Fat depot‐specific differences in leptin mRNA expression and its relation to adipocyte size in steers

ABSTRACT This experiment was conducted to investigate leptin mRNA expression, adipocyte size, and their relationship in several adipose tissues of fattening steers. Subcutaneous, perirenal, intermuscular and intramuscular adipose tissues were collected from three crossbred steers (Japanese Black cattle X Holstein) aged 21 months. The mRNA level and adipocyte diameter were determined in these adipose tissues. The intramuscular adipose tissue had a lower leptin mRNA level than the intermuscular and perirenal adipose tissues (P < 0.05). Leptin mRNA level was lower in the subcutaneous depot than in the intermuscular depot (P < 0.05). Adipocyte diameter was larger in the intermuscular adipose tissue than in the subcutaneous and intramuscular adipose tissues (P < 0.05). Leptin mRNA level was positively correlated with adipocyte diameter (r² = 0.81, P < 0.05). These results suggest that the cattle have fat depot‐specific differences in leptin gene expression, which are a result of a difference in adipocyte size.     

Lipogenic enzyme activities in different adipose depots of Pirenaican and Holstein bulls and heifers taking into account adipocyte size

The effects of sex, genotype, and adipose depot on lipogenic enzyme activity have been investigated in Holstein and Pirenaican bulls and heifers, taking into account differences in adipocyte size. Fifteen Pirenaican bulls and 15 heifers and 15 Holstein bulls and 13 heifers were fattened until slaughter (12 to 13 mo old and 450 to 500 kg of body weight). During the fattening period, animals had ad libitum access to commercial concentrates and straw. The 10th rib was dissected to determine the fat content. Adipocyte size and activities of the following lipogenic enzymes were determined: glycerol 3-phosphate dehydrogenase, fatty acid synthase, nicotinamide adenine dinucleotide phosphate (NADP)-malate dehydrogenase, glucose 6-phosphate dehydrogenase, and NADP-isocitrate dehydrogenase, in the omental, perirenal, subcutaneous, and intermuscular adipose depots, respectively. Because adipocyte mean cell volume varied with sex, breed, and depot, regression analyses of log(e) activity per cell and log(e) cell volume were used to compare activities per unit volume. Sex, breed and depot had no effect (P > 0.05) on the gradients of regressions, which did not differ significantly from 1. Thus, activity per unit volume did not vary with cell size. Consequently, sex, breed, and depot effects on the regression analyses were equivalent to effects on activity per unit volume. Females had greater amounts of fat in the 10th rib (P < 0.001), larger adipocytes (P < 0.001) and, in general, greater (P < 0.05) lipogenic activity per cell, even when adjusted for cell size, than males. These findings suggest that differences in adiposity between sexes are mainly due to females having a greater capacity for lipid synthesis, and hence, hypertrophy, than males. When adjusted for differences in carcass weight, Holsteins had larger adipocytes than Pirenaicans. The abdominal depots, omental and perirenal, had a greater adipocyte size (P < 0.001) and, in general, greater lipogenic enzyme activities per cell (P < 0.05) than the subcutaneous and intermuscular carcass depots. However, when activity per cell was adjusted for cell size, subcutaneous depots had greater fatty acid synthae, glucose 6-phosphate dehydrogenase, and NADP-malate dehydrogenase activities than omental and perirenal, indicating that other factors such as nutrient supply may restrict hypertrophy of carcass adipocytes.     

Adipogenic gene expression and fatty acid composition in subcutaneous adipose tissue depots of Angus steers between 9 and 16 months of age

We have demonstrated that among carcass adipose tissue depots, brisket subcutaneous adipose tissue contains the greatest concentration of MUFA and lowest concentration of SFA. Therefore, we hypothesized that brisket subcutaneous adipose tissue depots would exhibit greater adipogenic gene expression over time than other major subcutaneous adipose tissue depots. Four Angus steers, each at 9, 12, 14, and 16 mo of age, were harvested and fresh subcutaneous adipose tissue samples were collected from over the brisket, chuck, rib, loin, sirloin, round, flank, and plate. Relative gene expression for C/EBPβ, PPARγ, carnitine palmitoyltransferase-1 beta (CPT-1β), stearoyl-coenzyme A desaturase (SCD), AMP-activated protein kinase alpha (AMPKα), and G-coupled protein receptor 43 (GPR43) was analyzed by quantitative real-time PCR. Expression of C/EBPβ, PPARγ, and CPT-1β was greatest at 12 to 14 mo of age (all P < 0.0001) and declined to very low abundance by 16 mo of age in all depots. Expression of PPARγ and CPT-1β was greater (P < 0.03) in flank, rib, and sirloin subcutaneous adipose tissues than in brisket and round adipose tissues. The expression of the SCD gene did not differ among the 4 age groups (P = 0.95). The palmitoleic:stearic acid ratio (an estimate of SCD activity) was greater (P < 0.001) in the subcutaneous adipose tissues from brisket, plate, and round than in the loin, rib, and sirloin. Conversely, subcutaneous adipose tissue from the loin, rib, and sirloin had greater (P < 0.001) SCD gene expression than the brisket, plate, and round. In general, subcutaneous adipose tissues with the highest concentration of MUFA and least SFA consistently exhibited the least SCD gene expression and adipogenic gene expression. We conclude that MUFA in the brisket and other depots with large SCD indices were deposited before 9 mo of age, during a time when the subcutaneous adipocytes were highly differentiated.     

