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YAO Xin, CHEN Nan, MA Chun-Hua, TAO Jing, BAO Jian-An, CHENG Zong-Qi, CHEN Zu-Tao, MIAO Li-Yan. Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways[J]. 中国天然药物, 2015, 13(1): 52-58.
引用本文: YAO Xin, CHEN Nan, MA Chun-Hua, TAO Jing, BAO Jian-An, CHENG Zong-Qi, CHEN Zu-Tao, MIAO Li-Yan. Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways[J]. 中国天然药物, 2015, 13(1): 52-58.
YAO Xin, CHEN Nan, MA Chun-Hua, TAO Jing, BAO Jian-An, CHENG Zong-Qi, CHEN Zu-Tao, MIAO Li-Yan. Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways[J]. Chinese Journal of Natural Medicines, 2015, 13(1): 52-58.
Citation: YAO Xin, CHEN Nan, MA Chun-Hua, TAO Jing, BAO Jian-An, CHENG Zong-Qi, CHEN Zu-Tao, MIAO Li-Yan. Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways[J]. Chinese Journal of Natural Medicines, 2015, 13(1): 52-58.

Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways

Ginkgo biloba extracts attenuate lipopolysaccharide-induced inflammatory responses in acute lung injury by inhibiting the COX-2 and NF-κB pathways

  • 摘要: In the present study, we analyzed the role of Ginkgo biloba extract in lipopolysaccharide(LPS)-induced acute lung injury (ALI). ALI was induced in mice by intratracheal instillation of LPS. G. biloba extract (12 and 24 mgkg-1) and dexamethasone (2 mgkg-1), as a positive control, were given by i.p. injection. The cells in the bronchoalveolar lavage fluid (BALF) were counted. The degree of animal lung edema was evaluated by measuring the wet/dry weight ratio. The superoxidase dismutase (SOD) and myeloperoxidase (MPO) activities were assayed by SOD and MPO kits, respectively. The levels of inflammatory mediators, tumor necrosis factor-, interleukin-1, and interleukin-6, were assayed by enzyme-linked immunosorbent assay. Pathological changes of lung tissues were observed by HE staining. The levels of NF-B p65 and COX-2 expression were detected by Western blotting. Compared to the LPS group, the treatment with the G. biloba extract at 12 and 24 mgkg-1 markedly attenuated the inflammatory cell numbers in the BALF, decreased NF-B p65 and COX-2 expression, and improved SOD activity, and inhibited MPO activity. The histological changes of the lungs were also significantly improved. The results indicated that G. biloba extract has a protective effect on LPS-induced acute lung injury in mice. The protective mechanism of G. biloba extract may be partly attributed to the inhibition of NF-B p65 and COX-2 activation.

     

    Abstract: In the present study, we analyzed the role of Ginkgo biloba extract in lipopolysaccharide(LPS)-induced acute lung injury (ALI). ALI was induced in mice by intratracheal instillation of LPS. G. biloba extract (12 and 24 mgkg-1) and dexamethasone (2 mgkg-1), as a positive control, were given by i.p. injection. The cells in the bronchoalveolar lavage fluid (BALF) were counted. The degree of animal lung edema was evaluated by measuring the wet/dry weight ratio. The superoxidase dismutase (SOD) and myeloperoxidase (MPO) activities were assayed by SOD and MPO kits, respectively. The levels of inflammatory mediators, tumor necrosis factor-, interleukin-1, and interleukin-6, were assayed by enzyme-linked immunosorbent assay. Pathological changes of lung tissues were observed by HE staining. The levels of NF-B p65 and COX-2 expression were detected by Western blotting. Compared to the LPS group, the treatment with the G. biloba extract at 12 and 24 mgkg-1 markedly attenuated the inflammatory cell numbers in the BALF, decreased NF-B p65 and COX-2 expression, and improved SOD activity, and inhibited MPO activity. The histological changes of the lungs were also significantly improved. The results indicated that G. biloba extract has a protective effect on LPS-induced acute lung injury in mice. The protective mechanism of G. biloba extract may be partly attributed to the inhibition of NF-B p65 and COX-2 activation.

     

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