Cargando…
Doxorubicin-induced ovarian toxicity
BACKGROUND: Young cancer patients may occasionally face infertility and premature gonadal failure. Apart from its direct effect on follicles and oocytes, chemotherapy may induce ovarian toxicity via an impact on the entire ovary. The role of doxorubicin in potential ovarian failure remains obscure....
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838903/ https://www.ncbi.nlm.nih.gov/pubmed/20202194 http://dx.doi.org/10.1186/1477-7827-8-20 |
_version_ | 1782178912337395712 |
---|---|
author | Ben-Aharon, Irit Bar-Joseph, Hadas Tzarfaty, Galia Kuchinsky, Lital Rizel, Shulamith Stemmer, Salomon M Shalgi, Ruth |
author_facet | Ben-Aharon, Irit Bar-Joseph, Hadas Tzarfaty, Galia Kuchinsky, Lital Rizel, Shulamith Stemmer, Salomon M Shalgi, Ruth |
author_sort | Ben-Aharon, Irit |
collection | PubMed |
description | BACKGROUND: Young cancer patients may occasionally face infertility and premature gonadal failure. Apart from its direct effect on follicles and oocytes, chemotherapy may induce ovarian toxicity via an impact on the entire ovary. The role of doxorubicin in potential ovarian failure remains obscure. Our intention was to elucidate doxorubicin-related toxicity within ovaries. METHODS: Female mice were injected intraperitoneally with 7.5 or 10 mg/kg doxorubicin and their ovaries were visualized in vivo by high resolution MRI, one day and one month following treatment. Ovaries of other treated mice were excised and weighed at the same post-treatment intervals. Ovarian histological sections were stained for TUNEL or active caspase-3 and follicles were counted and categorized. Ovulation rates were evaluated in superovulated female mice treated with doxorubicin. RESULTS: A single injection of doxorubicin resulted in a major reduction in both ovarian size and weight that lasted even one month post treatment. A dramatic reduction in ovulation rate was observed one week after treatment, followed by a partial recovery at one month. Histological examination revealed positive staining of TUNEL and active caspase-3. We observed a significant reduction in the population of secondary and primordial follicles one month following treatment. CONCLUSIONS: Our results may imply a mechanism of chemotherapy-induced ovarian toxicity, manifested by reduced ovulation and accompanied by a reduction in ovarian size, caused probably by an acute insult to the ovary. |
format | Text |
id | pubmed-2838903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28389032010-03-16 Doxorubicin-induced ovarian toxicity Ben-Aharon, Irit Bar-Joseph, Hadas Tzarfaty, Galia Kuchinsky, Lital Rizel, Shulamith Stemmer, Salomon M Shalgi, Ruth Reprod Biol Endocrinol Research BACKGROUND: Young cancer patients may occasionally face infertility and premature gonadal failure. Apart from its direct effect on follicles and oocytes, chemotherapy may induce ovarian toxicity via an impact on the entire ovary. The role of doxorubicin in potential ovarian failure remains obscure. Our intention was to elucidate doxorubicin-related toxicity within ovaries. METHODS: Female mice were injected intraperitoneally with 7.5 or 10 mg/kg doxorubicin and their ovaries were visualized in vivo by high resolution MRI, one day and one month following treatment. Ovaries of other treated mice were excised and weighed at the same post-treatment intervals. Ovarian histological sections were stained for TUNEL or active caspase-3 and follicles were counted and categorized. Ovulation rates were evaluated in superovulated female mice treated with doxorubicin. RESULTS: A single injection of doxorubicin resulted in a major reduction in both ovarian size and weight that lasted even one month post treatment. A dramatic reduction in ovulation rate was observed one week after treatment, followed by a partial recovery at one month. Histological examination revealed positive staining of TUNEL and active caspase-3. We observed a significant reduction in the population of secondary and primordial follicles one month following treatment. CONCLUSIONS: Our results may imply a mechanism of chemotherapy-induced ovarian toxicity, manifested by reduced ovulation and accompanied by a reduction in ovarian size, caused probably by an acute insult to the ovary. BioMed Central 2010-03-04 /pmc/articles/PMC2838903/ /pubmed/20202194 http://dx.doi.org/10.1186/1477-7827-8-20 Text en Copyright ©2010 Ben-Aharon et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ben-Aharon, Irit Bar-Joseph, Hadas Tzarfaty, Galia Kuchinsky, Lital Rizel, Shulamith Stemmer, Salomon M Shalgi, Ruth Doxorubicin-induced ovarian toxicity |
title | Doxorubicin-induced ovarian toxicity |
title_full | Doxorubicin-induced ovarian toxicity |
title_fullStr | Doxorubicin-induced ovarian toxicity |
title_full_unstemmed | Doxorubicin-induced ovarian toxicity |
title_short | Doxorubicin-induced ovarian toxicity |
title_sort | doxorubicin-induced ovarian toxicity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838903/ https://www.ncbi.nlm.nih.gov/pubmed/20202194 http://dx.doi.org/10.1186/1477-7827-8-20 |
work_keys_str_mv | AT benaharonirit doxorubicininducedovariantoxicity AT barjosephhadas doxorubicininducedovariantoxicity AT tzarfatygalia doxorubicininducedovariantoxicity AT kuchinskylital doxorubicininducedovariantoxicity AT rizelshulamith doxorubicininducedovariantoxicity AT stemmersalomonm doxorubicininducedovariantoxicity AT shalgiruth doxorubicininducedovariantoxicity |