Growing goats of different sexes have distinct metabolic responses to continuous feed restriction

2018 ◽  
Vol 58 (5) ◽  
pp. 818
Author(s):  
Nhayandra C. D. Silva ◽  
Carla J. Härter ◽  
Fernanda O. M. Figueiredo ◽  
Rafael F. Leite ◽  
José M. Santos Neto ◽  
...  
Keyword(s):  
Growth Factor ◽  
Aspartate Aminotransferase ◽  
Protein Body ◽  
Fat Deposition ◽  
Feed Restriction ◽  
Insulin Like Growth Factor ◽  
Body Retention ◽  
Ad Libitum ◽  
The Difference ◽  
Growing Goats

The objective of the present study was to investigate the effect of sex on the hormonal and metabolic changes in growing goats subjected to levels of feed restriction. We used 72 Saanen kids, including 24 intact males, 24 castrated males and 24 females with initial bodyweight of 15.76 ± 0.174 kg and initial age of 108.4 ± 18.86 days respectively. A split-plot design was employed (3 sexes = intact males, castrated males, and females; 3 levels of feed restriction = 0% (ad libitum), 25% and 50%). Groups of three goat kids were formed by sex (each goat eating one level of feed restriction); goats of each group were slaughtered when animals fed ad libitum reached 30 kg bodyweight. Fat and protein deposition were calculated by the difference between the determinations performed on samples of homogenates of control animals slaughtered at the start of the experiment and the experimental animals. Blood samples were collected every 10 days to evaluate glucose, total protein, albumin, urea, creatinine, cholesterol, non-esterified fatty acid, β-hydroxybutyrate, aspartate aminotransferase, gamma glutamyltransferase, creatine kinase, triiodothyronine (T3), thyroxine and insulin-like growth factor. Females presented greater fat deposition than did castrated and intact males, regardless of feed restriction (P < 0.0001). Protein body retention (kg) was affected only by feed restriction (P < 0.0001). In females, aspartate aminotransferase activity was greater in those subjected to 50% feed restriction (83.83 ± 4.96 U/L). Regardless of sex, the greatest serum β-hydroxybutyrate concentration was observed when animals were subjected to 50% feed restriction (P < 0.0149). Plasma concentration of insulin-like growth factor 1 was similar in castrated and females, being lower than in intact males. Intact males showed lower plasma T3 concentration than did females (P < 0.05). Females changed their glycolytic metabolism to retain fat deposition even under feed restriction, whereas males mainly changed their protein metabolism to retain protein synthesis, and were less affected by feed restriction.

Effects of growth hormone-releasing factors and cottonseed meal on hormones and metabolites in plasma from lambs fed lucerne chaff ad libitum

1994 ◽  
Vol 45 (6) ◽  
pp. 1125 ◽  
Author(s):  
RD Sainz ◽  
BJ Hosking ◽  
FJ Hart ◽  
GSG Spencer
Keyword(s):  
Fatty Acids ◽  
Growth Hormone ◽  
Growth Factor ◽  
Cottonseed Meal ◽  
Metabolic Effects ◽  
Insulin Like Growth Factor ◽  
Plasma Urea ◽  
Blood Samples ◽  
Esterified Fatty Acids ◽  
Ad Libitum

This study was part of an experiment on the effects of cottonseed meal (CSM) and growth hormone-releasing factor (GRF) on growth in lambs fed lucerne chaff. Forty-eight crossbred lambs were fed lucerne chaff ad libitum, alone or with a cottonseed meal supplement (CSM; 300 g/day). Eight lambs from each group were injected twice daily with recombinant or synthetic GRF (rGRF and sGRF respectively; 30 8g per kg body weight/day) or excipient only for 28 or 30 days. Jugular blood samples were obtained on days 0, 7, 14, 21 and 28. On day 29, blood samples were taken from selected lambs (n = 2/group) at 0, 20, 40, 60, 80, 100, 120, 160 and 240 min after injection. Supplementation of lucerne chaff with CSM generally increased glucose and urea concentrations in plasma, reflecting improved energy and protein status. However, concentrations of growth hormone, insulin-like growth factor-1 and insulin were unaffected by CSM, as were plasma proteins, triacylglycerols and non-esterified fatty acids. Injection of rGRF and sGRF stimulated secretion of growth hormone (GH), insulin-like growth factor-1 (IGF-1) and insulin. Peak GH concentrations (20 min) following injection of GRF appeared to be higher in lambs fed CSM than in those receiving lucerne chaff alone. In contrast, maximal concentrations of IGF-1 were seen after 14 days of treatment. These changes were accompanied by increased plasma glucose, with no changes in triacylglycerols, non-esterified fatty acids and protein. Plasma urea was reduced by GRF, indicating that amino acids were diverted away from catabolism towards protein synthesis. These two sources of GRF were very similar in their endocrine and metabolic effects. This confirms similar observations regarding their effects on growth performance and carcass composition.

