Feed restriction reduces short-chain fatty acid absorption across the reticulorumen of beef cattle independent of diet.

The objective of this study was to evaluate the effects of the forage-to-concentrate ratio (F:C) of diets fed before and during short-term feed restriction (FR) on rumen fermentation, absorptive capacity of the reticulorumen, and apparent total tract digestibility. Twenty ovariectomized and ruminally cannulated Angus × Hereford heifers were blocked by BW and individually penned in box stalls (9 m(2)), having free access to water throughout the study. Heifers were randomly assigned to 1 of 2 dietary treatments, receiving either a high forage diet (HF; F:C of 92:8) or a moderate forage diet (MF; F:C of 60:40). Diets were fed ad libitum for 14 d before 5 d of baseline measurements (BASE) followed by 5 d of FR where heifers were restricted to 25% of ad libitum DMI relative to BASE. Dry matter intake was measured daily and ruminal pH was recorded every 2 min throughout the study. Ruminal fluid and blood samples were collected on d 3 of BASE and FR whereas short-chain fatty acid (SCFA) absorption was assessed in vivo using the isolated washed reticulorumen technique on d 5 of BASE and FR. Indigestible NDF was used as a marker to estimate apparent total tract digestibility. Diet × period interactions (P = 0.030 and 0.025) were detected for DMI and ruminal SCFA concentration, respectively. The interaction was the result of greater DMI and numerically greater SCFA concentration for MF than HF during BASE, with a reduction observed for both during FR, although treatment effects were no longer present. Period effects (BASE vs. FR) but not treatment effects (P > 0.05) were detected for mean ruminal pH (P < 0.001) and the total SCFA absorption rate (mmol/h; P = 0.038). During BASE, mean pH was reduced (6.4 vs. 6.9) and the SCFA absorption rate was greater relative to FR (674.5 vs. 554.8 mmol/h). Diet (P < 0.001) and period (P < 0.001) effects were detected for DM and OM digestibility with greater digestibility occurring for heifers fed MF than HF (70.5 vs. 63.3% for DM and 73.0 vs. 66% for OM) and greater digestibility during FR than BASE (69.5 vs. 64.3% for DM and 71.7 vs. 67.2% for OM). During FR, NDF digestibility was also greater than during BASE (P < 0.001; 62.4 vs. 55.8%). The effect of FR on serum NEFA differed by diet (diet × period, P < 0.001) with NEFA being greater for heifers fed HF than MF during FR (474.4 vs. 377.7 μEq/mL, respectively) with no differences observed between HF and MF during BASE. It can be concluded that severe short-term FR had a negative impact on ruminal SCFA absorption and energy balance and that altering the F:C of the diet does not mitigate these effects.

[1]  D. Barreda,et al.  Short-term feed restriction impairs the absorptive function of the reticulo-rumen and total tract barrier function in beef cattle. , 2013, Journal of animal science.

[2]  D. Bohnert,et al.  Effects of twenty-four hour transport or twenty-four hour feed and water deprivation on physiologic and performance responses of feeder cattle. , 2012, Journal of animal science.

[3]  K. Schwartzkopf-Genswein,et al.  Benchmarking study of industry practices during commercial long haul transport of cattle in Alberta, Canada. , 2012, Journal of animal science.

[4]  M. Steele,et al.  Ruminant Nutrition Symposium: Molecular adaptation of ruminal epithelia to highly fermentable diets. , 2011, Journal of animal science.

[5]  F. Stumpff,et al.  Ruminant Nutrition Symposium: Role of fermentation acid absorption in the regulation of ruminal pH. , 2011, Journal of animal science.

[6]  O. Alzahal,et al.  Rumen epithelial adaptation to high-grain diets involves the coordinated regulation of genes involved in cholesterol homeostasis. , 2011, Physiological genomics.

[7]  R. Baldwin,et al.  Gene expression in the digestive tissues of ruminants and their relationships with feeding and digestive processes. , 2010, Animal : an international journal of animal bioscience.