Effects of selection for rapid postweaning gain on maturing patterns of fat depots in mice

Correlated responses to selection for rapid 3 to 6-wk postweaning gain in male mice were estimated for five fat depots weighed at specific degrees of maturity in body weight (37.5, 50.0, 62.5, 75, 87.5 and 100%). Fat pads measured were from regions of the subcutaneous hindlimb, subcutaneous forelimb, epididymides, mesentery and kidneys. At the same degree of maturity, selected mice (M16) were older (P less than .01) than controls (ICR). M16 had heavier (P less than .01) fat depots than ICR for all sites at each degree of maturity. From 62.5 to 100% maturity, M16 was larger than ICR in fat depot weight as a percentage of body weight at all sites. Mesenteric fat made up the largest percentage of total fat in both lines and perirenal fat the smallest percentage. Development of degree of maturity in each fat depot relative to degree of maturity in body weight was studied using the constrained quadratic and standardized allometric models. Both models showed similar trends, but the latter identified more significant line differences. The standardized allometric analysis indicated that total fat and all individual fat depots except mesenteric fat matured at a slower rate (P less than .01) in M16 than in ICR. Bivariate allometric analyses of ln fat depot weight on ln body weight showed that M16 exceeded (P less than .01) ICR in relative growth of all fat depots except mesenteric fat; at lower body weights, ICR had larger fat depots than M16, but the reverse was true at higher body weights.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effects of metabolizable energy intake on body fat depots of adult Pelibuey ewes fed roughage diets under tropical conditions

The objective of this work was to evaluate the effect of metabolizable energy intake (MEI) on changes in fat depots of adult Pelibuey ewes fed roughage diets under tropical conditions. Eighteen 3-year-old Pelibuey ewes with similar body weight (BW) of 37.6 ± 4.0 kg and body condition score (BCS) of 2.5 ± 0.20 were randomly assigned to three groups of six ewes each in a completely randomized design. Ewes were housed in metabolic crates and fed three levels of MEI: low (L), medium (M), and high (H) for 65 days to achieve different BW and BCS. At the end of the experiment, the ewes were slaughtered. Data recorded at slaughter were: weights of viscera and carcass. Internal fat (IF, internal adipose tissue) was dissected, weighed, and grouped as pelvic (around kidneys and pelvic region), omental, and mesenteric regions. Carcass was split at the dorsal midline in two equal halves, weighed, and chilled at 6°C during 24 h. After refrigeration, the left half of the carcass was completely dissected into subcutaneous and intermuscular fat (carcass fat). Dissected carcass fat (CF) of the left carcass was adjusted as whole carcass. At low levels of MEI, proportion of IF and CF was approximately 50%; however, as the MEI was increased, the proportion of IF was increased up to 57% and 60% for M and H, respectively. Omental and pelvic fat depots were those which increased in a larger proportion with respect to the mesenteric fat depot. Regression equations between the weight of each body fat depot and BW had a coefficient of determination (r ²) that ranged between 0.37 for mesenteric fat and 0.87 for CF. The regression with BCS had a r ² that ranged between 0.57 for mesenteric and 0.71 for TBF. BW was the best predictor for TBF, CF, omental fat, and pelvic fat; whereas, BCS was better than BW in predicting IF and mesenteric fat. Inclusion of both BW and BCS in multiple regressions improved the prediction for all fat depots, except for pelvic fat, which was best estimated by BCS alone. The greater slope of the regression for the pelvic fat depot equation, relative to TBF (1.40), EBW (4.02), and BCS (2.36), suggested that pelvic fat has a greater capacity to accumulate and mobilize fat. These results indicated that adult Pelibuey ewes seem to store a considerable proportion of absorbed energy in the IF depots rather than in the carcass.     

