The role of endogenous opioids and the dopaminergic system on the inhibition of luteinizing hormone (LH) secretion during early and late anoestrus, together with its modulation by the plane of nutrition were investigated in ewes with a short anoestrous season. In early anoestrus (22 March; day 0), two groups of ovariectomized, oestradiol-treated adult Rasa Aragonesa ewes, maintained under natural photoperiod at 41°N, were given enough food to provide 1·4 × (high; H; no. = 6) or 0·5 × (low; L; no. = 6) energy requirements for maintenance. The effects of administration of the opiate receptor antagonist naloxone (1 mg/kg at four 1-h intervals) (day 15) and of the dopaminergic2 receptor antagonist pimozide (0·08 mg/kg) (day 21) on LH secretion were assessed. A second experiment was carried out in late anoestrus (21 June) using the same protocol. A significant increase in LH pulse frequency after naloxone treatment for both H and L groups was detected in late anoestrus. Number ofLH pulses after naloxone injections in early anoestrus also increased in H (P < 0·05) and L ewes (P = 0·08). The effect of pimozide injection on mean LH pulse frequency was greater in early than in late anoestrus, especially in ewes receiving a high plane of nutrition (P < 0·05 and P = 0·07 for H and L ewes, respectively in April and P = 0·07 for H ewes in July). A significant increase of LH pulse amplitude was also detected in early anoestrus in H ewes (P < 0·01). These results provide evidence that endogenous opioid mechanisms are involved in the inhibition ofLH pulsatile release both in early and late anoestrus in ewes with a short seasonal anoestrus. The ability of pimozide to increase LH pulse frequency in early anoestrus could be enhanced by a high plane of nutrition in the breed studied.

The effectiveness of different gonadotropin releasing hormone analogues (GnRHa) and/or pimozide for inducing ovulation in Arctic charr was investigated at two different temperatures: 5 °C, a temperature suitable for spontaneous ovulation in Arctic charr and 10 °C, a temperature which inhibited ovulation in Arctic charr. At 5 °C all the different GnRH analogues tested were able to induce and synchronize ovulation. At 10 °C a sustained release preparation of D-tryptophan6 luteinizing hormone releasing hormone (D-Trp6LH-RH) at 20 μg.kg−1 and an acute release preparation of D-arginine6salmon GnRH (D-Arg6 sGnRH) at 100 μg.kg−1 were able to induce ovulation in 80% of the females within 15 days (versus 2% in controls). Pimozide alone or in combination with a low dose of D-Arg6sGnRH was able to induce some ovulation at 10 °C, suggesting that a dopamine inhibition of gonadotropin secretion could occur at 10 °C. Egg survival in groups receiving GnRHa at 5 °C was comparable to controls (73%) except in the group receiving GnRHa in combination with pimozide (45%). At 10 °C, egg survival was significantly lower than controls at 5 °C, except for the group receiving pimozide alone. At both temperatures, egg survivals of each spawn were negatively correlated with the plasma gonadotropin (GtH2) level of the reproducing females except in groups receiving a sustained release preparation of D-Trp6LH-RH.