Responses to intravenous glucose challenge (no. = 26) and basal metabolite and hormone concentrations (no. = 68) were determined in dairy cows selected for high (HFI) or low (LFI) milk-fat concentration but with similar 40 g/kg fat-corrected milk (FCM) yields. All cows were given a mixed diet ad libitum. Following a glucose challenge the insulin release was higher (P < 0·05) and the glucose clearance rate faster (P < 0·05) in the HFI cows compared with the LFI cows. Basal plasma concentrations of the metabolites alanine, β -hydroxybutyrate, glucose, non-esterified fatty acids and urea and the hormones insulin-like growth factor-1 (IGF-1), insulin and leptin were not influenced by selection line.

Coopworth sheep selected for low (lean) or high (fat) backfat have large differences in plasma GH profiles. Fat genotype ram lambs (5 months old) were treated with growth hormone (GH) to simulate the plasma GH profiles of lean sheep and investigate whether exogenous GH could modify carcass fatness. For 77 days, bovine GH was administered at 25 Uglkg live weight per day either as a single, daily subcutaneous bolus (fat bolus) or via portable pulsatile infusion pumps (fat pump) which delivered GH solution at 90-min intervals into a jugular catheter. Measurements of body composition were made by computed tomography (CT) and ultrasonic scanning during the trial, with linear carcass measurements and proximate analysis undertaken at the end of the experiment.

Before treatments began, mean plasma GH levels were lower (P < 0·01) in fat control (0·34 ugll) than in lean lambs (1·1 μg/l). Several weeks after the start of the trial, mean plasma GH had increased in both fat bolus (1·2 μg/l) and fat pump (0·45 μg/l) treatment lambs with major changes in the pulsatility relative to the fat control lambs. Although these changes were maintained in the fat bolus lambs, by the end of the trial there was no significant difference in mean plasma GH between fat pump and fat control sheep. Throughout the trial, plasma 1GF-1 levels were higher in fat bolus, fat pump and lean lambs than in fat control lambs. Analysis of body composition data over the GH treatment period revealed that the slope of the allometric equation for total fat relative to empty body weight was lower in the fat bolus lambs (1·07) than in the lean lambs (1·50) with fat control and fat pump treatment lambs intermediate (1·30 and 1·36, respectively). Subcutaneous fat was later maturing in lean lambs than in fat control and bolus treatment lambs when regressed against total fat, with the fat pump treatment lambs being intermediate. Linear carcass measurements revealed changes due to GH administration in the distribution of subcutaneous fat and eye muscle dimensions.

It is concluded that sheep from the fat genotype show physiological responses to exogenous GH. Increasing plasma GH levels of fat sheep increased plasma IGF-1 and had variable effects on carcass fatness. The change in body composition may be affected by the mode of administration of exogenous GH.

The aim of the study was to investigate the influence of different energy levels during a 4-week lactation on the regulation of the metabolic hormones somatotropin (GH), prolactin, insulin and insulin-like growth factor-1 (IGF-1). A total of 21 crossbred sows (German Landrace × Duroc) were cannulated for daily blood collection from 3 weeks before parturition until 2 weeks after weaning and for weekly window sampling (every 20 min for 10 h). Nineteen sows were given 2·8 kg food during late gestation, 5·0 kg food during lactation and 2·8 kg food per day after weaning and two sows were given food at a restricted level (3·0 kg) during lactation. In the 19 sows, the different energy balance was induced by allocation of different numbers of sucking piglets to the respective sows. One group of sows suckled seven piglets and served as a control (C; no. = 7) and another group suckled 10 to 12 piglets and was energy deficient (D). After the study, the sows of the deficient group were, based on their litter weight gain from parturition until weaning, divided into low (D-L; no. = 6) or high (D-H; no. = 6) litter weight gain. The D-H sows lost more body weight during lactation than C and had lower glucose and higher nonesterified fatty acids levels before morning feeding. GH and prolactin increased around parturition and their secretory profiles during lactation were altered by the frequent sucking stimulus, whereby the access of the piglets to their dams was not controlled. During lactation, GH and prolactin were highest in D-H sows. The results suggest a possible role of not only GH but also of prolactin in nutrient partitioning to the mammary gland just before the start of lactation and for minimizing the adverse effects of a negative energy balance. Furthermore, insulin and IGF-1 increased around parturition in all sows. Insulin was higher before and after feeding and the highest levels were found in C and D-L sows. The regulation patterns of insulin and IGF-1 indicate that the lactating sow is able to mobilize enough energy from body reserves to prevent metabolic disorders, even during a period with deficient energy supply. This is contrary to the regulation in the dairy cow, where the negative energy balance is coupled with a severe glucose deficit during phases of high milk yield, which causes decreased levels of insulin and IGF-1. In the sow, the glucose intake with the food meets the glucose requirement for metabolic pathways also during a deficient lactational energy intake. Therefore, in sows IGF-1 can be stimulated by increased GH levels via the GH receptor in the liver during a state of nutritional energy deficiency and the fact that sows can compensate a deficient metabolic state much better than cows is also reflected in the respective endocrinology.

