Dexmedetomidine Promotes Alveolar Fluid Clearance by Upregulating Na,K-ATPase Expression in a Rat Model of Acute Lung Injury via α2 AR/PI3K/Akt Pathway


 Our previous studies have shown that Dexmedetomidine (Dex), α2 adrenergic receptor (α2AR) agonist, reduces pulmonary edema in LPS-induced acute lung injury (ALI), but the mechanism is not clear. The purpose of this study is to explore whether Dex promotes AFC by upregulating the expression of Na,K-ATPase in LPS-induced ALI and possible molecular mechanisms. Histology of the lungs was assayed with H-E staining, and the lung injury score was calculated. PaO2, PaO2/FiO2 , the lung index, wet/dry (W/D) ratio of the lung tissues and alveolar fluid clearance(AFC) was measured; The concentrations of TNF-α, IL-1β, IL-6 in bronchoalveolar lavage fluid (BALF) and serum were measured. Myeloperoxidase (MPO) activity in lung tissues were determined. The apoptosis rate of A549 cells and the expression of Bcl-2 and Bax were evaluated. The expression of Na,K-ATPase , p-PI3K and p-Akt in vivo and in vitro were evaluated. Dex significantly alleviated lung tissue injury induced by LPS. Dex treatment reduced the W/D, lung index and MPO activity, increased PaO2, PaO2/FiO2 and AFC in LPS-induced ALI. In addition, Dex reduced the concentrations of TNF-α, IL-β and IL-6 in BALF and serum. Dex reduced the apoptosis rate, up-regulated the expression of Bcl-2 and down-regulated the expression of Bax in LPS-stimulated A549 cells. Furthermore, Dex increased the expression of α1Na,K-ATPase, β1 Na,K-ATPase and p-PI3K , p-Akt in vivo and vitro. However, these effects of Dex were partially reversed by the α2AR inhibitor yohim-bine or PI3K inhibitor LY294002. Collectively, these results suggest that Dex attenuates pulmonary edema by stimulating AFC via upregulating the Na,K-ATPase expressi-on in LPS-induced acute lung injury by modulating the α2AR/PI3K/Akt signaling pathway.


Introduction
Pulmonary edema is the central link in the pathogenesis of acute lung injury (ALI) (Schlapfer et al. 2012).If pulmonary edema cannot be eliminated as soon as possible, it will lead to gas exchange disturbance and progressive hypoxaemia, which eventually results in multiple organ damage. Although the mechanism of pulmonary edema is complex in ALI, it is attribute to the imbalance between the formation and clearance of pulmonary edema uid. Research has shown that the uid transport function of alveolar epithelium cells is normal or only slightly impaired, and generally there is no pulmonary edema or only slight pulmonary interstitial edema. Severe alveolar edema is often associated with signi cantly reduced alveolar uid clearance (AFC) (Mutlu and Sznajder 2005).
AFC is related to aquaporin (AQP) and sodium ion transport (Zhang et al. 2018). Sodium ions are actively transported into the cell, and then enter the cell stroma under the action of the sodium potassium ATP enzyme (Na,K-ATPase) to form an osmotic gradient. Water is then transferred from the water channel to the pulmonary interstitium, and nally absorbed by lymphatic vessels or capillaries. Therefore, Na, K-ATPase plays an important role in alveolar uid transport (Sznajder et al. 2012).Current research suggests that pulmonary edema may be attributed to the in ammatory response during ALI. Ramia et al. (2010) and Berger et al. (2011) reported that several in ammatory cytokines, including TNF-α and IL-1β may impair the function of the alveolar epithelial cells and affect Na,K-ATPase expression. Lan et al. (2017) and Zhuo et al. (2018) demonstrated that inhibiting the release of in ammatory cytokines may promote alveolar uid clearance (AFC) by increasing the expression of Na,K-ATPase. Therefore, inhibition of the in ammatory response may be bene cial for upregulating Na,K-ATPase expression and reducing pulmonary edema in LPS-induced ALI.
Dexmedetomidine (DEX), a selective agonist of α 2 AR, has sedative properties, and has been used under general anaesthesia. Zhou et al.(2019)and Zhou et al.(2019) and Liu et al.(2016) reported that Dex has potential anti-in ammatory effects both in vivo and in vitro . In addition, Dex has been shown to alleviate pulmonary edema in ALI (Hancl et al. 2012). Consistent with these studies, our previous study found that Dex could reduce lipopolysaccharide (LPS)-induced pulmonary edema in ALI rats, increase the partial pressure of oxygen, reduce the in ammatory response of lung tissue, and increase the expression of aquaporin 1 and 5 (AQP1, AQP5) in lung tissue ( Jiang et al. 2015), suggesting that Dex may alleviate pulmonary edema by promoting AFC through increasing AQP expression. These results prompted us to hypothesize that the effect of Dex on pulmonary edema may be related to the expression of Na,K-ATPase.
In addition, the molecular mechanism by which Dex reduces pulmonary edema has not been fully elucidated. Therefore, this study investigated whether Dex regulates the expression of Na,K-ATPase through the α2AR /PI3K/Akt pathway, thereby stimulating AFC and alleviating pulmonary edema.