Effect of source and amount of energy and rate of growth in the growing phase on adipocyte cellularity and lipogenic enzyme activity in the intramuscular and subcutaneous fat depots of Holstein steers

Seventy-three Holstein steers (initial BW 138.5 +/- 4.3 kg; approximately 3 mo of age) were allotted by BW to one of three growing-phase treatments to determine the effect of source and amount of energy on feedlot performance, and characteristics of subcutaneous (s.c.) and intramuscular (i.m.) adipose tissue. Treatment diets were 1) high concentrate fed ad libitum (ALC); 2) high forage fed ad libitum for 55 d, then a mid-level forage diet fed ad libitum for 98 d (ALF); or 3) limit-fed high concentrate to achieve a gain of 0.8 kg/d for 55 d, then to achieve a gain of 1.2 kg/d for 98 d (LFC). All steers were fed the ALC diet from d 154 to slaughter. Eight steers per treatment were selected after an average of 145 and 334 d on feed for determination of adipocyte cellularity and lipogenic enzyme activity at the end of the growing and finishing phases, respectively. Remaining steers were slaughtered after an average of 334 d on feed. At initial slaughter, ALC steers had a two- to threefold greater (P < 0.05) s.c. fat depth, and 1.9-fold greater (P < 0.01) longissimus muscle ether extract than steers in other groups. At final slaughter, LFC steers had a greater fat depth than ALF steers (P < 0.10) and had the greatest (P < 0.10) longissimus muscle ether extract. Increased fat depth for ALC steers at initial slaughter was a result of a greater (P < 0.05) mean adipocyte diameter in the s.c. depot. Mean i.m. adipocyte diameter followed the same trend (P < 0.16). The number of adipocytes per gram of s.c. fat was least for ALC and greatest for ALF (P < 0.10) at initial slaughter. Mean diameter and number of adipocytes per gram of i.m. and s.c. fat did not differ among treatments at final slaughter (after 180 d on a common finishing diet). High energy (ALC) increased activities of ATP-citrate lyase, fatty acid synthase, 6-phosphogluconate dehydrogenase, glucose-6-phosphate dehydrogenase, and malate dehydrogenase (P < 0.05), in the s.c. depot, and increased activities of ATP-citrate lyase and glucose-6-phosphate dehydrogenase (P < 0.10) in the i.m. depot at initial slaughter. Lipogenic enzyme activity in the s.c. depot at final slaughter did not differ among treatments. Glucose-6-phosphate dehydrogenase activity in the i.m. depot at final slaughter was lowest (P < 0.10) in ALF. Hypertrophy made a greater contribution to fat tissue growth than hyperplasia. Hypertrophy was affected by amount of energy, whereas hyperplasia was affected by source of energy. Differences diminished when cattle were fed the common finishing diet.     

Development and evaluation of empirical equations to interconvert between twelfth-rib fat and kidney, pelvic, and heart fat respective fat weights and to predict initial conditions of fat deposition models for beef cattle

The Davis growth model (DGM) simulates growth and body composition of beef cattle and predicts development of 4 fat depots. Model development and evaluation require quantitative data on fat weights, but sometimes it is necessary to use carcass data that are more commonly reported. Regression equations were developed based on published data to interconvert between carcass characteristics and kilograms of fat in various depots and to predict the initial conditions for the DGM. Equations include those evaluating the relationship between the following: subcutaneous fat (SUB, kg) and 12th-rib fat thickness (mm); visceral fat (VIS, kg) and KPH (kg); DNA (g) in intermuscular, intramuscular, subcutaneous, and visceral fat depots and empty body weight; and contributions of fat (kg) in intramuscular (INTRA), SUB, and VIS fat depots and total body fat (kg). The intermuscular fat (INTER, kg) contribution was found by difference. The linear regression equations were as follows: SUB vs. 12th-rib fat thickness (n = 75; P < 0.01) with R(2) = 0.88 and SE = 10.00; VIS vs. KPH (kg; n = 78; P < 0.01) with R(2) = 0.95 and SE = 2.82; the DNA (g) equations for INTER, INTRA, SUB, and VIS fat depots vs. empty body weight (n = 6, 5, 6, and 6; P = 0.08, P < 0.01, P < 0.01, and P = 0.05) with R(2) = 0.57, 0.93, 0.93, and 0.66, and SE = 0.03, 0.003, 0.02, and 0.03, respectively; and initial contribution of INTRA, SUB, and VIS fat depots vs. total body fat (n = 23; P < 0.01) for each depot, with R(2) = 0.97, 0.99, and 0.97, and SE = 0.61, 0.93, and 1.41, respectively. All empirical equations except for DNA were challenged with independent data sets (n = 12 and 10 for SUB and VIS equations and n = 9 for the initial INTER, INTRA, SUB, and VIS fat depots). The mean biases were -2.21 (P = 0.12) and 2.11 (P < 0.01) kg for the SUB and VIS equations, respectively, and 0.05 (P = 0.97), -0.37 (P = 0.27), 1.82 (P = 0.08), and -1.50 (P = 0.06) kg for the initial contributions of INTER, INTRA, SUB, and VIS fat depots, respectively. The random components of the mean square error of prediction were 73 and 26% for the SUB and VIS equations, respectively, and similarly were 99, 85, 62, and 61% for the initial contributions of INTER, INTRA, SUB, and VIS fat depots, respectively. Both the SUB and VIS equations predicted accurately within the bounds of experimental error. The equations to predict initial fat contribution (kg) were considered adequate for initializing the fat depot differential equations for the DGM and other beef cattle simulation models.     

