Biomedical subjects

G C Fahey

Publications and source records attributed to G C Fahey.

At least 91 records · Page 5Linked to original sources

PubMed1994

Effects of cobalt on in vitro fiber digestion of forages and by-products containing fiber.

Cobalt glucoheptonate as a source of Co to enhance ruminal fiber digestion was evaluated in two in vitro digestibility experiments. In Experiment 1, Co supplementation (0, 5, and 10 ppm) of five substrates (leaf and stem fractions of alfalfa and orchardgrass hays and ground corn) was evaluated under two dietary conditions (ruminal fluid taken from steers fed alfalfa hay or a high concentrate diet) for 24 or 48 h of fermentation in a 3 x 5 x 2 x 2 factorial arrangement. In Experiment 2, four concentrations of Co (0, 10, 20, and 30 ppm) were added to five substrates (alfalfa hay, orchardgrass hay, corn cobs, recycled newsprint treated with HCl, and cellulose casings) and were incubated with ruminal fluid from steers fed alfalfa hay for 24 or 48 h of fermentation in a 4 x 5 x 2 factorial arrangement. No interactions among treatments were observed for digestibilities of DM, OM, or NDF in both experiments or for VFA concentrations in Experiment 1. Supplementation with Co did not increase digestibilities of DM, OM, or NDF in either experiment or concentrations of VFA in Experiment 1. In Experiment 1, in vitro digestibilities of DM, OM, and NDF were higher for inoculum from steers fed alfalfa versus concentrate. In Experiment 2, digestibilities of DM, OM, and NDF were highest for alfalfa hay and lowest for recycled newsprint treated with HCl. Cobalt concentrations that were above minimum requirements did not improve digestion of DM, OM, or fiber.

Animals↗

PubMed1994

Effects of reduced phenolic acids on metabolism of propionate and palmitate in bovine liver tissue in vitro.

Benzoic acid, 3-phenylpropionic acid, trans-cinnamic acid, and 3-(4-hydroxyphenyl)propionic acid in ruminal fluid are presumed to be the products of chemical reduction of dietary phenolic monomers by ruminal microorganisms. Effects of reduced phenolics on metabolism in bovine liver tissue were evaluated by measurement of 1) conversion of propionate to glucose and CO2, 2) conversion of palmitate to oxidized products, and 3) leakage of lactate dehydrogenase from liver slices in vitro. In Experiment 1, .4 mM benzoic, 3-phenylpropionic, trans-cinnamic, or 3-(4-hydroxyphenyl)propionic acids decreased conversion of propionate to glucose and decreased conversion of palmitate to total oxidation products. At .2 mM, 3-(4-hydroxyphenyl)propionic acid did not inhibit conversion of propionate to glucose compared with that of controls, but the other reduced phenolics did. In Experiment 2, the same reduced phenolics inhibited conversion of propionate to glucose. Of the reduced phenolics tested, cinnamic acid inhibited conversion of propionate to glucose at the lowest concentration, .1 mM. Additionally, when present at > or = .4, .1, or .005 mM, benzoic, 3-phenylpropionic, or trans-cinnamic acids, respectively, increased leakage of lactate dehydrogenase from liver tissue. The reduced phenolics tested, which are representative of those in ruminal fluid, inhibited metabolism of bovine liver tissue in vitro at supraphysiological concentrations. Data at physiological concentrations were inconclusive.

Animals↗

PubMed1993

AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet.

