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纸质出版日期:2009
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[1].Protective Effect of Emodin against Lipopolysaccharides-induced Corneal Injury in Rats[J].Chinese Medical Sciences Journal,2009,24(04):236-240.
Guo-ling Chen1, Zhi-yu Liu2, Jing Wang1, et al. Protective Effect of Emodin against Lipopolysaccharides-induced Corneal Injury in Rats[J]. Chinese medical sciences journal, 2009, 24(4): 236-240.
[1].Protective Effect of Emodin against Lipopolysaccharides-induced Corneal Injury in Rats[J].Chinese Medical Sciences Journal,2009,24(04):236-240. DOI:
Guo-ling Chen1, Zhi-yu Liu2, Jing Wang1, et al. Protective Effect of Emodin against Lipopolysaccharides-induced Corneal Injury in Rats[J]. Chinese medical sciences journal, 2009, 24(4): 236-240. DOI:
Objective To investigate the effect of emodin on lipopolysaccharides(LPS)-induced corneal injury in rats.Methods Three parallel incisions on the central surface of corneal epithelium were made and LPS was applied on them to induce corneal injury in Wistar rats.All rats were randomly divided into emodin group(n=40) and keratitis group(n=40).Rats in the emodin group received subconjunctival injection of emodin and rats in the keratitis group received its vehicle 30 minutes before LPS exposure.At different time points-1
3
6
12
and 24 hours after LPS exposure
the symptoms of all rats were observed and the severity of their ocular inflammation was examined with a slit lamp microscope
then 8 rats in each group were killed through cervical dislocation and their eyes were enucleated and prepared to observe pathological changes of corneal tissue under a light microscope.The activation of nuclear factor-κB(NF-κB) under different conditions was determined by Western blot.Immunocytochemistry staining with an antibody against intercellular adhesion molecule-1(ICAM-1) was performed to identify positive cells in corneal tissues.Results The model of acute keratitis was successfully established in Wistar rats.LPS could induce a typical corneal inflammatory response
such as hyperemia
corneal edema and opacity
which were observed in model rats.Compared with keratitis group
both ocular behaviors and damages of the corneal structure were improved in emodin group.Furthermore
the activation of NF-кB and the expression of ICAM-1 induced by LPS were markedly inhibited in emodin group.Conclusion Emodin can inhibit the activation of NF-κB and the expression of ICAM-1 induced by LPS in corneas
protect against acute corneal injury
and improve symptoms in rats.
Objective To investigate the effect of emodin on lipopolysaccharides(LPS)-induced corneal injury in rats.Methods Three parallel incisions on the central surface of corneal epithelium were made and LPS was applied on them to induce corneal injury in Wistar rats.All rats were randomly divided into emodin group(n=40) and keratitis group(n=40).Rats in the emodin group received subconjunctival injection of emodin and rats in the keratitis group received its vehicle 30 minutes before LPS exposure.At different time points—1
3
6
12
and 24 hours after LPS exposure
the symptoms of all rats were observed and the severity of their ocular inflammation was examined with a slit lamp microscope
then 8 rats in each group were killed through cervical dislocation and their eyes were enucleated and prepared to observe pathological changes of corneal tissue under a light microscope.The activation of nuclear factor-κB(NF-κB) under different conditions was determined by Western blot.Immunocytochemistry staining with an antibody against intercellular adhesion molecule-1(ICAM-1) was performed to identify positive cells in corneal tissues.Results The model of acute keratitis was successfully established in Wistar rats.LPS could induce a typical corneal inflammatory response
such as hyperemia
corneal edema and opacity
which were observed in model rats.Compared with keratitis group
both ocular behaviors and damages of the corneal structure were improved in emodin group.Furthermore
the activation of NF-кB and the expression of ICAM-1 induced by LPS were markedly inhibited in emodin group.Conclusion Emodin can inhibit the activation of NF-κB and the expression of ICAM-1 induced by LPS in corneas
protect against acute corneal injury
and improve symptoms in rats.
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