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pubmed-article:3337226pubmed:abstractTextThe metabolic clearance rate (MCR) of gonadal or adrenal steroid hormones in rabbits often does not bear the expected inverse relationship with hormone binding to testosterone-binding globulin (TeBG) or corticosteroid-binding globulin (CBG). This suggests TeBG or CBG may not impede steroid hormone delivery to tissues. The effects of rabbit plasma proteins on the influxes of 3H-labeled steroids from the circulation into the rabbit uterus were measured in vivo using a tissue sampling single-injection technique. In the absence of plasma proteins, estradiol (E2) and testosterone (T) were freely diffusible through the uterine microvasculature (i.e., extraction greater than 80%). The extractions of dihydrotestosterone (DHT) and corticosterone (B) ranged from 60 to 72%, while that of cortisol (F) was reduced at 40%. Rabbit serum exerted no inhibition of the influxes of the steroids tested. The influxes of T and B greatly exceeded the rates that would be expected if only the free and albumin-bound fractions estimated in vitro were diffusible in vivo. However, the extraction of [3H]corticosteroid-binding globulin or bovine [3H]albumin were low, consistent with little, if any, extravascular uptake of the plasma proteins. The results indicate both albumin-bound and globulin-bound steroid hormone are available for transport into the uterus in the rabbit in vivo without significant exodus of the plasma protein, per se.lld:pubmed
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pubmed-article:3337226pubmed:paginationE79-83lld:pubmed
pubmed-article:3337226pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:3337226pubmed:year1988lld:pubmed
pubmed-article:3337226pubmed:articleTitleTeBG- and CBG-bound steroid hormones in rabbits are available for influx into uterus in vivo.lld:pubmed
pubmed-article:3337226pubmed:affiliationDepartment of Obstetrics and Gynecology, School of Medicine, University of California, Los Angeles 90024.lld:pubmed
pubmed-article:3337226pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3337226pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed