). These expression changes were partially reversed in the T+LPS and P+LPS groups, and most significantly reversed in the T+LPS+P group (P<0.05; Fig. 4B, C, E, F and I). In addition, the expression levels of NF-κB p65 and phosphorylated JNK increased (P<0.05; Fig. 4G and H), and the expression of TIPE2 decreased, in mice in the LPS group compared with the sham group (P<0.05; Fig. 4D). The expression levels of NF-κB p65 and p-JNK decreased (P<0.05; Fig. 4G and H), and the expression of TIPE2 increased (P<0.05; Fig. 4D), in mice in the T+LPS, P+LPS and T+LPS+P groups compared with the LPS group.

 Discussion

The pathological changes of ALI are mainly associated with alveolar damage and the release of neutrophil and inflammatory cytokines (29). At present, no specific drugs are used for the treatment of ALI (1). In addition to controlling the primary disease, inhibiting systemic inflammation is an important measure to prevent and treat ALI (30). In the present study, it was found that LPS stimulation could worsen histological changes of lung tissues and dysfunctions of gas exchange.

PHC is a novel anticholinergic drug that can inhibit biomembrane lipid peroxidation and decrease the levels of cytokines and oxyradicals in patients with sepsis (31). Previous research has demonstrated that PHC plays a protective role against sepsis through inhibiting the expression of inflammatory factors and inducible nitric oxide synthase mRNA (32). Some previous studies (33,34) have shown that it plays a protective role in ischemia-reperfusion injury, but the role in transplant surgery has not yet been reported in the literature, thus the related dosage and clinical effects need to be further investigated. A study reported that the protective effect of PHC may involve the inhibition of NF-κB activation via inhibition of the p38MAPK and ERK signaling pathways (35). In the present study, it was found that PHC pretreatment ameliorated pulmonary edema in mice with LPS-induced ALI, as evaluated by a significant decrease in the lung wet/dry ratio. At the same time, PMNs/total cells and total protein concentration in the BALF, which are the common indicators to detect pulmonary vascular permeability (36), were significantly increased in LPS group and decreased in the P+LPS group. PHC pretreatment also alleviated lung histological damage and improved gas exchange dysfunction induced by LPS. TNF-α is the earliest proinflammatory factor that plays a central role in stress response and is the initiator of the occurrence and development of ALI (37). The present results showed that PHC could significantly inhibit the expression of TNF-α, IL-6 and IL-1β, which indicated that PHC has anti-inflammatory properties. At the same time, PHC pretreatment could decrease the Bax/Bcl-2 ratio, as well as the expression of cleaved caspase 3 and cleaved caspase 9 protein, indicating a potential antiapoptotic effect. Recent studies have also demonstrated that PHC can decrease the expression of phosphorylated JNK in mice and rats with cerebral ischemia-reperfusion and myocardial ischemia-reperfusion injury, and provided protective effects in the brain (38) and heart (39), respectively, which is consistent with the present experimental results in the lung tissues of mice.

TIPE2 is predominantly expressed in immune cells of the myeloid and lymphoid lineages (40), which provides TIPE2 with an important role in the maintenance of immune homeostasis (41). Therefore, the abnormal expression of TIPE2 can lead to diseases such as systemic autoimmunity, diabetic nephropathy and hepatitis B in humans (42). In the present study, it was demonstrated that TIPE2 overexpression could inhibit the expression of TNF-α, IL-6 and IL-1β compared with the LPS group, which was concomitant with a decrease in NF-κB activation. Some studies have found that TIPE2 is a negative regulator of MAPK and NF-κB signaling pathways (14,15), However, the underlying mechanisms are currently unknown. Thus, the present study explored the expression of related proteins and the underlying relationship between them. It was found that TIPE2 overexpression significantly reduced the expression of pro-apoptotic proteins such as Bax, cleaved caspase-9, cleaved caspase-3 and p-JNK, at the same time, the expression of anti-apoptotic protein Bcl-2 was increased. These data suggested that the effect of TIPE2 overexpression on cell apoptosis may be associated with suppression of JNK activation. Furthermore, treatment with PHC and TIPE2 overexpression at the same time led to a more obvious protective effect compared with PHC or TIPE2 alone. In our previous experiment, we found that TIPE2 overexpression markedly inhibited inflammation and cell apoptosis induced by LPS (20), and the present results suggested that the expression of TIPE2 was increased after the mice received intraperitoneal injection with PHC. These findings indicate that TIPE2 may be linked to the protective mechanism of PHC in mice with LPS-induced ALI.

