Sl. Monfort et al., URINARY 3-ALPHA,17-BETA-ANDROSTANEDIOL GLUCURONIDE IS A MEASURE OF ANDROGENIC STATUS IN ELD DEER STAGS (CERVUS-ELDI-THAMIN), Biology of reproduction, 53(3), 1995, pp. 700-706
To determine the primary excretory by-products of testosterone (T), 85
mu Ci [H-3]T was administered i,v, to two adult Eld's deer stags, Blo
od (10 mi) was collected by jugular venipuncture at 0, 5, 10, 15, 30,
45, 60, 90, 120, 150, 180, 240, and 480 min after isotope infusion, an
d all urine and feces were collected for 96 h after injection. Seventy
percent of labeled circulating steroid was conjugated by 30 min posti
nfusion. The majority (80.4 +/- 3.2%) of T metabolites were excreted i
nto urine, and 95.0 i: 0.9% of these were conjugated, 95.8 +/- 0.2% be
ing hydrolyzable with glucuronidase. Seven urinary androgen metabolite
s, including androstanediol (5 alpha-androstan-3 alpha-17 beta-diol an
d 5 beta-androstan-3 alpha-17 beta-diol), were identified in glucuroni
dase-hydrolyzed, ether-extracted Eld's deer urine pools after gas chro
matography/ mass spectrometry, A double-antibody I-125 RIA for 5 alpha
-androstanediol-3 alpha,17 beta-diol, 17-glucuronide (3 alpha-diol-G)
was validated for unprocessed urine, Longitudinal assessments of urine
samples collected from 13 stags for 3 yr revealed biological concorda
nce between fluctuations in urinary 3 alpha-diol-G and serum T,as well
as seasonal changes in secondary sexual characteristics. Overall corr
elation between ''same-day'' matched serum T and urinary 3 alpha-diol-
G was 0.58, (n = 6; p < 0.001). Thus, monitoring urinary 3 alpha-diol-
G provides a noninvasive, alternative method for characterizing male e
ndocrine interrelationships in an endangered ungulate species.