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Ovarian hormones modulate multidrug resistance transporters in the ovary

  • Brayboy, Lynae M1, 2, 3, 4
  • Knapik, Laura O1
  • Long, Sokunvichet5
  • Westrick, Mollie4
  • Wessel, Gary M3
  • 1 Women & Infants Hospital of Rhode Island, Department of Obstetrics and Gynecology then Division of Reproductive Endocrinology and Infertility, 101 Dudley Street, Providence, RI, 02905, USA , Providence (United States)
  • 2 Alpert Medical School of Brown University, 222 Richmond Street, Providence, RI, 02903, USA , Providence (United States)
  • 3 Brown University, Department of Molecular Biology, Cell Biology and Biochemistry, 60 Olive Street, Providence, RI, 02912, USA , Providence (United States)
  • 4 University of Pennsylvania, Biological Basis of Behavior Department, Room 122 425 South University Avenue, Philadelphia, PA, 19104, USA , Philadelphia (United States)
  • 5 Brown University, 60 Olive Street, Providence, RI, 02912, USA , Providence (United States)
Published Article
Contraception and Reproductive Medicine
BioMed Central
Publication Date
Nov 15, 2018
DOI: 10.1186/s40834-018-0076-7
Springer Nature


BackgroundMultidrug resistance transporters (MDRs) are transmembrane proteins that efflux metabolites and xenobiotics. They are highly conserved in sequence and function in bacteria and eukaryotes and play important roles in cellular homeostasis, as well as in avoidance of antibiotics and cancer therapies. Recent evidence also documents a critical role in reproductive health and in protecting the ovary from environmental toxicant effects. The most well understood MDRs are MDR-1 (P-glycoprotein (P-gp) also known as ABCB1) and BCRP (breast cancer resistance protein) and are both expressed in the ovary. We have previously shown that MDR-1 mRNA steady state expression changes throughout the murine estrous cycle, but expression appears to increase in association with the surge in estradiol during proestrus.MethodsHere we test the model that MDR-1 and BCRP are regulated by estrogen, the major hormonal product of the ovary. This was performed by administering 6-week-old female mice either sesame oil (vehicle control) or oral ethinyl estradiol at 1 μg, 10 μg, and 100 μg or PROGESTERONE at 0.25mg, 0.5 mg or 1 mg or a combination of both for 5 days. The mice were then sacrificed, and the ovaries were removed and cleaned. Ovaries were used for qPCR, immunoblotting, and immnunolabeling.ResultsWe found that oral ethinyl estradiol did not influence the steady state mRNA of MDR-1 or BCRP. Remarkably, the effect on mRNA levels neither increased or decreased in abundance upon estrogen exposures. Conversely, we observed less MDR-1 protein expression in the groups treated with 1 μg and 10 μg, but not 100 μg of ethinyl estradiol compared to controls. MDR-1 and BCRP are both expressed in pre-ovulatory follicles. When we tested progesterone, we found that MDR-1 mRNA increased at the dosages of 0.25 mg and 0.5 mg, but protein expression levels were not statistically significant. Combined oral ethinyl estradiol and progesterone significantly lowered both MDR-1 mRNA and protein.ConclusionsProgesterone appears to influence MDR-1 transcript levels, or steady state levels. This could have implications for better understanding how MDR-1 can be modulated during times of toxic exposure. Understanding the normal physiology of MDR-1 in the ovary will expand the current knowledge in cancer biology and reproduction.

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