Includes bibliographical references (leaves 59-79) Examines the metabolism of volatile fatty acid and formic acid in fed sheep. Develops a method for analysing and qualifying volatile fatty acids with special reference to formic acid in biological fluids by High-Performance Liquid Chromatography.

Three experiments were conducted to study the influence of dietary fatty acids on the production performance and immune response of chickens. In experiment I, forty day-old broiler chicks were fed diets containing 5% of either animal fat + conjugated linoleic acid (CLA) (Diet I), sunflower oil (Diet II), flax oil (Diet III) or fish oil (Diet IV). No significant differences (P>0.05) were observed between the live weight of birds. The liver tissue total fat content was lower (P<0.05) in treatment I and II. The fatty acid composition of breast and thigh muscle, liver, heart, pericardial fat, plasma, splenocytes and gut associated lymphoid tissue differed (P<0.05) between treatments. The thiobarbituric acid reactive substances (TBARS) of breast and thigh muscle, liver and heart tissue were lower (P<0.05) in Diet I fed birds. Serum antibody activity was decreased (P<0.05) in Diet II fed birds. In experiment II, 120 day-old broiler chicks were fed diets containing 3.5% of either animal fat + conjugated linoleic acid (CLA) (Diet I), sunflower oil (Diet II), linseed oil (Diet III) or fish oil (Diet IV). Body weight gain was higher (P<0.05) in Diets III and IV compared to Diets I and II fed birds. Feed intake was increased (P<0.05) in Diet IV fed birds. Birds fed Diets III and IV had higher (P<0.05) n-3 fatty acids in all tissues studied. A preferential incorporation of CLA was observed in spleen mononuclear cells. TBARS were higher (P<0.05) in the breast and thigh muscle of Diet IV fed birds. Serum anti-BSA antibody content was higher (P<0.05) in birds fed Diets III and IV. Delayed type hypersensitivity (DTH) response was increased (P<0.05) in Diets IV and III fed birds. Lymphocyte and spleen mononuclear cell CD4⁺, CD8⁺ and IgM⁺ cell population did not differ (P>0.05) among treatments. In experiment III, 120 layer birds were fed diets containing 3% of CLA+animal fat (Diet I), sunflower oil (Diet II), canola+flax oil (Diet III) or fish oil (Diet IV). Egg production, feed consumption and feed efficiency did not differ (P>0.05) among treatments. Birds fed Diets III and IV had higher content of n-3 fatty acids in eggs. Eggs from hens fed Diet I incorporated higher (P<0.05) CLA and saturated fatty acids with a concomitant reduction in (P<0.05) monounsaturated fatty acid content. A preferential incorporation of CLA was observed in eggs over other tissues. TBARS were higher (P<0.05) in breast and thigh muscle of Diet IV fed birds. Egg TBARS content did not differ (P>0.05) among treatments. Serum and yolk anti-BSA antibody contents were higher (P<0.05) in birds fed Diets III and IV. DTH response was increased (P<0.05) in Diets IV and III fed birds. Lymphocyte and spleen mononuclear cell CD4⁺, CD8⁺ and IgM⁺ cell population did not differ (P>0.05) among treatments. Feeding n-3 fatty acids increased antibody mediated immune response while n-6 fatty acids and CLA increased cell mediated immune response. / Graduation date: 2003

Graduation date: 1995

The effects of conjugated linoleic acid (CLA) on lipogenesis and preadipocyte proliferation in young pigs were evaluated in two separate experiments. The first compared dietary effects of linoleic acid, beef tallow, and CLA on composition, lipogenesis, and DNA synthesis. Eighteen pigs weaned at 17 d of age were allotted randomly to corn-based diets supplemented with 1.5% corn oil, 1.5% tallow, or 1.5% CLA. The second experiment evaluated the effects of CLA included with diets high in polyunsaturated fat or beef tallow. Twenty-four pigs weaned at 17 d of age were allotted randomly to one of four corn-based diets supplemented with: 15% corn oil, 12% corn oil + 3% CLA, 15% tallow, and 12% tallow + 3% CLA. The piglets in both trials were fed a basal diet for 7 d and their respective diet for 35 d. [U-14C]Glucose incorporation into total lipids was (experiment 1): 10.64, 11.04, 13.64; (experiment 2): 21.15, 17.54, 21.34, and 19.52 nmol/(105 cells per h) for subcutaneous (s.c.) adipose tissue from corn oil, tallow, CLA; corn oil, corn oil + CLA, tallow, and tallow + CLA-fed piglets, respectively. Tritiated thymidine incorporation into DNA was not different in s.c. adipocytes across treatment groups, but was 5,581, 2,794, 6,573, and 3,760 dpm/(105 cells per h) in s.c. stromal vascular cells from corn oil, corn oil + CLA, tallow, and tallow + CLA-fed piglets, respectively (CLA main effect p<0.034). Additionally, there was a greater proportion of s.c. adipocytes in the smaller, 180-pL cell fraction from the corn oil + CLA-fed pigs (p<0.0074). CLA in the diet increased the s.c. adipose tissue concentration of 18:0 and decreased 16:1 and 18:1 (p<0.05), suggesting depression of stearoyl-coenzyme A desaturase (SCD) enzyme activity in the CLA-fed pigs. The concentration of CLA isomers was raised only slightly in s.c. adipose tissue with the addition of CLA to the diets even though the CLA oil contained 62% CLA isomers. No effects on the growth of young pigs were observed. However, CLA caused a more saturated fatty acid composition and may suppress preadipocyte proliferation, apparent SCD activity, and lipid filling of smaller cells.

