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Article

Evaluation of LPS-Induced Acute Lung Injury Attenuation in Rats by Aminothiazole-Paeonol Derivatives

by
Pin-Kuei Fu
1,2,3,
Chi-Yu Yang
4,
Su-Chin Huang
5,
Yu-Wen Hung
4,
Kee-Ching Jeng
6,
Ying-Pei Huang
7,
Hong Chuang
7,
Nai-Chun Huang
5,
Jui-Ping Li
5,
Ming-Hua Hsu
8 and
Jen-Kun Chen
5,9,10,*
1
Department of Critical Care Medicine, Taichung Veterans General Hospital, Taichung 40705, Taiwan
2
Department of Biotechnology, Hungkuang University, Taichung 43302, Taiwan
3
School of Chinese Medicine, China Medical University, Taichung 40447, Taiwan
4
Animal Technology Laboratory, Agriculture Technology Research Institute, Miaoli 35053, Taiwan
5
Institute of Biomedical Engineering and Nanomedicine, National Health Research Institutes, Miaoli 35053, Taiwan
6
Department of Medical Research, Tungs’ Taichung MetroHarbor Hospital, Taichung 43503, Taiwan
7
Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan
8
Department of Chemistry, National Changhua University of Education, Changhua County 50007, Taiwan
9
Graduate Institute of Life Sciences, National Defense Medical Center, Taipei 11490, Taiwan
10
School of Dentistry, National Defense Medical Center, Taipei 11490, Taiwan
*
Author to whom correspondence should be addressed.
Molecules 2017, 22(10), 1605; https://doi.org/10.3390/molecules22101605
Submission received: 1 September 2017 / Revised: 20 September 2017 / Accepted: 21 September 2017 / Published: 25 September 2017
(This article belongs to the Special Issue Focusing on Sulfur in Medicinal Chemistry)
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Abstract

:
Paeonol is a key phenolic compound in the root bark of Moutan Cortex Radicis that has been used in traditional Chinese Medicine to ameliorate inflammation. A series of aminothiazole-paeonol derivatives (APDs) were synthesized in this work and subjected to preliminary evaluation in cells followed by verification in animals. Quantification of monocyte chemotactic protein-1 (MCP-1) and interleukin-6 (IL-6) in culture media of LPS-activated A549 cells, a lung epithelial adenocarcinoma cell line, were used to investigate the anti-inflammatory capability of APDs. ALI-bearing rats were employed to verify therapeutic efficacy of APDs according to observations of total cells, protein amounts, MCP-1 and IL-6 in bronchoalveolar lavage fluid (BALF). Histopathological examinations of lung tissues were consequently applied for validation of APDs. Among these compounds, 2-(2-aminothiazol-4-yl)-5-methoxyphenol (4) had the most potent activity, showing comparable inhibition of MCP-1/IL-6 and superior elimination of neutrophil infiltration and protein exudation in lungs compared to others as well as dexamethasone. This study demonstrated a comprehensive strategy to evaluate APDs through integration of cell-based screening and animal-based verification. In order to fulfill unmet needs of treating acute lung injury (ALI) and acute respiratory distress syndrome (ARDS), APDs introduced in this work could be promising lead compounds to develop high potent anti-inflammation agents.

Graphical Abstract

1. Introduction

Herbal medicine and plant-derived compounds have been used to alleviate inflammatory diseases [1,2,3]. Paeonol is a representative phenolic compound found in the root bark of Moutan Cortex Radicis (MCR), reported to inhibit proinflammatory cytokines, cell surface adhesion molecules, and reactive oxygen species (ROS) [4,5,6,7,8]. Both MCR and purified paeonol were capable of attenuating LPS-induced ALI in rats by eliminating expression of myeloperoxidase (MPO) activity, iNOS, interleukin-1β (IL-1β), interleukin-6 (IL-6) and macrophage-inflammatory peptide-2 (MIP-2) [9,10]. Recently, paeonol derivatives have been synthesized and assessed for their potential anti-atherogenic, anti-cancer, anti-oxidant, and anti-virus properties [11,12,13,14]. The 2-aminothiazole moiety not only serves as a stable bioisostere of phenol groups but provides lipophilicity to improve oral availability [15]. Indeed, the 2-aminothiazole moiety has been identified to be an effective pharmacophore for different therapeutic purposes [16,17].
In the present work, we coupled 2-aminothiazole moieties with paeonol to prepare aminothiazole-paeonol derivatives (APDs) in order to treat acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). The ALI and ARDS present severe inflammatory cascades and in conjunction with injury in the respiratory tract, are major health concerns that lead to high mortality and morbidity in critically ill patients [18,19,20]. Many clinical trials using drugs such as aspirin, β2-agonists, omega-3 fatty acids, prostaglandin E1, glucocorticoids, N-acetylcysteine and statins, were frustrated due to poor results whereby these treatments neither prevented nor healed ALI/ARDS [21,22,23].
Since ALI/ARDS is a complex disease associated with many biological responses, it is important to utilize not only in vitro experiments in cell lines but to also verify the results seen in animal models in order to better evaluate the effect of the most potent APDs. Several animal models, for example in vivo intratracheal administration of LPS [24,25,26], are clinically relevant and have been successfully used in previous studies. Neutrophil extracellular traps (NETs) accompanied by disruption of epithelial integrity and leakage of protein and fluid in the lungs are commonly observed in both patients and LPS-induced ALI animal models [27,28,29]. Migration and accumulation of neutrophils in airspaces are associated with up-regulation of adhesion molecules, chemotaxis, and proinflammatory cytokines in ALI and ARDS [29,30,31]. Various pro-inflammatory cytokines, including IL-1β, IL-6 and tumor necrosis factor (TNF-α), were involved in the recruitment of neutrophils to promote inflammation.
The levels of pro-inflammatory cytokines are strongly correlated with survival in ALI/ARDS patients [32,33]. A previous study indicated monocyte chemoattractant protein (MCP)-1 was an activating factor in the LPS-induced ALI animal model [34]. The MCP-1 regulated through the JNK signaling pathway might participate in lung injury by modulating adhesion of inflammatory cells and activation of monocytes [35,36]. Yong et al. suggested using plasma MCP-1 to predict the severity of patients with pneumonia [37]. Chen et al. have demonstrated the MCP-1 in BALF could be used as a critical marker for pulmonary inflammation [38]. The MCP-1 was also employed to evaluate bleomycin-induced lung injury [39]. As for IL-6, Liang et al. have reported IL-6 could promote type 2 alveolar epithelial cells (AEC2) renewal [40]. Therefore, we aimed to use MCP-1 and IL-6 as preliminary markers for cell-based screening to evaluate anti-inflammation potency.
In this study, LPS-activated A549 cells for preliminary screening could be integrated with LPS-induced ALI-bearing rats for verification. Changes of MCP-1 and IL-6 in culture media of LPS-activated A549 cells were employed to evaluate the anti-inflammatory activities of APDs compared to reference compounds (paeonol and dexamethasone). Furthermore, relatively high potent APDs were subjected to verification in ALI-bearing rats. Comprehensive investigation of cell infiltration, protein accumulation and inflammatory markers secretion in both of bronchoalveolar lavage fluid (BALF) and lung tissues demonstrate an effective strategy to explore optimal APDs for the therapy of ALI/ARDS.

