Abstract

Aim: This study co-evaluated the 2 quoted histologic variables after erythropoietin (Epo) administration. The calculation was based on the results of 2 preliminary studies, each one evaluating a respective histologic variable of endometrial karyorrhexis (EK) or uterus congestion (UC) in an induced ischemia reperfusion (IR) animal experiment.

Highlights

  • Erythropoietin (Epo) was investigated whether having antioxidant capacities. 2 histologic variables in a uterine ischemia reperfusion (UIR) experiment were tested for this purpose

  • The one variable was that of endometrial karyorrhexis (EK) which was recessed by without lesions 0.2727273 ± 0.17222171 (p-value=0.1102) [1]

  • TLR4 has a regulatory role for two antiinflammatory cytokines: the interferon-B1 decreased in wildtype mice and the interleukin-10 increased in TLR4-deficient mice (P

Read more

Summary

Introduction

Erythropoietin (Epo) was investigated whether having antioxidant capacities. 2 histologic variables in a uterine ischemia reperfusion (UIR) experiment were tested for this purpose. Erythropoietin (Epo) was investigated whether having antioxidant capacities. 2 histologic variables in a uterine ischemia reperfusion (UIR) experiment were tested for this purpose. The one variable was that of endometrial karyorrhexis (EK) which was recessed by without lesions 0.2727273 ± 0.17222171 (p-value=0.1102) [1]. The other variable was that of uterus congestion (UC) and was restored by without lesions 0.0090909 ± 0.12689199 (p-value=0.9414) [2]. Epo is met in over 29,895 published biomedical studies, only a 3.51% of them negotiate its antioxidant capacities. The present experimental work tried to co-evaluate these EK and UC variables together and to compare its outcome with each one separately, from the same rat induced UIR protocol

Objectives
Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.