In the present study, LPS-induced ALI in mice led to the increased expression of NF-κB and promoted the activation of JNK protein, subsequently causing the excessive release of pro-inflammatory cytokines and the activation of pro-apoptotic proteins, which was inhibited following PHC pretreatment-induced upregulation of TIPE2 expression. TIPE2 can negatively regulate TLR signaling, thereby inhibiting activation of NF-κB and JNK and reducing apoptosis (20). Thus, based on these findings, it was speculated that PHC inhibits these effects by upregulating the expression of TIPE2, thereby alleviating lung inflammation and apoptosis. The current study preliminarily investigated the effects of TIPE2 and PHC drug treatment on mice with LPS-induced ALI. However, the specific underlying mechanism of PHC treatment on TIPE2 expression also needs to be verified by knockout mice. At present, we have carried out the cultivation of gene knockout mice, but the number of mice was not enough to be included in the present study, so research on specific pathways will be investigated in future research.

In conclusion, the present study provided evidence that TIPE2 contributes to the protective effects of PHC pretreatment against LPS-induced ALI through decreasing the expression of NF-κB and inhibiting the activation of JNK in the lungs of mice. However, the potential underlying mechanisms will be further elucidated in depth in the future through the use of gene knockout mice.

 Acknowledgements

Not applicable.

 Funding

This study was supported by the National Natural Science Foundation of China (grant nos. 81571941 and 81901952).

 Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

 Authors' contributions

XMS and XJW participated in the design of the study and reviewed the manuscript. MY and QK carried out the experiments. GQJ and TQM performed the data analyses. MY wrote and revised the manuscript. XMS and XJW confirm the authenticity of all the raw data. All authors read and reviewed the final manuscript.

 Ethics approval and consent to participate

Ethics approval was provided by the Medical Ethics Committee of Renmin Hospital of Wuhan University (Wuhan, China). All surgical procedures were performed in accordance with Wuhan University Animal Care and Use committee.

 Patient consent for publication

Not applicable.

 Competing interests

The authors declare that they have no competing interests.