2. Results

2.1. Synthesis

The preparation of the vaminothiazole-paeonol derivatives is shown in Scheme 1. Paeonol (1) was treated with 2-chloroethylmorpholine to generate morpholine-o-paeonol (2). Compound 2 was reacted with thiourea and iodine to obtain morpholine-o-paeonol aminothiazole (3). Additionally, paeonol (1) could be treated with thiourea and iodine to construct the 2-aminothiazole scaffold 4 through the condensation–cyclization of thiourea. Compound 4 was reacted with excess hydrochloric acid gas to generate the aminothiazole-paeonol salt 4.HCl. Paeonol-2-aminothiazole-phenylsulfonyl derivatives 5a–5g were obtained reacting compound 4 with substituted phenylsulfonyl chlorides. These products were obtained in sufficient yields and purified by using recrystallization for the subsequent cell-based and animal-based experiments.

2.2. MCP-1 and IL-6 Secretion in LPS-Activated A549 Cells

Low and high concentrations of paeonol, dexamethasone (Dexa) and APDs (1.0 µg/mL and 10 µg/mL) were used to treat LPS-activated A549 cells following the protocols shown in Figure 1. A549 is a lung epithelial adenocarcinoma cell line. The MCP-1 in conditioned media was quantified to survey anti-inflammatory capability of APDs. Secretion of MCP-1 was significantly inhibited by compound 4 and Dexa at 1.0 µg/mL and 10 µg/mL (Table 1 and Figure 2A). The compound 4.HCl at 10 µg/mL could inhibit of MCP-1 secretion (Figure 2A). Only compound 4 at 10 µg/mL suppressed IL-6 secretion but others didn't at neither high nor low concentrations (Figure 2B).

2.3. Cell Viabilities for APDs Treatments

Cell viabilities for APDs against A549 cells were determined by WST-1 assays. Compound 4 and compound 4.HCl are very biocompatible because of more than 90% cell survive a 50 µg/mL treatment (Figure 3). Compound 5c, showing an IC50 value of 39 µg/mL (127 µM) is the most cytotoxic APD prepared in this study.

2.4. Comparison of BALF Collected from ALI-Bearing Rats

Compound 4 and Compound 4.HCl are promising APDs based on our preliminary screening in a LPS-activated A549 cell model. To further verify therapeutic efficacy, paeonol, compound 4, compound 4.HCl and Dexa were injected i.p. into the ALI-bearing rat model following the protocols shown in Figure 4.
Previous studies have indicated both of endotoxin-induced ALI animal models and endotoxin-treated human showed time-dependent changes in either peripheral inflammatory responses or accumulation of immune cells, total proteins, and cytokines in BALF associated with pathological lung injury within 48 h after endotoxin-challenge [41,42]. The severity peak was observed in ALI-bearing rats at 8 h after LPS challenge [43]. Therefore, changes of total cell counts, cytokines (IL-6 and MCP-1) and total proteins in BALF were determined in order to validate therapeutic efficacy of APDs (Figure 5).
Paeonol and Dexa proved ineffective at inhibiting cell infiltration in lungs of ALI-bearing rats (Figure 5A). Notably, compound 4 eliminated total cell counts in BALF at both 25 mg/kg and 50 mg/kg treatment. As for compound 4.HCl, effective inhibition of cell infiltration in lungs was observed at 50 mg/kg treatment. Compound 4 was thus superior to paeonol, Dexa, and compound 4.HCl and substantially inhibited protein infiltration in lungs of ALI-bearing rats (Figure 5B). Paeonol (50 mg/kg), compound 4 (25 and 50 mg/kg), compound 4.HCl (50 mg/kg) and Dexa (1 and 5 mg/kg) suppressed IL-6 secretion in BALF (Figure 5C), in which compound 4 and Dexa presented comparable efficacies for the two dosages. The compound 4.HCl and paeonol presented comparable efficacies merely at 50 mg/kg. Paeonol, 4, and 4.HCl were comparable at inhibiting MCP-1 secretion at both of low and high dosages (Figure 5D).

2.5. Comparison of Compound 4 and Compound 4.HCl by Histopathological Examinations

Lung tissues for histopathological examination were collected at 8 h after LPS administration. No prominent neutrophil infiltration, red blood cells and protein exudates were observed in the negative control group (Figure 6A). ALI-bearing rats presented extremely severe protein exudation and cells infiltration in lungs (Figure 6B), which could be eliminated after treatment with Dexa (Figure 6C), paeonol (Figure 6D), compound 4 (Figure 6E) and compound 4.HCl (Figure 6F). Compound 4 is superior to Dexa, paeonol and compound 4.HCl at alleviating LPS-induced acute lung injury.

