{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,13]],"date-time":"2026-02-13T14:05:43Z","timestamp":1770991543253,"version":"3.50.1"},"reference-count":53,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2004,7,20]],"date-time":"2004-07-20T00:00:00Z","timestamp":1090281600000},"content-version":"vor","delay-in-days":49,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Birth Defects Research Pt B"],"published-print":{"date-parts":[[2004,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:bold>BACKGROUND:<\/jats:bold> Lasofoxifene is a nonsteroidal selective estrogen receptor modulator (SERM) with greater than 100\u2010fold selectivity against all other steroid receptors and is a potentially superior treatment for postmenopausal osteoporosis. The purpose of this study was to evaluate the effects of lasofoxifene on male reproduction in rats in light of the known effects of estrogen modulating compounds on male reproductive ability. <jats:bold>METHODS:<\/jats:bold> Lasofoxifene was administered to adult male rats at doses of 0.1, 1, 10, and 100\u2009mg\/kg for 66\u201370 consecutive days. After 28 days of dosing, male rats were cohabited with untreated female rats. Female rats were euthanized on gestation day 14 and a uterine examination was carried out for evaluation of reproductive parameters and embryo viability. Male rats were euthanized after 66\u201370 days of dosing and epididymal sperm motility and concentration were assayed. The testes, epididymides, prostate, and seminal vesicles were weighed and microscopically examined. <jats:bold>RESULTS:<\/jats:bold> The duration of cohabitation was increased for 100\u2009mg\/kg males by 0.7 days. The number of males copulating and the number of implantation sites produced per copulation were reduced in the 10 and 100\u2009mg\/kg groups. Weights of the seminal vesicles and epididymides were reduced for all groups, although the testes weight and epididymal sperm motility and concentration were not affected by treatment. There were no microscopic findings in the male reproductive tissues. <jats:bold>CONCLUSION:<\/jats:bold> The changes in male fertility and reproductive tissue weights after exposure to lasofoxifene are consistent with those previously described for estrogen receptor\u2010modulating compounds. <jats:italic>Birth Defects Res B<\/jats:italic> 71:142\u2013149, 2004. \u00a9 2004 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/bdrb.20008","type":"journal-article","created":{"date-parts":[[2004,7,20]],"date-time":"2004-07-20T15:08:35Z","timestamp":1090336115000},"page":"142-149","source":"Crossref","is-referenced-by-count":9,"title":["Reproductive toxicity assessment of lasofoxifene, a selective estrogen receptor modulator (SERM), in male rats"],"prefix":"10.1002","volume":"71","author":[{"given":"Gregg 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