Adipogenic differentiation state-specific gene expression as related to bovine carcass adiposity

Genetic regulation of the site of fat deposition is not well defined. The objective of this study was to investigate adipogenic differentiation state-specific gene expression in feedlot cattle (>75% Angus; <25% Simmental parentage) of varying adipose accretion patterns. Four groups of 4 steers were selected via ultrasound for the following adipose tissue characteristics: low subcutaneous-low intramuscular (LSQ-LIM), low subcutaneous-high intramuscular (LSQ-HIM), high subcutaneous-low intramuscular (HSQ-LIM), and high subcutaneous-high intramuscular (HSQ-HIM). Adipose tissue from the subcutaneous (SQ) and intramuscular (IM) depots was collected at slaughter. The relative expression of adipogenic genes was evaluated using quantitative PCR. Data were analyzed using the mixed model of SAS, and gene expression data were analyzed using covariate analysis with ribosomal protein L19 as the covariate. No interactions (P > 0.10) were observed between IM and SQ adipose tissue depots for any of the variables measured. Therefore, only the main effects of high and low accretion within a depot and the effects of depot are reported. Steers with LIM had smaller mean diameter IM adipocytes (P < 0.001) than HIM steers. Steers with HSQ had larger mean diameter SQ adipocytes (P < 0.001) than LSQ. However, there were no differences (P > 0.10) in any of the genes measured due to high or low adipose accretion. Preadipogenic delta-like kinase1 mRNA was greater in the IM than the SQ adipose tissue; conversely, differentiating and adipogenic genes, lipoprotein lipase, PPARγ, fatty acid synthetase, and fatty acid binding protein 4 were greater (P < 0.001) in the SQ than the IM depot. Intramuscular adipocytes were smaller than SQ adipocytes and had greater expression of the preadipogenic gene, indicating that more hyperplasia was occurring. Meanwhile, SQ adipose tissue contained much larger (P < 0.001) adipocytes that had a greater expression (P < 0.001) of differentiating and adipogenic genes than did the IM adipose tissue, indicating more cells were undergoing differentiation and hypertrophy. Adipogenic differentiation state-specific gene expression was not different in cattle with various phenotypes, but adipogenesis in the SQ and IM adipose tissues seems to occur independently.     

Effects of acute fasting and age on leptin and peroxisome proliferator‐activated receptor gamma production relative to fat depot in immature and mature pigs

Leptin and peroxisome proliferator‐activated receptor gamma (PPARγ) are adipogenic proteins that are actively involved in metabolic homeostasis of fat. Recently, it was reported that fat tissue in humans and rodents differs in metabolic activity relative to anatomical location of the fat tissue (i.e. depots) and animal age. Hence, we hypothesized that leptin and PPARγ production in various fat depots in female pigs differs in response to acute fasting, and that these responses vary with physiological maturity of the animal. Sixteen intact crossbred immature female pigs [prepubertal (PP); 132.2 ± 4.1 days] and 16 sexually mature female pigs (M; 224 ± 7.4 days) housed in an open‐air, concrete slab, sheltered barn were randomly assigned to either Control or Fasted treatments. Control pigs (PP, n = 8; M, n = 8) had ad libitum access to feed, while Fasted pigs (PP, n = 8; M, n = 8) were denied access to feed from the onset of the study (0 h) to euthanasia at 72 h. Immediately post‐mortem, fat samples were collected from the subcutaneous, pelvic, kidney, and heart (M pigs only) fat depots and analysed for leptin and PPARγ mRNA and protein content. Acute fasting decreased mean leptin mRNA tissue content in a depot specific manner in M pigs (p < 0.01), while mean leptin protein concentrations in fat tissues did not differ with fat depot or age of the pig. Furthermore, acute fasting did not affect mean PPARγ mRNA tissue content in a fat depot or age dependent manner. Mean concentrations of PPARγ protein in fat depots tended to be greater in M vs. PP pigs (p = 0.07). We suggest that these data provide evidence that acute fasting has a greater effect on leptin than PPARγ production in a fat depot dependent manner in M pigs, which may be indicative of changing physiological demands as an animal matures.     

