Evaluation of the rates of mineral accretion per kilogram of body weight gain and net energy intake for two genetic lines of barrows and gilts from 20 to 125 kilograms body weight1

2012 ◽  
Vol 28 (4) ◽  
pp. 387-394
Author(s):  
A.P. Schinckel ◽  
D.C. Mahan ◽  
T.G. Wiseman ◽  
M.E. Einstein
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Intake ◽  
Body Weight Gain ◽  
Net Energy ◽  
Net Energy Intake

scholarly journals Individual housing of male C57BL/6J mice after weaning impairs growth and predisposes for obesity

2019 ◽  
Author(s):  
Lidewij Schipper ◽  
Steffen van Heijningen ◽  
Giorgio Karapetsas ◽  
Eline M. van der Beek ◽  
Gertjan van Dijk
Keyword(s):  
Body Weight ◽  
Adipose Tissue ◽  
Weight Gain ◽  
Energy Intake ◽  
White Adipose Tissue ◽  
Body Weight Gain ◽  
Tissue Mass ◽  
Individual Housing ◽  
Adipose Tissue Mass ◽  
Obesogenic Diet

AbstractIndividual housing from weaning onwards resulted in reduced growth rate during adolescence in male C57Bl/6J mice that were housed individually, while energy intake and energy expenditure were increased compared to socially housed counterparts. At 6 weeks of age, these mice had reduced lean body mass, but significantly higher white adipose tissue mass compared to socially housed mice. Body weight gain of individually housed animals exceeded that of socially housed mice during adulthood, with elevations in both energy intake and expenditure. At 18 weeks of age, individually housed mice showed higher adiposity and higher mRNA expression of UCP-1 in inguinal white adipose tissue. Exposure to an obesogenic diet starting at 6 weeks of age further amplified body weight gain and adipose tissue deposition. This study shows that post-weaning individual housing of male mice results in impaired adolescent growth and higher susceptibility to obesity in adulthood. Mice are widely used to study obesity and cardiometabolic comorbidities. For (metabolic) research models using mice, (social) housing practices should be carefully considered and regarded as a potential confounder due to their modulating effect on metabolic health outcomes.

scholarly journals Effects of Consuming Sugar-Sweetened Beverages for 2 Weeks on 24-h Circulating Leptin Profiles, Ad Libitum Food Intake and Body Weight in Young Adults

Nutrients ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3893 ◽  
Author(s):  
Desiree M. Sigala ◽  
Adrianne M. Widaman ◽  
Bettina Hieronimus ◽  
Marinelle V. Nunez ◽  
Vivien Lee ◽  
...  
Keyword(s):  
Young Adults ◽  
Body Weight ◽  
Weight Gain ◽  
Food Intake ◽  
Energy Intake ◽  
Body Weight Gain ◽  
Energy Requirement ◽  
Area Under The Curve ◽  
Sugar Sweetened Beverage ◽  
Ad Libitum

Sugar-sweetened beverage (sugar-SB) consumption is associated with body weight gain. We investigated whether the changes of (Δ) circulating leptin contribute to weight gain and ad libitum food intake in young adults consuming sugar-SB for two weeks. In a parallel, double-blinded, intervention study, participants (n = 131; BMI 18–35 kg/m2; 18–40 years) consumed three beverages/day containing aspartame or 25% energy requirement as glucose, fructose, high fructose corn syrup (HFCS) or sucrose (n = 23–28/group). Body weight, ad libitum food intake and 24-h leptin area under the curve (AUC) were assessed at Week 0 and at the end of Week 2. The Δbody weight was not different among groups (p = 0.092), but the increases in subjects consuming HFCS- (p = 0.0008) and glucose-SB (p = 0.018) were significant compared with Week 0. Subjects consuming sucrose- (+14%, p < 0.0015), fructose- (+9%, p = 0.015) and HFCS-SB (+8%, p = 0.017) increased energy intake during the ad libitum food intake trial compared with subjects consuming aspartame-SB (−4%, p = 0.0037, effect of SB). Fructose-SB decreased (−14 ng/mL × 24 h, p = 0.0006) and sucrose-SB increased (+25 ng/mL × 24 h, p = 0.025 vs. Week 0; p = 0.0008 vs. fructose-SB) 24-h leptin AUC. The Δad libitum food intake and Δbody weight were not influenced by circulating leptin in young adults consuming sugar-SB for 2 weeks. Studies are needed to determine the mechanisms mediating increased energy intake in subjects consuming sugar-SB.

