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A combined treatment with selective androgen and estrogen receptor modulators prevents bone loss in orchiectomized rats

Purpose Enobosarm (EN), a selective androgen receptor modulator and raloxifene (RAL), a selective estrogen receptor modulator, have been shown to improve bone tissue in osteoporotic males. The present study evaluated the effects of a combination therapy of EN and RAL on bone properties in orchiectom...

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Published in:Journal of endocrinological investigation 2022-12, Vol.45 (12), p.2299-2311
Main Authors: Komrakova, M., Büchler, G., Böker, K. O., Lehmann, W., Schilling, A. F., Roch, P. J., Taudien, S., Hoffmann, D. B., Sehmisch, S.
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creator Komrakova, M.
Büchler, G.
Böker, K. O.
Lehmann, W.
Schilling, A. F.
Roch, P. J.
Taudien, S.
Hoffmann, D. B.
Sehmisch, S.
description Purpose Enobosarm (EN), a selective androgen receptor modulator and raloxifene (RAL), a selective estrogen receptor modulator, have been shown to improve bone tissue in osteoporotic males. The present study evaluated the effects of a combination therapy of EN and RAL on bone properties in orchiectomized rats compared to the respective single treatments. Methods Eight-month-old male Sprague–Dawley rats were either left intact (Non-Orx) or orchiectomized (Orx). The Orx rats were divided into four groups (n = 15 each): 1) Orx, 2) EN treatment (Orx + EN), 3) RAL treatment (Orx + RAL), 4) combined treatment (Orx + EN + RAL). EN and RAL (0.4 mg and 7 mg/kg body weight/day) were applied immediately after Orx with a soy-free pelleted diet for up to 18 weeks. The lumbar spine and femora were examined by micro-CT, biomechanical, histomorphological, ashing, and gene expression analyses. Results EN exhibited an anabolic effect on bone, improving some of its parameters in Orx rats, but did not affect biomechanical properties. RAL exhibited antiresorptive activity, maintaining the biomechanical and trabecular parameters of Orx rats at the levels of Non-Orx rats. EN + RAL exerted a stronger effect than the single treatments, improving most of the bone parameters. Liver weight increased after all treatments; the kidney, prostate, and levator ani muscle weights increased after EN and EN + RAL treatments. BW was reduced due to a decreased food intake in the Orx + RAL group and due a reduced visceral fat weight in the Orx + EN + RAL group. Conclusion The EN + RAL treatment appeared to be promising in preventing male osteoporosis, but given the observed side effects on liver, kidney, and prostate weights, it requires further investigation.
doi_str_mv 10.1007/s40618-022-01865-9
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O. ; Lehmann, W. ; Schilling, A. F. ; Roch, P. J. ; Taudien, S. ; Hoffmann, D. B. ; Sehmisch, S.</creator><creatorcontrib>Komrakova, M. ; Büchler, G. ; Böker, K. O. ; Lehmann, W. ; Schilling, A. F. ; Roch, P. J. ; Taudien, S. ; Hoffmann, D. B. ; Sehmisch, S.</creatorcontrib><description>Purpose Enobosarm (EN), a selective androgen receptor modulator and raloxifene (RAL), a selective estrogen receptor modulator, have been shown to improve bone tissue in osteoporotic males. The present study evaluated the effects of a combination therapy of EN and RAL on bone properties in orchiectomized rats compared to the respective single treatments. Methods Eight-month-old male Sprague–Dawley rats were either left intact (Non-Orx) or orchiectomized (Orx). The Orx rats were divided into four groups (n = 15 each): 1) Orx, 2) EN treatment (Orx + EN), 3) RAL treatment (Orx + RAL), 4) combined treatment (Orx + EN + RAL). EN and RAL (0.4 mg and 7 mg/kg body weight/day) were applied immediately after Orx with a soy-free pelleted diet for up to 18 weeks. The lumbar spine and femora were examined by micro-CT, biomechanical, histomorphological, ashing, and gene expression analyses. Results EN exhibited an anabolic effect on bone, improving some of its parameters in Orx rats, but did not affect biomechanical properties. RAL exhibited antiresorptive activity, maintaining the biomechanical and trabecular parameters of Orx rats at the levels of Non-Orx rats. EN + RAL exerted a stronger effect than the single treatments, improving most of the bone parameters. Liver weight increased after all treatments; the kidney, prostate, and levator ani muscle weights increased after EN and EN + RAL treatments. BW was reduced due to a decreased food intake in the Orx + RAL group and due a reduced visceral fat weight in the Orx + EN + RAL group. Conclusion The EN + RAL treatment appeared to be promising in preventing male osteoporosis, but given the observed side effects on liver, kidney, and prostate weights, it requires further investigation.