Effects of early- to mid-gestational undernutrition with or without protein supplementation on offspring growth, carcass characteristics, and adipocyte size in beef cattle

Angus × Gelbvieh cows with 2 to 3 previous pregnancies were used to evaluate effects of maternal nutrient restriction on offspring adipose tissue morphology at standard production endpoints. At 45 d after AI to a single sire, pregnancy was confirmed and cows randomly allotted into groups and fed a control (Con, 100% of NRC recommendations), nutrient-restricted (NR, 70% of Con diet), or nutrient-restricted + protein-supplemented (NRP, 70% of Con + essential AA supply to the small intestine equal to Con) diet. At d 185 of gestation, cows were commingled and received the Con diet thereafter. Bull calves were castrated at 2 mo of age. Calves were weaned at 210 d, backgrounded for 28 d, and then placed in the feedlot for 195 d. Steers and heifers were slaughtered at an average 12th-rib fat thickness of 7.6 mm. Adipose tissue from selected depots was collected for adipocyte size analysis. There was no significant difference in BW or BCS between Con, NRP, and NR cows at d 45 of gestation, which averaged 489.7 ± 17.7 kg and 5.35 ± 0.13, respectively. At d 185 of gestation, Con and NRP groups had similar BW (566.1 ± 14.8 and 550.2 ± 14.8 kg) and BCS (6.34 ± 0.27 and 5.59 ± 0.27), but NR cows exhibited reduced (P < 0.05) BW (517.9 ± 14.8 kg) and BCS (4.81 ± 0.27). Among offspring (steers and heifers) at slaughter, there were no significant differences in BW or organ weights among treatment groups. Yield grade was reduced (P < 0.05) and semitendinosus weight/HCW tended (P = 0.09) to be reduced in NR offspring compared with Con and NRP offspring. Average adipocyte diameter was increased (P < 0.05) in subcutaneous, mesenteric, and omental adipose tissue and tended (P = 0.09) to increase in perirenal adipose tissue in NR compared with Con offspring with NRP offspring adipocyte diameter being either intermediate or similar to Con calves. The adipocyte size alterations observed in NR offspring were confirmed by DNA concentration of the adipose tissue depots. There also was an increased mRNA expression (P < 0.05) of fatty acid transporter 1 in subcutaneous adipose tissue from NR offspring compared with Con and NRP offspring. Nutritional restriction during early and mid gestation increased or tended to increase (P < 0.09) adipocyte diameter in all adipose tissue depots in finished steer and heifer calves.     

Fat depot‐specific effects of body fat distribution and adipocyte size on intramuscular fat accumulation in Wagyu cattle

Ectopic fats have been recognized as a new risk factor for metabolic syndrome. In obese humans, ectopic fat accumulations are affected by body fat distribution. Intramuscular adipose tissue is categorized as one of the ectopic fats. Japanese black cattle (Wagyu) are characterized by the ability to accumulate high amounts of intramuscular adipose tissue. In Japan, the marbling level is indicated by the beef marbling standard number (BMS No.), which reflects the intramuscular fat content of longissimus muscle. We hypothesized that the intramuscular fat accumulation is affected by the body fat distribution in Wagyu cattle. In this study, we showed that the BMS No. was not correlated with the subcutaneous and visceral adipocyte diameter. In contrast, the BMS No. was positively correlated with intramuscular adipocyte diameter. These results indicate that the intramuscular adipocyte diameter of Wagyu is hypertrophied with an increase in the intramuscular fat accumulation. In addition, we showed that the BMS No. was positively correlated with the subcutaneous fat percentage. In contrast, the BMS No. was negatively correlated with the visceral fat percentage. These results indicate that highly marbled Wagyu cattle have a higher percentage of subcutaneous fat and a lower percentage of visceral fat.     

