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      Voluntary Exercise Improves Estrous Cyclicity in Prenatally Androgenized Female Mice Despite Programming Decreased Voluntary Exercise: Implications for Polycystic Ovary Syndrome (PCOS)

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          Abstract

          Prenatal androgen (PNA) exposure in mice produces a phenotype resembling lean polycystic ovary syndrome. We studied effects of voluntary exercise on metabolic and reproductive parameters in PNA vs vehicle (VEH)-treated mice. Mice (8 wk of age) were housed individually and estrous cycles monitored. At 10 weeks of age, mice were divided into groups (PNA, PNA-run, VEH, VEH-run, n = 8–9/group); those in the running groups received wheels allowing voluntary running. Unexpectedly, PNA mice ran less distance than VEH mice; ovariectomy eliminated this difference. In ovary-intact mice, there was no difference in glucose tolerance, lower limb muscle fiber types, weight, or body composition among groups after 16 weeks of running, although some mitochondrial proteins were mildly up-regulated by exercise in PNA mice. Before running, estrous cycles in PNA mice were disrupted with most days in diestrus. There was no change in cycles during weeks 1–6 of running (10–15 wk of age). In contrast, from weeks 11 to 16 of running, cycles in PNA mice improved with more days in proestrus and estrus and fewer in diestrus. PNA programs reduced voluntary exercise, perhaps mediated in part by ovarian secretions. Exercise without weight loss improved estrous cycles, which if translated could be important for fertility in and counseling of lean women with polycystic ovary syndrome.

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          Author and article information

          Journal
          Endocrinology
          Endocrinology
          endo
          endoc
          endo
          Endocrinology
          Endocrine Society (Washington, DC )
          0013-7227
          1945-7170
          December 2015
          10 September 2015
          1 December 2016
          : 156
          : 12
          : 4618-4628
          Affiliations
          Departments of Obstetrics and Gynecology (L.D.H., S.M.M.), Molecular and Integrative Physiology (L.L.B., A.J.C., D.E.M., S.M.M.), and Internal Medicine (D.E.M., S.M.M.), University of Michigan, Ann Arbor, Michigan 48109-5622
          Author notes
          Address all correspondence and requests for reprints to: Suzanne M. Moenter, Department of Obstetrics and Gynecology, University of Michigan, 7725 Medical Sciences II, 1137 East Catherine Street, Ann Arbor, MI 48109-5622. E-mail: smoenter@ 123456umich.edu .
          Article
          PMC4655213 PMC4655213 4655213 EN-15-1593
          10.1210/en.2015-1593
          4655213
          26360506
          57ce64af-5d05-4ea5-b511-d79b56bab79f
          Copyright © 2015 by the Endocrine Society
          History
          : 7 July 2015
          : 3 September 2015
          Categories
          Original Research
          Neuroendocrinology

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