Responses of rufous hummingbirds to midday fasts

1985 ◽  
Vol 63 (10) ◽  
pp. 2249-2253 ◽  
Author(s):  
Zena J. Tooze ◽  
Clifton Lee Gass
Keyword(s):  
Body Weight ◽  
Energy Balance ◽  
Food Intake ◽  
Energy Intake ◽  
Laboratory Tests ◽  
Net Energy ◽  
Energy Reserves ◽  
Metabolic Costs ◽  
Net Energy Intake ◽  
Highly Correlated

This study investigates how rufous hummingbirds regain energy balance after experimentally imposed midday fasts reduce their energy reserves. Net energy balance calculated from food intake, activity budgets, and allometric equations for the costs of flying and perching was highly correlated with change in body weight in laboratory tests of 3 h or more. Individuals accumulated energy and body weight at the same rate after fasts as before, resulting in energy deficits at the end of the day compared with control conditions. Energy balance relative to control values was regained by the following morning, primarily by reducing metabolic costs in the dark through torpor. Net energy intake increased the following day, but this increase was relatively unimportant to reestablishing equilibrium.

Effect of energy intake on the performance of different types of pig from 45 to 100 kg body weight. 2. Tissue gain

1996 ◽  
Vol 63 (2) ◽  
pp. 289-296 ◽  
Author(s):  
N. Quiniou ◽  
J. Noblet ◽  
J.-Y. Dourmad
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Intake ◽  
Body Weight Gain ◽  
Energy Levels ◽  
Metabolizable Energy ◽  
Large White ◽  
Different Types ◽  
Ad Libitum ◽  
The Relationship

AbstractThe effect of energy supply on physical composition of body weight gain between 45 and 100 kg was studied in Large White castrated males (cLW), crossbred Pietrain × Large White castrated males (cPPX) and boars (bPPX). The pigs were either given food ad libitum and kept in individual pens in experiment 1, or allocated to four energy levels (0·70, 0·80, 0·90, and 1·00 ad libitum) and kept in metabolism cages in experiment 2. Daily protein supplies were calculated to be the same at the four energy levels within each type of pig and non-limiting for growth. Five additional animals for each type of pig were slaughtered at 45 kg. Daily tissue gain was measured according to the comparative slaughter technique. The daily lean gain increased with metabolizable energy (ME) intake according to a linear-plateau relationship whereas the daily fat gain increased linearly. The type of pig significantly affected the slope of the relationship between lean gain and ME intake (from 15 to 22 g per extra MJ ME) but not the slope of the relationship between fat gain and ME intake (10 g per extra MJ ME on average). Increased energy intake was associated with increased fatness of body-weight gain, which was higher in cLW and cPP× than in bPP×.

scholarly journals Energy utilization for body weight gain of ram-lambs fed differently processed breadfruit (Artocarpus altilis) meal in total mixed rations.

