Effect of mifepristone on COX-2 both in eutopic and ectopic endometrium in mouse endometriotic model

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Mifepristone reduced COX-2 mRNA and protein in a mouse endometriosis model but did not alter ectopic lesion size or serum PGE2 levels.

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This paper studied the effect of the antiprogesterone mifepristone on cyclooxygenase-2 (COX-2) mRNA and protein expression in both eutopic and ectopic endometrium in a mouse endometriosis model, using 30 mice allocated to mifepristone or control groups evaluated at 1, 4, and 6 weeks. Ectopic lesion size was monitored by small animal optical imaging, while COX-2 mRNA and protein were measured by RT-PCR and western blot, and serum PGE2 was assessed by ELISA. Mifepristone did not significantly change fluorescent intensity (ectopic lesion size) at any time point, but it decreased COX-2 mRNA transcription at 1 and 4 weeks and decreased COX-2 protein at 4 and 6 weeks, with a non-significant trend toward lower serum PGE2. This paper is centrally about endometriosis—specifically, mifepristone’s impact on COX-2 and its prostaglandin product in eutopic versus ectopic endometrial tissue in a mouse endometriotic model.

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Abstract

ObjectiveTo study the influence of mifepristone on the expression of cyclooxygenase 2 (COX-2) protein and COX-2 mRNA and then to evaluate the mechanism.MethodsAfter the establishment of 30 mice endometriosis models, the mice were randomly divided into six groups with 5 mice each group and assigned to experimental and control groups of 1-, 4- and 6-week circle according to whether mifepristone (0.13 mg d(-1)) was taken or not. Small animal optical imaging system was used to detect the fluorescent intensity of the ectopic tissue. Reverse transcript-polymerase chain reaction and western blot was used to examine COX-2 protein and COX-2 mRNA expression. ELISA was used to examine concentration of PGE(2) in serum.Result(s)Mifepristone could not affect the fluorescent intensity of the ectopic endometrium after it was taken 1, 4, and 6 (P > 0.05). However, it could decrease the transcription of COX-2 mRNA in the 1 and 4 week groups (P 0.05). It could decrease the expression of COX-2 protein after it was taken 4 and 6 weeks (P 0.05).Conclusion(s)This study showed that mifepristone could not affect the size of the ectopic endometrium, but it could decrease the transcription of COX-2 gene and then reduce the expression of COX-2 protein and its product PGE(2) which is an important factor which mediate pain. This maybe another mechanism that mifepristone takes effect through anti-inflammatory path.
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Abstract

Objective To study the influence of mifepristone on the expression of cyclooxygenase 2 (COX-2) protein and COX-2 mRNA and then to evaluate the mechanism.

Methods

After the establishment of 30 mice endometriosis models, the mice were randomly divided into six groups with 5 mice each group and assigned to experimental and control groups of 1-, 4- and 6-week circle according to whether mifepristone (0.13 mg d−1) was taken or not. Small animal optical imaging system was used to detect the fluorescent intensity of the ectopic tissue. Reverse transcript-polymerase chain reaction and western blot was used to examine COX-2 protein and COX-2 mRNA expression. ELISA was used to examine concentration of PGE2 in serum. Result(s) Mifepristone could not affect the fluorescent intensity of the ectopic endometrium after it was taken 1, 4, and 6 (P > 0.05). However, it could decrease the transcription of COX-2 mRNA in the 1 and 4 week groups (P 0.05). It could decrease the expression of COX-2 protein after it was taken 4 and 6 weeks (P 0.05). Conclusion(s) This study showed that mifepristone could not affect the size of the ectopic endometrium, but it could decrease the transcription of COX-2 gene and then reduce the expression of COX-2 protein and its product PGE2 which is an important factor which mediate pain. This maybe another mechanism that mifepristone takes effect through anti-inflammatory path. Similar content being viewed by others

References

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Condition tags

endometriosis

MeSH descriptors

Cyclooxygenase 2 Endometriosis Endometrium Menstruation-Inducing Agents Mifepristone Animals Cyclooxygenase 2 Dinoprostone Dinoprostone Drug Evaluation, Preclinical Endometriosis Endometriosis Endometrium Endometrium Female Fluorescence Menstruation-Inducing Agents Menstruation-Inducing Agents Mice Mice, Inbred C57BL

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