A highly purified FSH preparation has been used to develop a specific homologous radioimmunoassay for chicken FSH which is sufficiently sensitive and precise to measure the hormone in small sample (10-100 microliter) of plasma. The assay was used to measure plasma FSH in the chicken and turkey. The FSH concentration was higher in sexually mature chickens than in juvenile birds and further elevated after castration or ovariectomy. In turkeys, it was lower in birds held on a short daily photoperiod than in birds held on a long daily photoperiod. FSH rose in sexually quiescent female turkeys after injection of synthetic LH-releasing hormone and was increased in laying hens after injection of progesterone. No major changes were observed in FSH concentration during the chicken ovulatory cycle, although there was a small increase 15 and 14 h before ovulation.

1. Concentrations of prolactin, growth hormone, testosterone, progesterone, thyroxine and triiodothyronine were measured in the blood plasma of female turkeys during successive periods of egg laying, a decline in lay, a moult induced by a short photoperiod (6 light: 18 dark) and a resumption of egg laying induced by a long photoperiod (16L:8D). 2. Concentrations of prolactin, growth hormone, testosterone and progesterone were higher in laying birds than in birds which were moulting or not laying. 3. The concentration of testosterone, but not of the other hormones studied, increased significantly during the period of profuse moult. 4. Concentrations of the thyroid hormones did not change with the varying physiological condition of the birds. However, the concentration of thyroxine was depressed by the long photoperiod.

1. Circulating immunoreactive luteinising hormone (LH) and follicle stimulating hormone (FSH) concentrations have been measured during photoperiodically-induced changes in the reproductive state of turkeys. 2. In a period of sexual quiescence on short photoperiods (6L: 18D) LH concentrations were higher during the hours of darkness in both sexes. 3. Transfer to long photoperiods (16L: 8D) stimulated a rapid increase in LH and FSH concentrations. This was maintained for between 2 to 3 months when the concentrations of both gonadotrophins decreased as the birds became photorefractory. 4. Return to short photoperiods had no immediate effect on the concentrations of LH and FSH in females. The concentration of LH was increased during the 3rd week of short photoperiods when the hens were moulting. 5. LH concentrations fluctuated during the ovulatory cycle and were highest about 6 h before ovulation.

Three enzymes used for the determination of cytochrome P-448 activity, namely aryl hydrocarbon hydroxylase, biphenyl 2-hydroxylase and ethoxyresorufin O-de-ethylase, were evaluated with respect to their specificity, sensitivity and inducibility. Purified cytochrome P-448 (LM4), but not cytochrome P-450 (LM2), catalysed the O-de-ethylation of ethoxyresorufin in a reaction that was markedly inhibited by 9-hydroxyellipticine. After the administration of 3-methylcholanthrene to rats all three activities were induced, the extent of induction being highest for ethoxyresorufin O-de-ethylase. Administration of very small doses of benzo[a]pyrene (50 micrograms/kg) to rats to induce cytochrome P-448 specifically increased only the O-de-ethylation of ethoxyresorufin. 3-Hydroxybenzo[a]pyrene, the major metabolite determined by the aryl hydrocarbon hydroxylase assay, undergoes further NADPH-dependent oxygenation leading to loss of fluorescence. On the basis of these observations and those by other workers, we conclude that ethoxyresorufin O-de-ethylase provides the most specific, sensitive and reproducible means of determining cytochrome P-448 activity.

The concentrations of circulating GH were low in 1-week-old birds (male plasma pool 30 ng/ml, female 32 ng/ml), reached a maximum at 7 weeks in male birds (142 +/- 26 SEM ng/ml) or 4 weeks in females (185 +/- 32 ng/ml) and then decreased to 17-3 +/- 2-8 ng/ml in males and 8-7 +/- 0-6 ng/ml in females at 17 weeks. 2. Significant inverse correlations between GH concentration and age or body weight were found (male, r = -0-693), female, r = -0-623). 3. In males, but not females, the weekly increase in body weight was correlated with the plasma GH concentration (r = 0-291).