Animals
Twenty-four 6 to 8 weeks old Wistar rats weighing 220-250g were provided by the Guangdong Medical Animal Experiment Center (China). The rats were housed in an environmentally controlled animal care facility, where they were fed ad libitum, and exposed to 12-h light/dark cycles. The protocol was approved by the Animal Care Committee of the Second Clinical Medical College of Jinan University(Shenzhen, China), and was carried out according to institutional guidelines for animal care and by the Guide for Care and Use of Laboratory Animals published by the United States National Institutes of Health.

Experimental protocol
The rats were anaesthetized with sodium pentobarbital (50 mg/kg, i.p. injection). The left femoral vein of each rat were punctured with catheters (PE-50) for administration of drugs. A tracheostomy was performed, and a 14-gauge angiocather was inserted as a tracheostomy tube to keep the airway unobstructed. After tracheostomy, anaesthesia was maintained by supplementary injections of pentobarbital (approximately 1-3 mg/kg, i.v.), as required.
The animals were randomly assigned to four groups (n = 6): Control group (Control), ALI model group (LPS group), Dex treatment group (LPS + Dex), and LPS + Dex + yohimbine group (LPS + Dex + YOH). Rats in the Control group were treated with 0.9% normal saline (5ml/kg, i.p.). LPS (20 mg/kg, i.p. ) was administered to induce the ALI model. Rats in the LPS + Dex group received Dex (100 µg/kg,i.p.) immediately after LPS treatment.The Dex dose was determined based on previous studies (Hancl et al. 2012). Rats in the LPS + Dex + YOH group received yohimbine (0.1 mg/kg, i.p.) 30 min prior to LPS administration and then received the same treatment as the LPS + Dex group. At the end of the experiment, 1.0 mL of blood was collected for blood gas analysis. Another sample of blood (1.5mL) and the bronchoalveolar lavage uid (BALF) was collected to measure in ammatory cytokines. All rats were sacri ced by bloodletting. The samples of lung tissues were removed for further examination.

Histological examinations
After the rats are sacri ced,the lung tissues were taken. The specimens were routinely xed and embedded in para n. Sections were stained with haematoxylin and eosin (H&E) for light microscopy analysis. The histological lung injury was scored based on the alveolar congestion, haemorrhage, neutrophil in ltration into the airspace or vessel wall, and thickness of the alveolar wall, and the thickness of the alveolar septum in ve random elds in a blinded manner using light microscopy. Lung sections were scored as 1 (no or very slight pathological changes), 2 (slight pathological changes), 3 (moderate pathological changes), or 4 (severe pathological changes). Evaluation scores were added to the total injury score.
Measurement of arterial oxygen tension (PaO 2 ) and oxygenation index(PaO 2 /FiO 2 ) A 1.0-mL blood sample was collected from the right common carotid artery before the rats were sacri ced, and PaO 2 was immediately measured with a blood gas analyser (Stat Pro le pHOx, Nova Biomedical Corporation; Waltham, MA, USA). PaO 2 /FiO 2 was calculated according to the concentration of inhaled oxygen.

Measurement of lung index and wet/dry weight ratio (W/D)
At the end of the experiments, the rats were sacri ced, thoracotomy was performed immediately, and the whole lungs were removed and weighed. The ratio of whole lung wet weight to body weight is the lung index. The upper lobe of the right lung was removed, and the measured weight indicates the wet weight.Then it was placed in an oven at 75℃, and baked for 24 hours, and the measured weight represented the dry weight, the degree of pulmonary edema was evaluated by calculating the ratio of W/D .

