Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Mar 18:23:1355-1362.
doi: 10.12659/msm.900523.

Protective Effects of Cucurbitacin B on Acute Lung Injury Induced by Sepsis in Rats

Affiliations

Protective Effects of Cucurbitacin B on Acute Lung Injury Induced by Sepsis in Rats

Shu Hua et al. Med Sci Monit. .

Abstract

BACKGROUND The aim of this study was to investigate the protective effects of cucurbitacin B (CuB) on sepsis-induced acute lung injury (ALI) in rats. MATERIAL AND METHODS An ALI model was made by cecal ligation and puncture (CLP) in SD rats. Rats were randomly divided into 5 groups (n=15 per group): animals undergoing a sham CLP (sham group); animals undergoing CLP (CLP control group); animals undergoing CLP and treated with CuB at 1 mg/kg of body weight (bw) (low-dose CuB [L-CuB] group), animals undergoing CuB at 2 mg/kg of bw (mid-dose CuB [M-CuB] group); and animals undergoing CuB at 5 mg/kg of bw (high-dose CuB [H-CuB] group). Samples of blood and lung tissue were harvested at different time points (6, 12, and 24 hour post-CLP surgery) for the detection of indicators which represented ALI. Five rats were respectively sacrificed at each time point. Pathological changes of lung tissue were observed by H&E staining. Another 50 rats were distributed into the same five groups to record the 72 hour survival rates. RESULTS Treatment with CuB significantly increased the blood gas PaO2 levels and decreased lung wet/dry (W/D) ratio (p<0.05). It significantly reduced protein concentration, accumulation of the inflammatory cells, and levels of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), (p<0.05), in the bronchoalveolar lavage fluid (BALF). Pulmonary pathological damage and survival rates at 72 hours were found to be effectively improved by CuB. In addition, CuB performed its pulmonary protection effects in a dose-depended manner. CONCLUSIONS CuB can effectively improve the pulmonary gas exchange function, reduce pulmonary edema, and inhibit the inflammatory response in the lung, revealing that CuB may serve as a potential therapeutic strategy for sepsis-induced ALI.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(A, B) CuB increased PaO2 levels and reduced the lung W/D ratio in CLP-induced ALI rats. Data are presented as mean ±SD, n=5. * P<0.05 compared to sham rats and # p<0.05, compared to CLP rats.
Figure 2
Figure 2
(A–D) CuB decreased the protein content and cell (total cells, neutrophils and lymphocytes) counting in the BALF of CLP-induced ALI rats. Data are presented as mean ±SD, n=5; * p<0.05 compared to sham rats and # p<0.05 compared to CLP rats.
Figure 3
Figure 3
(A, B) CuB inhibited TNF-α and IL-6 expression in the BALF of CLP-induced ALI rats. Data are presented as mean ±SD, n=5; * p<0.05 compared to sham rats and # p<0.05 compared to CLP rats.
Figure 4
Figure 4
CuB ameliorated histopathological changes in lung tissues of CLP-induced ALI rats (12 hours after CLP).

References

    1. Schlichting D, McCollam JS. Recognizing and managing severe sepsis: A common and deadly threat. South Med J. 2007;100:594–600. - PubMed
    1. Matuschak GM, Lechner AJ. Acute lung injury and the acute respiratory distress syndrome: pathophysiology and treatment. Mo Med. 2010;107:252–58. - PMC - PubMed
    1. Rubenfeld GD, Caldwell E, Peabody E, et al. Incidence and outcomes of acute lung injury. N Engl J Med. 2005;353:1685–93. - PubMed
    1. Ware LB, Matthay MA. The acute respiratory distress syndrome. N Engl J Med. 2000;342:1334–49. - PubMed
    1. Slutsky AS, Tremblay LN. Multiple system organ failure. Is mechanical ventilation a contributing factor? Am J Respir Crit Care Med. 1998;157:1721–25. - PubMed

MeSH terms