Jl. Brown et al., EFFECTS OF GNRH ANALOGS ON PITUITARY-TESTICULAR FUNCTION IN FREE-RANGING AFRICAN ELEPHANTS (LOXODONTA-AFRICANA), Journal of Reproduction and Fertility, 99(2), 1993, pp. 627-634
We tested the ability of several GnRH analogues to suppress pituitary-
testicular activity and potentially musth in free-ranging African elep
hants (Loxodonta africana). In Study I, adult bulls were given 4 or 12
mg GnRH antagonist (Detirelix) or saline i.m. on day 0 (n = 3 bulls p
er treatment). Animals were then recaptured on day 2 (about 48 h later
) and given 300 mu g GnRH i.v. to assess the ability of the antagonist
to block pituitary activity. Detirelix reduced (P < 0.05) basal conce
ntrations of serum LH and testosterone on day 2 compared with day 0, w
ith no effect of dose. Similarly LH and testosterone release induced b
y GnRH were also reduced (P < 0.05) in the Detirelix-treated bulls (50
-70% reduction in peak concentrations). In Study 2, elephants were giv
en 30 mg of a structurally similar GnRH antagonist (103-201-40; n = 6)
, 22.5 mg of a long-acting GnRH agonist (Lupron Depot; n = 4) or D-man
nitol carrier (n = 4) i.m. on day 0. All bulls were recaptured and giv
en GnRH on day 2 (103-201-40 treatment) or on days 2 and 20 (Lupron De
pot treatment) after the initial injection. In contrast to Detirelix,
103-201-40 did not inhibit basal or GnRH-induced LH or testosterone se
cretion. Pituitary-testicular responses to Lupron Depot were initially
stimulatory, as evidenced by increased (P < 0.05) LH and testosterone
secretion on days 0 and 2. By day 20, basal LH concentrations had ret
urned to baseline values and the response to GnRH was markedly reduced
(P < 0.05), indicating that the pituitary was at least partially dese
nsitized. Basal testosterone concentrations had also returned to basel
ine values by day 20 after Lupron Depot treatment. However, despite th
e attenuated LH response to GnRH, subsequent testosterone secretion wa
s increased (P < 0.05) compared with controls, suggesting the testes o
f agonist-treated bulls had instead, become hyper-responsive to small
increases in LH secretion. These results suggest that GnRH analogues c
an suppress the pituitary-gonadal axis in African elephants; however,
longer treatment periods, more frequent injection intervals or higher
doses are probably needed to inhibit testosterone secretion completely
and, thus, musth.