 References HodderRCritical care in the ED: Potentially fatal asthma and acute lung injury syndromeOpen Access Emerg Med45368201227147862 GalaniVTatsakiEBaiMKitsoulisPLekkaMNakosGKanavarosPThe role of apoptosis in the pathophysiology of acute respiratory distress syndrome (ARDS): An up-to-date cell-specific reviewPathol Res Pract206145150201010.1016/j.prp.2009.12.00220097014 LinSWuHWangCXiaoZXuFRegulatory T cells and acute lung injury: Cytokines, uncontrolled inflammation, and therapeutic implicationsFront Immunol91545201810.3389/fimmu.2018.0154530038616 BhatiaMZemansRLJeyaseelanSRole of chemokines in the pathogenesis of acute lung injuryAm J Respir Cell Mol Biol46566572201210.1165/rcmb.2011-0392TR22323365 XieKYuYHuangYZhengLLiJChenHHanHHouLGongGWangGMolecular hydrogen ameliorates lipopolysaccharide-induced acute lung injury in mice through reducing inflammation and apoptosisShock37548555201210.1097/SHK.0b013e31824ddc8122508291 EricksonSEMartinGSDavisJLMatthayMAEisnerMDNIH NHLBI ARDS NetworkRecent trends in acute lung injury mortality: 1996–2005Crit Care Med3715741579200910.1097/CCM.0b013e31819fefdf19325464 KangelarisKNPrakashALiuKDAouizeratBWoodruffPGErleDJRogersASeeleyEJChuJLiuTIncreased expression of neutrophil-related genes in patients with early sepsis-induced ARDSAm J Physiol Lung Cell Mol Physiol308L1102L1113201510.1152/ajplung.00380.201425795726 ChuangCYChenTLCherngYGTaiYTChenTGChenRMLipopolysaccharide induces apoptotic insults to human alveolar epithelial A549 cells through reactive oxygen species-mediated activation of an intrinsic mitochondrion-dependent pathwayArch Toxicol85209218201110.1007/s00204-010-0585-x20848084 FoncecaAMZoskyGRBozanichEMSutantoENKicicAMcNamaraPSKnightDASlyPDTurnerDJStickSMAccumulation mode particles and LPS exposure induce TLR-4 dependent and independent inflammatory responses in the lungRespir Res1915201810.1186/s12931-017-0701-z29357863 SunKHuangRYanLLiDTLiuYYWeiXHCuiYCPanCSFanJYWangXHanJYSchisandrin attenuates lipopolysaccharide-induced lung injury by regulating TLR-4 and Akt/FoxO1 signaling pathwaysFront Physiol91104201810.3389/fphys.2018.0110430177885 DingXTongYJinSChenZLiTBilliarTRPittBRLiQZhangLMMechanical ventilation enhances extrapulmonary sepsis-induced lung injury: Role of WISP1-αvβ5 integrin pathway in TLR4-mediated inflammation and injuryCrit Care22302201810.1186/s13054-018-2237-030445996 BordoloiDBanikKShabnamBPadmavathiGMonishaJArfusoFDharmarajanAMaoXLimLHKWangLTIPE family of proteins and its implications in different chronic diseasesInt J Mol Sci192974201810.3390/ijms1910297430274259 LouYLiuSThe TIPE (TNFAIP8) family in inflammation, immunity, and cancerMol Immunol4947201110.1016/j.molimm.2011.08.00621924498 OhoMNakanoRNakayamaRSakuraiWMiyamotoAMasuhiroYHanazawaSTIPE2 (Tumor Necrosis Factor α-induced Protein 8-like 2) is a novel negative regulator of TAK1 signalJ Biol Chem2912265022660201610.1074/jbc.M116.73345127601471 ZhangYMeiSZhouYYangDPanTChenZWangQTIPE2 negatively regulates mycoplasma pneumonia-triggered immune response via MAPK signaling pathwaySci Rep713319201710.1038/s41598-017-13825-y29042627 XiaoHTLiaoZTongRSPenehyclidine hydrochloride: A potential drug for treating COPD by attenuating Toll-like receptorsDrug Des Devel Ther6317322201210.2147/DDDT.S3655523139625 SunHGongSCarmodyRJHilliardALiLSunJKongLXuLHilliardBHuSTIPE2, a negative regulator of innate and adaptive immunity that maintains immune homeostasisCell133415426200810.1016/j.cell.2008.03.02618455983 ChenCWangYZhangZWangCPengMToll-like receptor 4 regulates heme oxygenase-1 expression after hemorrhagic shock induced acute lung injury in mice: Requirement of p38 mitogen-activated protein kinase activationShock31486492200910.1097/SHK.0b013e318188f7e118827744 ChambersERoundsSLuQPulmonary endothelial cell apoptosis in emphysema and acute lung injuryAdv Anat Embryol Cell Biol2286386201810.1007/978-3-319-68483-3_429288386 WuXKongQZhanLQiuZHuangQSongXTIPE2 ameliorates lipopolysaccharide-induced apoptosis and inflammation in acute lung injuryInflamm Res68981992201910.1007/s00011-019-01280-631486847 HanXYLiuHLiuCHWuBChenLFZhongBHLiuKLSynthesis of the optical isomers of a new anticholinergic drug, penehyclidine hydrochloride (8018)Bioorg Med Chem Lett1519791982200510.1016/j.bmcl.2005.02.07115808451 