2021 ◽  
Vol 43 (2) ◽  
pp. 147-154
Author(s):  
M. I Okoruwa
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Intake ◽  
Feed Intake ◽  
Body Weight Gain ◽  
Energy Utilization ◽  
Daily Weight Gain ◽  
Energy Output ◽  
Initial Body Weight ◽  
Ram Lambs

The study was carried out to estimate the energy utilization for body weight gain in West African dwarf ram-lambs fed differently processed breadfruit meal in total mixed rations. Twenty non-castrated ram-lambs, about 7months of age with an average-initial body weight of 6.00 ± 0.55kg, were randomly assigned to four dietary treatments with five ram-lambs per treatment group in a completely randomized design. Ficus foliage with differently processed breadfruit meals and concentrate diet were used as treatment diets. Diet A (50% unpeeled raw breadfruit meal +20% Ficus foliage + 30% concentrate diet) B (50% peeled raw breadfruit +20% Ficus foliage + 30% concentrate diet), C (50% unpeeled soaked breadfruit meal +20% Ficus foliage + 30% concentrate diet) and D (50% unpeeled boiled breadfruit meal + 20% Ficus foliage + 30% concentrate diet). Results showed that faecal energy output (999.41MJ/g/day DM) was significantly (P< 0.05) highest in treatment diet Acompared with other treatment diets. Ram-lambs on treatment diets B and C had the significantly highest (P < 0.05) on digestible energy intake (1310.84 and 1295.62 MJ/g/day DM), metabolizable energy intake (1074.89 and 1062.41MJ/g/day DM), average total weight gain (4.18 and 4.13kg) and average daily weight gain (87.08 and 86.04g) compared with treatment diets A and D. Gross energy intake (4503.00MJ/g/day), average total feed intake (13.68kg), average daily feed intake (285.00g) and feed conversion ratio (4.44) were significantly (P < 0.05) better in ram-lambs on treatment diet D. There were no significant (P > 0.05) differences in urinary energy loss, metabolizability and initial body weight of ram-lambs. It was therefore concluded that diets B and C enhanced efficiency of energy utilization for body weight gain of ram-lambs.

The long-acting amylin/calcitonin receptor agonist ZP5461 suppresses food intake and body weight in male rats

2021 ◽  
Author(s):  
Lauren M. Stein ◽  
Lauren E McGrath ◽  
Rinzin Lhamo ◽  
Kieran Koch-Laskowski ◽  
Samantha M. Fortin ◽  
...  
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Balance ◽  
Food Intake ◽  
Energy Intake ◽  
Receptor Agonist ◽  
Body Weight Gain ◽  
Male Rats ◽  
Calcitonin Receptor ◽  
Long Acting

The peptide hormone amylin reduces food intake and body weight, and is an attractive candidate target for novel pharmacotherapies to treat obesity. However, the short half-life of native amylin and amylin analogs like pramlintide limits these compounds' potential utility in promoting sustained negative energy balance. Here, we evaluate the ability of the novel long-acting amylin/calcitonin receptor agonist ZP5461 to reduce feeding and body weight in rats, and also test the role of calcitonin receptors (CTRs) in the dorsal vagal complex (DVC) of the hindbrain in the energy balance effects of chronic ZP5461 administration. Acute dose-response studies indicate that systemic ZP5461 (0.5-3 nmol/kg) robustly suppresses energy intake and body weight gain in chow- and high-fat diet (HFD)-fed rats. When HFD-fed rats received chronic systemic administration of ZP5461 (1-2 nmol/kg), the compound initially produced reductions in energy intake and weight gain, but failed to produce sustained suppression of intake and body weight. Using virally-mediated knockdown of DVC CTRs, the ability of chronic systemic ZP5461 to promote early reductions in intake and body weight gain was determined to be mediated in part by activation of DVC CTRs, implicating the DVC as a central site of action for ZP5461. Future studies should address other dosing regimens of ZP5461 to determine whether an alternative dose/frequency of administration would produce more sustained body weight suppression.