Winter growth of young male red deer can be increased by exposure to 16 h of light (L) and 8 h of dark (D) per day (16L: 8D). This study tested the duration of photoperiod required for this growth response, determined if the time to reach slaughter weight can be reduced and monitored plasma IGF-1, prolactin and reproductive development. Fifty male calves were allocated to five equal groups. Four groups were housed indoors and for 33 weeks from the winter solstice (22 June, southern hemisphere) until 11 February were placed under either 16L: 8D (16L), 13·25L: 10·75D (13L), 10·751:13·25D (111) or 8L: 16D (8L) photoperiods. The fifth group of deer (OC) remained outside in a gravelled enclosure. All groups were given a pelleted diet ad libitum. Group food intake was recorded daily, individual live weight was measured weekly and testes diameter and blood samples taken at weekly or 2-week intervals.

Plasma prolactin concentrations in 16L increased within 4 weeks of treatment and were different (P < 0·001) between groups from 14 August to 4 September. IGF-1 increased in both 16L and 13L 4 weeks after treatments and then increased further in 16L above that of 13L (P < 0·01). All groups grew at the same rate for the first 7 weeks. 16L then gained more weight (P < 0·001) than the other groups over the next 19 weeks (50·7 kg v. 38·5 for 13L, 35·7 for 11L, 37·0 for 8L and 37·4 for OC; s.e.d. 3·76). Food intake was positively related to growth rate in a similar way among the inside groups (P < 0·001), however there was a higher energy requirement outdoors (P < 0·05). A target live weight for slaughter of 95 kg was reached 7 weeks earlier for 16L than the other groups (P < 0·01). Testes diameter of 16L was larger than in the other groups from 13 November until 24 December (P < 0·001). The growth oflSL slowed from 1 January while that of OC increased and the live weight ofOC was equal to 16L by the end of the experiment. OC also had the largest testes diameter from 5 February onwards (P < 0·01). The live-weight increase in OC was associated with increases in both prolactin and IGF-1 levels.

This study confirmed that 16L: 8D stimulates rapid growth of young male red deer during winter for sufficient time to achieve an earlier slaughter date. The live-weight advantage was lost by late summer however. The increased growth rate was mediated by food intake and associated with increases in IGF-1 and prolactin and earlier reproductive development. Photoperiods of 13 h of light per day or less did not stimulate growth and increases in IGF-1 and prolactin were of a lower amplitude than under 16L: 8D.

Texel (T) and Suffolk (S) sired ram, wether and ewe lambs (no = 180) were kept at grass with their dams until weaned at 20 weeks and then taken to slaughter weights of 40, 44 and 48 kg, also at grass. Sex type, but not sire breed, affected lamb growth rate (rams 293, wethers 253, ewes 224 g/day; P < 0·001). Both T and S ewe lambs were fatter at slaughter in all fat depots compared with their ram and wether siblings such that rams could be slaughtered at a calculated 7·7 kg greater live weight than ewes at equal carcass fat cover. T carcasses were greater than S carcasses in eye-muscle area (793 v. 732 mm2; P < 0·001) and killing-out proportion (481 v. 476 g/kg; P < 0·05) but not in any fat measurement. Slaughter weight influenced killing-out proportion (P < 0·001) and all fat measurements (P < 0·01) but did not significantly affect eye-muscle area.

Mean serum insulin-like growth factor-1 (IGF-1) concentrations (μig/l), determined during weeks 8,11, 14, 17 and 20 in a balanced subset of 84 lambs, were higher in T than in S lambs (P < 0·05), in singles than in twins (P < 0·01; rams and wethers only) and in rams than in either wethers or ewes (P < 0·001). Mean serum IGF-1 concentration decreased between week 8 and week 20 with a greater rate of decline in singles than in twins (P < 0·001). IGF-1 was more strongly correlated with live weight at 8 weeks (r = 0·629; P< 0·001) than at 20 weeks (r = 0·293; P < 0·05). Mean IGF-1 (weeks 8 to 20) was correlated with rate of live-weight change (r = 0·576; P < 0·001). Significant differences for T and S lambs were found in the relationships between mean serum IGF-1 (weeks 8 to 20) and daily live-weight gain (weeks 8 to 20) and between mean IGF-1 and eye-muscle area at slaughter. Metabolite concentrations differed little between sire breeds and not at all between sex types.

