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Effect of safflor yellow injection on inhibiting lipopolysaccharide-induced pulmonary inflammatory injury in mice

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Abstract

Objective

To observe the effect of Safflor Yellow (SY) Injection on acute lung injury (ALI) induced by lipopolysaccharide (LPS) in mice.

Methods

Seventy-two mice were divided into six groups: control (saline + saline); LPS (LPS + saline); SY Injection [LPS + SY (10, 20 or 40 mg/kg, intravenously)] and anisodamine (AD) (LPS + AD). Thirty minutes after SY or AD administration, 15 mg/kg LPS was given intraperitoneally. All animals were sacrificed 4 h after LPS injection. Arterial blood gas and lung water content index (LWCI) were measured. Lung tissue myeloperoxidase (MPO) activity was assayed. mRNA expression of inflammatory cytokines was assayed by reverse-transcription polymerase chain reaction. Lung morphological and nuclear factor (NF)-κB p65-positive cell changes were observed by HE and immunohistochemical staining. p38 mitogen-activated protein kinase (MAPK) phosphorylation was observed by Western blotting.

Results

After LPS administration, all animals displayed increased arterial carbon dioxide partial pressure (PaCO2) and decreased arterial oxygen partial pressure (PaO2), arterial oxygen saturation (SO2), HCO3 concentration and pH, and increased LWCI, MPO activity, interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α mRNA expression, NF-κB p65-positive staining and p38 MAPK activation compared with normal controls (all P<0.01). SY Injection significantly mitigated the LPS-induced increase in arterial PaCO and the decreases in arterial PaO2, SO2 and pH, and attenuated increases in LWCI and lung tissue MPO activity (all P<0.01). Moreover, SY Injection inhibited the increases in NF-κB p65 staining and in TNF-α, IL-1β and IL-6 mRNA expression (all P<0.01), and promoted the expression of the antiinflammatory cytokine IL-10 (P<0.05) following LPS injection. LPS-induced pulmonary p38 MAPK phosphorylation was suppressed by pretreatment with SY Injection (P<0.01).

Conclusion

SY Injection ameliorates inflammatory ALI induced by LPS in mice.

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References

  1. Ware LB, Matthay MA. The acute respiratory distress syndrome. N Eng J Med 2000;342:1334–1349.

    Article  CAS  Google Scholar 

  2. Bosma K, Fanelli V, Ranieri VM. Acute respiratory distress syndrome: update on the latest developments in basic and clinical research. Curr Opin Anaesthesiol 2005;18:137–145.

    Article  PubMed  Google Scholar 

  3. Jin M, Li JR, Wu W. Study on the antioxidative effect of Safflor Yellow. Chin J Chin Mater Med (Chin) 2004;29:447–449.

    CAS  Google Scholar 

  4. Wu W, Jin M, Piao YZ, Li JR. Inhibition of safflor yellow against myocardial ischemia in jury of rats. Chin Tradit Herbal Drugs (Chin) 2007;37:1373–1375.

    Google Scholar 

  5. Zhang Q, Chen ZY, Wu LB, Wang SC, Zheng QS. Clinical non-feriority evaluation on the efficacy and safety of safflower yellow pigment lyophilized power & dripping solution in the treatment of patients with angina. Chin J Evid-Based Med (Chin) 2005;15:276–285.

    Google Scholar 

  6. Pei CQ, Sun CY, Jin M. Mitigation of Safflor Yellow Injection on acute lung injury of rats induced by oleic acid. Chin Tradit Herbal Drugs (Chin) 2010;41:596–601.

    CAS  Google Scholar 

  7. Koroush K, Jean-Pierre G, Chen MH, Chen DF, Zhang DX. Characterization of a murine model of endotoxin-induced acute lung injury. Shock 2002;17:300–303.

    Article  Google Scholar 

  8. Chen TT, Du YJ, Liu XL, Zhu HB. Inhibitory action of hydroxysafflor yellow A on inflammatory signal transduction pathway related factors in rats with cerebral cortex ischemia. Acta Pharm Sin (Chin) 2008;43:570–575.

    CAS  Google Scholar 

  9. Sun CY, Pei CQ, Zang BX, Wang, Jin M. The ability of hydroxysafflor yellow A to attenuate lipopolysaccharideinduced pulmonary. Phytotherapy Res 2010;24:1788–1795.

    Article  CAS  Google Scholar 

  10. Bhatia M, Moochhala S. Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome. J Pathol 2004;202:145–156.

    Article  PubMed  CAS  Google Scholar 

  11. Minamino T, Komuro I. Regeneration of the endothelium as a novel therapeutic strategy for acute lung injury. J Clin Invest 2006;116:2316–2319.

    Article  PubMed  CAS  Google Scholar 

  12. Blackwell TS, Christman JW. The role of nuclear factor kappa B in cytokine gene regulation. Am J Respir Cell Mol Biol 1997;17:3–9.

    Article  PubMed  CAS  Google Scholar 

  13. Garrean S, Gao XP, Brovkovych V, Shimizu J, Zhao YY, Vogel SM, et al. Caveolin-1 regulates NF-kappa B activation and lung inflammatory response to sepsis induced by lipopolysaccharide. J Immunol 2006;177:4853–4860.

    PubMed  CAS  Google Scholar 

  14. Schnyder-Candrian S, Quesniaux VF, Di Padova F, Maillet I, Noulin N, Couillin I, et al. Dual effects of p38 MAPK on TNF-α dependent bronchoconstriction and TNF-α independent neutrophil recruitment in lipopolysaccharideinduced acute respiratory distress syndrome. J Immunol 2005;175:262–269.

    PubMed  CAS  Google Scholar 

Download references

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Correspondence to Ming Jin  (金 鸣).

Additional information

Supported by National Natural Science Foundation of China (No. 30572344), Natural Science Foundation of Beijing (No. 7102025), and Science and Technology Personnel Serve Enterprise Action (No. 2009GJA30001)

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Jin, M., Sun, Cy., Pei, Cq. et al. Effect of safflor yellow injection on inhibiting lipopolysaccharide-induced pulmonary inflammatory injury in mice. Chin. J. Integr. Med. 19, 836–843 (2013). https://doi.org/10.1007/s11655-012-1151-6

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  • DOI: https://doi.org/10.1007/s11655-012-1151-6

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