David L. Thompson , Roger S. Rittmaster , Angela M. Rodriguez , Perry H. Moore Jr , Pemmaraju N. Rao
{"title":"用于放射免疫测定的新型类固醇半抗原的合成- viii。血清5α-雄烷-3α,17β-二醇17-葡糖苷的特异性放射免疫测定方法的开发和验证","authors":"David L. Thompson , Roger S. Rittmaster , Angela M. Rodriguez , Perry H. Moore Jr , Pemmaraju N. Rao","doi":"10.1016/0022-4731(90)90227-J","DOIUrl":null,"url":null,"abstract":"<div><p>5α-Androstane-3α,17β-diol glucuronide (androstanediol-G) is a dihydrotestosterone metabolite whose serum levels are elevated in hirsute women. Current assay methods do not distinguish between the two androstanediol-G isomers, androstanediol 3-G and androstanediol 17-G. Since the production of these isomers may be influenced by different factors, we have developed a specific radioimmunoassay for androstanediol 17G. The antibody was raised against 5α-androstane-3α,17β-diol 17-G conjugated to bovine serum albumin (BSA). [9,11-<sup>3</sup>H]5α-Androstane-3α,17β-diol 17-G was used for determination of procedural losses and as the labeled ligand in the assay. Unlabeled androstanediol 17-G was used as assay standard.</p><p>Serum levels of total androstanediol-G, androstanediol 3-G and androstanediol 17-G were measured in 8 normal men. Total androstanediol-G levels were 16.5 ± 5.2 nmol/l, androstanediol 17-G levels were 12.9 ± 5 nmol/l, and androstanediol 3-G levels were 30.3 ± 1.8 nmol/l. 77 ± 13% of total androstanediol-G was androstanediol 17-G.</p><p>These results confirm our previous findings that androstanediol 17-G is the predominant androstanediol-G isomer in human serum and suggests that 5α-dihydrotestosterone (DHT) is preferentially metabolized to androstanediol 17-G.</p></div>","PeriodicalId":17138,"journal":{"name":"Journal of steroid biochemistry","volume":"36 4","pages":"Pages 345-349"},"PeriodicalIF":0.0000,"publicationDate":"1990-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0022-4731(90)90227-J","citationCount":"13","resultStr":"{\"title\":\"Synthesis of new steroid haptens for radioimmunoassay—VIII. Development and validation of a specific radioimmunoassay for serum 5α-androstane-3α,17β-diol 17-glucuronide\",\"authors\":\"David L. Thompson , Roger S. Rittmaster , Angela M. Rodriguez , Perry H. Moore Jr , Pemmaraju N. Rao\",\"doi\":\"10.1016/0022-4731(90)90227-J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>5α-Androstane-3α,17β-diol glucuronide (androstanediol-G) is a dihydrotestosterone metabolite whose serum levels are elevated in hirsute women. Current assay methods do not distinguish between the two androstanediol-G isomers, androstanediol 3-G and androstanediol 17-G. Since the production of these isomers may be influenced by different factors, we have developed a specific radioimmunoassay for androstanediol 17G. The antibody was raised against 5α-androstane-3α,17β-diol 17-G conjugated to bovine serum albumin (BSA). [9,11-<sup>3</sup>H]5α-Androstane-3α,17β-diol 17-G was used for determination of procedural losses and as the labeled ligand in the assay. Unlabeled androstanediol 17-G was used as assay standard.</p><p>Serum levels of total androstanediol-G, androstanediol 3-G and androstanediol 17-G were measured in 8 normal men. Total androstanediol-G levels were 16.5 ± 5.2 nmol/l, androstanediol 17-G levels were 12.9 ± 5 nmol/l, and androstanediol 3-G levels were 30.3 ± 1.8 nmol/l. 77 ± 13% of total androstanediol-G was androstanediol 17-G.</p><p>These results confirm our previous findings that androstanediol 17-G is the predominant androstanediol-G isomer in human serum and suggests that 5α-dihydrotestosterone (DHT) is preferentially metabolized to androstanediol 17-G.</p></div>\",\"PeriodicalId\":17138,\"journal\":{\"name\":\"Journal of steroid biochemistry\",\"volume\":\"36 4\",\"pages\":\"Pages 345-349\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1990-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0022-4731(90)90227-J\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of steroid biochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/002247319090227J\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of steroid biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/002247319090227J","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of new steroid haptens for radioimmunoassay—VIII. Development and validation of a specific radioimmunoassay for serum 5α-androstane-3α,17β-diol 17-glucuronide
5α-Androstane-3α,17β-diol glucuronide (androstanediol-G) is a dihydrotestosterone metabolite whose serum levels are elevated in hirsute women. Current assay methods do not distinguish between the two androstanediol-G isomers, androstanediol 3-G and androstanediol 17-G. Since the production of these isomers may be influenced by different factors, we have developed a specific radioimmunoassay for androstanediol 17G. The antibody was raised against 5α-androstane-3α,17β-diol 17-G conjugated to bovine serum albumin (BSA). [9,11-3H]5α-Androstane-3α,17β-diol 17-G was used for determination of procedural losses and as the labeled ligand in the assay. Unlabeled androstanediol 17-G was used as assay standard.
Serum levels of total androstanediol-G, androstanediol 3-G and androstanediol 17-G were measured in 8 normal men. Total androstanediol-G levels were 16.5 ± 5.2 nmol/l, androstanediol 17-G levels were 12.9 ± 5 nmol/l, and androstanediol 3-G levels were 30.3 ± 1.8 nmol/l. 77 ± 13% of total androstanediol-G was androstanediol 17-G.
These results confirm our previous findings that androstanediol 17-G is the predominant androstanediol-G isomer in human serum and suggests that 5α-dihydrotestosterone (DHT) is preferentially metabolized to androstanediol 17-G.