The impact of dietary protein source on observed and predicted metabolizable energy of dry extruded dog foods.

Fifty-five observations were used to determine the ME content of 8 foods containing different protein sources. The major protein sources tested included low-oligosaccharide whole soybeans; 2 low-oligosaccharide, low-phytate whole soybeans; 2 conventional soybean meals; low-ash poultry meal; low-oligosaccharide, low-phytate soybean meal; and conventional whole soybeans. The ME content of all foods ranged from 3,463 to 4,233 kcal/kg of DM. The first objective was to utilize the observed ME data and test the accuracy of the modified Atwater equation. In this study, the modified Atwater equation generally underpredicted ME compared with the observed ME (residual mean = 247 kcal/kg). The second objective was to use individual data to develop an equation, based on the chemical composition of the food, to predict the ME content of the foods. A multivariate regression analysis was used to predict ME content based on chemical composition. Five models were fitted to the data. Model 1 included CP, ether extract (EE), and crude fiber (CF). Because the foods varied in protein sources, and the ratio of total AA (TAA) to non-AA (NAA) CP ranged from 3.5:1 to 14.4:1, it was hypothesized that accounting for the proportion of TAA and NAA in CP would improve the fit of the model. Therefore, model 2 included TAA, NAA, EE, and CF. Defining CP in terms of TAA and NAA improved the r2 of the model from 0.46 to 0.79. Subsequently, models 3, 4, and 5 replaced the CF term with ADF, NDF, and hemicellulose (HEM). Model 3 included TAA, NAA, EE, and NDF. Model 4 included TAA, NAA, EE, ADF, and HEM. Model 5 included TAA, NAA, EE, and HEM. Defining dietary fiber in terms of HEM improved the r2 of model 2 from 0.79 to 0.81. Residual analysis suggested that replacing the CF term with HEM (model 5) improved the prediction of ME content. In contrast, defining fiber in terms of NDF (model 3) did not result in an improvement over model 2, whereas the ADF term (model 4) did not (P > 0.34) contribute to the overall model. Fractionating CP into TAA and NAA components further defined the chemical composition of the food. These data suggest that defining protein composition improves the accuracy of predicting the ME content of dog foods.

Nutritional modification of inflammatory diseases.

Regulation of the immune system is extremely complex. We are only starting to understand how the immune system coordinates the body's response to a disease or invading pathogen. Immunomodulation, as the term implies, can be used to designate either a suppression or an augmentation of an immune response. Suppressing the function of the immune system may be important in cases of inflammation and augmenting the immune response when increased resistance to disease is required. Nutrition does and can play an important role in modulation of the animal's immune system. The majority of scientific literature published on the interaction of nutrition and the immune system correlates the effects of nutrient deficiency and modulation of an immune response. These studies have evaluated deficiencies of protein; energy; the fat soluble vitamins A, D, and E; the B-complex vitamins; vitamin C; and the minerals selenium, iron, zinc, and copper and their relationship to immune dysfunction. Most recently, researchers have concentrated efforts on evaluating the impact specific fatty acids have on modulation of the immune system. Undoubtedly, the nutritional status of the animal plays an important role in resistance mechanisms against disease causing organisms and may influence the outcome of disease in infected animals. The focus of this chapter is to concentrate on the role specific polyunsaturated fatty acids have on the immune response of animals and to consider the potential for nutritional modification of diseases related to inflammation.

Nutritional management of osteoarthritis.

Nutrition can influence developmental orthopedic diseases and the inflammatory process of arthritis. Developmental skeletal disease is a group of skeletal abnormalities that primarily affect fast-growing, large-breed dogs. Nutrient excesses (calcium and energy) and rapid growth (overfeeding and excess energy) are known risk factors. Inflammation can be directly or indirectly affected by nutritional influences. A direct effect can be achieved by modulating the immune response and inflammatory process with fatty acids. Weight control can indirectly influence the degenerative joint disease process by reducing the stresses on the joint.

Volatile compound content and fatty acid composition of pork as influenced by linoleic acid content of the diet.