scholarly journals The Differential Effects of pp120 (Ceacam 1) on the Mitogenic Action of Insulin and Insulin-Like Growth Factor 1 Are Regulated by the Nonconserved Tyrosine 1316 in the Insulin Receptor

2000 ◽  
Vol 20 (11) ◽  
pp. 3896-3905 ◽  
Author(s):  
Payal Soni ◽  
Montaha Lakkis ◽  
Matthew N. Poy ◽  
Mats A. Fernström ◽  
Sonia M. Najjar
Keyword(s):  
Growth Factor ◽  
Insulin Receptor ◽  
Site Directed Mutagenesis ◽  
Insulin Like Growth Factor ◽  
Β Subunit ◽  
Conserved Domain ◽  
C Terminus ◽  
Mitogenic Action ◽  
The Difference ◽  
Differential Phosphorylation

ABSTRACT pp120 (Ceacam 1) undergoes ligand-stimulated phosphorylation by the insulin receptor, but not by the insulin-like growth factor 1 receptor (IGF-1R). This differential phosphorylation is regulated by the C terminus of the β-subunit of the insulin receptor, the least conserved domain of the two receptors. In the present studies, deletion and site-directed mutagenesis in stably transfected hepatocytes derived from insulin receptor knockout mice (IR−/−) revealed that Tyr1316, which is replaced by the nonphosphorylatable phenylalanine in IGF-1R, regulated the differential phosphorylation of pp120 by the insulin receptor. Similarly, the nonconserved Tyr1316 residue also regulated the differential effect of pp120 on IGF-1 and insulin mitogenesis, with pp120 downregulating the growth-promoting action of insulin, but not that of IGF-1. Thus, it appears that pp120 phosphorylation by the insulin receptor is required and sufficient to mediate its downregulatory effect on the mitogenic action of insulin. Furthermore, the current studies revealed that the C terminus of the β-subunit of the insulin receptor contains elements that suppress the mitogenic action of insulin. Because IR−/− hepatocytes are derived from liver, an insulin-targeted tissue, our observations have finally resolved the controversy about the role of the least-conserved domain of insulin and IGF-1Rs in mediating the difference in the mitogenic action of their ligands, with IGF-1 being more mitogenic than insulin.

Regulation and localization of the insulin-like growth factor system in small bowel during altered nutrient status

1995 ◽  
Vol 268 (4) ◽  
pp. G631-G640 ◽  
Author(s):  
D. E. Winesett ◽  
M. H. Ulshen ◽  
E. C. Hoyt ◽  
N. K. Mohapatra ◽  
C. R. Fuller ◽  
...  
Keyword(s):  
Growth Factor ◽  
Small Bowel ◽  
Lamina Propria ◽  
Elemental Diet ◽  
Nutrient Status ◽  
Insulin Like Growth Factor ◽  
Nutrient Regulation ◽  
Igf I ◽  
Ad Libitum ◽  
Igfbp 3

Insulin-like growth factor-I (IGF-I) may regulate small bowel growth. Analyses here in ad libitum-fed, fasted, and refed rats demonstrate that during fasting and refeeding changes in jejunal mass correlate with changes in serum IGF-I and jejunal IGF-I mRNAs. These data indicate that circulating and locally expressed IGF-I contribute to nutrient regulation of jejunal mass. During refeeding, jejunal IGF binding protein 3 (IGFBP-3) mRNA abundance was reduced relative to that of IGF-I, possibly amplifying enterotrophic actions of IGF-I. Localization of IGFBP-3 to subepithelial cells in lamina propria of jejunum indicates that IGFBP-3 derived from lamina propria may modulate IGF-I action on adjacent epithelium. Ileum differed from jejunum in that refeeding did not increase bowel mass or IGF-I mRNA to ad libitum values. Differences in exposure to luminal nutrient may underlie distinct responses of the two segments. Rats fed elemental diet intravenously showed reduced jejunal mass but not reduced jejunal IGF-I mRNA compared with rats fed oral elemental diet. Elemental nutrient given intravenously or orally therefore does not differ in effects on jejunal IGF-I expression. Complex luminal nutrient may, however, regulate jejunal IGF-I expression.