3. Discussion

Herbal medicines are invaluable resources to construct plant-derived compound libraries for preventing and treating diseases. For example, paeonol (1, Scheme 1) is a one of the remarkable molecules in Moutan Cortex Radicis (MCR) that has been used in traditional Chinese medicine to promote blood circulation and eliminate blood stasis [44,45]. Our previous work described an animal model treated with MCR to alleviate ALI through inhibiting MCP-1 and IL-8 secretion [10]. In addition to MCP-1 and IL-8, elimination of TNF-α, IL-1β, IL-6, and PAI-1 in BALF were observed in ALI-bearing rats that were treated with paeonol purified from MCR [9]. Paeonol derivatives may also have extensive biomedical applications. Zhu et al. reported thiosemicarbazone paeonol derivatives were potential inhibitors of mushroom tyrosinase [46]. Tsai et al. recently demonstrated a series of aminothiazole paeonol derivatives (APDs) as anticancer agents with relatively high potency against gastrointestinal adenocarcinoma (AGS and HT-29 cells) [14]. The thiazole ring of APDs may contribute to a variety of biological effects, which encourage us to evaluate anti-inflammatory responses for a series of APDs.
ALI and ARDS present acute respiratory failure with severe inflammation in the respiratory tract, leading to high mortality in critically ill patients [18,47]. Inflammation disrupting lung epithelial and endothelial barriers cause damage of alveolar-capillary membrane integrity, excessive trans-epithelial neutrophil migration, and release of pro-inflammatory/cytotoxic mediators. Many therapeutics involved in different underlying mechanisms have been applied to treat ALI/ARDS; however, most of them rarely reduce mortality [21,48,49].
In this work, we have established a workflow consisting of primary cell-based screening (Figure 1) followed by animal-based verification (Figure 4) to propel evaluation of potential APDs against ALI. Figure 3 presents MCP-1 rather than IL-6 in conditioned media is a relatively sensitive marker to monitor how LPS-activated A549 cells responsive to APDs treatments because concentration of MCP-1 is approximately 10-fold higher than that of IL-6 in conditioned media. The MCP-1 in conditioned media of negative control group (without challenge of LPS) was 1411 pg/mL versus 4164 pg/mL in that of LPS-activated group (positive control), showing a 2.95-fold increase of MCP-1 caused by LPS challenge. On the other hand, IL-6 in conditioned medium showed a 2.42-fold increase (from 136 pg/mL to 329 pg/mL) caused by LPS challenge. 2-(2-Aminothiazol-4-yl)-5-methoxyphenol (4) and 2-(2-aminothiazol-4-yl)-5-methoxyphenol hydrochloride (4.HCl) significantly suppressed MCP-1 secretion (Figure 2A) and showed comparable efficacy to Dexa, a synthetic corticosteroid for treating inflammatory and autoimmune symptoms. Figure 2B shows that 10 µg/mL of compound 4 could effectively inhibit IL-6 secretion in culture media of LPS-activated A549 cells. Both compound 4 and compound 4.HCl are superior to compound 5c because of very mild cytotoxicity shown in Figure 3, which suggests compound 4 and compound 4.HCl could be safely used for anti-inflammatory medications for ALI/ARDS.
Compound 4 and compound 4.HCl were subsequently verified in ALI-bearing rats. The compound 4 is excellent at reducing cell infiltration and protein exudation in the alveolar space and simultaneously inhibits secretion of MCP-1 and IL-6 in BALF (Figure 5). However, compound 4.HCl shows limited effects (effective at the high dose: 50 mg/kg) in reducing cell infiltration (Figure 5A) and IL-6 secretion in lungs (Figure 5C) despite effective elimination of MCP-1 (Figure 5D) compared to compound 4. In comparison with compound 4 and compound 4.HCl, Dexa presents very effective elimination of IL-6 and MCP-1 in BALF (Figure 5C,D); but Dexa is less responsive for reduction of cell infiltration and protein exudation (Figure 5A,B).
To further validate therapeutic efficacy of compounds 4 and 4.HCl, histopathological examination of lung tissues (Figure 6) was employed to identify optimal APDs for treating ALI/ARDS. Infiltration of neutrophils, exudation of red blood cells and protein were extremely severe in ALI-bearing rats (Figure 6B) compared with non-challenged rats (Figure 6A), as determined by the extensive presence of cellular debris and proteinaceous material in lung tissues. The remarkable characteristic of ALI/ARDS is neutrophils recruited from the peripheral blood to the alveoli during active infections [50,51,52], which was simultaneously observed in ALI-bearing rats (Figure 6B). Neutrophil infiltration into the lungs is mediated through a complex network of chemokines/cytokines secreted by alveolar macrophages. Chemokines and cytokines including TNF-α, IL-1β, IL-6, IL-8, IL-10, and MCP-1 can promote chemotaxis and recruit more neutrophils into injured lungs [4,18,53,54,55,56]. Infiltration of neutrophils and red blood cells associated with protein exudates are alleviated to different levels by treating either Dexa (Figure 6C), paeonol (Figure 6D), compound 4 (Figure 6E) or compound 4.HCl (Figure 6F). Despite the dramatic inhibition of MCP-1 caused by Dexa (Figure 5D), it does not effectively eliminate protein exudation (Figure 5B) and neutrophil infiltration, which is again proved by the histopathological examination (Figure 6C). Treatment of compound 4 (Figure 6E) presents effective response to eliminate neutrophil infiltration and protein exudation compared to treatments of compound 1 (Figure 6D) and compound 4.HCl (Figure 6F). We therefore suggest the compound 4 is highly efficacious for treating ALI/ARDS because of its comprehensive activity to eliminate neutrophil infiltration, protein exudation and chemokine/ cytokine secretion.