Eighty pigs (average weight of 60 kg) were allotted by weight and sex to pens and treatments. There were four dietary treatments, five pens per treatment, and four pigs per pen. Diets consisted of a typical corn-soybean mix containing 9% total fat, 3% from the corn-soybean mix and 6% added. The four dietary treatments included 1) 6% safflower oil, 2) 4% safflower oil and 2% tallow, 3) 2% safflower oil and 4% tallow, and 4) 6% tallow, resulting in 6.1, 4.6, 3.2, and 1.76% linoleic acid, respectively, in the diet. Pigs were slaughtered at an average weight of 100 kg. Proximate composition, tristimulus color coordinates (L, a, and b values), pH, and flavor difference of the longissimus muscle (LM) were evaluated. Fatty acid content (milligrams per 100 grams of tissue) of the subcutaneous fat and LM and headspace volatile content of the LM were determined by capillary gas liquid chromatography. Proximate composition, color, pH, and flavor of the LM were not influenced by diet. Fatty acid content of the subcutaneous fat and LM and volatile content of the LM were influenced by diet. Increased levels of safflower oil in the diet resulted in less C16:0 and C18:1 and more C18:2, C20:2, and C20:3 in the subcutaneous fat. The LM contained more C18:2 and less C18:3 and C24:0 due to increased levels of safflower oil in the diet. Compared with the 6% tallow diet, LM from pigs fed the 4 or 6% safflower diets contained more pentanal, hexanal, 2-heptanone, trans-2-heptenal, 2-pentyl furan, 2-ethyl-1-hexanol, decanal, and undecanal.(ABSTRACT TRUNCATED AT 250 WORDS)

The effects of dietary fat or fiber addition on yield and composition of milk from sows housed in a warm or hot environment.

Sixty sows were individually penned in a thermoneutral (20 degrees C) or hyperthermal (32 degrees C) environment and fed a basal (corn-soybean meal), high-fiber (48.5% wheat bran) or high-fat (10.6% choice white grease) diet from d 100 of gestation through a 22-d lactation. The diets were determined to contain 3.28, 2.76 and 3.75 Mcal ME/kg, respectively. All pigs received 8.0 Mcal of ME and 17.5 g of lysine daily prior to parturition and were allowed to consume their respective diets ad libitum after parturition. Litter size was standardized at 9 to 10 pigs by d 2 postpartum. Milk yields were determined for five, 4-d periods from about d 2 through 22 of lactation via a D2O dilution technique. Daily milk yield and litter weight gain began to plateau, and the efficiency of utilizing milk DM and milk energy for gain was depressed (P less than .01), in the latter stages of the lactation. Heat exposure (32 degrees C) reduced (P less than .05) voluntary ME intake and milk energy yield of the sow and increased (P less than .05) the sow's weight loss during lactation. In the hot environment, increasing dietary energy concentration resulted in a linear (P less than .08) increase in milk fat content and milk energy yield over the duration of the 22-d lactation. In the latter stages of lactation, pigs consuming high-fat milk required more (P less than .09) milk and milk energy per unit of weight gain. In the warm environment, milk energy yield was increased by dietary fat or fiber additions in early lactation, but not in late lactation. These results indicate that the effects of thermal heat stress on sow milk energy yield and litter weight gain are aggravated by dietary fiber addition and minimized by dietary fat addition.

The effects of dietary fat or fiber addition on energy and nitrogen digestibility in lactating, primiparous sows housed in a warm or hot environment.

Thirty primiparous sows were individually penned in a thermoneutral (20 degrees C) or hyperthermal (32 degrees C) environment and fed a high-starch (corn-soybean meal basal), high-fiber (48.5% wheat bran) or high-fat (10.6% choice white grease) diet from d 100 of gestation through a 22-d lactation to determine the effects of thermal environment and dietary energy source on energy and N digestibility in lactating sows. Voluntary feed intake and total feces and urine output were determined from d 12 through d 14 postpartum. Heat exposure (32 degrees C) depressed (P less than .05) voluntary feed, ME and N intake and lowered (P less than .05) apparent daily N retention. Heat exposure did not alter (P greater than .15) digestibility, expressed as percentage of intake, of dietary energy or N. Dietary additions of wheat bran depressed (P less than .05) the proportion of gross energy retained as ME by 12 and 14 percentage units and the apparent digestibility of N by 2.5 and 4.5 percentage units at 20 and 32 degrees C, respectively, compared with those of the basal diet. Dietary additions of choice white grease did not alter (P greater than .15) energy digestibility but increased (P less than .05) the proportion of N digested and retained in both environments. Apparent ME of the wheat bran, corn-soybean meal mix and choice white grease (determined by difference) was 2.72, 3.70 and 8.43 Mcal/kg DM and was independent of thermal environment. Digestibility of fibrous and starchy feedstuffs was similar in lactating sows and growing pigs allowed to consume feed ad libitum, whereas fat was more digestible in the sows.