For sixteen years, the American Institute of Nutrition Rodent Diets, AIN-76 and AIN-76A, have been used extensively around the world. Because of numerous nutritional and technical problems encountered with the diet during this period, it was revised. Two new formulations were derived: AIN-93G for growth, pregnancy and lactation, and AIN-93M for adult maintenance. Some major differences in the new formulation of AIN-93G compared with AIN-76A are as follows: 7 g soybean oil/100 g diet was substituted for 5 g corn oil/100 g diet to increase the amount of linolenic acid; cornstarch was substituted for sucrose; the amount of phosphorus was reduced to help eliminate the problem of kidney calcification in female rats; L-cystine was substituted for DL-methionine as the amino acid supplement for casein, known to be deficient in the sulfur amino acids; manganese concentration was lowered to one-fifth the amount in the old diet; the amounts of vitamin E, vitamin K and vitamin B-12 were increased; and molybdenum, silicon, fluoride, nickel, boron, lithium and vanadium were added to the mineral mix. For the AIN-93M maintenance diet, the amount of fat was lowered to 40 g/kg diet from 70 g/kg diet, and the amount of casein to 140 g/kg from 200 g/kg in the AIN-93G diet. Because of a better balance of essential nutrients, the AIN-93 diets may prove to be a better choice than AIN-76A for long-term as well as short-term studies with laboratory rodents.

Animals↗

PubMed1993

Vegetable fiber fermentation by human fecal bacteria: cell wall polysaccharide disappearance and short-chain fatty acid production during in vitro fermentation and water-holding capacity of unfermented residues.

Dietary fiber from eight vegetables (broccoli, carrot, cauliflower, celery, cucumber, lettuce, onion and radish) was analyzed for chemical composition and potential in vitro fermentation by human fecal bacteria. Total dietary fiber concentration of substrates ranged from 34.9 (broccoli) to 5.8 (cucumber) g/kg edible matter. Substrate fiber fractions were composed primarily of pectic substances and cellulose with smaller concentrations of hemicelluloses and lignin. Total dietary fiber residues isolated from substrates were fermented in vitro for 24 h with fecal bacteria obtained from each of three human volunteers. Substrate dry matter disappearance during fermentation was highest for carrot (63.7%) and lowest for cucumber (49.4%). Averaged across all substrates, disappearances of arabinose, galactose, glucose, mannose, xylose and uronic acids during fermentation were 96, 90, 54, 68, 51 and 97%, respectively. Short-chain fatty acid (SCFA) production during substrate fermentation averaged 10.5 mmol SCFA/g dry matter fermented. Averaged across all substrates, production of the major SCFA, acetate, propionate and butyrate, occurred in the molar ratio 76:14:10. Potential water-holding capacity of substrates was not influenced by fiber source and averaged 2.04 g H2O/g original substrate dry matter. Extent of substrate fermentation, SCFA production and substrate potential water-holding capacity were significantly different among inoculum donors, indicating that considerable inter-individual variation exists in the potential in vivo fermentation of vegetable fiber.

Adult↗

PubMed1993

The accumulation of alpha- and beta-carotene in serum and tissues of preruminant calves fed raw and steamed carrot slurries.

The preruminant calf model was used to evaluate the effects of mild heat treatment on the serum and tissue accumulation of alpha- and beta-carotene from carrots. Twenty-four 1-wk-old Holstein male calves were assigned to one of four groups and fed a milk replacer diet. Negative control animals received no additional supplement. The three remaining groups received an additional 20 mg beta-carotene/d from either water-soluble beadlets, homogenized raw carrots or homogenized steamed carrots. Serum samples were obtained daily, and calves were killed after 7 d and samples of serum, liver and adrenal collected. Tissue and serum alpha- and beta-carotene concentrations were not significantly higher in steamed carrot-fed animals than in raw carrot-fed animals. The molar ratios of beta-carotene to alpha-carotene in both raw carrot-fed and steamed carrot-fed groups were highest in adrenal tissues, intermediate in serum and lowest in the diets. None of these differences were statistically significant. When the serum, liver and adrenal beta-carotene data were pooled, the mean relative accumulation of beta-carotene, expressed as a percentage of the mean response of calves receiving water-soluble beadlets, was 46.8% for calves fed raw carrots and 74.0% for calves fed steamed carrots. These results suggest a small enhancing effect of mild heat treatment of carrots on the serum and tissue accumulation of carotenoids.