4. Materials and Methods

4.1. Chemicals and General Procedures

Solvents, including dichloromethane, ethanol, ethyl acetate, hexane, methanol and tetrahydrofuran were purchased from Mallinckrodt Pharmaceuticals (St. Louis, MO, USA). Ethyl acetate was dried and distilled from CaH2. Tetrahydrofuran was dried by distillation from sodium and benzophenone under an atmosphere of nitrogen. Benzenesulfonyl chloride, 4-bromobenzenesulfonyl chloride, 4-chlorobenzenesulfonyl chloride, 4-fluorobenzenesulfonyl chloride, 4-methoxybenzene-sulfonyl chloride, 4-nitrobenzenesulfonyl chloride, potassium carbonate, and p-toluenesulfonyl chloride were purchased from Sigma-Aldrich (St. Louis, MO, USA). All reactions were carried out in oven-dried glassware (120 °C) under an atmosphere of nitrogen unless as indicated otherwise. The lipopolysaccharide (LPS) from E. coli (serotype O55:B5) was purchased from Sigma-Aldrich. Dexamethasone-21-phosphate disodium (Dexa) was purchased from Standard Chem. & Pharm. Co., Ltd. (Tainan, Taiwan).
Analytical thin layer chromatography was performed on pre-coated plates (silica gel 60 F-254), purchased from Merck (Merck KGaA, Darmstadt, Germany). Proton (1H)-NMR spectra were obtained on Mercury-400 (400 MHz) (Varian, Palo Alto, CA, USA) AC-400 (400 MHz) (Bruker Biospin GmbH, Rheinstetten, Germany) or Avance 500 (500 MHz) (Bruker) spectrometers using chloroform-d (CDCl3), dimethylsulfoxide-d6 (DMSO-d6) and deuterium oxide (D2O) as the solvents. Chemical shifts of 1H-NMR were referenced to residual protonated solvents (δ 7.24 for chloroform, δ 2.49 for dimethylsulfoxide and 4.79 for deuterium oxide). Carbon-13 NMR spectra were obtained on a Varian Mercury-400 (100 MHz) or Bruker Avance 500 (125 MHz) spectrometer using chloroform-d (CDCl3), dimethylsulfoxide-d6 (DMSO-d6) and methanol-d4 (CD3OD) as the solvents. Chemical shifts of 13C-NMR were referenced to the center of the CDCl3 triplet (δ 77.0 ppm), DMSO septet (δ 39.5 ppm) and methanol septet (δ 49.0 ppm). Multiplicities were recorded by following abbreviations: s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; J, coupling constant (hertz). NMR spectra are presented in the Supplementary Materials (Figures S1–S20). High-resolution mass spectra were obtained by a JMS-700 mass spectrometer (JEOL Ltd., Tokyo, Japan).

4.2. Procedure for the Preparation of Morpholine-O-Paeonol (2)

A solution containing paeonol (1, 1.0 equiv.), 2-chloroethylmorpholine (1.2 equiv.), potassium carbonate (3.0 equiv.) and ammonium chloride (1.5 equiv.) in acetone (30.0 mL) was refluxed for 12 h. Then the mixture was extracted with dichloromethane for three times, and dried over MgSO4(s). After concentration of the solvent, the residue was purified by column chromatography over silica gel using methanol and dichloromethane as eluent to afford 1-(4-methoxy-2-(2-morpholinoethoxy)- phenyl)ethanone (2) as a white solid. Yield 90%; 1H-NMR (500 MHz, CDCl3): δ = 7.81 (d, J = 8.5 Hz, 1H), 6.51 (dd, J = 2, 8.5 Hz, 1H), 6.42 (d, J = 2 Hz, 1H), 4.14 (t, J = 5.5 Hz, 2H), 3.83 (s, 3H), 3.70 (t, J = 4.5 Hz, 4H), 2.83 (t, J = 5.5 Hz, 2H), 2.54 (t, J = 4.5 Hz, 4H); 13C-NMR (125 MHz, CDCl3): δ = 197.5, 164.3, 160.0, 132.5, 121.2, 105.3, 98.9, 66.7, 65.9, 57.2, 55.4, 53.8, 31.9; HRMS (ESI+): m/z [M]+ calc. for C15H21NO4 279.1471, found 280.1578 for [M + H]+.

4.3. Procedure for the Preparation of Morpholine-O-Paeonol Aminothiazole (3)

To obtain aminothiazole paeonol 3, compound 2 (1.0 equiv) was reacted with iodine (1.1 equiv) and thiourea (3.0 equiv) in ethanol under reflux condition for 12–16 h. Then, the mixture was quenched with NaOH(aq) (2.0 equiv) and the ethanol was removed under reduced pressure. The residue was extracted with ethyl acetate and the combined organic layer was washed brine and dried over MgSO4(s). After being filtered and condensed under reduced pressure, the crude product was purified by column chromatography on silica gel (ethyl acetate and hexane as eluent) to obtain compound 4-(4-methoxy-2-(2-morpholinoethoxy)phenyl)thiazol-2-amine (3) as a whit solid. Yield 49%; 1H-NMR (500 MHz, DMSO-d6): δ = 7.93 (d, J = 10 Hz, 1H), 7.30 (s, 1H), 6.85 (s, 2H), 6.62 (s, 1H), 6.54 (d, J = 10 Hz, 1H), 4.15 (s, 1H), 3.76 (s, 3H), 3.57 (s, 4H), 2.76 (s, 2H); 13C-NMR (125 MHz, DMSO-d6): δ = 166.0, 159.2, 156.8, 145.7, 129.9, 116.7 105.1, 103.7, 99.4, 66.3, 65.1, 56.9, 55.2, 53.3; HRMS (ESI+): m/z [M]+ calc. for C16H21N3O3S 335.1298, found 336.1375 for [M + H]+.

4.4. Procedure for the Preparation of Aminothiazole-Paeonol (4)

To obtain aminothiazole-paeonol (4), paeonol (1, 1.0 equiv) was reacted with iodine (1.1 equiv) and thiourea (3.0 equiv) in ethanol under reflux condition for 12–16 h. Then, the mixture was quenched with NaOH(aq) (2.0 equiv) and the ethanol was removed under reduced pressure. The residue was extracted with ethyl acetate and the combined organic layer were washed brine and dried over MgSO4(s). After being filtered and condensed under reduced pressure, the crude product was purified by column chromatography on silica gel (ethyl acetate and hexane as eluent) to give compound 2-(2-aminothiazol-5-yl)-5-methoxyphenol (4). 1H-NMR (400 MHz, CDCl3): δ 7.40 (d, J = 8.4 Hz, 1H, H-3), 6.54 (s, 1H, CH), 6.47 (s, 1H, H-6), 6.42 (dd, J = 8.4, 2.0 Hz, 1H, H-4), 5.05 (s, 2H, NH2), 3.78 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 166.8, 161.0, 157.3, 148.9, 126.6, 111.0, 106.8, 101.6, 98.9, 55.2 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C10H10N2O2S1 222.0458, found 223.0562 for [M + H]+.