<p>Several abnormal conditions, including some cancers, have been associated with changes in the membrane lipid and FA composition. Dietary fat serves as a major source of lipids and FA, particularly the polyunsaturated fatty acids (PUFA), n-6 and n-3. High intakes of n-6 PUFA have been linked to the development of colon cancer in association with low n-3 PUFA intake. Therefore understanding the differences in the lipid and FA profiles between cancer and normal cells in the colon, and the role diet plays in these factors may be invaluable in understanding their role in carcinogenesis. This study compares the lipid profile of azoxymethane (AOM) induced colon polyps to that of the surrounding mucosa tissue in rats fed a diet high in n-6 PUFA. Male Fischer rats were fed the AIN-76A diet containing sunflower oil that has high n-6 PUFA content for a period of nine months. Results indicate that the lipid and FA content of the colon polyps differs significantly from the surrounding mucosa. Colon polyps had an increase in membrane phopholipids phosphatidylcholine (PC) and phosphatidylethanolamine (PE). Changes in membrane fluidity were indicated by the decrease (p&lt / 0.05) in the PC/PE and cholesterol/phospholipids (chol/PL) ratios, and increase (p&lt / 0.05) in the polyunsaturated FA/saturated FA (P/S) ratio. Metabolism of FA was significantly altered in the polyps favouring n-6 FA metabolism and the production of prostaglandin E2. No clear indication of impaired &Delta / 6-desauturase enzyme activity was noticed. Increases in the n-6 PUFA content could be a reflection of the dietary FA intake that increases FA incorporation in the polyps. Changes in the FA parameters of the polyps, particularly an increase in C20:4n-6 and the n6/n3 ratio have been shown to contribute to the rapid growth of cancer tissue. These lipid changes associated with the development of colon polyps could provide unique targets for developing strategies in chemoprevention by dietary manipulation.</p>

The primary objective of this study was to determine if the intake of omega-3 fatty acids (O3FA), from self-selected foods and supplements, was associated with a reduction in muscle soreness in collegiate rowers. Several groups of collegiate rowers were identified as potential subjects and, using an IRB-approved protocol, 61 volunteers from this subject pool agreed to participate in the study. At the end of the first week of fall practice, subjects were asked to provide information on age, weight, height, ethnicity, rowing level, sun exposure, exercise regimen, pre- and peak-soreness and exertion levels, hydration status, and food/supplement intake. A Talag scale was used to determine the severity of muscle soreness, and a modified Borg scale was used to determine the exertion intensity level. A food frequency questionnaire using a 10-point Likert scale was used to assess food and supplement intake, with a special focus on O3FA. Subjects with a higher intake of EPA/DHA rich bottled supplemental fish oil, taken by spoon, had significantly higher soreness levels than those with lower intakes (p = 0.028). Higher soreness was also significantly associated with higher intake of EPA/DHA rich fish oil capsules (p < 0.001). Lower soreness was significantly associated with higher fruit intake (p = 0.030). These findings suggest that high intakes of O3FA from fish oils, regardless of liquid or capsule form, may be contraindicated for collegiate rowers wishing to reduce muscle soreness. Recommending fruit intake may be warranted for rowers wishing to reduce muscle soreness.

Heat exposure causes several physiological and metabolic alterations. Although lipids are vital in sustaining energy production, heat-induced alterations in lipid metabolism have not been clearly established. CHAPTER 1 reviews the known metabolic alterations resulting from heat stress, with a specific focus on changes in whole-body lipid utilization and plasma lipids. CHAPTER 1also outlines the physiological changes caused by heat stress, and their role in reducing exercise performance. The study presented in CHAPTER 2 has shown that, compared to thermoneutral conditions, NEFA concentrations were 37% higher following passive heating and 34% higher following exercise in the heat, without significant changes in whole-body lipid utilization. In addition, the level of hyperthermia attained during passive pre-heating and exercise in the heat resulted in a 13% decrease in total external work and a significantly higher rate of perceived exertion. CHAPTER 3 summarizes the study results and presents the limitations and applications of the study.