Animals↗

PubMed1993

Fermentation of dietary fibre by human colonic bacteria: disappearance of, short-chain fatty acid production from, and potential water-holding capacity of, various substrates.

Several dietary fibre-rich substrates were fermented in vitro with human colonic bacteria obtained from each of three adult male subjects to assess the extent of substrate fermentation short-chain fatty acid (SCFA) production, and the potential effect of fermented residues on faecal bulk. Substrates tested were two varieties of oat hull fibre, gum arabic, carboxymethylcellulose (CMC), soy fibre, psyllium, and six blends containing oat fibre, gum arabic, and CMC in various proportions. All substrates contained greater than 900 g/kg of total dietary fibre except for CMC (816 g) and soy fibre (778 g). In vitro organic matter disappearance during fermentation was greatest for gum arabic (69.5%), intermediate for soy fibre (56.4%), and less than 20% for the two oat fibres, CMC, and psyllium. Averaged across substrates, acetate, propionate, and butyrate were produced in the molar proportion of 64:24:12. Potential water-holding capacity (PWHC) of substrates, a measure of faecal bulking potential, was greatest for CMC (13.5 g H2O/g substrate) and lowest for gum arabic (1.92 g) and soy fibre (1.71 g). Organic matter disappearance and SCFA production of blends were directly proportional to their gum arabic content. Blend PWHC was proportional to CMC content. In vitro procedures are useful in predicting the actions of fibre blends formulated to produce desirable effects in vivo.

Adult↗

PubMed1992

Evaluation of the preruminant calf as a model for the study of human carotenoid metabolism.

This study evaluated the preruminant calf as an animal model for the study of human carotenoid metabolism. Fifteen newborn male Holstein calves were fed a carotenoid-free milk replacer diet to maintain them in the preruminant state. After a 7-d adjustment period, three calves were killed and 12 calves received a single oral dose (20 mg) of beta-carotene in the form of water-soluble beadlets. Blood samples were collected periodically and samples of various tissues were collected when the calves were killed. Three animals each were killed by exsanguination at 1, 3, 6 and 11 d post-dosing. Serum beta-carotene concentrations peaked between 12 and 30 h post-dosing and declined slowly afterwards. Serum data were fitted to a two-compartment model and yielded an elimination constant (k2) that was similar to reported human values. Adrenal tissue showed significant concentrations of beta-carotene by 24 h post-dosing, and levels were still elevated at 264 h. Liver, spleen and lung beta-carotene concentrations were significantly elevated by 24 h and rapidly declined thereafter. Adipose and kidney peak beta-carotene concentrations were observed at 72 and 144 h, respectively. Heart and muscle did not display significant changes in beta-carotene concentrations. The preruminant calf shows promise as an animal model for the study of absorption and metabolism of carotenoids by humans.

Adipose Tissue↗

PubMed1992

Short-chain fatty acid production and fiber degradation by human colonic bacteria: effects of substrate and cell wall fractionation procedures.

Three dietary fiber sources (corn fiber, oat bran, wheat bran) were analyzed for chemical composition and potential fermentation by human colonic bacteria in vitro. Total dietary fiber (TDF) concentration of substrates was 64.3, 11.1 and 50.4 g/100 g dry matter for corn fiber, oat bran and wheat bran, respectively. Original material (ORIG), TDF fractions and simulated (SIM) cell wall fractions (produced by combining cellulose, hemicelluloses and pectic substances in proportions they represented in the cell wall) from each substrate were fermented in vitro for 6, 12, 18, 24 or 48 h using inoculum prepared from freshly voided feces from each of three human volunteers. Substrate dry matter remaining after 48 h of fermentation was 87.8, 39.8 and 73.5% for TDF fractions of corn fiber, oat bran and wheat bran, respectively. Disappearance of ORIG fractions was considerably greater than that of TDF due to fermentation of nonfibrous material. Disruption of cell wall structure during isolation of polysaccharide fractions allowed for dramatically increased fermentability of SIM relative to TDF. Averaged across all treatments, production of the short-chain fatty acids, acetate, propionate and butyrate, occurred in the molar ratio 63:21:16; however, profiles of short-chain fatty acids produced were influenced by both treatment and inoculum source. Extent of substrate fermentation varied among inoculum donors, implying that colonic microbial activities differ among individuals. Potential colonic fermentability of fiber sources was influenced by substrate, method of fiber preparation and inoculum source.