4.5. Procedure for the Preparation of Aminothiazole-Paeonol salt (4.HCl)

To obtain aminothiazole-paeonol salt 4.HCl, compound 4 (1.0 equiv) dissolved in acetone (20 mL) was reacted with excess hydrochloric acid gas that was produced by adding concentrated H2SO4 with an addition funnel to excess NaCl(s). When precipitation nearly stopped, the precipitate was collected using suction filtration and washed with cold acetone to obtain the pure 4-(2-hydroxy-4-methoxyphenyl)thiazol-2-aminium chloride (4.HCl) as a yellow solid. Yield 87%; 1H-NMR (D2O, 400 MHz): δ 7.37 (d, J = 8.4 Hz, 1H), 6.80 (s, 1H), 6.58 (dd, J = 6.8, 1.6 Hz, 1H), 6.48 (d, 2.0 Hz, 1H), 3.81 (s, 3H) ppm. 13C-NMR (CD3OD, 100 MHz): δ 171.4, 163.6, 157.0, 138.1, 130.1, 130.0, 109.0, 107.7, 102.5, 55.8 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C10H11ClN2O2S1 258.0224, found 223.0556 for [M + H − HCl]+.

4.6. Procedures for the Preparation of Aminothiazole-Paeonol Derivatives 5a–5g

The solution containing aminothiazole-paeonol (4, 1.0 equiv) in anhydrous THF (2.0–3.0 mL) was added potassium carbonate (1.3 equiv) and a sulfonyl chloride (1.1 equiv). After the reaction mixture was stirred at 25 °C for 2–3 h, it was diluted with dichloromethane (5.0 mL). Inorganic solids were filtered off and the filtrate was concentrated under reduced pressure to afford the residue. It was then purified by use of column chromatography on silica gel (various ratio of methanol to dichloromethane) to give the desired conjugates 5a–5g.
N-[4-(2-Hydroxy-4-methoxyphenyl)thiazol-2-yl]benzenesulfonamide (5a): Yield 80%. Green solid. IR (film): ν 3569.1, 2811.2, 1560.1, 1481.2, 1374.2, 1131.6, 853.4 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.62–7.52 (m, 2H, 2 × ArH), 7.43–7.31 (m, 1H, H-6), 7.28–7.25 (m, 3H, 3 × ArH), 6.98 (d, J = 2.0 Hz, 1H, H-3), 6.89–6.79 (m, 1H, H-5), 6.68 (s, 1H, SCH), 3.70 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 164.1, 129.7, 125.9, 113.9, 113.7, 105.0, 56.0 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C16H14N2O4S2 362.0390, found 363.0396 for [M + H]+.
N-[4-(2-Hydroxy-4-methoxyphenyl)thiazol-2-yl]-4-methylbenzenesulfonamide (5b): Yield 84%. Off-white solid. IR (film): ν 3579.1, 2921.2, 1580.1, 1491.2, 1384.1, 1141.6, 843.4 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.44 (d, J = 8.8 Hz, 1H, H-6), 7.39 (d, J = 8.2 Hz, 2H, 2 × ArH), 7.06 (d, J = 8.2 Hz, 2H, 2 × ArH), 6.81 (d, J = 2.4 Hz, 1H, H-3), 6.74 (dd, J = 8.8, 2.4 Hz, 1H, H-5) 6.52 (s, 1H, SCH), 3.72 (s, 3H, OMe), 2.29 (s, 3H, CH3) ppm. 13C-NMR (100 MHz, CDCl3): δ159.3, 147.0, 145.3, 144.4, 130.5, 129.1, 128.2, 120.9, 113.1, 108.7, 105.9, 55.4 (OMe), 21.4 (CH3) ppm; HRMS (ESI+): m/z [M]+ calc. for C17H16N2O4S2 376.0546, found 377.0551 for [M + H]+.
N-[4-(2-Hydroxy-4-methoxyphenyl)thiazol-2-yl]-4-methoxybenzenesulfonamide (5c): Yield 83%. Off-white solid. IR (film): ν 3672.1, 2931.1, 1560.6, 1473.2, 1388.1, 1142.7, 817.4 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.46–7.42 (m, 3H, H-6 + 2 × ArH), 6.86 (d, J = 2.8 Hz, 1H, H-3), 6.76–6.72 (m, 3H, H-5 + 2 × ArH), 6.57 (s, 1H, SCH), 3.75 (s, 3H, OMe), 3.74 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 166.8, 163.9, 159.4, 147.1, 144.7, 130.5, 125.9, 121.0, 113.7, 113.2, 108.8, 106.2, 55.6 (OMe), 55.5 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C17H16N2O5S2 392.0495, found 393.0498 for [M + H]+.
4-Fluoro-N-[4-(2-hydroxy-4-methoxyphenyl)thiazol-2-yl]benzenesulfonamide (5d): Yield 81%. White solid. IR (film): ν 3695.5, 2943.3, 1589.7, 1493.9, 1378.3, 1157.7, 837.7 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.51–7.48 (m, 2H, 2 × ArH), 7.41 (d, J = 8.8 Hz, 1H, H-6), 6.95–6.91 (m, 2H, 2 × ArH), 6.86 (d, J = 2.6 Hz, 1H, H-3), 6.75 (dd, J = 8.8, 2.6 Hz, 1H, H-5), 6.46 (s, 1H, SCH), 3.74 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 167.3, 167.1, 164.5, 159.4, 146.8, 144.5, 131.2, 130.6, 120.9, 115.9, 115.6, 113.3, 108.9, 105.8, 55.5 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C16H13FN2O4S2 380.0295, found 381.0302 for [M + H]+.
4-Chloro-N-[4-(2-hydroxy-4-methoxyphenyl)thiazol-2-yl]benzenesulfonamide (5e): Yield 81%. White solid. IR (film): ν 3708.8, 2796.7, 1566.74, 1459.55, 1314.15, 1256.54, 984.95 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.53 (d, J = 8.8 Hz, 1H, H-6), 7.48–7.46 (m, 2H, 2 × ArH), 7.29–7.27 (m, 2H, 2 × ArH), 6.94 (d, J = 2.4 Hz, 1H, H-3), 6.82 (dd, J = 8.8, 2.4 Hz, 1H, H-5), 6.56 (s, 1H, SCH), 3.81 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 167.2, 159.5, 146.8, 144.7, 140.7, 133.2, 130.7, 129.6, 128.7, 120.9, 113.5, 109.1, 106.0, 55.6 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C16H13ClN2O4S2 395.9999, found 397.0076 for [M + H]+.
4-Bromo-N-[4-(2-hydroxy-4-methoxyphenyl)thiazol-2-yl]benzenesulfonamide (5f): Yield 83%. White solid. IR (film): ν 3691.2, 2838.7, 1591.3, 1479.1, 1362.1, 1143.7, 821.7 cm−1. 1H-NMR (400 MHz, CDCl3): δ 7.36–7.33 (m, 3H, H-5 + 2 × ArH), 7.28–7.26 (m, 2H, 2 × ArH), 6.80 (d, J = 1.6 Hz, 1H, H-3), 6.71 (dd, J = 8.8, 1.6 Hz, 1H, H-5), 6.35 (s, 1H, SCH), 3.69 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 166.2, 159.6, 146.9, 145.1, 133.8, 121.0, 113.7, 109.1, 106.7, 55.7 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. C16H13BrN2O4S2 439.9495, found 440.9502 for [M + H]+.
N-[4-(2-Hydroxy-4-methoxyphenyl)thiazol-2-yl]-4-nitrobenzenesulfonamide (5g): Yield 84%. Orange solid. IR (film): ν 3607.7, 2685.6, 1554.65, 1360.65, 1325.25, 1267.54, 964.95 cm−1. 1H-NMR (400 MHz, CDCl3): δ 8.06 (d, J = 8.0 Hz, 2H, 2 × ArH), 7.59 (d, J = 8.0 Hz, 2H, 2 × ArH), 7.29 (d, J = 8.6 Hz, 1H, H-6), 6.90 (s, 1H, H-3), 6.77 (d, J = 8.6 Hz, 1H, H-5), 6.32 (s, 1H, SCH), 3.76 (s, 3H, OMe) ppm. 13C-NMR (100 MHz, CDCl3): δ 166.2, 159.9, 150.5, 146.6, 131.1, 129.7, 124.8, 114.0, 109.4, 106.7, 55.8 (OMe) ppm; HRMS (ESI+): m/z [M]+ calc. for C16H13N3O6S2 407.0240, found 408.0247 for [M + H]+.

