C. Estupina et al., VARIATIONS IN HYPOTHALAMIC SOMATOSTATIN RELEASE AND CONTENT DURING THE ESTROUS-CYCLE IN THE RAT - EFFECTS OF OVARIECTOMY AND ESTROGEN SUPPLEMENTATION, Neuroendocrinology, 63(2), 1996, pp. 181-187
To investigate the secretory pattern of somatostatin (SS) from the med
ian eminence (ME) in the female rat, as well as estrogenic influence o
n this secretion, we measured both SS release and hypothalamic content
in cycling, 10-day ovariectomized, and ovariectomized rats treated wi
th estradiol for 3 days before. Animals were stereotaxically implanted
with a push-pull cannula into the ME, and 10 days later the hypothala
mic structure was perfused with artificial cerebrospinal fluid for 120
-150 min at a regular flow rate of 17 mu l/min. Secretion peaks were o
bserved in the pattern of SS release, whatever the stage of the estrou
s cycle. The mean amplitude of SS peaks was similar throughout the cyc
le: 11.7 +/- 4.0, 8.6 +/- 1.5 and 10.5 +/- 1.3 pg at proestrus, estrus
and diestrus, respectively, and it was affected neither by ovariectom
y (7.4 +/- 1.3 pg) nor by estrogen replacement (5.5 +/- 1.0 pg). By co
ntrast, mean SS release levels in the proestrus phase were significant
ly higher than those measured in the other phases: 21.6 +/- 2.1 vs. 17
.7 +/- 1.2 pg/15 min in diestrus (p < 0.05) and vs. 12.0 +/- 0.7 pg/15
min in estrus (p < 0.001). Hypothalamic SS content showed variations
quite similar to those observed during its release, i.e. with the high
est values corresponding to the proestrus phase (1,170.5 +/- 224.9 pg/
mg of tissue) and to the diestrus (1,156.5 +/- 332.1 pg/mg of tissue)
and the lowest values in the estrus (511.5 +/- 52.9 pg/mg of tissue; p
< 0.05 vs. proestrus and diestrus). In addition, the lowest SS conten
t and secretion values were found in ovariectomized animals: 95.5 +/-
5.1 pg/mg of tissue (p < 0.001 compared to the values obtained for eac
h stage of the estrous cycle) and 10.0 +/- 0.9 pg/15 min (p < 0.001 vs
. proestrus and diestrus), respectively. Patterns of SS release and SS
hypothalamic content were not modified by estradiol treatment in ovar
iectomized animals. Our results suggest that (1) whatever the stage of
the estrous cycle, SS release from the ME is not uniform and exhibits
irregular peaks; (2) mean SS release levels were subjected to gonadal
influence; (3) the occurrence of SS peaks seems to be estrogen-indepe
ndent, and (4) variations in hypothalamic SS content were generally in
good agreement with those of neurohormone release.