Adult↗

PubMed1992

Dietary fiber for dogs: III. Effects of beet pulp and oat fiber additions to dog diets on nutrient intake, digestibility, metabolizable energy, and digesta mean retention time.

The objective of this experiment was to determine whether alkaline hydrogen peroxide-treated oat hulls (termed oat fiber; OF) are nutritionally efficacious as a source of dietary fiber in meat-based dog foods. Thirty female English Pointers were assigned in a completely randomized design to isonitrogenous diets. Treatments were 1) control diet, 2) 7.5% added beet pulp (BP), and 3) 2.5, 4) 5.0, and 5) 7.5% added OF. Inclusion of 7.5% BP increased (P less than .05) DM intake and decreased (P less than .05) digestibility of DM and OM compared with the control. Dry matter intake increased (P less than .05) with increasing level of OF and digestibility of DM, OM, and total dietary fiber (TDF) decreased (P less than .05). Digestibility of DM, OM, and TDF were higher for dogs fed the 7.5% BP than for those fed the 7.5% OF treatment. Digestible energy, expressed as a percentage of GE, was greater for the control treatment than for the 7.5% BP treatment. A linear decrease in DE (percentage of GE) was noted as the concentration of OF increased, and the DE value (percentage of GE) for the 7.5% BP treatment was greater (P less than .05) than that for the 7.5% OF treatment. A linear decrease (P less than .05) was noted in ME, expressed as a percentage of GE, as the level of OF increased. Frequency of defecation and mean retention time were unaffected (P greater than .05) by treatment. Oat fiber was an effective substitute for BP in dog diets.

Animal Feed↗

PubMed1991

Fermentability of various fiber sources by human fecal bacteria in vitro.

Certain beneficial effects of fiber in the human diet may be mediated by short-chain fatty acids (SCFAs) produced during anaerobic fermentation in the colon. Two studies, both involving in vitro incubations with human fecal bacteria as inoculum, were conducted to assess fermentation of various fiber sources and to quantitate the SCFAs produced. In experiment 1, substrate fermentability based on total SCFA production ranked as follows: citrus pectin greater than soy fiber greater than sugarbeet fiber greater than pea fiber greater than oat fiber. Fermentation of soy fiber led to higher proportions of propionate and butyrate than did fermentation of other substrates. In experiment 2, fermentation of gum arabic, a mixture of arabic and guar, and apple pectin resulted in greater SCFA production than did fermentation of either oat fiber or corn bran. Fermentation of gums led to more propionate and butyrate production than did that of apple pectin. It may be possible to select fiber sources capable of supporting stipulated amounts of both total and individual SCFA production in the human colon.

Bacteria↗

PubMed1991

Utilization of alkaline hydrogen peroxide-treated wheat straw in cattle growing and finishing diets.