4.7. Cell Culture

Human lung adenocarcinoma A549 (BCRC-60074) cell line was purchased from the Bioresource Collection and Research Center (BCRC, Hsinchu, Taiwan). The cell line was initially established through explant cultures of lung carcinomatous tissue from a 58-year-old Caucasian male. The A549 cells were cultured in 10% fetal bovine serum (HyClone, GE Healthcare Life Science, Logan, UT, USA) and 90% Ham's F12K medium (Gibco, Thermo Fisher Scientific, Waltham, MA, USA) containing L-glutamine (2.0 mM) and sodium bicarbonate (1.5 g/L). Cells were cultured in a T-75 flask with a feeding cycle of 2 days. The humidified atmosphere with 5% CO2 kept at 37 °C was provided in cell incubator.

4.8. Cytotoxicity of APDs

A549 cells were seeded into 96-well tissue culture plates at a concentration of 5 × 103 cells/well for overnight growth to evaluate the cytotoxicity of APDs. Subsequently, A549 cells were treated with serial concentrations of eleven APDs. After 24 h of incubation, cell viability was determined using WST-1 assays (Abcam, Cambridge, MA, USA). Briefly, 10 µL of WST-1 reagent was added to each well and incubated for 2 h at 37 °C prior to quantification. The absorbance at 450 nm was measured by a VersaMax™ ELISA Microplate Reader (Molecular Devices, Sunnyvale, CA, USA) using a reference absorbance at 600 nm for each well.

4.9. Preliminary Screening of APDs Against LPS-Activated A549 Cells

Preliminary screening procedure to evaluate a series of APDs against LPS-induced inflammation was established with activated A549 cells. Before challenge with LPS, A549 cells were seeded into 24-well plate (5 × 104 cells/well) for overnight. Twenty-four hours after challenge with LPS (1.0 µg/mL), low and high doses of APDs, Dexa, and paeonol (1.0 and 10 μg/mL) were added to activated A549 cells. Forty-eight hours after challenge with LPS, the secreted MCP-1 and IL-6 in the conditioned media from this system was measured by a commercial ELISA kit (R&D Systems, Minneapolis, MN, USA) according to the manufacturer’s instructions.

4.10. Animal Model of Acute Lung Injury

Adult male Sprague-Dawley rats weighing 250–300 g were obtained from the BioLASCO Breeding Center (Yi-Lan, Taiwan). Animals were housed in isolated ventilation cabinets (kept at 22–26 °C with 30–70% humidity) with a 12 h light/dark cycle and free access to food and water. Animal experiments were performed according to principles stated in the “Guide for the Care and Use of Laboratory Animals” and were approved by the Institutional Animal Care and Use Committee (IACUC) of the Agricultural Technology Research Institute (approved protocol number: 104033). Animals were randomly assigned to ten groups. Each group comprised six rats, including a negative control group (non-challenged; PBS group), a positive control group (8 mg LPS /kg; LPS group), and Dexa (1.0 and 5.0 mg/kg; Dexa (1) and Dexa (5) groups), paeonol (25 and 50 mg/kg; P (25) and P (50) groups), compound 4 (25 and 50 mg/kg; P-4 (25) and P-4 (50) groups) and compound 4.HCl (25 and 50 mg/kg; P-4.HCl (25) and P-4.HCl (50) groups) as treatment groups. Figure 4 shows experimental design and groups. Animals were anesthetized using inhaled 2% isoflurane (Halocarbon Laboratories, River Edge, NJ, USA) in 0.5 L/min of air before challenge. Intratracheal administration of LPS (0.5 mL/rat) was performed by inserting a MicroSprayer® Aerosolizer (Model IA-1B, Penn-Century, Wyndmoor, PA, USA) into the trachea. The microsprayer was subsequently removed, and animals were then placed in the vertical position and gently rotated for 30 s to distribute the spray homogenously throughout the lungs. The rats were treated with testing chemicals (APDs, Dexa and paeonol) through intraperitoneal (i.p.) injection at one hour after the LPS challenge and sacrificed at 8 h after the LPS challenge. The other two control groups (PBS and LPS group) were administered with vehicle (DMSO) through i.p. injection.