WengJChenMLinQChenJWangSFangDPenehyclidine hydrochloride defends against LPS-induced ALI in rats by mitigating endoplasmic reticulum stress and promoting the Hes1/Notch1 pathwayGene721144095201910.1016/j.gene.2019.14409531476403 LiHQianZLiJHanXLiuMEffects of early administration of a novel anticholinergic drug on acute respiratory distress syndrome induced by sepsisMed Sci Monit17BR319BR325201110.12659/MSM.88204122037734 WuXJLiuHMSongXMZhaoBLengYWangEYZhanLYMengQTXiaZYPenehyclidine hydrochloride inhibits TLR4 signaling and inflammation, and attenuates blunt chest trauma and hemorrhagic shock-induced acute lung injury in ratsMol Med Rep1763276336201829488614 LiYCaoYZengZLiangMXueYXiCZhouMJiangWAngiotensin-converting enzyme 2/angiotensin-(1–7)/Mas axis prevents lipopolysaccharide-induced apoptosis of pulmonary microvascular endothelial cells by inhibiting JNK/NF-kB pathwaysSci Rep58209201510.1038/srep0820925644821 ZekeAMishevaMRemenyiABogoyevitchMAJNK signaling: Regulation and functions based on complex protein-protein partnershipsMicrobiol Mol Biol Rev80793835201610.1128/MMBR.00043-1427466283 HuangCHeJChenYZhangYChenCPenehyclidine hydrochloride inhibits the LPS-induced inflammatory response in microgliaJ Surg Res188260267201410.1016/j.jss.2013.12.01124439132 National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory AnimalsGuide for the Care and Use of Laboratory Animals, 8th editionNational Academies Press (US)Washington (DC)2011 Z'GraggenBRTornicJMuller-EdenbornBReyesLBooyCBeck-SchimmerBAcute lung injury: Apoptosis in effector and target cells of the upper and lower airway compartmentClin Exp Immunol161324331201020456415 StandifordTJWardPATherapeutic targeting of acute lung injury and acute respiratory distress syndromeTransl Res167183191201610.1016/j.trsl.2015.04.01526003524 WangYGaoYMaJPleiotropic effects and pharmacological properties of penehyclidine hydrochlorideDrug Des Devel Ther1232893299201810.2147/DDDT.S17743530323561 ZhanJWangYWangCLiJZhangZJiaBProtective effects of penehyclidine hydrochloride on septic mice and its mechanismShock28727732200710.1097/shk.0b013e31805565b117621260 LiuZLiYYuLChangYYuJPenehyclidine hydrochloride inhibits renal ischemia/reperfusion-induced acute lung injury by activating the Nrf2 pathwayAging (Albany NY)121340013421202010.18632/aging.10344432652517 WangYLinDTanHGaoYMaJPenehyclidine hydrochloride preconditioning provides pulmonary and systemic protection in a rat model of lung ischaemia reperfusion injuryEur J Pharmacol839111201810.1016/j.ejphar.2018.09.01230201378 ShenWGanJXuSJiangGWuHPenehyclidine hydrochloride attenuates LPS-induced acute lung injury involvement of NF-kappaB pathwayPharmacol Res60296302200910.1016/j.phrs.2009.04.00719386282 XingJYuZZhangXLiWGaoDWangJMaXNieXWangWEpicatechin alleviates inflammation in lipopolysaccharide-induced acute lung injury in mice by inhibiting the p38 MAPK signaling pathwayInt Immunopharmacol66146153201910.1016/j.intimp.2018.11.01630453148 LiuSFengGWangGLLiuGJp38MAPK inhibition attenuates LPS-induced acute lung injury involvement of NF-kappaB pathwayEur J Pharmacol584159165200810.1016/j.ejphar.2008.02.00918328478 ShuYYangYZhangPNeuroprotective effects of penehyclidine hydrochloride against cerebral ischemia/reperfusion injury in miceBrain Res Bull121115123201610.1016/j.brainresbull.2016.01.00826802510 FengMWangLChangSYuanPPenehyclidine hydrochloride regulates mitochondrial dynamics and apoptosis through p38MAPK and JNK signal pathways and provides cardioprotection in rats with myocardial ischemia-reperfusion injuryEur J Pharm Sci121243250201810.1016/j.ejps.2018.05.02329860115 PadmavathiGBanikKMonishaJBordoloiDShabnamBArfusoFSethiGFanLKunnumakkaraABNovel tumor necrosis factor-α induced protein eight (TNFAIP8/TIPE) family: Functions and downstream targets involved in cancer progressionCancer Lett432260271201810.1016/j.canlet.2018.06.01729920292 FreundtECBidereNLenardoMJA different TIPE of immune homeostasisCell133401402200810.1016/j.cell.2008.04.01718455981 ZhangSZhangYWeiXZhenJWangZLiMMiaoWDingHDuPZhangWExpression and regulation of a novel identified TNFAIP8 family is associated with diabetic nephropathyBiochim Biophys Acta180210781086201010.1016/j.bbadis.2010.08.00320699119