Ovarian and hepatic insulin-like growth factor-I gene expression and associated metabolic responses in prepubertal gilts subjected to feed restriction and refeeding

1993 ◽  
Vol 139 (1) ◽  
pp. 143-152 ◽  
Author(s):  
S. T. Charlton ◽  
J. R. Cosgrove ◽  
D. R. Glimm ◽  
G. R. Foxcroft
Keyword(s):  
Gene Expression ◽  
Growth Factor ◽  
Follicular Fluid ◽  
Feed Restriction ◽  
Insulin Like Growth Factor ◽  
Factor I ◽  
Igf I ◽  
Growth Factor I ◽  
Plasma Gh ◽  
I Gene

ABSTRACT The effects of feed restriction and refeeding on ovarian and hepatic insulin-like growth factor-I (IGF-I) gene expression, systemic and ovarian IGF-I concentrations and on associated metabolic changes were measured in prepubertal gilts. Eleven pairs of littermate gilts (70·7 ± 4·7 kg) were placed on a maintenance level of feeding for 7 days (days 1–7). On day 8, littermates were either fed at a maintenance level of energy or fed to appetite for a further 6 days. Blood samples were taken on day 13 (07.00–16.00 h) to determine plasma insulin and IGF-I, and on day 14 (02.00–06.00 h) to determine plasma GH levels. Following slaughter on day 14, one ovary from each animal was retained to measure follicular fluid IGF-I and oestradiol concentrations. The remaining ovary and a sample of liver were retained for IGF-I mRNA analysis using a ribonuclease protection assay. Six days of refeeding significantly increased plasma IGF-I (P<0·005) and basal insulin (P<0·05) but there was no effect on plasma GH. Ovarian follicular volume and diameter were significantly larger after refeeding (P<0·05), with no effect on follicular fluid oestradiol concentrations. Mean follicular fluid IGF-I concentrations were unaffected by treatment. However, the relationships between individual follicular IGF-I concentrations, absolute follicular fluid IGF-I contents and follicle volume were affected by feeding level (P<0·05). Regression analysis of the same data also revealed that at this stage of maturity, small follicles had greater follicular fluid concentrations of IGF-I than larger follicles. Refeeding increased the amount of IGF-I mRNA in hepatic but not ovarian tissue. We conclude that there is differential regulation of the IGF-I gene in porcine hepatic and ovarian tissues, and that ovarian factors other than, or as well as, IGF-I are involved in the regulation of ovarian responses to refeeding. Journal of Endocrinology (1993) 139, 143–152

Insulin-like growth factor I responses to recombinant bovine growth hormone during feed restriction in heifers

1989 ◽  
Vol 120 (6) ◽  
pp. 735-744 ◽  
Author(s):  
H. Ronge ◽  
J. Blum
Keyword(s):  
Growth Factor ◽  
Feed Intake ◽  
Feed Restriction ◽  
Insulin Like Growth Factor ◽  
Urea Nitrogen ◽  
Blood Concentrations ◽  
Factor I ◽  
Esterified Fatty Acids ◽  
Low Glucose ◽  
Growth Factor I

Abstract. Insulin-like growth factor I, other hormones and blood metabolites were measured in growing heifers before, during and after a 3-day period of normal feed intake and a corresponding period of reduced feed intake. In addition, 0.1 or 0.5 mg recombinant bovine GH/kg was injected daily for 5 days during normal or during and following reduced feed intake. During reduced feed intake blood concentrations of insulin-like growth factor I, insulin, T4, T3, glucose and urea-nitrogen decreased, whereas those of non-esterified fatty acids, albumin and protein increased (P< 0.05). GH, insulin-like growth factor I and insulin increased, whereas urea-nitrogen decreased in response to exogenous GH when heifers were adequately fed (P< 0.05). In contrast, insulin-like growth factor I did not change during GH injections while heifers received reduced amounts of feed. Therefore, during insufficient energy and (or) protein intake, characterized by low glucose, insulin and thyroid hormone levels and increased non-esterified fatty acid concentrations, insulin-like growth factor I concentrations and responses to GH administration were markedly reduced.

