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Betamethasone (\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      ) is a glucocorticoid used in clinical practice for antenatal therapy. We previously reported changes to testicular morphology, altered sperm quality, and fertility in adult rats following intrauterine administration of\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      Given that high levels of corticosteroids during gestation lead to fetal androgen depletion, and the essential role of testosterone during epididymal development, here we investigated epididymal morphology and physiology in the F1 and F2 male offspring of female rats treated with\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      during gestation.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and methods<\/jats:title>\n                    <jats:p>\n                      Pregnant rats were randomly divided into two experimental groups: control (saline vehicle,\n                      <jats:italic>n\u00a0<\/jats:italic>\n                      =\n                      <jats:italic>\u00a0<\/jats:italic>\n                      11) and\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      \u2010treated group (0.1\u00a0mg\/kg betamethasone 21\u2010phosphate disodium,\n                      <jats:italic>n\u00a0<\/jats:italic>\n                      =\n                      <jats:italic>\u00a0<\/jats:italic>\n                      13). Rats received an intramuscular injection of vehicle or\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      on gestational days 12, 13, 18, and 19. This encompasses the beginning of the critical window of male rat reproductive tract development. A subset of three males from each litter (\n                      <jats:italic>n\u00a0<\/jats:italic>\n                      =\n                      <jats:italic>\u00a0<\/jats:italic>\n                      5 litters\/group) was used: One rat per litter was euthanized at puberty, one was euthanized at adulthood, while the others were mated with a non\u2010treated female to obtain the F2 generation. The same protocol described for the F1 was applied for F2, except for the mating protocol.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In both F1 and F2 generations, prenatal\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      exposure resulted in delayed differentiation of the cauda epididymal epithelium, characterized by increased cribriform appearance on\n                      <jats:styled-content style=\"fixed-case\">PND<\/jats:styled-content>\n                      45, and displayed weaker or non\u2010detectable Cx43 immunostaining. Furthermore, in the F1 generation only, immunostaining of\n                      <jats:styled-content style=\"fixed-case\">TP<\/jats:styled-content>\n                      63, a transcription factor expressed in basal cells, appeared more intense with a greater number of\n                      <jats:styled-content style=\"fixed-case\">TP<\/jats:styled-content>\n                      63\u2010positive cells observed in the cauda epididymis. In adults, the epithelial area was reduced in the F1\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      rats. The contractile activity of isolated epididymal ducts was comparable between groups.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion and Conclusion<\/jats:title>\n                    <jats:p>\n                      Prenatal\n                      <jats:styled-content style=\"fixed-case\">BM<\/jats:styled-content>\n                      exposure leads to intergenerational impairment in the development and structure of the rat epididymis.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/andr.12657","type":"journal-article","created":{"date-parts":[[2019,6,28]],"date-time":"2019-06-28T01:54:04Z","timestamp":1561686844000},"page":"719-729","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["Prenatal exposure to betamethasone causes intergenerational impairment of epididymal development in the rat"],"prefix":"10.1111","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2112-5123","authenticated-orcid":false,"given":"W. 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