Two experiments were conducted to evaluate alkaline hydrogen peroxide-treated wheat straw (AHPWS) in cattle growing (Exp. 1) and finishing (Exp. 2) diets. In Exp. 1, 162 crossbred steers (257 kg) were fed 66% roughage diets in an 84-d growth trial to compare AHPWS to corn silage (CS) and to evaluate different supplemental CP sources and levels. A completely randomized design with a 3 x 3 factorial arrangement of treatments was used. Factors were roughage source (CS, a 1:1 mixture of CS:AHPWS [MIX] and AHPWS) and CP treatment (13 and 11% CP with supplemental CP provided by soybean meal [13-SBM] and [11-SBM] and 11% CP with a combination of urea, corn gluten meal, and fish meal [UGF]). Lasalocid was fed at the rate of 200 mg per steer daily. Steers fed AHPWS had decreased (P less than .01) DMI compared with steers fed MIX and CS. This may be due to increased dietary Na from residual Na in AHPWS. With each incremental increase in AHPWS, ADG and gain/feed decreased (P less than .01). Dry matter intakes (kg/d), ADG (kg), and gain/feed for CS, MIX, and AHPWS were 8.0, 1.56, and .19; 8.2, 1.33, and .16; and 7.5, 1.08, and .14, respectively. Decreased performance by steers fed AHPWS may be due, in part, to a negative interaction between the lasalocid and dietary minerals. There were no differences in performance due to CP supplementation. In Exp. 2, AHPWS was compared to alfalfa hay (AH) and CS at 10 and 20% of dietary DM (2 x 3 factorial) in a 127-d finishing trial with 108 crossbred steers (341 kg).(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

PubMed1991

Effects of supplemental protein source and level of urea on intestinal amino acid supply and feedlot performance of lambs fed diets based on alkaline hydrogen peroxide-treated wheat straw.

Two experiments were conducted to determine the effects of supplemental CP source and level of urea on intestinal amino acid (AA) supply and feedlot performance of lambs fed diets based on alkaline hydrogen peroxide-treated wheat straw (AHPWS). In Exp. 1, five cannulated (ruminal, duodenal, and ileal) crossbred wethers (61 kg) were used in a 5 x 5 Latin square design. Treatments consisted of different sources of CP and included soybean meal (SBM), a combination of urea, distillers dried grains (DDG), and fish meal, each provided an equal portion of supplemental CP (UDF), and three levels of urea (17, 33, and 50% of supplemental CP) fed in combination with DDG (U17, U33, and U50). Organic matter and N digestibilities decreased (P less than .05) when lambs were fed U17 compared with those fed SBM. There were no differences (P greater than .05) in bacterial N or AA flows to the duodenum due to CP source despite large differences in ruminal NH3 N concentrations and lower ruminal OM digestion when lambs were fed U17. Duodenal nonbacterial N and AA flows were highest (P less than .05) in lambs fed U17 and UDF and lowest when lambs were fed U50 and SBM. Lysine concentration in duodenal digesta decreased with incremental increases in DDG. In Exp. 2, 30 individually penned ram lambs (33 kg) were allotted to five CP treatments in a randomized complete block design. Treatments were similar to those of Exp. 1, with the exception that U17 was replaced by a 14% CP diet with SBM as the supplemental CP source; all other diets were formulated to contain 12% CP. Lambs fed U50 had decreased (P less than .08) ADG and gain/feed compared with all other treatments, and lambs fed UDF had greater (P less than .05) ADG and gain/feed than lambs fed U33. It was concluded that 17% of the supplemental CP from urea seems adequate to maximize bacterial protein synthesis and that no more than 33% of the supplemental CP should be provided by urea in diets based on AHPWS. Feeding a combination of ruminally resistant protein sources with complementary AA profiles of lysine and methionine (UDF) may enhance quality of protein entering the duodenum and feedlot performance.

Amino Acids↗

PubMed1991

Effects of increasing crude protein level on nitrogen retention and intestinal supply of amino acids in lambs fed diets based on alkaline hydrogen peroxide-treated wheat straw.