Comparing mRNA levels of genes encoding leptin,leptin receptor,and lipoprotein lipase between dairy and beef cattle

Body weight and fat mass vary distinctly between German Holstein (dairy cattle) and Charolais (beef cattle). The aim of this study was to determine whether the expression of the obese (Ob) gene and lipoprotein lipase (LPL) gene in fat tissues and expression of the long isoform leptin receptor (Ob-Rb) gene in the hypothalamus were different between these two cattle breeds. Body weight and the area of longissimus muscle cross-section of German Holstein were lower (P<0.001), while body fat content, as well as the omental and perirenal fat mass were higher (P<0.001), compared to Charolais. Plasma insulin and leptin levels between two cattle breeds were determined by radioimmunoassay. Compared to Charolais, plasma insulin concentrations were significantly higher (P<0.01), and plasma leptin levels were tended to be higher (P<0.1) in German Holstein. Ob mRNA levels in subcutaneous and perirenal fat depots, but not in the omental fat depot, were significantly higher (P<0.05) in German Holstein than in Charolais. LPL mRNA expression in the perirenal fat depot of German Holstein was greater in abundance than that of Charolais. No significantly different LPL mRNA levels were found in subcutaneous and omental fat depots, and Ob-Rb mRNA levels in the hypothalamus between these two cattle breeds (P<0.05). Both Ob and LPL expression was greater in perirenal and omental fat depots than in the subcutaneous fat depot (P<0.05). Data indicated that in bovine the Ob and LPL gene expression levels in perirenal fats are an important index that is associated with body fat content, while Ob-Rb in hypothalamus is not.     

Growth of adipose tissues in cattle; partitioning between depots,chemical composition and cellularity. A review

This review article deals with the various aspects of development of adipose tissues: fat partitioning between depots, chemical composition and cellularity of the various fatty tissues.Particular attention is paid to the changes between birth and maturity of these different characteristics. Total body fat (TBF) increases from 5% empty body weight at birth to approximately 26% in adult Friesian males. Fat partitioning between depots changes greatly during growth, with an increasing proportion of omental fat (7–13% of TBF), Kidney fat (4–9% TBF) and subcutaneous fat (6–17% of TBF) while intermuscular fat decreases (41–59%). All these changes are accompanied by increases in percentage of lipids in fatty tissues and in adipose cell diameter from 45 to 135 μ m, still in Friesian bulls.The fatness of animals of different breeds may vary from 48 kg to 85 kg carcass fat, when compared at the same body weight (450 kg). In the same breed, heifers have 26 to 60% more fat than bulls, while steers are intermediate between the two. These variations are accompanied by differences in cell size and also in fat partitioning, animals with a higher rate of fattening having a higher proportion of subcutaneous fat.Nutritional control of the rate of fat deposition is also discussed. This review is based on recent results from our laboratory together with those of other authors.     

Factors influencing intermuscular fat and other measures of beef chuck composition.

Carcasses from 59 steers produced from the mating of Braford, Simbrah, Senepol, and Simmental bulls to Brahman- and Romana Red-sired cows and Brahman bulls mated to Angus cows were used in this study. Effects of sire breed and feeding calves vs yearlings on fat depots in the chuck, when steers were fed to 1.0 cm external fat, were determined. Breed of sire and feeding calves vs yearlings had no effect (P greater than .05) on percentage of intermuscular fat. However, carcasses from Braford-sired steers had a higher (P less than .05) percentage of dissectable subcutaneous fat on the chuck than did those from other breed groups. Carcasses from Simmental-sired steers were superior (P less than .05) to those from Braford-sired steers in USDA yield grade and had a higher average marbling score (P less than .05) than the Simbrah-sired group. Estimated kidney, pelvic, and heart (KPH) fat was higher (P less than .05) in carcasses from Brahman-, Simbrah-, and Senepol-sired steers than in Braford-sired steers. Steers fed as calves had higher percentages (P less than .05) of KPH fat and major chuck muscles than did those fed as yearlings. The best single predictor of percentage of intermuscular fat within the chuck was adjusted fat over the ribeye (R2 = .46).     

Genetic correlations between live yearling bull and steer carcass traits adjusted to different slaughter end points. 2. Carcass fat partitioning

