Effect of Emodin on Intestinalmucosa Mast Cells in Mice with Intestine Ischemia-Reperfusion
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Effect of Emodin on Intestinalmucosa Mast Cells in Mice with Intestine Ischemia-Reperfusion
Chinese Journal of Experimental Traditional Medical FormulaeVol. 17, Issue 16, Pages: 167-170(2011)
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Published:2011
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WEI Zhi-jun, WU Xian-ping, GAN Xiao-liang, et al. Effect of Emodin on Intestinalmucosa Mast Cells in Mice with Intestine Ischemia-Reperfusion[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(16): 167-170.
DOI:
WEI Zhi-jun, WU Xian-ping, GAN Xiao-liang, et al. Effect of Emodin on Intestinalmucosa Mast Cells in Mice with Intestine Ischemia-Reperfusion[J]. Chinese journal of experimental traditional medical formulae, 2011, 17(16): 167-170.DOI:
Effect of Emodin on Intestinalmucosa Mast Cells in Mice with Intestine Ischemia-Reperfusion
Objective: To investigate the effect of emodin on intestinalmucosa mast cells (IMMC) in mice with intestine ischemia-reperfusion (I/R). Method: Twenty-eight mice were randomly divided into four groups (n=7 each): group A (sham operation group)
group B(superior mesenteric artery was clamped for 30 minutes followed by reperfusion)
group D1 and D2 (in which emodin 60 or 120 mg·kg-1 was given via gastric tube every day for 3 days before I/R). Intestinalmucosa pathology structure
the ultramicrostructure of IMMC were observed under electron microscope
and tryptase expression was compared for IMMC counting
histamine and tumor necrosis factor (TNF-α) were determined. Result: Compared with that of group A
Chiu’s score and IMMC number
histamine
TNF-α in group B were increased significantly (P<0.05 or P<0.01). Compared with that of group B
IMMC number of group D1
D2 and TNF-α of group D2 were decreased markedly (P<0.05). IMMC ultrastructure in group A was normal
and there was some degranulation phenomenon in group B
such as mast cell envelope coalition and intracellular vacuoles. There was more less intracellular vacuoles in group D1 and D2. Conclusion: Emodin can decrease intestinalmucosa disorganization in mice by inhibiting IMMC activation and degranulation.
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