The effects of increasing dietary CP level on N retention (Exp. 1) and intestinal supply of amino acids (AA; Exp. 2) were studied in lambs fed diets based on alkaline hydrogen peroxide-treated wheat straw (AHPWS). Soybean meal (SBM) was substituted for corn to increase CP level in both experiments. In Exp. 1, an incomplete design for the two-way elimination of error was used to allot 24 ram lambs (mean BW = 25 kg) within breed to six CP levels (6, 8, 10, 12, 14, and 16% of DM). Neutral detergent fiber digestibility and N retention increased quadratically (P = .06 and P less than .01, respectively) with increasing CP level. Nitrogen retention, expressed as a percentage of N intake, was greatest for lambs fed 12% CP (20.7%) but was greatest for lambs fed 14% CP when expressed as grams per day (4.0 g/d). In Exp. 2, five multicannulated St. Croix lambs (34 kg) were used in a 5 x 5 Latin square design. Treatments were 8.5, 11, 13.5, 16, and 18.5% dietary CP. Chromic oxide was used as a digesta flow marker and purines were used as a bacterial marker. Protein level had no effect on extent of dietary CP degradation in the rumen (69 +/- 3.2%). True ruminal OM digestibility increased (P less than .01) linearly and ruminal fluid NH3 N concentration increased (P less than .01) quadratically with increasing CP level. Total, bacterial, and nonbacterial N and AA flows to the duodenum increased (P less than .05) linearly with increasing CP level. Duodenal AA profile (g/100 g total AA) was altered slightly. The essential AA valine, isoleucine, phenylalanine, lysine, and arginine increased (P less than .05) and methionine decreased (P less than .05) in proportion to other AA with increasing CP level. Flows of all essential AA increased with increasing CP level. Apparent small intestinal N and AA disappearance increased linearly (P less than .05) and apparent total tract N digestibility increased (P less than .01) quadratically with increasing CP level. These data are interpreted to indicate that maximal N retention and fiber digestibility in diets based on AHPWS are obtained at 12% CP, even though the intestinal supply of AA continues to increase with increasing CP level. Supplementation of diets based on AHPWS with an extensively degraded protein source (SBM) does not substantially alter the profile of AA entering the duodenum compared to the AA profile of bacterial protein.

Amino Acids↗

PubMed1991

Degradation of wheat straw and alkaline hydrogen peroxide-treated wheat straw by Ruminococcus albus 8 and Ruminococcus flavefaciens FD-1.

Degradation of wheat straw (WS) and alkaline hydrogen peroxide (AHP)-treated wheat straw (AHPWS) by Ruminococcus albus 8 and Ruminococcus flavefaciens FD-1 was determined by measuring the growth (OD600) of each bacterium and determining DM disappearance (DMD) of the substrate. Complex medium and defined medium with or without the addition of phenylpropanoic acid (PPA) and phenylacetic acid (PAA) were used. Tubes were incubated at 39 degrees C for 8 d. Both OD600 and DMD indicated that AHPWS was degraded to a much greater extent by either bacterium (R. flavefaciens FD-1, 60.8 +/- 1.8% and R. albus 8, 42.3 +/- 3.5%) vs untreated WS (R. flavefaciens FD-1, 16.5 +/- 1.8% and R. albus 8, 8.6 +/- 6%) in the complex medium. Most degradation occurred between d 1 and 4. With the complex medium, addition of PPA and PAA did not stimulate degradation by either bacterium. When the defined medium was used, the addition of PPA and PAA enhanced (P less than .05) degradation of AHPWS (39.6 +/- 2.6%) vs AHPWS with no added PPA and PAA (24.9 +/- 7.6%) by R. albus 8. There was no synergistic effect on degradation when the two species were co-cultured with either WS or AHPWS as the substrate. No effect of PPA and PAA on disappearance of AHPWS was observed for R. flavefaciens FD-1 or when the two bacteria were grown together. Dry matter disappearance analysis showed that R. flavefaciens FD-1 degraded AHPWS more rapidly (6.1 mg/d) than R. albus 8 did (4.2 mg/d) in complex medium.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1991

Isolation and chemical analyses of nonfermented fiber fractions of oat hulls and cottonseed hulls.