PHC pretreatment and TIPE2 overexpression ameliorates lung injury in mice with acute lung injury. (A) Histological assessments of lung tissues under light microscope. Scale bar, 100 µm. (B) The corresponding lung injury score. (C) The wet/dry weight ratio. (D) Protein concentration in the BALF. (E) PMNs/total cells in the BALF. (F) MPO activity. n=8/group. *P<0.05 vs. sham group; #P<0.05 vs. LPS group; &P<0.05 vs. T+LPS group; !P<0.05 vs. P+LPS group. PHC/P, penehyclidine hydrochloride; TIPE2/T, tumor necrosis factor α-induced protein 8-like protein 2; BALF, bronchoalveolar lavage fluid; MPO, myeloperoxidase; PMNs, polymorphonuclear neutrophils; LPS, lipopolysaccharide.

PHC pretreatment and TIPE2 overexpression improves gas exchange in the lungs of mice. Arterial blood gas analysis was performed to determine (A) pH, (B) PaO2, (C) PaCO2, (D) PaO2/FiO2. n=8/group. *P<0.05 vs. sham group; #P<0.05 vs. LPS group; &P<0.05 vs. T+LPS group; !P<0.05 vs. P+LPS group. PHC/P, penehyclidine hydrochloride; TIPE2/T, tumor necrosis factor α-induced protein 8-like protein 2; LPS, lipopolysaccharide; PaO2, partial pressure of oxygen; FiO2, fraction of inspired oxygen; PaCO2, partial pressure of carbon dioxide.

PHC pretreatment and TIPE2 overexpression attenuates the expression of pro-inflammatory cytokines. The BALF concentrations of (A) TNF-α, (B) IL-6 and (C) IL-1β. n=8/group. *P<0.05 vs. sham group; #P<0.05 vs. LPS group; &P<0.05 vs. T+LPS group; !P<0.05 vs. P+LPS group. PHC/P, penehyclidine hydrochloride; TIPE2/T, tumor necrosis factor α-induced protein 8-like protein 2; LPS, lipopolysaccharide; BALF, bronchoalveolar lavage fluid.

Effects of PHC pretreatment and TIPE2 overexpression on the expression of different proteins in the lung tissues of mice. (A) Western blotting analysis of protein expression levels. Semi-quantification of (B) Bax, (C) Bcl-2, (D) TIPE2, (E) cleaved caspase 3, (F) cleaved caspase 9, (G) NF-κB p65, (H) p-JNK/total JNK and (I) Bax/Bcl-2 ratio. n=8/group. *P<0.05 vs. sham group; #P<0.05 vs. LPS group; &P<0.05 vs. T+LPS group; !P<0.05 vs. P+LPS group. PHC/P, penehyclidine hydrochloride; TIPE2/T, tumor necrosis factor α-induced protein 8-like protein 2; LPS, lipopolysaccharide; p-, phosphorylated.