The influence of pre-slaughter nutrition on the potency of foetal serum in cell culture was studied. Ewes carrying late-gestation foetuses (120-day gestation) were either fasted for 66 h (F), fasted for 66 h but drenched with Ketol, a propylene glycol preparation, (5 × 120 ml doses; FK), given food ad libitum (A), or given food ad libitum and drenched with Ketol (5 × 120 ml doses; AK). Following slaughter foetal blood was collected for the determination of potency in cell culture using industry-standard cell culture bioassays: cloning efficiency, plating efficiency and a 96 h cell proliferation assay. Foetal serum insulin-like growth factor (IGF) concentrations were also measured. Pre-slaughter fasting or drenching with Ketol had no effect on the potency of foetal serum in any of the cell culture bioassays. Fasting significantly lowered foetal plasma IGF-1 levels (F < 0·01). Foetal IGF-2 levels were unaffected by fasting or drenching with Ketol.

The work described was carried out to study the expression of insulin-like growth factor 1 (IGF-1) and growth hormone-receptor (GHR) mRNA in liver, skeletal muscle and adipose tissue from three breeds of pig with varying growth characteristics. The three breeds studied were the Large Wlrite, noted for its lean tissue; the Duroc, characterized by its high intramuscular fat content; and the Meishan × Landrace (0·5 Meishan), noted for its fat, poorly conformed carcass and slower growth rate. The probes used were designed to monitor promoter usage for IGF-1 expression and also expression of the extra-cellular domain of the GHR. Eighteen gilts, six of each breed, were given a barley/wheat diet (158 g crude protein, 10·7 g lysine and 13·9 MJ energy per kg), to appetite, for 1 to 2 weeks until they reached about 85 kg. Samples of liver, longissimu s dorsi (LD) muscle and three adipose tissue depots (subcutaneous (SC), perirenal (PR) and omental (OM)) were collected immediately after slaughter and frozen in liquid nitrogen (total time of sample collection to plunging of sample into liquid nitrogen was <3 min), prior to extraction of total RNA and ribonuclease protection assays. Individual serum samples collected at exsanguination were frozen prior to IGF-1 radioimmunoassay. There were no breed differences in the serum IGF-1 concentrations (range 49 to 134 μg/l), or in expression of the GHR gene or either class of IGF-1 transcript in the liver. However, there was a significant difference between the breeds in expression of IGF-1 mRNA in the LD muscle (P < 0·001), the order being Duroc > Wliite > Meishan, with only class 1 transcripts of IGF-1 being found. GHR expression in LD muscle was lower in White than in the other tivo breeds (P = 0·022). There was a significant difference between the breeds in expression of IGF-1 mRNA (only class 1 transcripts present) in the adipose tissue (P = 0-006), the order being Wliite · Duroc · Meishan, and also a significant depot difference, with expression being highest in the SC depot (P < 0·001). There were no differences between the breeds or depots in expression of GHR mRNA in adipose tissue. The observed differences in muscle and adipose tissue IGF-1 expression may relate to the overall growth of the animal.

This study was performed to assess the relationship between serum growth hormone (GH) and insulin-like growth factor 1 (IGF-1) levels, slaughter weight, and myogenic satellite cell growth kinetics of Targhee rams. Serum was collected from 19 rams at 15-min intervals over a period of 4h. Radioimmunoassays of serum samples for GH revealed considerable variation (within individual rams) over the sampling period, with mean values ranging from 0·63 to 4·88 μg/l (mean overall 2·3 (s.e. 0·33) μg/l; no. = 19). There was no significant correlation between GH levels and slaughter weight (r = −0·11; P > 0·05) at 155 (s.e. 1·08) days. Serum IGF-1 levels of (individual) rams were invariant over the sampling period, with individual means ranging from 62 to 233 μg/l (mean overall of 117 (s.e. 45·6) ugll; no. = 19). IGF-1 was not strongly correlated with slaughter weight (r = +0·35; P > 0·05). Satellite cells were isolated from the left m. semimembranosus of all rams at slaughter and grown in culture to evaluate proliferation amount and differentiation extent. The correlations between serum GH levels and satellite cell proliferation and differentiation in vitro were r = −0·53 (P < 0·05) and r = −0·52 (P < 0·05), respectively. Serum IGF-1 showed no significant correlations to proliferation (r = +0·07; P > 0·05) or to differentiation (r = −0·07; P > 0·05) of the satellite cells. These data suggest that serum GH levels in Targhee rams may not reflect muscle growth potential if correlated to body weight of 155 days. Furthermore, as IGF-1 was not correlated significantly with slaughter weight or to variables of satellite cell proliferation and differentiation, another mode of satellite cell regulation (possibly paracrine controllers) is more likely at play to coordinate the satellite cell involvement in muscle growth in Targhee rams at 155 days.