</description><identifier>ISSN: 1720-8386</identifier><identifier>ISSN: 0391-4097</identifier><identifier>EISSN: 1720-8386</identifier><identifier>DOI: 10.1007/s40618-022-01865-9</identifier><identifier>PMID: 35867330</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Androgen receptors ; Androgens ; Biomechanics ; Body weight ; Bone loss ; Computed tomography ; Endocrinology ; Estrogen receptors ; Estrogens ; Food intake ; Gene expression ; Internal Medicine ; Kidneys ; Liver ; Mechanical properties ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases ; Original ; Original Article ; Osteoporosis ; Prostate ; Raloxifene ; Spine (lumbar)</subject><ispartof>Journal of endocrinological investigation, 2022-12, Vol.45 (12), p.2299-2311</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-7b7731c719611a2348a74d203f68ea71e7503569a664ad99b6f0b2c1caea9fc33</citedby><cites>FETCH-LOGICAL-c451t-7b7731c719611a2348a74d203f68ea71e7503569a664ad99b6f0b2c1caea9fc33</cites><orcidid>0000-0002-6225-4378</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids></links><search><creatorcontrib>Komrakova, M.</creatorcontrib><creatorcontrib>Büchler, G.</creatorcontrib><creatorcontrib>Böker, K. O.</creatorcontrib><creatorcontrib>Lehmann, W.</creatorcontrib><creatorcontrib>Schilling, A. F.</creatorcontrib><creatorcontrib>Roch, P. J.</creatorcontrib><creatorcontrib>Taudien, S.</creatorcontrib><creatorcontrib>Hoffmann, D. B.</creatorcontrib><creatorcontrib>Sehmisch, S.</creatorcontrib><title>A combined treatment with selective androgen and estrogen receptor modulators prevents bone loss in orchiectomized rats</title><title>Journal of endocrinological investigation</title><addtitle>J Endocrinol Invest</addtitle><description>Purpose Enobosarm (EN), a selective androgen receptor modulator and raloxifene (RAL), a selective estrogen receptor modulator, have been shown to improve bone tissue in osteoporotic males. The present study evaluated the effects of a combination therapy of EN and RAL on bone properties in orchiectomized rats compared to the respective single treatments. Methods Eight-month-old male Sprague–Dawley rats were either left intact (Non-Orx) or orchiectomized (Orx). The Orx rats were divided into four groups (n = 15 each): 1) Orx, 2) EN treatment (Orx + EN), 3) RAL treatment (Orx + RAL), 4) combined treatment (Orx + EN + RAL). EN and RAL (0.4 mg and 7 mg/kg body weight/day) were applied immediately after Orx with a soy-free pelleted diet for up to 18 weeks. The lumbar spine and femora were examined by micro-CT, biomechanical, histomorphological, ashing, and gene expression analyses. Results EN exhibited an anabolic effect on bone, improving some of its parameters in Orx rats, but did not affect biomechanical properties. RAL exhibited antiresorptive activity, maintaining the biomechanical and trabecular parameters of Orx rats at the levels of Non-Orx rats. EN + RAL exerted a stronger effect than the single treatments, improving most of the bone parameters. Liver weight increased after all treatments; the kidney, prostate, and levator ani muscle weights increased after EN and EN + RAL treatments. BW was reduced due to a decreased food intake in the Orx + RAL group and due a reduced visceral fat weight in the Orx + EN + RAL group. Conclusion The EN + RAL treatment appeared to be promising in preventing male osteoporosis, but given the observed side effects on liver, kidney, and prostate weights, it requires further investigation.