4.11. Total Cell Counts in BALF

Rats were euthanized at 8 h after the LPS challenge, and bronchoalveolar lavage fluid (BALF) was collected as previously described [9,10]. Briefly, the right main bronchus was ligated, and a catheter was inserted into the trachea. Double-lavage procedures were performed using 0.5 mL of normal saline to pass through the catheter twice. The BALF samples were kept on ice prior to cell counting. Total cell counts in the BALF were determined with a cell counter (Coulter Inc., Miami, FL, USA).

4.12. Total Proteins, IL-6 and MCP-1 in BALF

Quantification of total proteins in the BALF samples was performed by a BCA protein assay (Thermo Scientific, Rockford, IL, USA) with bovine serum albumin solution as calibration standard. For quantification of chemokines and cytokines in BALF, commercial ELISA kits for rat MCP-1 and IL-6 were purchased from Bioscience Systems (San Diego, CA, USA).

4.13. Histopathological Examination

The right lung tissues from 3 lobes of each rat were collected randomly and fixed with 10% neutral buffered paraformaldehyde (PFA) for 18 h. Fixed tissues were embedded in paraffin and dissected into 3-µm thick sections. Hematoxylin and eosin (H&E) staining was used for histopathological examination. Protein exudation, infiltration of red blood cells, mononuclear, and neutrophilic cells were examined by a pathologist and a medical doctor in pulmonary medicine using an Eclipse Ni-U microscope (Nikon, Tokyo, Japan) at 100× magnification.

4.14. Statistical Analysis

All data are presented as the mean ± standard deviation (SD). Figures and statistical analysis were plotted and performed by GraphPad Prism 5 (GraphPad Software Inc., La Jolla, CA, USA). The Mann-Whitney test was used for comparisons between two groups, including differences between particularly experimental group and positive control (LPS-activated) group. Statistical analysis was performed using non-parametric statistics by IBM SPSS Statistics (Version 22.0, Armonk, NY, USA). All comparisons were considered significantly different at p values less than 0.05.

5. Conclusions

To evaluate a series of APDs for treating ALI, eleven APDs were prepared in this work and evaluated using LPS-activated A549 cell model for preliminary screening integrated with ALI-bearing rat model for verification. The best compound, 2-(2-aminothiazol-4-yl)-5-methoxyphenol (4), can effectively alleviate ALI in rats through comprehensively inhibition of chemokines/cytokines, attenuating neutrophil infiltration and eliminating protein exudation in alveolar space. The achievement of this study gives us insight into developing plant-derived compounds to avoid human from suffering lethal ALI and ARDS.

Supplementary Materials

The following are available online, Figure S1-S20: The 1H- and 13C-NMR Spectra of compounds 2, 3, 4, 5a, 5b, 5c, 5d, 5e, 5f and 5g.

Acknowledgments

Authors are grateful to have financial supports from Taichung Veterans General Hospital (TCVGH-1034101B and TCVGH-1044101B for PKF), National Health Research Institutes (NHRI-BN-105-PP-27 for JKC), Agriculture Technology Research Institute (105AS-6.2.1-ST-al for CCY), and Ministry of Science and Technology (MOST 103-2113-M-400-001 for JKC and MOST-104-2119-M-007-017 for MHH). Authors thank Miss Ya-Ting Yang for technical support of intratracheal instillation and are grateful for animal care provided by Animal Molecular Imaging Core Facility (Mr. Chien-Hong Chen and Wei-Neng Liao) in NHRI.

Author Contributions

P.-K.F., M.-H.H. and J.-K.C. conceived and designed the experiments; Y.-W.H., Y-.P.H., S.-C.H., H.C. and N.-C.H. performed the experiments; P.-K.F., J.-P.L. and J.-K.C. analyzed the data; C.-Y.Y., M.-H.H. and J.-K.C. contributed reagents/materials/analysis tools; P.-K.F., K.-C.J., M.-H.H. and J.-K.C. prepared the manuscript and J.-K.C. supervised whole research~project.

Conflicts of Interest

The authors declare no conflict of interest.

