DIFFERENTIAL-EFFECTS OF ESTROGEN AND MEDROXYPROGESTERONE ON BASAL ANDSTRESS-INDUCED GROWTH-HORMONE RELEASE, IGF-1 LEVELS, AND CELLULAR-IMMUNITY IN POSTMENOPAUSAL WOMEN
Wb. Malarkey et al., DIFFERENTIAL-EFFECTS OF ESTROGEN AND MEDROXYPROGESTERONE ON BASAL ANDSTRESS-INDUCED GROWTH-HORMONE RELEASE, IGF-1 LEVELS, AND CELLULAR-IMMUNITY IN POSTMENOPAUSAL WOMEN, ENDOCRINE, 7(2), 1997, pp. 227-233
We evaluated the influence of continual estrogen replacement therapy (
ERT) as presently practiced by postmenopausal women with conjugated es
trogens and medroxyprogesterone acetate (MPA) on the growth hormone/in
sulin-like growth factor-1 (GH/IGF-1) axis and cellular immunity. Thir
ty-nine postmenopausal women were evaluated (12 on no replacement, 14
on estrogen only, and 13 on estrogen and MPA). In the women receiving
only conjugated estrogens, increased GH levels and decreased IGF-1 lev
els were found, which replicated previous research and probably reflec
ted estrogen inhibition of hepatic IGF-1 production with a secondary i
ncrease in GH release because of reduced feedback inhibition. In women
taking both MPA and estrogen, GH was increased and the previously obs
erved estrogen induced decrease in IGF-1 levels was inhibited. In orde
r to determine the influence of ERT on psychosocial stress-induced GH
release, math (mental stress) and speech (social stress) challenges we
re utilized, and they produced significant increases in heart rate in
all three groups. The heart rate following stress was significantly en
hanced by estrogen replacement. These stressors also led to increased
GH secretion in the women taking estrogen and MPA, but not in the othe
r two groups. Gonadal steroids and GH can influence cellular immunity.
We observed that ERT in both groups was associated with significantly
enhanced lymphocyte responsiveness to the T-cell mitogens phytohemagl
utinin (PHA) and Conconavalin A (Con A), and basal GH levels were corr
elated with the PHA response in the estrogen only group. ERT did not i
nfluence natural killer (NK) cell activity. We also found significant
differences in the steady-state expression of lat ent Epstein-Barr vir
us (EBV) with increased antibody titers in the women in the estrogen o
nly group and lower antibody titers in the MPA plus estrogen group. GH
levels were correlated with EBV antibody titers in the estrogen plus
MPA group. This study supports the hypothesis that GH and immune modul
ation can be influenced by ERT in postmenopausal woman. Given the exta
nt literature on the immune-enhancing effects of CH, these data sugges
t that ERT may slow the decline of GH secretion with aging, an event t
hat has been implicated in immunosenescence.