Myeloperoxidase (MPO) activity analysis
The lung tissues were homogenized and centrifuged, and the supernatant was incubated in a water bath (60°C) for 2 h for subsequent determination of MPO activity according to the manufacturer's instructions of the assay kits.
Detection of TNF-α, IL-1β, IL-6 in BALF and serum After the rats were sacri ced, the main bronchus was exposed. The right bronchus was ligated, and a homemade tracheal catheter was inserted into the main bronchus. Then, 2 mL cold phosphate-buffered saline (PBS) was infused into the left lung and extracted three times. The bronchoalveolar lavage uid (BALF) was centrifuged at 1200×g for 10 min at 4°C. The supernatant was separated into aliquots and stored at -70°C. An aliquot of BALF supernatant was used to assay the levels of TNF-α, IL-1β, IL-6 by ELISA according to the manufacturer's instructions. Blood samples from the common arteries were collected and serum levels of TNF-α, IL-1β, IL-6 were measured by ELISA according to the manufacturer's instructions.

Immunohistochemical analyses
Lung tissues were xed in 10 neutral formaldehyde solution, and para n tissue sections were produced. The para n sections were then baked overnight in a 60°C oven, dewaxed with dimethyl benzene, dehydrated in gradient ethanol solutions, repaired with 500 ml EDTA antigen repair solution, treated with 50 µl 3% hydrogen peroxide solution at room temperature for 20 min to block endogenous peroxidase activity and rinsed with TBS 3 times (3 min each time). Then, 5% normal goat serum solution was added at room temperature for 20 min, and the super uous liquid was discarded without washing. Diluted primary antibody was added, and the tissues were incubated at room temperature for 30 min and washed with TBS 3 times (3 min each time). Secondary antibody (biotinylated goat anti-rabbit IgG) was added, and the tissues were incubated at room temperature for 30 min and washed with TBS 3 times (3 min each time). After that, the cells were stained with 3,3-diaminobenzidine for 3 ~ 5 min. PBS was used instead of primary antibody for the negative control group. The average optical densities (AODs) of α 1 Na,KATPase, β 1 Na,KATPase were measured by an imaging analysis system.

Measurement of alveolar uid clearance
The AFC was determined by measuring the Evans blue-labeled albumin concentration. First, 5% bovine serum albumin perfusion solution labeled with Evans blue was injected (5 ml/kg) into the left lung via the trachea, and 2 ml oxygen was injected to facilitate distribution. The rats were ventilated with 100% oxygen, and the positive end expiratory pressure was kept at 2 ~ 3 cm H 2 O during the baseline period to maintain lung tension. These tissue units were wrapped with plastic wrap and then incubated in a 37°C water bath for 1 h. The alveolar uid was immediately aspirated, and labeled albumin was measured by a spectrophotometer at 620 nm. AFC was calculated based on the following formula: where Ci represents the concentration of injected Evans blue-labeled 5% albumin and C f represents the nal concentration of Evans blue-labeled 5% albumin.
Cell culture and treatment A549 cells (Cell Bank of the Chinese Academy of Sciences, Shanghai, China) were seeded in culture dishes at a density of 1× 10 6 cells/cm 2 and cultured in a 5% CO 2 and 95% air atmosphere in Dulbecco's modi ed Eagle medium (DMEM) with 10% fetal bovine serum, 0.1 mg/ml streptomycin, and 100 U/ml penicillin. The culture medium was changed every two days. For all experiments, the cells were subcultured in six-well plates. Once the cells reached 80% con uence, they were serum-starved for 24 h.

Cell viability assay
The CCK8 assay was performed to measure cell viability. The cells (100 µl/well) were cultured in a 96-well plate for 24 h. Then, 10 µl CCK8 solution was added to each well, the culture plate was incubated in the incubator for 2 h under 5% CO2 at 37°C, and the absorbance at 490 nm was measured with a microplate reader.

LDH activity assay
The cells (100 µl/well) were cultured in a 96-well plate for 24 h. The supernatant was collected to measure lactate dehydrogenase (LDH) activity by using an LDH assay kit according to the manufacturer's instructions. The absorbance at 490 nm was measured with a microplate reader.