The purpose of this study was to isolate, using both in situ and in vivo methodology, the nonfermented fiber fraction of oat hulls (OH) and cottonseed hulls (CSH) and to compare the concentrations of alkali-labile phenolic monomers, nitrobenzene oxidizable phenolic monomers, and neutral monosaccharides, as well as the cross polarization/magic angle spinning (CP/MAS) carbon-13 (13C) nuclear magnetic resonance (NMR) spectra, of the nonfermented fraction with the original OH or CSH. The in situ isolation procedure involved a 30-h ruminal pretreatment and an 8-h acid:pepsin pretreatment followed by 1 to 7 additional days of incubation in the rumen. Fractions not fermented in vivo were isolated from duodena, ileal, and fecal material obtained from a site and extent of digestion trial in which these byproducts were fed to sheep at 80% of the diet (as-fed basis) and they represented the sole source of dietary fiber. Based on nonfermented fraction composition, both in situ and in vivo, all components analyzed were degraded to some extent. Also, all components present in original byproduct material were present in both the in situ and in vivo nonfermented fractions. Based on NMR analysis, cellulose crystallinity did not change during either long-term in situ or in vivo fermentation. However, CSH cellulose was more crystalline than that of OH. The ADL content of OH and CSH was 6.1% and 19.4%, respectively, and very little (15%) of the ADL disappeared during either in situ or in vivo fermentation. Much of the p-coumaric and ferulic acid of OH, associated with the cell wall matrix as lignin-carbohydrate and phenolic-carbohydrate complexes, was recovered in the fermented fractions. Data are interpreted to indicate that lignin encrustation and cellulose crystallinity are factors affecting CSH fermentation. Lignin encrustation and the presence of lignin-carbohydrate/phenolic-carbohydrate complexes are factors that inhibit OH fermentation.

Animal Feed↗

PubMed1991

Effects of defaunation and various nitrogen supplementation regimens on microbial numbers and activity in the rumen of sheep.

Five sheep (average BW 62 kg) were fed 65% roughage: 35% concentrate diets (CP = 15%) in a 5 x 5 Latin square design to study the effects of combinations of defaunation and N supplements (soybean meal [SBM], corn gluten meal [CGM], blood meal [BM], urea, and casein) differing in ruminal degradation on ruminal microbial numbers and activity. Diets were fed twice daily (DM intake 1,759 g/d). Defaunation was accomplished with doses of 30 ml of alkanate 3SL3.sheep-1.d-1 for 3 d with 2 d of fasting. Treatment 1 (control) involved feeding faunated sheep a diet in which the supplemental N was 67% SBM N and 33% urea N. Treatment 2 involved feeding defaunated sheep the same diet as the control. Treatments 3, 4, and 5 involved feeding defaunated sheep diets in which the supplemental N source was either 67% CGM-BM N (CGM and BM combined on a 1:1 N ratio): 33% urea N, or 33% CGM-BM N:67% urea N or 33% CGM-BM N:33% urea N:33% casein N, respectively. Compared with the faunated control, defaunation (Treatments 2, 3, 4, and 5) increased (P less than .05) total direct counts of ruminal bacteria (2.7 vs 1.3 x 10(11)/ml), fungal zoospores (2.8 vs 1.4 x 10(5)/ml), and ruminal microbial protease activity (1.4 vs 1.0 mg azocasein/[ml ruminal fluid.h]). Defaunation did not have a consistent effect on ruminal microbial deaminase activity. Compared with the control, defaunation resulted in lower (P less than .05) total perchloric acid-soluble amino N in ruminal fluid at 4 and 10 h after the morning feeding. Defaunation did not decrease (P greater than .05) total free amino acid concentrations in ruminal fluid, but it altered the profile of free amino acids. Although defaunation increased (P less than .05) ruminal bacterial numbers, no increases in total microbial CP or OM concentrations in ruminal contents were observed.

Amino Acids↗

PubMed1991

Manipulation of nitrogen digestion by sheep using defaunation and various nitrogen supplementation regimens.

