SEASONAL AND PHOTOPERIOD-INDUCED CHANGES IN THE SECRETION OF ALPHA-MELANOCYTE-STIMULATING HORMONE IN SOAY SHEEP - TEMPORAL RELATIONSHIPS WITH CHANGES IN BETA-ENDORPHIN, PROLACTIN, FOLLICLE-STIMULATING-HORMONE,ACTIVITY OF THE GONADS AND GROWTH OF WOOL AND HORNS
Ga. Lincoln et Bi. Baker, SEASONAL AND PHOTOPERIOD-INDUCED CHANGES IN THE SECRETION OF ALPHA-MELANOCYTE-STIMULATING HORMONE IN SOAY SHEEP - TEMPORAL RELATIONSHIPS WITH CHANGES IN BETA-ENDORPHIN, PROLACTIN, FOLLICLE-STIMULATING-HORMONE,ACTIVITY OF THE GONADS AND GROWTH OF WOOL AND HORNS, Journal of Endocrinology, 144(3), 1995, pp. 471-481
Blood plasma concentrations of alpha-melanocyte-stimulating hormone (a
lpha-MSH), beta-endorphin (beta-END), prolactin and follicle-stimulati
ng hormone (FSH), and associated changes in the size of the testes, an
d growth of the hems and pelage were measured in male (n=8), castrated
male (n=5) and female (n=9) Soay sheep. The animals were born in Apri
l and kept outdoors near Edinburgh (56 degrees N) during the first two
years of life. In all groups there was a close association between th
e weekly changes in the plasma concentrations of alpha-MSH and beta-EN
D; the molar ratio in mean concentrations was close to 1:1. The blood
plasma concentrations of both hormones varied markedly with season wit
h a 3- to 10-fold increase in concentrations fr om the minimum in wint
er to the maximum in autumn. The seasonal peak occurred in September i
n the first year of life as juveniles, and between July (males) and Se
ptember (females) in the second year when the animals were sexually ma
ture. The plasma concentrations of ACTH did not vary in parallel with
the seasonal changes in the concentrations of alpha-MSH (measured only
in males); the molar ratio for the concentrations of alpha-MSH:ACTH w
as 1:012. The seasonal increase in the concentrations of alpha-MSH occ
urred 1-3 months after the seasonal increase in the concentrations of
prolactin and the associated growth in hems and pelage, and slightly b
efore, or coincident with the seasonal increase in the concentrations
of FSH and the growth in the testes. In a second experiment, the same
parameters were measured in a group of adult male Soay sheep (n=8) hou
sed indoors under an artificial lighting regimen of alternating 16-wee
k periods of long (16 h light:8 h darkness) and short days (8 h light:
16 h darkness). In this situation, there was a clearly defined photope
riod-induced cycle in the plasma concentrations of alpha-MSH with a 25
-fold increase from a minimum under long days to a maximum under short
days. The concentrations of beta-END varied in close parallel with th
e changes in alpha-MSH, and the temporal associations with the changes
in the other pituitary hormones were similar to those observed in ani
mals housed outdoors. Overall, the results support the view that alpha
-MSH is co-secreted with beta-END from the melanotrophs in the pars in
termedia of the pituitary gland, and that the secretory activity of th
e melanotrophs changes markedly with season, increasing in summer and
autumn, and decreasing in winter and spring. The annual cycle in dayle
ngth is likely to be the principle environmental cue timing the cycle
in alpha-MSH and beta-END. alpha-MSH is known to have biological effec
ts in the brain (neuroendocrine control of prolactin and FSH), and in
the adrenal gland (secretion of glucocorticoids), adipose tissue (fat
storage), and skin (melanogenesis and secretion of sebum). Thus the se
asonal increase in the secretion of alpha-MSH may regulate multiple ph
ysiological changes in autumn in preparation for winter.