Hoechst 33258 staining
The A549 cell suspension was added at a density of 1×10 5 cells/well into 6-well plates. A549 cells were treated with PBS, LPS (1 µg/ml), LPS + Dex (10 µΜ), LPS + Dex + Yohimbime (100 µΜ). After 24 h, cells were washed twice with TBST and xed with 4% formaldehyde for 10 min at room temperature.Then, four groups of cells were stained with Hoechst 33258 for 30 min at 37˚C. Cell damage was observed under a uorescence microscope.

Western blot analysis in vivo and vitro
Proteins were obtained with RIPA lysis buffer (50 mM Tris [pH 7.4], 150 mM NaCl, 1% Triton X-100, 1% sodium deoxycholate, 0.1% SDS, sodium orthovanadate, sodium uoride, EDTA, and leupeptin) and PMSF. The protein concentrations of the supernatants were determined by using a BCA protein assay kit.
The proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to PVDF membranes. Tris buffer solution containing 5% skim milk powder was used to block the membrane for 1 h at room temperature. The membrane was permeabilized with PBS containing 0.05% Tween 20 and washed with PBST 5 times (5 min each time). Then, the membrane was incubated overnight at 4°C with the following primary antibodies: α 1 Na,KATPase, β 1 Na,KATPase, p-PI3K,p-AKT and β-actin.The membrane was incubated with a horseradish peroxidase (HRP)-labeled goat anti-rabbit antibody at room temperature for 3 h, and the membrane was washed with PBST 5 times (5 min each time). Finally, the bands were visualized using an enhanced chemiluminescence kit (ECL) with a UVP gel imaging system. The band intensities were analyzed with Image J software.

Statistical analysis
All data are expressed as the mean ± standard deviation (SD). The signi cance of the differences among the four groups was tested using one-way ANOVA, and Dunnett's test was used for multiple comparison.A two-side p value less than 0.05 was considered statistically signi cant.

Effects of Dex on acute lung injury induced by LPS
Firstly, HE staining was performed to observe LPS-induced pathological pulmonary changes.In the Control group, the lung structure was intact, and the alveolar cavity was clear and free from in ammatory cell in ltration. Compared with Control group, LPS induced signi cant changes in lung injury, namely, interstitial edema, alveolar septum thickening, and a large amount of in ammatory cell in ltration, as evidenced by an increase in the lung injury score. Dex treatment signi cantly alleviated but yohimbine aggravated the pathological alterations and lung injury scores induced by LPS (Fig. 1a-b, P < 0.01). Subsequently, arterial blood samples were obtained for blood gas analysis and showed that PaO 2 and PaO 2 /FiO 2 was signi cantly lower in the LPS group than in the control group. Dex treatment signi cantly increased but yohimbine decreased the PaO 2 and PaO 2 /FiO 2 (Fig. 1c-d, P < 0.01or 0.05). In addition, the degree of pulmonary edema and lung tissue MPO activity were performed to further assess the lung injury. W/D, lung index, MPO activity in the LPS group were increased compared with control group, Dex treatment signi cantly increased but yohimbine decreased the W/D, lung index, MPO activity ( Fig. 1e-g, P < 0.01or 0.05) .

Effects of Dex on Alveolar uid clearance(AFC)
Compared with control group, AFC was decreased in LPS group. Compared with LPS group, AFC was increased in LPS + Dex group,while α 2 AR inhibitor yohimbine reversed the effect of Dex (Fig. 2, p < 0.01 ).
Effects of Dex on the concentrations of TNF-α, IL-β, IL-6 in BALF and serum Compared with control group, the concentration of TNF-a, IL-β and IL-6 were increased in BALF and serum in LPS group. Compared with LPS group, the concentration of TNF-a, IL-β and IL-6 were decreased in BALF and serum in LPS + Dex group, while α 2 AR inhibitor yohimbine reversed the effect of Dex (Fig. 3a-f, P < 0.01 ).
Effects of Dex on α 1 Na,KATPase and β 1 Na,KATPase expression in vivo Immunohistochemical analysis was used to determine the expression of α 1 Na,KATPase and β 1 Na,KATPase. Immunostained cells appeared brown. The expression of α 1 Na,KATPase and β 1 Na,KATPase were decreased in the LPS group compared with the control group, but were increased in the LPS + Dex group compared with the LPS group, while α 2 AR inhibitor yohimbine reversed the effect of Dex (Fig. 4a-d, P < 0.01).
To further con rm that Dex stimulates AFC by increasing the expression of Na,KATPase, the expression levels of α 1 Na,KATPase and β 1 Na,KATPase in lung tissues were detected by western blotting. Compared with Control group, the expression of α 1 Na,KATPase and β 1 Na,KATPase were decreased in LPS group.
Dex attenuated LPS-induced A549 cell injury Different concentrations of dexmedetomidine alone did not affect cell viability (Fig. 5a, p > 0.05). Compared with the control group, LPS expoure reduced the cell viabilitiy and increased the LDH release, which was alleviated by 0.1-100µm Dex treatment. The use of 10µm and 100µm Dex had the best therapeutic effect (Fig. 5b-c, p < 0.05 or 0.01). Therefore, Dex (10 µm) was used in subsequent cell experiments.