</description><subject>Androgen receptors</subject><subject>Androgens</subject><subject>Biomechanics</subject><subject>Body weight</subject><subject>Bone loss</subject><subject>Computed tomography</subject><subject>Endocrinology</subject><subject>Estrogen receptors</subject><subject>Estrogens</subject><subject>Food intake</subject><subject>Gene expression</subject><subject>Internal Medicine</subject><subject>Kidneys</subject><subject>Liver</subject><subject>Mechanical properties</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metabolic Diseases</subject><subject>Original</subject><subject>Original Article</subject><subject>Osteoporosis</subject><subject>Prostate</subject><subject>Raloxifene</subject><subject>Spine (lumbar)</subject><issn>1720-8386</issn><issn>0391-4097</issn><issn>1720-8386</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kUtv1TAQhS1ERUvhD7CyxIZNwK_4sUGqKl5SpW7o2nKcyb2uEvtiO7eCX49LKl6LrnysOfN5xgehV5S8pYSod0UQSXVHGOsI1bLvzBN0RhUjneZaPv1Ln6LnpdwSwhXX6hk65b2WinNyhu4usE_LECKMuGZwdYFY8V2oe1xgBl_DEbCLY047iPcCQ6nbJYOHQ00ZL2lcZ9dUwYcMxwYoeEgR8JxKwSHilP0-NFZawo_2Tna1vEAnk5sLvHw4z9HNxw9fLz93V9efvlxeXHVe9LR2alCKU6-okZQ6xoV2SoyM8ElqcIqC6gnvpXFSCjcaM8iJDMxT78CZyXN-jt5v3MM6LDD6Nlx2sz3ksLj83SYX7L-VGPZ2l47WSCF7IRvgzQMgp29rW94uoXiYZxchrcUyabhSmjLVrK__s96mNce2nm1VIQVVQjQX21w-t-_JMP0ehhJ7n6vdcrUtV_srV2taE9-aSjPHHeQ_6Ee6fgLFjac7</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Komrakova, M.</creator><creator>Büchler, G.</creator><creator>Böker, K. 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O.</creatorcontrib><creatorcontrib>Lehmann, W.</creatorcontrib><creatorcontrib>Schilling, A. F.</creatorcontrib><creatorcontrib>Roch, P. J.</creatorcontrib><creatorcontrib>Taudien, S.</creatorcontrib><creatorcontrib>Hoffmann, D. B.</creatorcontrib><creatorcontrib>Sehmisch, S.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of endocrinological investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komrakova, M.</au><au>Büchler, G.</au><au>Böker, K. O.</au><au>Lehmann, W.</au><au>Schilling, A. F.</au><au>Roch, P. J.</au><au>Taudien, S.</au><au>Hoffmann, D. B.</au><au>Sehmisch, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A combined treatment with selective androgen and estrogen receptor modulators prevents bone loss in orchiectomized rats</atitle><jtitle>Journal of endocrinological investigation</jtitle><stitle>J Endocrinol Invest</stitle><date>2022-12-01</date><risdate>2022</risdate><volume>45</volume><issue>12</issue><spage>2299</spage><epage>2311</epage><pages>2299-2311</pages><issn>1720-8386</issn><issn>0391-4097</issn><eissn>1720-8386</eissn><abstract>Purpose Enobosarm (EN), a selective androgen receptor modulator and raloxifene (RAL), a selective estrogen receptor modulator, have been shown to improve bone tissue in osteoporotic males. The present study evaluated the effects of a combination therapy of EN and RAL on bone properties in orchiectomized rats compared to the respective single treatments. Methods Eight-month-old male Sprague–Dawley rats were either left intact (Non-Orx) or orchiectomized (Orx). The Orx rats were divided into four groups (n = 15 each): 1) Orx, 2) EN treatment (Orx + EN), 3) RAL treatment (Orx + RAL), 4) combined treatment (Orx + EN + RAL). EN and RAL (0.4 mg and 7 mg/kg body weight/day) were applied immediately after Orx with a soy-free pelleted diet for up to 18 weeks. The lumbar spine and femora were examined by micro-CT, biomechanical, histomorphological, ashing, and gene expression analyses. Results EN exhibited an anabolic effect on bone, improving some of its parameters in Orx rats, but did not affect biomechanical properties. RAL exhibited antiresorptive activity, maintaining the biomechanical and trabecular parameters of Orx rats at the levels of Non-Orx rats. EN + RAL exerted a stronger effect than the single treatments, improving most of the bone parameters. Liver weight increased after all treatments; the kidney, prostate, and levator ani muscle weights increased after EN and EN + RAL treatments. BW was reduced due to a decreased food intake in the Orx + RAL group and due a reduced visceral fat weight in the Orx + EN + RAL group. Conclusion The EN + RAL treatment appeared to be promising in preventing male osteoporosis, but given the observed side effects on liver, kidney, and prostate weights, it requires further investigation.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>35867330</pmid><doi>10.1007/s40618-022-01865-9</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-6225-4378</orcidid><oa>free_for_read</oa></addata></record>
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subjects Androgen receptors
Androgens
Biomechanics
Body weight
Bone loss
Computed tomography
Endocrinology
Estrogen receptors
Estrogens
Food intake
Gene expression
Internal Medicine
Kidneys
Liver
Mechanical properties
Medicine
Medicine & Public Health
Metabolic Diseases
Original
Original Article
Osteoporosis
Prostate
Raloxifene
Spine (lumbar)
title A combined treatment with selective androgen and estrogen receptor modulators prevents bone loss in orchiectomized rats
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