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Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model

BACKGROUND: Undescended testis is an absence of testis in the scrotum, the incidence was 15 cases per 1000 from 1974 to 1996 in Europe. At Saiful Anwar Regional Hospital East Java, from January 2015 to July 2019 there were 60 boys diagnosed with undescended testis. A temperature rise of testis locat...

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Autores principales: Ardiani, Astarin, Purnomo, Basuki B., Kurnia Penta, S., Kenty Wantri, A., Wardhani, Viera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8385726/
https://www.ncbi.nlm.nih.gov/pubmed/34483444
http://dx.doi.org/10.5455/medarh.2021.75.168-173
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author Ardiani, Astarin
Purnomo, Basuki B.
Kurnia Penta, S.
Kenty Wantri, A.
Wardhani, Viera
author_facet Ardiani, Astarin
Purnomo, Basuki B.
Kurnia Penta, S.
Kenty Wantri, A.
Wardhani, Viera
author_sort Ardiani, Astarin
collection PubMed
description BACKGROUND: Undescended testis is an absence of testis in the scrotum, the incidence was 15 cases per 1000 from 1974 to 1996 in Europe. At Saiful Anwar Regional Hospital East Java, from January 2015 to July 2019 there were 60 boys diagnosed with undescended testis. A temperature rise of testis located in the abdominal triggers production of reactive oxygen species, causing impairment of the testicular epithelial germ cells and spermatogenesis, leading to many complications. Erythropoietin is a glycoprotein hormone that circulates in the body and has a positive effect on ischemic injury/gonadal reperfusion. OBJECTIVE: To find out ROS involvement in undescended testis and efficacy of EPO as an additional therapy for undescended testis. METHODS: This study is an experimental study with a post-test only control group design, using 18 male Wistar mice conditioned to be undescended testis for 7 days and underwent orchidopexy and some are given additional erythropoietin 1000iu/Kg 3 times a week. RESULTS: Before and after the intervention, the mean body weight of mice did not experience a significant difference, meanwhile testicular volume showed a significant difference between the orchidopexy and EPO groups (p = 0.005 and 0.001). Johnsen’s score were found significant in the EPO group. Malone dialdehyde level in EPO and orchidopexy group showed significant difference p = 0.01 and 0.009 when compared to undescended testis group. CONCLUSION: There was the involvement of ROS in undescended testis and additional EPO improve impairment of germinal epithelial cells and spermatogenesis process due to undescended testis.
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spelling pubmed-83857262021-09-02 Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model Ardiani, Astarin Purnomo, Basuki B. Kurnia Penta, S. Kenty Wantri, A. Wardhani, Viera Med Arch Original Paper BACKGROUND: Undescended testis is an absence of testis in the scrotum, the incidence was 15 cases per 1000 from 1974 to 1996 in Europe. At Saiful Anwar Regional Hospital East Java, from January 2015 to July 2019 there were 60 boys diagnosed with undescended testis. A temperature rise of testis located in the abdominal triggers production of reactive oxygen species, causing impairment of the testicular epithelial germ cells and spermatogenesis, leading to many complications. Erythropoietin is a glycoprotein hormone that circulates in the body and has a positive effect on ischemic injury/gonadal reperfusion. OBJECTIVE: To find out ROS involvement in undescended testis and efficacy of EPO as an additional therapy for undescended testis. METHODS: This study is an experimental study with a post-test only control group design, using 18 male Wistar mice conditioned to be undescended testis for 7 days and underwent orchidopexy and some are given additional erythropoietin 1000iu/Kg 3 times a week. RESULTS: Before and after the intervention, the mean body weight of mice did not experience a significant difference, meanwhile testicular volume showed a significant difference between the orchidopexy and EPO groups (p = 0.005 and 0.001). Johnsen’s score were found significant in the EPO group. Malone dialdehyde level in EPO and orchidopexy group showed significant difference p = 0.01 and 0.009 when compared to undescended testis group. CONCLUSION: There was the involvement of ROS in undescended testis and additional EPO improve impairment of germinal epithelial cells and spermatogenesis process due to undescended testis. Academy of Medical Sciences of Bosnia and Herzegovina 2021-06 /pmc/articles/PMC8385726/ /pubmed/34483444 http://dx.doi.org/10.5455/medarh.2021.75.168-173 Text en © 2021 Astarin Ardiani, Basuki B. Purnomo, Kurnia Penta S., Kenty Wantri A., Viera Wardhani https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Ardiani, Astarin
Purnomo, Basuki B.
Kurnia Penta, S.
Kenty Wantri, A.
Wardhani, Viera
Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title_full Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title_fullStr Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title_full_unstemmed Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title_short Erythropoietin Effect on Testicular Germinal Epithelium Cells in Undescended Testis Mice Model
title_sort erythropoietin effect on testicular germinal epithelium cells in undescended testis mice model
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8385726/
https://www.ncbi.nlm.nih.gov/pubmed/34483444
http://dx.doi.org/10.5455/medarh.2021.75.168-173
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