Partial carcass dissection data from 1,031 finished crossbred beef steers were used to calculate heritabilities and genetic correlations among subcutaneous, intermuscular, and body cavity fat percentage and marbling score adjusted to slaughter age-, HCW-, fat depth-, and marbling score-constant endpoints. Genetic correlations were also calculated among these fat partitions with live growth and ultrasound traits evaluated in yearling beef bulls (n = 2,172) and steer carcass measurements. Heritabilities of the different fat partitions ranged from 0.22 (marbling score-constant body cavity fat) to 0.46 (HCW-constant marbling score). Genetic correlations between subcutaneous fat and intermuscular fat (rg = 0.16 to 0.32) and between intermuscular fat and body cavity fat (rg = 0.38 to 0.50) were more highly associated than subcutaneous fat and body cavity fat (rg = -0.08 to 0.05), indicating that fat depots are not under identical genetic control. Adjusting fat depots to different end points affected the magnitude but usually not the sign of the genetic correlations. Bull postweaning gain was associated with intermuscular (-0.24 to -0.35), body cavity (-0.24 to -0.29), and marbling fat (-0.24 to -0.39) in steers. Bull hip height was associated with body cavity (-0.20 to -0.29) and marbling fat (-0.20 to -0.47) in steers. Bull ultrasound fat depth was associated with subcutaneous (0.11 to 0.29), intermuscular (0.05 to 0.36), body cavity (0.27 to 0.49), and marbling fat (0.27 to 0.73) in steers. Bull ultrasound intramuscular fat percentage was associated with subcutaneous (-0.22 to -0.44) and intermuscular fat (-0.06 to 0.31) in steers. Bull ultrasound LM area was associated with body cavity (-0.25 to -0.31) and marbling fat (-0.25 to -0.30) in steers. Ultrasound LM width measurements were negatively correlated with subcutaneous fat (rg = -0.09 to -0.18), intermuscular fat (rg = -0.53 to -0.61), body cavity fat (rg = -0.63 to -0.69), and marbling score (rg = -0.75 to -0.87) at slaughter age-, HCW-, and fat depth-constant endpoints; correlations were generally lower at a marbling score-constant end point (rg = 0.07 to -0.49). Ultrasound indicator traits measured in seedstock may be useful in altering fat partitioning in commercial beef carcasses.     

Molecular and histological evidence of brown adipose tissue in adult cats

Brown adipose tissue (BAT) can influence glucose, lipid, and energy metabolism in rodents. Active BAT is now known to be present in adult humans, and interventions targeting BAT are being investigated for the treatment of human obesity and disorders of glucose and lipid metabolism. Domestic cats, like humans, are at increasing risk for obesity and diabetes but little is known about the presence and role of BAT in adult cats. The purpose of this study was to determine if brown adipocytes, identifiable by histological features and molecular markers, were present in the fat depots of adult cats. Adipose tissue samples from intrascapular, perirenal, and subcutaneous depots of eleven 8–12 year old cats (6 lean, 5 obese), were analyzed by real-time PCR for brown adipocyte markers uncoupling protein 1 (UCP1) and Type II iodothyronine 5′deiodinase (D2), by histological examination and by immunohistochemistry for UCP1.UCP1 mRNA was detectable in interscapular and subcutaneous depots in all cats, and in the perirenal depot in 10/11 cats. D2 mRNA was detectable in all depots from all cats. Multilocular adipocytes were identified in the interscapular depots of 4/11 cats and these were positive for UCP1 immunoreactivity. The results demonstrate that UCP1-expressing brown adipocytes are present in multiple depots of adult lean and long-term obese cats, even at 8–12 years of age. It is possible that dietary components or pharmacological agents that influence brown fat activity could exert a relevant biological effect in cats.     

Fatty acid profiles and iodine value correlations between 4 carcass fat depots from pigs fed varied combinations of ractopamine and energy

A total of 54 finishing barrows (initial BW = 99.8 ± 5.1 kg; PIC C22 × 337) reared in individual pens were allotted to 1 of 6 dietary treatments in a 2 × 3 factorial arrangement of treatments with 2 levels of ractopamine (0 and 7.4 mg/kg) and 3 levels of dietary energy (high: 3,537, medium: 3,369, and low: 3,317 kcal/kg of ME) to determine the effects of feeding ractopamine and various dietary energy levels on the fatty acid profile of 4 carcass fat depots (jowl, belly, subcutaneous loin, and intramuscular) and the predictive relationships of calculated iodine value (IV) between these 4 fat depots. Carcasses were sampled for fat tissues at the anterior tip of the jowl, posterior to the sternum on the belly edge, three-quarters the distance around the LM (subcutaneous fat; SC), and within the LM (intramuscular fat; IMF). Feeding ractopamine diets reduced (P < 0.05) total SFA in SC and IMF and increased (P = 0.04) total MUFA in SC. Also, feeding ractopamine diets increased (P < 0.01) the IV of IMF. Total MUFA of belly fat was reduced (P < 0.05) when the low-energy diet was fed compared with the high-energy diet. Jowl fat total MUFA was reduced (P < 0.05) and total PUFA was increased (P < 0.05) when the medium-energy diet was fed compared with the high- and low-energy diets. Iodine values, independent of treatment, were 60.97, 64.51, 55.59, and 58.26 for belly, jowl, IMF, and SC fat depots, respectively. The IV correlations within fat depots were not consistent across dietary treatments because of the effect of treatments on carcass fatty acid characteristics. Feeding ractopamine diets shifted the fatty acid profile from SFA to MUFA in the SC depot. Feeding ractopamine diets did not change belly fat profiles, thus avoiding the potential negative effect of softening belly fat, which is detrimental to processing value. The IV of one fat depot may not be a good indication of IV of other fat depots because of weak correlation coefficients and the apparent influence of dietary treatment.     

