Andrographolide sulfonate ameliorates lipopolysaccharide-induced acute lung injury in mice by down-regulating MAPK and NF-κB pathways

详细信息    查看全文

• 作者：Shuang Peng^a ; Nan Hang^a ; Wen Liu^a ; Wenjie Guo^a ; Chunhong Jiang^b ; ^c ; Xiaoling Yang^b ; ^c ; Qiang Xu^a ; ^{molpharm@163.com" class="auth_mail" title="E-mail the corresponding author} ; Yang Sun^a ; ^{yangsun@nju.edu.cn" class="auth_mail" title="E-mail the corresponding author}
• 关键词：ALI ; acute lung injury ; ARDS ; acute respiratory distress syndrome ; BALF ; bronchoalveolar lavage fluid ; DSS ; dextran sulfate sodium ; H&E ; hematoxylin & eosin ; HRP ; horseradish peroxidase ; IL-6 ; interleukin-6 ; JNK ; c-Jun N-terminal kinase ; LPS ; lipopolysaccharide ; MAPK ; mitogen-activated protein kinase ; NF-κB ; nuclear factor-κB ; TNBS ; trinitrobenzenesulfonic acid ; TNF ; tumor necrosis factor
• 刊名：Acta Pharmaceutica Sinica B
• 出版年：2016
• 出版时间：May 2016
• 年：2016
• 卷：6
• 期：3
• 页码：205-211
• 全文大小：2945 K

文摘

Acute lung injury (ALI) or acute respiratory distress syndrome (ARDS) is a severe, life-threatening medical condition characterized by widespread inflammation in the lungs, and is a significant source of morbidity and mortality in the patient population. New therapies for the treatment of ALI are desperately needed. In the present study, we examined the effect of andrographolide sulfonate, a water-soluble form of andrographolide (trade name: Xi-Yan-Ping Injection), on lipopolysaccharide (LPS)-induced ALI and inflammation. Andrographolide sulfonate was administered by intraperitoneal injection to mice with LPS-induced ALI. LPS-induced airway inflammatory cell recruitment and lung histological alterations were significantly ameliorated by andrographolide sulfonate. Protein levels of pro-inflammatory cytokines in bronchoalveolar lavage fluid (BALF) and serum were reduced by andrographolide sulfonate administration. mRNA levels of pro-inflammatory cytokines in lung tissue were also suppressed. Moreover, andrographolide sulfonate markedly suppressed the activation of mitogen-activated protein kinase (MAPK) as well as p65 subunit of nuclear factor-κB (NF-κB). In summary, these results suggest that andrographolide sulfonate ameliorated LPS-induced ALI in mice by inhibiting NF-κB and MAPK-mediated inflammatory responses. Our study shows that water-soluble andrographolide sulfonate may represent a new therapeutic approach for treating inflammatory lung disorders.