Quantification of changes in body weight and body condition scores during lactation by modelling individual energy balance and total net energy intake

2001 ◽  
Vol 72 (2) ◽  
pp. 325-334 ◽  
Author(s):  
R. Schwager-Suter ◽  
C. Stricker ◽  
D. Erdin ◽  
N. Künzi
Keyword(s):  
Body Weight ◽  
Energy Balance ◽  
Energy Intake ◽  
Body Condition ◽  
Dairy Cow ◽  
Fixed Effects ◽  
Net Energy ◽  
Net Energy Intake ◽  
Gut Fill ◽  
Body Condition Scores

AbstractIndividual energy balances (EB) and total net energy intake (NEI) were modelled to quantify the energy content of the explanatory variables body-weight change corrected for gut fill (BWC) and body condition-score change (BCSC). A total of 6147 records from 213 lactating dairy cows, 71 Holstein-Friesians, 71 Jerseys and 71 HolsteinJersey F1-crosses was analysed (1st, 2nd and >2nd lactation). Data were collected during 210 days of lactation, from calving to week 30. Individual EB were calculated as total energy for lactation (MJ NEL) minus estimated energy necessary for maintenance and production. Body-weight changes were calculated as differences between weekly means of body weight corrected for gut fill (BWCw) as well as from polynomial regression (BWCp). BCSC were differences between assessed body condition scores. The study included analyses of 1- and of 4-week periods for BWCw and BWCp, of differences between measuring periods for BCSC as well as separate analyses of data from cows in either negative or positive energy balance.Analysis of repeated measurements were performed applying mixed model theory. Models for EB contained type of dairy cow, lactation and type of roughage as fixed effects, week of lactation and either BWCw, BWCp or BCSC. Models for NEI contained type of dairy cow, lactation and quality of roughage as fixed effects, week of lactation as well as energy corrected milk, metabolic body weight and either BWCw, BWCp or BCSC as covariates.Most plausible energy contents per unit body tissue change were estimated for BWCp from weekly data with either EB (with energy partitioned into milk production and maintenance fixed) or NEI (no restrictions concerning partitioning) as the response variable. The estimated energy contents for BWCp were 15·40 and 10·47 MJ NEL, respectively.

scholarly journals Routes to obesity: phenotypes, food choices and activity

2000 ◽  
Vol 83 (S1) ◽  
pp. S33-S38 ◽  
Author(s):  
John E. Blundell ◽  
John Cooling
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Energy Expenditure ◽  
Energy Intake ◽  
Body Weight Gain ◽  
Food Selection ◽  
Activity Level ◽  
Positive Energy ◽  
High Fat ◽  
Age Related

Gain in body weight over a number of years could be achieved through cumulative positive energy balances. These positive balances could come about through adjustments in the various components of energy expenditure or fuel utilization, together with shifts in food selection or eating patterns leading to adjustments in macronutrient intake. This means that many combinations of intake and expenditure could lead to a positive energy balance; these combinations can be called routes to body weight gain. However, these routes are difficult to trace by studying random samples of individuals. Previous investigations have found a clear association between high fat consumption and the occurrence of obesity, and although a high fat intake is a strong behavioural risk factor for weight gain, the relationship does not constitute a biological inevitability. Some normal-weight and lean individuals appear to eat a high-fat diet. To investigate reasons for this we have studied individuals initially defined by particular clusters of dietary characteristics related to fat and carbohydrate consumption. Habitual high-fat (HF) and low-fat (LF) consumers have been termed phenotypes. Various aspects of energy expenditure (physiological and behavioural) and energy intake were measured in these individuals with contrasting profiles. HF phenotypes had high intakes of fatty foods and an overall higher energy intake than LF. However, these groups of young adult males had similar BMIs and percentage body fat. The HF had a significantly higher resting metabolic rate (RMR) and a lower RQ, together with high plasma fasting leptin levels, and a higher sleeping heart rate. In HF individuals the physical activity level was somewhat lower and they had significantly more periods of sedentary behaviour than LF subjects. Although HF individuals appear to be more vulnerable to developing obesity, both phenotypes carry particular risk factors and protective factors for weight gain. The use of phenotypes has allowed the identification of different potential routes to weight gain. Different strategies are required to prevent age-related increase in body weight in these quite different individuals.

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