The growth hormone-insulin-like growth factor (GH-IGF) axis is involved in the control of postnatal growth in all animals studied to date. At birth, blood levels of IGF-1 are low, although levels of GH are high. Thus a switching occurs during the postnatal period, which involves an increase in liver GH-receptors (GHR). This study investigates the changes in serum IGF-1 and IGF-1 and GHR mRNA in liver and skeletal muscle of growing pigs. The period from birth to 20 days of age showed a gradual increase in both IGF-1 and GHR mRNA expression by the liver, thus accounting for the gradual increase in serum IGF-1. The IGF-1 mRNA expressed was found to be predominantly class 1 transcripts with very few class 2 transcripts. There was a plateau of liver IGF-1 mRNA levels after 20 days and up to 140 days, even though the expression of GHR mRNA continued to increase. The levels of expression of the two genes were found to correlate in the first 20-day period (r = 0·76, P < 0·005), but not in the later period (r = 0·44, P > 0·05).

Levels of expression of both genes in the LD muscle were highly variable, with no age related changes being observed. However, a significant negative correlation of expression of the two genes was observed (R = 0·60, P < 0·001), with the correlation still being significant in the two age periods.

The data are consistent with a likely initial dependence for postnatal growth upon GH-stimulated IGF-1 mRNA expression by the liver, up to 20 days of age. After this time, hepatic expression of IGF-1 mRNA reaches a plateau, even though the serum IGF-1 and hepatic GHR mRNA levels continue to rise. A possible explanation for this could be an increase in either turn-over or stability of IGF-1 mRNA, giving rise to increased levels of peptide with no apparent change in mRNA level. Another possibility is that an increased expression/production of the IGF-binding proteins leads to an increase in the half-life of the peptide in the circulation.

The effect of nutritional growth restriction on reproductive development in red deer stags reared in constant photoperiod was investigated and the correlation between reproductive status and circulating concentrations of growth hormone (GH) and insulin-like growth factor-1 (IGF-1) examined.

Stags were reared from birth in constant photoperiod (12 h light: 12 h dark). They were offered a ‘complete diet’ ad libitum until they reached 52-5 kg live weight (LW) and were then maintained at this LWby restricting daily food dry-matter intake (DMI)for either a long (LR, 26 to 51 weeks of age, no. = 5) or short (SR, 21 to 33 weeks, no. = 6) period before being returned to ad libitum feeding.

Relative to SR stags, antlers hardened later in LR stags (72·0 v. 57·5 weeks of age, P < 0·001); sustained elevations in plasma testosterone also began later (55·2 v. 38·5 weeks, P < 0·001) but at lower LW (54·0 v. 60·6 kg, P < 0·05). In both groups, the testosterone rise followed the return to ad libitum food by 4 to 5 weeks. Plasma IGF-1 was closely correlated with DMI (LR, r = 0·84, P < 0·001; SR, r = 0-93, P < 0·001) and with plasma testosterone (LR, r = 0·42, P < 0·001; SR, r = 0·38, P < 0·01). Also the increase in plasma IGF-1 preceded that of testosterone (by 2·8 (s.e. 0·94) weeks) and was associated with a transient plasma GH peak (P < 0·05) and elevated LH concentrations (SR, P < 0·01; LR, P < 0·05).

The timing of reproductive development in growth-restricted male red deer in constant photoperiod may therefore be more sensitive to DMI than LW, and changes in plasma IGF-1 concentrations are consistent with a putative permissive role in relaying this information.

Eight sets of identical twin heifers and their first three calf crops were used to determine effects of single-trait selection for blood serum insulin-like growth factor 1 (IGF-1). Twin heifers were offspring of Simmental sires and Hereford × Simmental or Hereford × Angus dams. All 16 heifers were mated with the same Simmental bull in each year of the study to produce calves born in 1989, 1990 and 1991 (no. = 16, 13 and 10, respectively). Although differences were noted in performance of progeny from the four twins with the highest v. the four with the lowest IGF-1 concentrations, they zoere not large enough to recommend single-trait selection for blood serum IGF-1 in beef heifers.