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Impact of matrine on inflammation related factors in rat intestinal microvascular endothelial cells

Update time: 7/8/2010 2:09:04 AM  Views: 22  【 Font: Large Medium Small 】【Print

Journal of Ethnopharmacology Volume 125, Issue 3, 25 September 2009, Pages 404-409

Zhanwei Suoa, b, Ye Liub, Miro Ferreria, Tao Zhangb, Zhongjie Liua, Xiang Mub, Corresponding Author Contact Information, E-mail The Corresponding Author and Bo Hana, Corresponding Author Contact Information, E-mail The Corresponding Author

aCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, PR China

bBeijing Key Laboratory of Traditional Chinese Veterinary Medicine, Beijing Agricultural College, Beijing 102206, PR China

Abstract

Ethnopharmacological relevance

Matrine (MT) is a main active ingredient of Sophora flavescens roots, which is used in Traditional Chinese Medicine (TCM) for the treatment of inflammations like enteritis, hepatitis and atopic dermatitis.

Aims of the study

Aim of the study is to gain insight into the effects of MT on nitric oxide (NO) release, intracellular NO production, and endothelial nitric oxide synthase (eNOS) level in second generation rat intestinal microvascular endothelial cells (RIMECs). Moreover, the effects of MT on soluble intercellular adhesion molecule-1 (sICAM-1), interleukin-6 (IL-6) and interleukin-8 (IL-8) production induced by lipopolysaccharide (LPS) in these cells were evaluated.

Material and Methods

Isolated and identified RIMECs cultures were exposed to different concentrations of matrine, and changes in extra- and intracellular NO concentrations were measured in dependance of time by Griess reaction or DAF-FM diacetate. Obtained cell cultures were solitude treated with lypopolysaccharide (LPS) or combined with MT to observe impacts on sICAM-1, IL-6 and IL-8 concentration in culture supernatants by ELISA.

Results

Matrine dose-dependently increased the concentration of NO in culture supernatant of RIMECs. Exposure of MT resulted in a steady intracellular NO increase pattern under different concentrations with different values and has an increasing effect on eNOS concentration at a long time exposure. Additionally, matrine reduced the increasing effect of LPS on the production of IL-6, IL-8, and sICAM-1 in RIMECs.

Conclusion

These results show that matrine may serve as a protective agent against tissue damage in inflammation by improving NO-dependent vasomotion and inhibiting inflammatory cytokines induced by LPS.

Graphical abstract


Keywords: Matrine; Microvascular endothelial cells; Nitric oxide; Intercellular adhesion molecule-1; Interleukin

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