Dex inhibits LPS-induced A549 cell apoptosis
The Hoechst staining results showed that LPS expoure increased the apoptosis rate, which was decreased by Dex treatment. Howere, α 2 AR inhibitor yohimbine reversed the effect of Dex. (Fig. 6a-b, p < 0.01 ). To further con rm the protective effects of Dex, the expression of Bax, Bcl-2 in the lung were evaluated by western blotting. We found that the expression of Bax increased and the expression of Bcl-2 decreased in LPS group, which was alleviated by Dex treatment.Howere, α 2 AR inhibitor yohimbine reversed the effect of Dex. (Fig. 6c-e, p < 0.01 ).
Effects of Dex on α 1 Na,KATPase and β 1 Na,KATPase expression in vitro To further con rm that Dex stimulates AFC by increasing the expression of Na,KATPase, we detected the expression levels of α 1 Na,KATPase and β 1 Na,KATPase in A549 cells.Compared with Control group, the expression of α 1 Na,KATPase and β 1 Na,KATPase were decreased in LPS group. Compared with LPS group, the expression of α 1 Na,KATPase and β 1 Na,KATPase were increased in LPS + Dex group, while α 2 AR inhibitor yohimbine reversed the effect of Dex (Fig. 7a-c, p < 0.01).

Effects of Dex on p-PI3K and p-Akt expression in vivo and vitro
Compared with control group, the expression of p-PI3K and p-Akt was decreased in LPS group in vivo.
Compared with LPS group, the expression of p-PI3K and p-Akt was increased in LPS + Dex groupin in vivo, while α 2 AR inhibitor yohimbine reversed the effect of Dex (Fig. 8a -c, p < 0.01 ).
To further con rm that whether Dex regulates the expression of Na,KATPase through the α 2 AR/PI3K/Akt signaling pathway. we administered PI3K inhibitors LY294002 as well as α 2 AR inhibitors yohimibine in LPS-stimulated A549 cell to observe the expression of p-PI3K and p-Akt. Compared with the control group, the expression of p-PI3K and p-Akt was decreased in LPS group in vitro. Compared with LPS group, the expression of p-PI3K and p-Akt was increased in LPS + Dex group in vitro, while α 2 AR inhibitor yohimbine and PI3K inhibitor LY294002 reversed the effect of Dex(p < 0.01) (Fig. 9a -c, p < 0.01 ).

