H. Tsukamura et al., Intracerebroventricular administration of melanin-concentrating hormone suppresses pulsatile luteinizing hormone release in the female rat, J NEUROENDO, 12(6), 2000, pp. 529-534
Melanin-concentrating hormone (MCH) has been reported to be involved in the
regulation of feeding behaviour in rats and mice. Because many neuropeptid
es that influence ingestive behaviour also regulate reproductive function,
the present study was designed to determine if central administration of MC
H changes pulsatile secretion of luteinizing hormone (LH) in the rats. Wist
ar-Imamichi strain female rats were ovariectomized and implanted with oestr
adiol to produce a moderate inhibitory feedback effect on LH release. The e
ffects of i.c.v. injections of MCH on LH release were examined in freely mo
ving animals. Blood samples were collected every 6 min for 3 h through an i
ndwelling cannula. After 1 h of sampling, MCH (0.1, 1 or 10 mu g/animal) or
vehicle (saline) was injected into the third cerebroventricle. Because MCH
is also reported to affect the hypothalamo-pituitary-adrenal (HPA) axis, w
hich in turn, can influence reproductive function, plasma corticosterone co
ncentrations were determined in the same animals at 30-min intervals during
the first and last hours and every 12 min during the second hour of the 3-
h sampling period. When expressed as per cent changes, mean plasma LH conce
ntrations after MCH administration were significantly tower in the animals
injected with all doses of the peptide compared with vehicle-treated animal
s; LH pulse frequency was significantly lowered by 1 mu g of MCH. Per cent
changes in mean plasma corticosterone levels were not significantly affecte
d by MCH administration. These results in oestradiol-treated ovariectomized
rats indicate that central MCH is capable of inhibiting pulsatile LH secre
tion. We have previously shown that 48-h fasting suppresses pulsatile LH re
lease in the presence of oestrogen, Take together, these results raise the
possibility that MCH could play a role in mediating the suppression of LH s
ecretion during periods of reduced nutrition.