4-hydroxyphenylacetic acid attenuated inflammation and edema via suppressing HIF-1αin seawater aspiration-induced lung injury in rats

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Abstract

4-Hydroxyphenylacetic acid (4-HPA) is an active component of Chinese herb Aster tataricus which had been widely used in China for the treatment of pulmonary diseases. The aim of this study is to investigate the effect of 4-HPA on seawater aspiration-induced lung injury. Pulmonary inflammation and edema were assessed by enzyme-linked immunosorbent assay (ELISA), bronchoalveolar lavage fluid (BALF) white cell count, Evans blue dye analysis, wet to dry weight ratios, and histology study. Hypoxia-inducible factor-1α(HIF-1α) siRNA and permeability assay were used to study the effect of 4-HPA on the production of inflammatory cytokines and monolayer permeability in vitro. The results showed that 4-HPA reduced seawater instillation-induced mortality in rats. In lung tissues, 4-HPA attenuated hypoxia, inflammation, vascular leak, and edema, and decreased HIF-1α protein level. In primary rat alveolar epithelial cells (AEC), 4-HPA decreased hypertonicity- and hypoxia-induced HIF-1α protein levels through inhibiting the activations of protein translational regulators and via promoting HIF-1α protein degradation. In addition, 4-HPA lowered inflammatory cytokines levels through suppressing hypertonicity- and hypoxia-induced HIF-1αin NR8383 macrophages. Moreover, 4-HPA decreased monolayer permeability through suppressing hypertonicity and hypoxia-induced HIF-1α, which was mediated by inhibiting vascular endothelial growth factor (VEGF) in rat lung microvascular endothelial cell line (RLMVEC). In conclusion, 4-HPA attenuated inflammation and edema through suppressing hypertonic and hypoxic induction of HIF-1α in seawater aspiration-induced lung injury in rats. © 2014 by the authors; licensee MDPI, Basel, Switzerland.

Figures

  • Figure 1. Effects of 4-hydroxyphenylacetic acid (4-HPA) on seawater instillation-induced mortality in rats. Drowning model rats were prepared with or without different does of 4-HPA (50, 100 or 150 mg/kg body weight, i.p.). 4-HPA was administered after seawater instillation for 10 min. The mortality of rats were recorded at 2, 4, 6, 8, 10, and 12 h after seawater instillation in each group (n = 20). * p < 0.05 vs. seawater group, # p < 0.01 vs. seawater group.
  • Figure 2. Effects of 4-HPA on PaO2 and PaCO2 after seawater instillation in rats. At 0, 0.5, 1, 2, 3, and 4 h after seawater instillation with or without 4-HPA treatment, blood samples were obtained from left carotid artery and then PaO2 (A) and PaCO2 (B) were measured by blood gas analyzer. Data are means ± standard deviation (SD) (n = 10), * p < 0.05 vs. seawater group.
  • Figure 3. Effects of 4-HPA on inflammatory cytokines, vascular leakage, and edema after seawater instillation in lungs. After instillation of seawater for 0, 2, 4, and 6 h in the absence or presence of 4-HPA, TNF-α (A); IL-1β (B); and IL-6 (C) contents in lung tissues were assessed by ELISA and white cells in brochoalveolar lavage fluid (BALF) were counted (D); Pulmonary vascular leakage was determined by Evans blue dye analysis (E); Lung edema was assessed by wet to dry weight ratios (F); Lung tissues were stained with hematoxilin and eosin to reveal histopathological changes at 4 h after seawater aspiration. (G) Control group; (H) 4-HPA group; (I) Seawater group; and (J) Seawater + 4-HPA group. The data are presented as means ± SD from three independent experiments, * p < 0.05 vs. control group, # p < 0.05 vs. seawater group.
  • Figure 3. Cont.
  • Figure 4. Effects of 4-HPA on seawater instillation-induced HIF-1α protein and mRNA levels in lungs. After instillation of seawater for 0, 2, 4, and 6 h in the absence or presence of 4-HPA, HIF-1α protein (C,D) and HIF-1α mRNA (A,B) levels of lung tissue were detected by Western blotting and RT-PCR. The ratios of HIF-1α to β-actin in protein and mRNA levels from three independent experiments were obtained by density scanning of the Western blotting and PCR band using an image analysis system. Data are means ± SD, * p < 0.05 vs. control group, # p < 0.05 vs. seawater group.
  • Figure 5. Effects of 4-HPA on hypertonicity, hypoxia, and both of the two induced HIF-1α protein and mRNA levels in primary AEC. Treated by hypertonicity, hypoxia, or both of the two with or without 4-HPA treatment for 4 h, primary rat alveolar epithelial cells (AEC) were harvested and HIF-1α protein and mRNA levels were assessed by Western blotting and RT-PCR. The ratios of HIF-1α to β-actin in protein and mRNA levels from three independent experiments were obtained by density scanning of the Western blotting and PCR band using an image analysis system. Data are means ± SD, * p < 0.05 vs. control group, # p < 0.05 vs. the groups with stimuli or stimulus in the absence of 4-HPA treatment.
  • Figure 6. Effects of 4-HPA on HIF-1α related protein translational regulators under hypertonicity and hypoxia conditions in primary AEC. Primary AEC were treated by hypertonicity and hypoxia in the absence or presence of 4-HPA for 4 h. Then, the cells were harvested for Western blotting and phosphorylation and total protein levels of HIF-1α related translational regulators, including p70S6K1 (A); S6 ribosomal protein (B); 4E-BP1 (C); and eIF4E (D) were detected. The ratios of HIF-1α related translational regulators to β-actin in protein levels from three independent experiments were obtained by density scanning of the Western blotting. Data are means ± SD, * p < 0.05 vs. control group, # p < 0.05 vs. hypertonicity + hypoxia group.
  • Figure 7. Effects of 4-HPA on HIF-1α protein degradation under hypertonicty and hypoxia conditions in primary AEC. AEC were treated with hypertonicity (C); hypoxia (B); or both of the two (A) with or without 4-HPA treatment for 4 h, followed by incubation with 100 μM cycloheximide (CHX, blocking ongoing protein synthesis) from 0–30 min. Cell lysates were subjected to Western blotting using antibodies against HIF-1α and β-actin (the left panel) and the intensity of HIF-1α protein relative content was quantified (the right panel). The plot represented means ± SD from three independent experiments, * p < 0.05 vs. groups with 4-HPA treatment; and (D) prolyl hydroxylase domain enzyme isoform-2 (PHD2) protein of AEC which were treated with both hypertonicity and hypoxia in the presence and absence of 4-HPA was detected by Western blotting. Data are means ± SD, & p < 0.01 vs. control group, # p < 0.05 vs. hypertonicity + hypoxia group.

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Liu, Z., Xi, R., Zhang, Z., Li, W., Liu, Y., Jin, F., & Wang, X. (2014). 4-hydroxyphenylacetic acid attenuated inflammation and edema via suppressing HIF-1αin seawater aspiration-induced lung injury in rats. International Journal of Molecular Sciences, 15(7), 12861–12884. https://doi.org/10.3390/ijms150712861

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