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Clomiphene citrate causes aberrant tubal apoptosis and estrogen receptor activation in rat fallopian tube: implications for tubal ectopic pregnancy.

Journal article
Authors Linus Ruijin Shao
Magdalena Nutu
Birgitta Weijdegård
Emil Egecioglu
Julia Fernandez-Rodriguez
Linda Karlsson-Lindahl
Kristina Gemzell-Danielsson
Christina Bergh
Håkan Billig
Published in Biology of reproduction
Volume 80
Issue 6
Pages 1262-71
ISSN 0006-3363
Publication year 2009
Published at Institute of Biomedicine, Department of Medical and Clinical Genetics
Institute of Neuroscience and Physiology, Department of Physiology
Institute of Clinical Sciences
Pages 1262-71
Language en
Links dx.doi.org/10.1095/biolreprod.108.0...
Keywords Animals, Apoptosis, drug effects, Body Weight, drug effects, Cell Movement, drug effects, Clomiphene, administration & dosage, adverse effects, Epithelial Cells, drug effects, Estradiol, pharmacology, Fallopian Tubes, cytology, drug effects, metabolism, pathology, Female, Gonadal Steroid Hormones, blood, Oocytes, drug effects, Organ Size, drug effects, Pregnancy, Pregnancy, Tubal, chemically induced, Rats, Rats, Sprague-Dawley, Receptors, Estrogen, metabolism, Selective Estrogen Receptor Modulators, administration & dosage, adverse effects, Superovulation
Subject categories Medical and Health Sciences

Abstract

Clomiphene citrate (CC) therapy for disorders of anovulatory infertility has been linked to an increased frequency of tubal ectopic pregnancy. Although CC enhances apoptotic processes in the ovaries, villi, and decidual tissues, its effect on apoptosis in the fallopian tube is unknown. Here, we show that chronic treatment with CC induces tubal apoptosis, but not necrosis, through an intrinsic mitochondria-dependent signaling pathway in vivo. The apoptosis was specific to epithelial cells in the isthmus, and the damage was reversed with 17beta-estradiol (E2); however, pretreatment or concomitant treatment with E2 did not protect against tubal apoptosis induced by chronic treatment with CC. Chronic treatment activated estrogen receptors (ESRs), particularly cilia-localized ESR2A (formerly ERbeta2). In contrast to E2, acute treatment of superovulating rats with a high dose of CC or the ESR2-selective agonist 2,3-bis (4-hydroxyphenyl)-propionitrile (DPN) significantly delayed the transport of oocyte-cumulus complexes through the fallopian tube. Our findings suggest that in response to chronic CC therapy, isthmus-specific apoptosis of epithelial cells and activation of cilia-ESR2A act in parallel to block gamete and embryo passage through the fallopian tube, eventually resulting in tubal ectopic pregnancy.

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