Effect of sodium selenite on growth, insulin-like growth factor-binding proteins and insulin-like growth factor-I in rats

1995 ◽  
Vol 145 (1) ◽  
pp. 105-112 ◽  
Author(s):  
H Grønbæk ◽  
J Frystyk ◽  
H Ørskov ◽  
A Flyvbjerg
Keyword(s):  
Growth Factor ◽  
Sodium Selenite ◽  
Insulin Like Growth Factor ◽  
Factor I ◽  
Igf I ◽  
Selenium Treatment ◽  
Group A ◽  
Ad Libitum ◽  
Group B ◽  
Igfbp 3

Abstract Selenium is an essential trace element although at higher doses it is also known to be a toxic agent causing a wide range of symptoms including growth retardation. In order to investigate the effect of sodium selenite on growth, insulin-like growth factor-binding proteins (IGFBPs) and insulin-like growth factor-I (IGF-I), 30 male Wistar rats were randomized into three groups. Group A was treated with sodium selenite in the drinking water (3·3 mg selenium/l). Group B was ad libitum fed with free access to standard fodder and tap water and group C was pair fed relative to the selenium-treated rats. Serum IGF-I and IGFBPs were determined on days 0, 14 and at the end of the study on day 35. Selenium-treated rats had significantly lower body weights compared with group B rats on day 9 and group C rats on day 14 (P<0·05). Tibia length was measured at the end of the study and no difference was observed between groups B and C (3·77 ± 0·04 cm vs 3·60±0·02 cm); however, selenium-treated rats had significantly shorter tibia lengths (3·46±0·03 cm) compared with rats in groups B (P<0·001) and C (P<0·05). Selenium treatment induced a significant reduction in circulating IGF-I by the end of the study compared with ad libitum and pair fed rats (P<0·05). Serum subjected to Western ligand blots showed four distinct IGFBP bands with apparent relative molecular weights of 38–47 kDa (doublet) (IGFBP-3), 30 kDa (IGFBP-1 and/or IGFBP-2) and 24 kDa (IGFBP-4). At the end of the study a significant reduction in IGFBP-3 was observed in group A compared with groups B and C (P<0·05). Selenium treatment also caused a reduction in IGFBP-1 and/or IGFBP-2 compared with ad libitum fed rats; in addition, a reduction was observed in pair fed controls. In conclusion, sodium selenite treatment leads to growth retardation accompanied by reduced circulating levels of IGF-I, IGFBP-3, and IGFBP-1 and/or IGFBP-2. The reduction in IGF-I and IGFBP-3 could not be attributed to reduced caloric intake but seems to be a specific action of selenium. Journal of Endocrinology (1995) 145, 105–112

Growth and serum thyroid hormone and insulin-like growth factor I (IGF-I) responses to natural passive immunization against somatostatin in the lamb

1993 ◽  
Vol 73 (3) ◽  
pp. 509-516 ◽  
Author(s):  
A. G. Van Kessel ◽  
R. S. Korchinski ◽  
B. Laarveld
Keyword(s):  
Growth Rate ◽  
Growth Factor ◽  
Thyroid Hormone ◽  
Serum Insulin ◽  
Passive Immunization ◽  
Insulin Like Growth Factor ◽  
Factor I ◽  
Igf I ◽  
Ad Libitum ◽  
Growth Factor I

The colostral transfer of maternal humoral immunity against somatostatin (SRIF) was examined as a mechanism of improving growth performance of the lamb. Lambs were the offspring of 15 ewes actively immunized against an SRIF-ovalbumin conjugate (SI; 14 male, 7 female) and of 13 ewes actively immunized against ovalbumin (C; 10 male, 5 female). At 5 d of age, lambs were removed from the ewes and received a 50:50 mixture of whole cow's milk and milk replacer ad libitum. At 46 d of age lambs were weaned and provided with an 18% crude protein pelleted grower ration ad libitum. Lamb weight was recorded and blood samples were obtained at regular intervals from 5 to 46 d of age and at 102 d of age. From 5 to 46 d of age, immunization increased growth rate of male (P < 0.001) but not female lambs. Serum thyroxine (T4) was lower (P < 0.001) in male than in female lambs. Serum triiodothyronine (T3) was higher (P < 0.05) in SI male than in C male lambs. SI female lambs initially demonstrated higher serum T3 levels than C female lambs, but this effect reversed after 19 d of age. Serum insulin-like growth factor I (IGF-I) levels were higher (P = 0.08) in SI than in C lambs without significant influence of sex. From 46 to 102 d of age, somatostatin immunization increased growth rate of male (P = 0.08) but not female lambs. Serum levels of T4, T3 and IGF-I at 102 d of age were not affected by immunization. Passive immunization against SRIF through colostral transfer of immunity may improve growth rate of the lamb via an influence on thyroid hormone metabolism. Key words: Sheep, somatostatin, immunoneutralization. growth, thyroid, IGF-I

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