Isoforskolin downregulates proinflammatory responses induced by Borrelia burgdorferi basic membrane protein A

被引:11
作者
Zhao, Hua [1 ]
Liu, Aihua [2 ,3 ]
Shen, Longqiang [2 ]
Xu, Cuiping [2 ]
Zhu, Ziwei [1 ]
Yang, Jiaru [2 ]
Han, Xinling [1 ]
Bao, Fukai [1 ,3 ]
Yang, Weimin [4 ,5 ]
机构
[1] Kunming Med Univ, Dept Microbiol & Immunol, 1186 Chunronxi Rd, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Med Univ, Dept Biochem & Mol Biol, Kunming 650500, Yunnan, Peoples R China
[3] Kunming Med Univ, Inst Trop Med, Kunming 650500, Yunnan, Peoples R China
[4] Kunming Med Univ, Sch Pharmaceut Sci, 1186 Chunrongxi Rd, Kunming 650500, Yunnan, Peoples R China
[5] Kunming Med Univ, Yunnan Key Lab Pharmacol Nat Prod, 1186 Chunrongxi Rd, Kunming 650500, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
isoforskolin; Borrelia burgdorferi; basic membrane protein A; Lyme disease; GENE-EXPRESSION; LYME ARTHRITIS; CELLS; BMPA;
D O I
10.3892/etm.2017.5300
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The plant Coleus forskohlii is distributed primarily in India, Thailand, China, Egypt and Brazil and has a history of use in the treatment of multiple diseases. Isoforskolin (ISOF) is the principle active component of C. forskohlii native to China and has previously been studied for its biological effects. The aim of the present study was to evaluate the effect of ISOF on the proinflammatory responses induced by recombinant Borrelia burgdorferi basic membrane protein A (rBmpA). In in vitro experiments, the proinflammatory effects of rBmpA and the anti-inflammatory function of ISOF were evaluated in murine macrophages, human macrophages and dendritic cells by detecting the transcription and expression of tumor necrosis factor (TNF)-alpha and interleukin (IL)-6. In in vivo experiments, mean arthritis index and X-ray and histopathological examinations were used to verify the role of ISOF in experimental Lyme arthritis in mice. The results indicated that rBmpA, which induced the transcription and expression of TNF-alpha and IL-6, activated proinflammatory responses in murine macrophages, human macrophages and dendritic cells. In turn, ISOF downregulated the transcription and expression of TNF-alpha and IL-6 induced by rBmpA. Additionally, the in vivo experiments demonstrated that ISOF could also inhibit the symptoms of experimental Lyme arthritis. These results suggest that ISOF may have a potential application as an anti-inflammatory agent for the treatment of Lyme arthritis.
引用
收藏
页码:5974 / 5980
页数:7
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