The objective of this study was to determine the effects of method of barley grain processing (dry-rolled vs. pelleted barley) and source of oilseed (ground canola vs. ground flaxseed), arranged as a 2 x 2 factorial, on feed intake, ruminal fermentation, nutrient flow to the duodenum, and milk production and composition in dairy cows. Eight Holstein cows (655 ± 69 kg; 83 ± 16 DIM) were used in a replicated 4 x 4 Latin square with 28-d periods. Cows in one square were fitted with ruminal and duodenal cannulae. Cows fed dry-rolled barley consumed 1.8 to 3.5 kg/d more (P = 0.02) DM than those fed pelleted barley; however, source of supplemental dietary fat had no effect on DM intake. Ruminal pH was lower (P = 0.045) in cows fed pelleted barley compared to those fed dry-rolled barley. Ruminal concentration of acetate was greater (P = 0.001), whereas ruminal concentration of propionate tended to be lower (P = 0.11), in cows fed dry-rolled barley compared to those fed pelleted barley; consequently, the acetate:propionate ratio was higher (P = 0.01) in cows fed dry-rolled barley compared to those fed pelleted barley. Ruminal concentration of total VFA was unaffected (P > 0.05) by diet. Source of dietary fat had no effect on ruminal digestion of OM, NDF, ADF or starch; however, ruminal starch digestion was slightly higher in cows fed pelleted barley compared to those fed dry-rolled barley (90.8 vs. 89.5%). Total dietary fatty acid intake was higher (P < 0.05) in cows consuming dry-rolled barley compared to those fed pelleted barley. Duodenal flow of C18:0 was lower, whereas that of C18:2n6c was higher (P < 0.05) in cows fed pelleted barley compared to those fed dry-rolled barley. Feeding flaxseed increased duodenal flows of C18:3n3, cis-9, trans-11 and trans-10, cis-12 conjugated linoleic acid compared to feeding canola. Milk yield was unaffected (P > 0.05) by diet; however, milk fat content was higher (P = 0.004) in cows fed dry-rolled barley compared to those fed pelleted barley. Milk fat content of C18:3 was higher (P = 0.005) in cows fed canola compared to those fed flax. Milk fat content of C18:3 and cis-9, trans-11 C18:2 were higher in cows fed pelleted barley compared to those fed dry-rolled barley with flax as the source of oilseed, but not with canola (interaction, P < 0.01). Milk fat content of saturated fatty acids decreased (P < 0.001) and that of polyunsaturated fatty acids increased (P = 0.003) in cows fed pelleted barley compared to those fed dry-rolled barley. In summary, milk fatty acid profiles were altered by method of grain processing and source of oilseed.

The conversion of stearic acid and lauric acid to unsaturated fatty acids by the desaturase system of Penicillium chrysogenum was investigated by incubating cell free fractions prepared from mycelial sonicates with the radioactively labeled fatty acids and analyzing the reaction products. In some experiments exogenous acyl carrier protein (ACP) or coenzyme A (Co.A) was added to the incubation mixtures. The percentage of radioactive label appearing in unsaturated fractions was regarded as a measure of the activity of the desaturase system.Desaturase activity was detected in both the 15,000 x g particulate and supernatant fractions. Only small percentages of 1-14C-stearyl-CoA were converted to unsaturated fatty acids; 1-14Clauryl-CoA was apparently more readily desaturated. The desaturase system was found to be inhibited by exogenous ACP, but not by exogenous CoA. This suggested that the fatty aryl-CoA thioesters were converted to thioesters of ACP prior to desaturation.Ball State UniversityMuncie, IN 47306

The elongation and desaturation of fatty acids was investigated by studying the fate of 1-14C lauric, myristic, and stearic acids added to submerged cultures of Aspergillus niger. The mycelium produced oleic and linoleio acids from 1-14C lauric and 1-14C steario acids and to only a slight extent from 1-14C myristic acid. Stearic acid was the principal labeled saturated fatty acid produced when laurio acid was the substrate; both palmitic and steario acids were produced in reduced amounts from myristic acid. Myristic acid has been reported to be a poor precursor for long chain fatty acids in Penicillium chrysogenum and Torulopsos bombicoli well. The absence of label in fatty acids shorter than the added substrates indicated that oxidation followed by do novo synthesis did not occur. Pariodate-permanganate oxidation data verified that do novo synthesis did not occur.When either 1-14C lauric acid or 1-14C myristic acid was the substrate, Schmidt decarboxylation data of the saturated fatty acids longer that the substrate indicated that the terminal acetate unit of the substrate was removed and used to elongate palmitio acid to steario acid. The rapid incorporation. of label into long chain fatty acids supports this conclusion. When 1- 4C steario acid was the substrate, decarboxylation data of the saturated fatty acids longer than stearicindicated that the terminal acetate unit of the substrate was removed and used to produce fatty acids with chain lengths longer than stearic acid.Ball State UniversityMuncie, IN 47306