In vitro effects of emodin on peritoneal macrophage intercellular adhesion molecule-3 in a rat model of severe acute pancreatitis/systemic inflammatory response syndrome

  • NI Q
  • ZHANG W
  • SUN K
  • et al.
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Abstract

Rhubarb is often used in Chinese herbal medicine for the treatment of systemic inflammatory response syndrome (SIRS). Emodin is the main active constituent of rhubarb. This study was performed to investigate the in vitro effects of emodin and dexamethasone on peritoneal macrophage (pMPhi) phagocytosis and the expression of intercellular adhesion molecule-3 (ICAM-3). A total of 40 Sprague-Dawley (SD) rats were randomly divided into sham surgery (n=10) and model groups (n=30). After 24 h, pMPhis were harvested and the model group was randomly divided into three subgroups (n=10 rats/subgroup): the 5 mug/ml emodin, 0.1 mumol/ml dexamethasone and control groups. The drugs were administered following macrophage (MPhi) adhesion for 24 h. pMPhi phagocytosis was significantly increased in the emodin group compared to that in the control group. Moreover, pMPhi phagocytosis was significantly increased in the emodin group compared to that in the dexamethasone group. The expression of ICAM-3 was significantly increased in the emodin group compared to that in the control group. The expression of ICAM-3 was significantly increased in the emodin group compared to that in the dexamethasone group. The expression of ICAM-3 was significantly increased in the emodin and dexamethasone groups compared to that in the control group. pMPhi phagocytosis and ICAM-3 expression were significantly increased following emodin treatment compared to those in the control and dexamethasone groups, indicating that emodin may enhance pMPhi phagocytosis and apoptotic cell clearance by altering ICAM-3 expression.

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NI, Q., ZHANG, W., SUN, K., YIN, C., AN, J., & SHANG, D. (2014). In vitro effects of emodin on peritoneal macrophage intercellular adhesion molecule-3 in a rat model of severe acute pancreatitis/systemic inflammatory response syndrome. Biomedical Reports, 2(1), 63–68. https://doi.org/10.3892/br.2013.178

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