Discussion
Our data clearly indicated that lung index and W/D ratio were signi cantly increased in LPS-induced ALI, while Dex reduced the lung index and W/D ratio, indicating that Dex alleviated pulmonary edema in LPSinduced ALI in rats.Consistent with the results, Dex signi cantly increased PaO 2 , PaO 2 /FiO 2 and improved lung histopathological changes. In addition, Dex treatment promotes AFC following LPS exposure, it seems possible that Dex reduces pulmonary edema by increasing AFC, which in turn increases PaO 2 . Our study also observed that Dex inhibited the down-regulation of Na,K-ATPase expression induced by LPS. So, it is likely that Dex reduce pulmonary edema by promoting AFC through the elevation of the Na,K-ATPase expression. Howere, these effects of Dex were partially reversed by α 2 AR inhibitor yohimbine, indicating that Dex acts through the α 2 AR. Furthermore, our study demonstrated that Dex increased the expression of P-PI3K and p-Akt, while a 2 AR inhibitor yohimbine partially reversed the effect of Dex, indicating that Dex reduced pulmonary edema through increasing Na,K-ATPase expression by a 2 AR/PI3K/Akt signaling pathway.
Although aquaporin (AQP) is important in water transport between alveolar cavity and capillaries, but the driving force for water transport is the osmotic gradient formed by Na + transmembrane transport (Matthay et al. 1996). Sodium ions are actively transported into alveolar epithelial cells, it then enters the alveolar stroma in the presence of Na, K-ATpase, forming an osmotic gradient, water is then transferred from the water channel to the pulmonary interstitial, and nally absorbed back by lymphatic vessels or capillaries. In this process, the function of Na,K-ATPase is to transport three sodium ions out of the cell and pump two potassium ions at the same time, thus forming the permeability gradient difference between inside and outside the cell membrane. The increased expression or activity of Na,K-ATPase on the alveolar epithelial cell membrane can promote alveolar uid clearance (Smith et al. 2013). On the contrary, Vadasz et al. (2014) and Wang et al. (2013) and Peteranderl et al. (2016) reported that the low expression of Na,K-ATPase on the alveolar epithelial cell membrane or inhibition of its activity leads to a decrease in alveolar uid clearance. Huang et al.(2014) and Wang et al.(2014) and Emr et al. (2015) found that the expression of Na,K-ATPase and AFC were decreased during the ALI, suggesting that inhibiting the decrease of Na,K-ATPase expression is a new way to promote AFC and alleviate pulmonary edema in ALI. In the previous study, we found that Dex alleviated pulmonary edema through up-regulating the expression of AQP (Jiang et al. 2015), but it is not clear whether its effect is related to increase the Na,K-ATPase expression. In this study, we observed that the expression of the α 1 Na,K-ATPase and β 1 Na,K-ATPase expression were decreased in LPS group,while Dex treatment enhanced the expression of the α 1 Na,K-ATPase and β 1 Na,K-ATPase in the lung tissues and alveolar epithelial cells. In addition, immunohisochemical analysis of lung tissue con rmed similar results. Moreover, this effect of Dex appears to occur through a a 2 AR. These ndings suggest that Dex promotes AFC and reduces pulmonary edema by increasing α 1 Na,K-ATPase and β 1 Na,K-ATPase expression.
The exact mechanism behind ALI remains unclear, but excessive in ammatory response is mainly responsible for the development of ALI. Studies have shown that in ammatory cytokines such as TNF-α, IL-1 β and IL-6 can inhibit the expression of Na,K-ATPase (Song et al.2016). Our study found that LPS induced the increase of pro-in ammatory cytokines TNF-α, IL-1 β and IL-6, suggesting that in ammatory response may be an important reason for the decreased expression of Na,K-ATPase in this study. Liu et al. (2016) and Tasdogan et al.(2008) and Peng et al.(2013) demonstrated that Dex has an antiin ammatory effect through inhibiting in ammatory cytokines such as TNF-a, IL-1β. In addition, Xu et al. (2015) and Gu et al.(2011) reported that Dex reduced pulmonary edema in ALI. Our study found that Dex decreased the concentration of TNF-α, IL-1 β and IL-6 in BALF and serum and reduced neutrophil in ltration in lung tissue, suggesting that Dex may increase the Na,K-ATPase expression to stimulate AFC and alleviate pulmonary edema through inhibiting in ammatory response in the LPS-induced ALI in rats.
