TY - JOUR
T1 - Doxorubicin-induced ovarian toxicity
AU - Ben-Aharon, Irit
AU - Bar-Joseph, Hadas
AU - Tzarfaty, Galia
AU - Kuchinsky, Lital
AU - Rizel, Shulamith
AU - Stemmer, Salomon M.
AU - Shalgi, Ruth
N1 - Funding Information:
We thank Hassida Orenstein for her skillful technical assistance, Ruth Kraicer for her valuable advice and Dr Inbal Biton for her useful assistance with the MRI experiments. This research was partially funded by the Israel Cancer Research Fund and by the Israel Cancer Association through donation from the Izraeli Family in memory of the late Prof. Dafna and the late Prof. Dov Izraeli. The MRI work was supported by the the Israel Science Foundation (ISF), the Raymond and Beverly Sackler Center for Biophysics, Tel Aviv University and the Alfredo Federico Strauss Center for Computational Neuro-Imaging, Tel Aviv University. This work was performed in partial fulfillment of the requirements for a Ph.D. degree of Hadas Bar Josef, Faculty of Medicine Tel Aviv University
PY - 2010/3/4
Y1 - 2010/3/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=77950466130&partnerID=8YFLogxK
U2 - 10.1186/1477-7827-8-20
DO - 10.1186/1477-7827-8-20
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AN - SCOPUS:77950466130
SN - 1477-7827
VL - 8
JO - Reproductive Biology and Endocrinology
JF - Reproductive Biology and Endocrinology
M1 - 20
ER -