Relative development of subcutaneous, intermuscular, and kidney fat in growing pigs with different body compositions

A total of 94 pigs from seven groups considered as lean (boars from a synthetic line and the Pietrain breed), conventional (boars, gilts, and barrows from the Large White breed), fat (barrows from the Meishan x Large White cross), or obese (Meishan barrows) were serially slaughtered between 12 and 110 kg BW. Carcasses were dissected into muscle, bone, skin, and fat, which was further separated into subcutaneous, intermuscular, and kidney fats. Subcutaneous fat accounted for 60 to 70% of body fat and intermuscular fat for 20 to 35% of body fat. Relative to total fat, intermuscular fat grew more slowly (allometric growth coefficients generally < 1), subcutaneous fat at the same rate (b close to 1), and kidney fat more rapidly (1.12 < b < 1.33). The leaner the animals genetically, the higher the proportion of intermuscular fat in total fat. The ratio of intermuscular to subcutaneous fat varied from .31 in Meishan barrows to .66 in Pietrain boars. Overall, the ratio of intermuscular fat to muscle weight or body weight was positively related to the development of total fat. However, Pietrain pigs were unique in having a high development of intermuscular fat. The present results suggest that 1) the genetic controls of the development of intermuscular and subcutaneous fat are partially independent and 2) the development of intermuscular fat may be determined at an early stage, before 20 kg BW.     

Fish oil-induced yellow fat disease in rats. I. Histological changes

Yellow fat disease was induced in young rats given a vitamin E-deficient diet supplemented with 15% fish oil. The changes in adipose tissue of this oil-induced disorder were different from those of natural yellow fat disease in horse, pig and mink. In the natural disease all fat depots had the early stage of yellow fat disease with interstitial lipofuscin-laden macrophages exclusively. In the rat, however, this change was seen only in the subcutaneous fat depot. Moreover, affected adipose tissue of animals with natural disease had extensive fibrosis, but in the rat fibrosis was always absent. Rats with fish oil-induced yellow fat disease had degenerative changes in various fat depots that occurred at various times but in the horse, pig and mink fat depots were affected simultaneously. Lipofuscin accumulated in the reticuloendothelial system in rats. Accumulation in spleen and liver was dependent on vitamin E deficiency, but only the accumulation in the Kupffer cells was correlated with yellow fat disease. Lipofuscin accumulation in the mesenteric lymph node did not depend on vitamin E deficiency.     

In vivo estimation of goat carcass composition and body fat partition by real-time ultrasonography

The accuracy of ultrasound measurements to assess goat carcass composition and the partition of body fat depots was evaluated. An ultrasound machine with a 5-MHz probe and image analysis was used to assess in vivo fat thickness and muscle depth in 56 Spanish Celtiberica adult goats, in lumbar and breast body regions. The goats were slaughtered and the weight of body fat depots recorded. Measurements corresponding to the in vivo ultrasound fat thickness and muscle depth were taken on carcasses. The left sides of carcasses were completely dissected into their components. The best relationships (r = 0.94, P < 0.01) between in vivo and carcass measurements of fat thickness were obtained when measurements were taken at the sternum, and the best anatomical point was located between the third and fourth sternebrae. The best correlation coefficients (r = 0.84) for muscle depth were found for measurements taken between the third and the fourth lumbar vertebrae at 2 cm from the middle of the vertebral column. Body weight and ultrasound measurements were used to fit the best multiple regression equations to predict carcass composition and the partition of body fat depots. All equations, with the exception of those for muscle quantity, omental, and total body fat depot amounts, were computed after performing a logarithmic transformation. Body weight in association with the ultrasound measurement taken at largest LM muscle depth, between the first and second lumbar vertebrae accounted for 90% of the muscle weight. Body weight was the first variable admitted into the prediction models of muscle, mesenteric fat, and total body fat and accounted for 82, 67, and 79% of the variation in tissue weights, respectively. The ultrasound measurement of fat thickness taken at the third sternebra was the first variable admitted into the prediction models for intermuscular fat, kidney and pelvic fat, and total carcass fat and accounted for by 73, 75, 71, and 79% of the variation in the weight of these fat depots, respectively. The ultrasound measurements taken in the breast region, particularly at the third and fourth sternebrae, were the most suitable for assessing fat thickness. The results of this experiment suggest that BW associated with some in vivo ultrasonic fat measurements allow the accurate prediction of goat carcass composition and body fat depots.