Apoptosis plays an important role in the pathogenesis of ALI(Zheng et al. 2020). Na,K-ATPase were expressed in alveolar epithelial cells. So, Apoptosis of alveolar epithelial cells may decrease the expression of Na,K-ATPase. Sun et al.(2019) improved that Dex inhibited the apoptosis of alveolar epithelial cells.Consistent with these studies, our study found that Dex signi cantly reduced LPS-induced alveolar epithelial cell apoptosis, while α 2 AR inhibitors yohimbine partially reversed the effect of Dex, suggesting that the effect of DEX on apoptosis was α 2 AR dependent. Bax and Bcl-2 play important roles in the regulation of apoptosis. High expressionof Bax (apoptosis-promoting) and low expression of Bcl-2 (anti-apoptosis) can result in apoptosis. In the present study, we found that Dex upregulated the expression of Bcl-2 and inhibited the expression of Bax, and α 2 AR inhibitors yohimbine partially reversed the effect of Dex, indicating that Dex acted in an α 2 AR-dependent manner.These results suggest that that Dex increases Na,K-ATPase expression by reducing the apoptosis of alveolar epithelial cells as well as inhibiting in ammatory response.
Our study con rmed that Dex alleviated pulmonary edema by up-regulating the expression of Na,K-ATPase, but the molecular mechanism was not clear. The lipid kinase PI3K generates phosphatidylinositol (3,4,5)-trisphosphate (PIP3), which is a second messenger that facilitates the translocation of Akt to the plasma membrane. At the membrane, Akt is phosphorylated and plays an important role in processes such as cell proliferation, differentiation, survival and apoptosis. Li et al. (2018) and Sun et al.(2019) reported that Dex has a protective effect on LPS or renal ischemiareperfusion induced alveolar epithelial cells and pulmonary microvascular endothelial cells by the activation of α2AR/PI3K /Akt pathway. Our previous studies have shown that Dex reduces pulmonary edema by activating the PI3K/Akt /Nedd4-2 pathway (Jiang et al. 2021). In addition, the increased expression of Na,K-ATPase is related to the activation of PI3K/Akt pathway (Bhargava et al. 2007). Therefore, it seems likely that Dex has a protective effect on LPS-induced ALI through activating PI3K/Akt pathway by stimulating α 2 AR. Our studies found that LPS inhibited the expression of p-PI3K and p-Akt, but Dex signi cantly increased the expression of p-PI3K and p-Akt, while α 2 AR inhibitor yohimbine partially reversed the effect of Dex. In vitro, We found that LY294002 (PI3K inhibitor) decreased the expression of p-PI3K and p-Akt as well as α 2 AR inhibitor yohimbine.These results furtherly suggest that Dex may enhance the Na,K-ATPase expression through α 2 AR-mediated activation of PI3K/Akt, and contribute to stimulate AFC to decrease lung edema.
In conclusion, Dex promotes AFC and attenuates pulmonary edema by up-regulating the expression of Na,K-ATPase in LPS induced ALI, which may be related to α 2 AR/PI3K/Akt signaling pathway. Our results provide new insight into alleviating pulmonary edema in LPSinduced ALI and suggest a new therapeutic use for Dex in patients with ALI. Zhou H, Zhou D, Lu J, Wu C, Zhu Z(2019). Effects of pre-cardiopulmonary bypass administration of dexmedetomidine on cardiac injuries and the in ammatory response in valve replacement surgery with a sevo urane postconditioning Protocol: A Pilot Study. J. Cardiovasc. Pharmacol 74 (2) Dex ameliorates LPS-induced ALI in rats. Represents histopathological images of lung tissues(a), histological injury scores for lung tissues (b), the PaO2(c), the PaO2/FiO2(d), the W/D (e), the lung index (f), the MPO of lung tissues (g). All data are expressed as mean ± standard deviation(n=6). **P<0.01vs. the control group; ##P<0.01 vs. the LPS group; &&P<0.01 vs. the LPS+Dex group. Dex reduces in ammatory response in LPS-induced ALI in rats. Represents the levels of TNF-α(a) , IL-1β(b), IL-6(c) in BALF and the levels of TNF-α(d) , IL-1β(e), IL-6(f) in serum. All data are expressed as mean ± standard deviation (n=6). **P<0.01, vs. control group; ##P<0.01 vs. the LPS group; &&P<0.01 vs. the LPS+Dex group . Effect of Dex on Na,K-ATPase of the lung tissues in LPS-induced ALI in rats. Represents the expression of α1Na,K-ATPase(a) and β1 Na,K-ATPase(b) assesed by immunoh-istochemistry ; Represents densitometric quanti cation of the level of α1Na,K-ATPase (c) and β1Na,K-ATPase (d). Represents the expression of α1Na,K-ATPase and β1 Na,K-ATPase(e) assesed by western blotting; Represents densitometric quanti cation of the level of α1Na,K-ATPase and β1Na,K-ATPase (f). All data are expressed as mean ± standard deviation (n=6). **P<0.01 vs. control group; ##P<0.01 vs. LPS group; &&P<0.01 vs. LPS+Dex group. and LDH activity(c) in A549 cells treated with LPS for 12 hours. All data are expressed as mean ± standard deviation. *P<0.05 or **P<0.01 vs. control group; #P<0.05 or ##P<0.01 vs. LPS group.