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Sample Availability: Samples of the compounds are available from the authors.
Molecules 22 01605 sch001 550
Scheme 1. Synthesis of aminothiazole-paeonol derivatives (APDs) as anti-inflammation agents in this study.
Scheme 1. Synthesis of aminothiazole-paeonol derivatives (APDs) as anti-inflammation agents in this study.
Molecules 22 01605 sch001
Molecules 22 01605 g001 550
Figure 1. Preliminary screening protocols for anti-inflammation potency of APDs using the LPS-activated A549 cell model.
Figure 1. Preliminary screening protocols for anti-inflammation potency of APDs using the LPS-activated A549 cell model.
Molecules 22 01605 g001
Molecules 22 01605 g002 550
Figure 2. Secretion of (A) MCP-1 and (B) IL-6 in conditioned media of LPS-activated A549 cells treated with Dexa (1.0 µg/mL and 10 µg/mL) and selected APDs (1.0 µg/mL and 10 µg/mL). Significant differences between each treatment group and LPS-activated (positive control) group at p values less than 0.05 were annotated with *.
Figure 2. Secretion of (A) MCP-1 and (B) IL-6 in conditioned media of LPS-activated A549 cells treated with Dexa (1.0 µg/mL and 10 µg/mL) and selected APDs (1.0 µg/mL and 10 µg/mL). Significant differences between each treatment group and LPS-activated (positive control) group at p values less than 0.05 were annotated with *.
Molecules 22 01605 g002
Molecules 22 01605 g003 550
Figure 3. Viabilities of A549 cells at 24 h post-treatment of selected APDs. The P-4, P-4.HCl and P-5c represented the Compound 4, 4.HCl and 5c shown in Figure 1.
Figure 3. Viabilities of A549 cells at 24 h post-treatment of selected APDs. The P-4, P-4.HCl and P-5c represented the Compound 4, 4.HCl and 5c shown in Figure 1.
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Molecules 22 01605 g004 550
Figure 4. Verification protocols of LPS-challenged ALI-bearing rats treated with testing chemicals (APDs, paeonol, and dexamethasone).
Figure 4. Verification protocols of LPS-challenged ALI-bearing rats treated with testing chemicals (APDs, paeonol, and dexamethasone).
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Molecules 22 01605 g005 550
Figure 5. Biological responses of ALI-bearing rats treated with Dexa, paeonol and selected APDs on (A) total cell counts, (B) total protein concentrations, (C) IL-6 and (D) MCP-1 in bronchoalveolar lavage fluid (BALF). Significant differences between each treatment group and LPS-treated (positive control) group at p values less than 0.05 were annotated with *.
Figure 5. Biological responses of ALI-bearing rats treated with Dexa, paeonol and selected APDs on (A) total cell counts, (B) total protein concentrations, (C) IL-6 and (D) MCP-1 in bronchoalveolar lavage fluid (BALF). Significant differences between each treatment group and LPS-treated (positive control) group at p values less than 0.05 were annotated with *.
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Molecules 22 01605 g006 550
Figure 6. Histopathological examination of H&E stained lung tissues collected from: (A) non-challenged (negative control), (B) LPS-challenged (positive control) rats without treatment and ALI-bearing rats treated with (C) Dexa, (D) paeonol, (E) Compound 4, and (F) Compound 4.HCl. Rats were consequently sacrificed at 8 h after intratracheal administration of LPS (8 mg/kg). The alveolar spaces (∗) filled with the mixture of red blood cells (→) and mononuclear/neutrophilic infiltrates (⇧) combined with biological responses observed in BALF were integrated to comprehensively evaluate therapeutic efficacy of APDs. (Scale bar: 100 µm).
Figure 6. Histopathological examination of H&E stained lung tissues collected from: (A) non-challenged (negative control), (B) LPS-challenged (positive control) rats without treatment and ALI-bearing rats treated with (C) Dexa, (D) paeonol, (E) Compound 4, and (F) Compound 4.HCl. Rats were consequently sacrificed at 8 h after intratracheal administration of LPS (8 mg/kg). The alveolar spaces (∗) filled with the mixture of red blood cells (→) and mononuclear/neutrophilic infiltrates (⇧) combined with biological responses observed in BALF were integrated to comprehensively evaluate therapeutic efficacy of APDs. (Scale bar: 100 µm).
Molecules 22 01605 g006
Table
Table 1. Secretion of MCP-1 in conditioned media of LPS-activated A549 cells treated with low (1.0 µg/mL) and high (10 µg/mL) concentrations of Dexa, paeonol, and APDs.
Table 1. Secretion of MCP-1 in conditioned media of LPS-activated A549 cells treated with low (1.0 µg/mL) and high (10 µg/mL) concentrations of Dexa, paeonol, and APDs.
Drugs (Symbols)Secretion of MCP-1 in Conditioned Media (pg/mL)
Low Dose TreatmentHigh Dose Treatment
Dexamethasone (Dexa)2669 ± 578 *2538 ± 343 *
Paeonol (P)3938 ± 1063584 ± 329
2 (P-2)4332 ± 3323610 ± 505
3 (P-3)3618 ± 2674446 ± 201
4 (P-4)2724 ± 254 *2077 ± 111 *
4.HCl (P-4.HCl)3323 ± 2612826 ± 362 *
5a (P-5a)3980 ± 4243225 ± 76
5b (P-5b)3983 ± 1203786 ± 131
5c (P-5c)4238 ± 4643793 ± 176
5d (P-5d)4140 ± 4164118 ± 372
5e (P-5e)4002 ± 1253893 ± 312
5f (P-5f)4050 ± 2.34334 ± 544
5g (P-5g)4354 ± 1554628 ± 89
Significant differences of MCP-1 secretion between positive control group and each treatment group at p values less than 0.05 were annotated with *. The MCP-1 concentration in positive control (LPS-activated) groups was 4163.5 pg/mL.

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MDPI and ACS Style

Fu, P.-K.; Yang, C.-Y.; Huang, S.-C.; Hung, Y.-W.; Jeng, K.-C.; Huang, Y.-P.; Chuang, H.; Huang, N.-C.; Li, J.-P.; Hsu, M.-H.; et al. Evaluation of LPS-Induced Acute Lung Injury Attenuation in Rats by Aminothiazole-Paeonol Derivatives. Molecules 2017, 22, 1605. https://doi.org/10.3390/molecules22101605

AMA Style

Fu P-K, Yang C-Y, Huang S-C, Hung Y-W, Jeng K-C, Huang Y-P, Chuang H, Huang N-C, Li J-P, Hsu M-H, et al. Evaluation of LPS-Induced Acute Lung Injury Attenuation in Rats by Aminothiazole-Paeonol Derivatives. Molecules. 2017; 22(10):1605. https://doi.org/10.3390/molecules22101605

Chicago/Turabian Style

Fu, Pin-Kuei, Chi-Yu Yang, Su-Chin Huang, Yu-Wen Hung, Kee-Ching Jeng, Ying-Pei Huang, Hong Chuang, Nai-Chun Huang, Jui-Ping Li, Ming-Hua Hsu, and et al. 2017. "Evaluation of LPS-Induced Acute Lung Injury Attenuation in Rats by Aminothiazole-Paeonol Derivatives" Molecules 22, no. 10: 1605. https://doi.org/10.3390/molecules22101605

APA Style

Fu, P. -K., Yang, C. -Y., Huang, S. -C., Hung, Y. -W., Jeng, K. -C., Huang, Y. -P., Chuang, H., Huang, N. -C., Li, J. -P., Hsu, M. -H., & Chen, J. -K. (2017). Evaluation of LPS-Induced Acute Lung Injury Attenuation in Rats by Aminothiazole-Paeonol Derivatives. Molecules, 22(10), 1605. https://doi.org/10.3390/molecules22101605

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