Five ruminally, duodenally, and ileally cannulated sheep (average BW 62 kg) were fed 65% roughage: 35% concentrate diets (CP = 15%) in a 5 x 5 Latin square design to study the applicability of using a combination of defaunation with N supplements (soybean meal [SBM], corn gluten meal [CGM], blood meal [BM], urea, and casein) with different extents of ruminal degradation to manipulate microbial protein synthesis and amount of ruminal escape protein. Diets were fed twice daily (1,759 g DM/d). Defaunation was accomplished with 30-ml doses of alkanate 3SL3 (active ingredient: sodium lauryl diethoxy sulfate)/sheep daily for 3 d with 2 d of fasting. Treatment 1 (control) involved feeding faunated sheep a diet in which the supplemental N (45% of total dietary N) was 67% SBM N and 33% urea N. Treatment 2 involved feeding defaunated sheep the same diet as the control. Treatments 3, 4, and 5 involved feeding defaunated sheep diets in which the supplemental N source was either 67% CGM-BM (1:1 N ratio) N:33% urea N, or 33% CGM-BM N:67% urea N or 33% CGM-BM N:33% urea N:33% casein N, respectively. Compared with the faunated control, defaunation decreased (P less than .05) ruminal ammonia concentration (19 vs 26 mg/dl) and increased (P less than .05) CP flow to the duodenum (253 vs 214 g/d) due to a trend for increases in both bacterial (BCP) and nonbacterial (NBCP) CP flows.(ABSTRACT TRUNCATED AT 250 WORDS)

Amino Acids↗

PubMed1991

Effects of urea and sodium bicarbonate supplementation of a high-fiber diet on nutrient digestion and ruminal characteristics of defaunated sheep.

Five sheep (average BW 48 kg) with ruminal, duodenal, and ileal cannulas were fed 63% roughage: 37% concentrate diets (CP = 14.5%) in a 5 x 5 Latin square design to study effects of urea and sodium bicarbonate supplementation on nutrient digestion and ruminal characteristics of defaunated sheep. Diets were fed twice daily (DMI = 1,076 g/d). Defaunation was accomplished with 25-ml doses of alkanate 3SL3/sheep daily for 3 d. Control sheep were faunated (Treatment 1) and fed soybean meal as the major N supplement. Remaining sheep were maintained defaunated and fed either the same diet as Treatment 1 (Treatment 2), Treatment 1 with urea replacing 30% of the soybean meal N (Treatment 3), or Treatment 1 with 2% sodium bicarbonate in the diet (Treatment 4). Treatment 5 was a combination of Treatments 3 and 4. Compared with the faunated control, defaunation decreased (P less than .05) total tract DM, OM, NDF, ADF, and CP digestibilities (71.5 vs 69.4, 73.8 vs 71.7, 64.6 vs 61.4, 58.7 vs 55.8, and 74.2 vs 70.6%, respectively) and average (2 to 12 h postfeeding) ruminal fluid ammonia (23.5 vs 13.7 mg/dl) and isobutyrate (.9 vs .7 mM) concentrations. However, defaunation increased (P less than .05) linoleic and linolenic acid flows (.58 vs .45 g C18:2/d; .17 vs .14 g C18:3/d) to and disappearance (.50 vs .39 g C18:2/d; .14 vs .11 g C18:3/d) from the small intestine. Urea supplementation increased (P less than .05) total tract DM (70.2 vs 68.6%) and OM (72.3 vs 71.0%) digestibilities of defaunated sheep but lowered (P less than .05) ruminal fluid isobutyrate concentration (.6 vs .8 mM). Sodium bicarbonate supplementation increased (P less than .05) ruminal fluid pH (6.4 vs 6.2), isobutyrate concentration (.75 vs .60 mM), total tract ADF digestibility (57.6 vs 54.2%), and ruminal NDF (41.6 vs 28.5%), ADF (36.6 vs 22.8%), and CP (-5.5 vs -26.8%) digestibilities in defaunated sheep. Dietary supplementation of urea or sodium bicarbonate increased nutrient digestion by defaunated sheep.

Absorption↗