N.A. Ciccone

Gonadotrophin Inhibitory Hormone Depresses Gonadotrophin α and Follicle-Stimulating Hormone β Subunit Expression in the Pituitary of the Domestic Chicken

Studies performed in vitro suggest that a novel 12 amino acid RF amide peptide, isolated from the quail hypothalamus, is a gonadotrophin inhibitory hormone (GnIH). The aim of the present study was to investigate this hypothesis in the domestic chicken. Injections of GnIH into nest‐deprived incubating hens failed to depress the concentration of plasma luteinizing hormone (LH). Addition of GnIH to short‐term (120 min) cultures of diced pituitary glands from adult cockerels depressed follicle‐stimulating hormone (FSH) and LH release and depressed common α and FSHβ gonadotrophin subunit mRNAs, with no effect on LHβ subunit mRNA. Hypothalamic GnIH mRNA was higher in incubating (out‐of‐lay) than in laying hens, but there was no significant difference in the amount of hypothalamic GnIH mRNA in out‐of‐lay and laying broiler breeder hens at the end of a laying year. It is concluded that avian GnIH may play a role in controlling gonadotrophin synthesis and associated constitutive release in the domestic chicken.

Lighting regimens and plasma LH and FSH in broiler breeders

1. Egg production by meat-type fowl is markedly inferior to that from commercial laying hens, and so, to assess the degree to which photorefractoriness might be a contributing factor, male- and female-line broiler breeders were maintained on 8-, 11- or 16-h photoperiods. In addition, to determine the age-related rate of change in response to an increment in photoperiod, other birds were transferred from 8- to 16-h photoperiods at 67 or 124 d. 2. Blood samples were taken from all groups, except those on constant 11-h photoperiods, in both genotypes at 67, 69, 124 and 126 d, and from all lighting groups in the female line at 58 weeks (end of trial), and the plasma was assayed for plasma luteinising hormone (LH) and follicle stimulating hormone (FSH) concentration to investigate possible correlations with rate of sexual maturity, total egg numbers and terminal rates of lay. 3. Prepubertal LH was consistently higher for the female line than for the male line, and higher for 16-h birds than for 8-h birds. At 69 and 126 d, LH values were not significantly different from those 2 d earlier for 8-h birds, but significantly reduced for 16-h birds. There was an increase in LH following photostimulation at 67 d, but no significant change after the 124-d light increase. 4. There were no significant differences in FSH between the two genetic lines, nor any effect of photostimulation at 67 or 124 d. There was a tendency for FSH in 8-h birds to be higher than for 16-h birds, and this difference became significant for male-line birds at 67 d. 5. At 58 weeks, LH was higher for constant 11- and 16-h birds and for birds photostimulated at 67 d than for constant 8-h controls or birds transferred from 8 to 16 h at 124 d. 6. Neither baseline nor photoinduced prepubertal changes in plasma LH nor FSH were found to be of value for predicting age at sexual maturity or subsequent rates of egg production. At 58 weeks, LH was not generally correlated with sexual maturity, total eggs or terminal rates of lay, however, there was a negative correlation with age at first egg in birds photostimulated at 124 d. 7. It must be concluded that plasma LH and FSH concentrations are of minimal value to the broiler breeder industry for predicting the degree of photorefractoriness, the age at sexual maturity, or subsequent egg production.

Light intensity can influence plasma FSH and age at sexual maturity in domestic pullets.

1. Shaver White and ISA Brown pullets were reared to 140 d in cage groups of 8 on a 10-h photoperiod of incandescent light and maintained at an illuminance of 3 or 25 lux, or transferred from 3 to 25 lux or from 25 to 3 lux at 63 or 112 d of age. 2. Plasma follicle stimulating hormone (FSH) concentration at 63 and 112 d was higher in both breeds for pullets maintained at an illuminance of 25 lux compared with 3 lux. After 2–4 d, and relative to constant-illuminance controls, plasma FSH increased significantly for ISA Brown transferred from 3 to 25 lux at 63 d and for Shaver White transferred at 112 d. Irrespective of genotype, plasma FSH for pullets given a decrease in illuminance at 63 or 112 d showed a tendency for less change than did constant-illuminance controls. 3. There was no significant difference in sexual maturity for ISA Brown maintained on 3 or 25 lux, but Shaver White pullets exposed to constant 3 lux matured later than those maintained on 25 lux. Shaver White matured later following an increase from 3 to 25 lux at 63 and 112 d, and earlier subsequent to a decrease from 25 to 3 lux at 112 d. ISA Brown pullets were not significantly affected by a change in illuminance at 63 or 112 d, though their responses were in the same direction as Shaver White. 4. Changes in plasma FSH in the 2- to 4-d period following a change in illuminance at 63 or 112 d were not significantly correlated with sexual maturity.

Does gonadotrophin inhibiting hormone (GnIH) play a functional role in avian reproduction

calculation of synthesis rate. Once this parameter was available, we were then able to deconvolute the heavy and light variants of the monovaline peptides to reveal the amount of newly synthesised material compared to residual protein synthesised before the labelling period. As expected, the amount of unlabelled material declined over time (degradation) and the amount of labelled protein increased over time (synthesis). This approach can be applied on a protein-by-protein basis and delivers an understanding of proteome dynamics to protein accretion in skeletal muscle.

2004 SPRING MEETING OF THE WPSA UK BRANCH PAPERS

calculation of synthesis rate. Once this parameter was available, we were then able to deconvolute the heavy and light variants of the monovaline peptides to reveal the amount of newly synthesised material compared to residual protein synthesised before the labelling period. As expected, the amount of unlabelled material declined over time (degradation) and the amount of labelled protein increased over time (synthesis). This approach can be applied on a protein-by-protein basis and delivers an understanding of proteome dynamics to protein accretion in skeletal muscle.

2004 SPRING MEETING OF THE WPSA UK BRANCH PAPERS: Does gonadotrophin inhibiting hormone (GnIH) play a functional role in avian reproduction?

calculation of synthesis rate. Once this parameter was available, we were then able to deconvolute the heavy and light variants of the monovaline peptides to reveal the amount of newly synthesised material compared to residual protein synthesised before the labelling period. As expected, the amount of unlabelled material declined over time (degradation) and the amount of labelled protein increased over time (synthesis). This approach can be applied on a protein-by-protein basis and delivers an understanding of proteome dynamics to protein accretion in skeletal muscle.