[8]  L. Baumgard,et al.  Effects of heat stress on energetic metabolism in lactating Holstein cows. , 2010, Journal of dairy science.

[9]  M. Oba,et al.  Epithelial capacity for apical uptake of short chain fatty acids is a key determinant for intraruminal pH and the susceptibility to subacute ruminal acidosis in sheep. , 2009, The Journal of nutrition.

[10]  M. Ranilla,et al.  Microbial protein synthesis, ruminal digestion, microbial populations, and nitrogen balance in sheep fed diets varying in forage-to-concentrate ratio and type of forage. , 2009, Journal of animal science.

[11]  K. Beauchemin,et al.  Effect of dietary forage to concentrate ratio on volatile fatty acid absorption and the expression of genes related to volatile fatty acid absorption and metabolism in ruminal tissue. , 2009, Journal of dairy science.

[12]  L. Baumgard,et al.  Effects of heat stress and plane of nutrition on lactating Holstein cows: I. Production, metabolism, and aspects of circulating somatotropin. , 2009, Journal of dairy science.

[13]  F. Stumpff,et al.  Bicarbonate-dependent and bicarbonate-independent mechanisms contribute to nondiffusive uptake of acetate in the ruminal epithelium of sheep. , 2009, American journal of physiology. Gastrointestinal and liver physiology.

[14]  D. Yáñez-Ruiz,et al.  Effects of forage:concentrate ratio and forage type on apparent digestibility, ruminal fermentation, and microbial growth in goats. , 2009, Journal of animal science.

[15]  H. Martens,et al.  Change of ruminal sodium transport in sheep during dietary adaptation , 2009, Archives of animal nutrition.

[16]  A. Trenkle,et al.  Prolonged, moderate nutrient restriction in beef cattle results in persistently elevated circulating ghrelin concentrations. , 2008, Journal of animal science.

[17]  M. Galyean,et al.  BOARD-INVITED REVIEW: Recent advances in management of highly stressed, newly received feedlot cattle , 2007, Journal of animal science.

[18]  H. Dann,et al.  Metabolic effects of abomasal L-carnitine infusion and feed restriction in lactating Holstein cows. , 2006, Journal of dairy science.

[19]  K. Beauchemin,et al.  An evaluation of the accuracy and precision of a stand-alone submersible continuous ruminal pH measurement system. , 2006, Journal of dairy science.

[20]  M. Galyean,et al.  REVIEW: Dietary Roughage Concentration and Health of Newly Received Cattle , 2005 .

[21]  S. Donkin,et al.  Feed restriction induces pyruvate carboxylase but not phosphoenolpyruvate carboxykinase in dairy cows. , 2005, Journal of dairy science.

[22]  C. Pedersen,et al.  The Effect of Subclinical Hypocalcaemia Induced by Na2EDTA on the Feed Intake and Chewing Activity of Dairy Cows , 2003, Veterinary Research Communications.

[23]  H. Martens,et al.  Short-chain fatty acids and CO2 as regulators of Na+ and Cl− absorption in isolated sheep rumen mucosa , 2004, Journal of Comparative Physiology B.

[24]  J. France,et al.  Rates of production of acetate, propionate, and butyrate in the rumen of lactating dairy cows given normal and low-roughage diets. , 2003, Journal of dairy science.

[25]  J. France,et al.  Effects of volatile fatty acid supply on their absorption and on water kinetics in the rumen of sheep sustained by intragastric infusions. , 2003, Journal of animal science.

[26]  Gary D. Schnitkey,et al.  ECONOMIC LOSSES FROM HEAT STRESS BY US LIVESTOCK INDUSTRIES , 2003 .

[27]  E. Nordheim,et al.  Animal and dietary factors affecting feed intake during the prefresh transition period in Holsteins. , 2002, Journal of dairy science.

[28]  J. Aschenbach,et al.  Influence of food deprivation on the transport of 3-O-methyl-alpha-D-glucose across the isolated ruminal epithelium of sheep. , 2002, Journal of animal science.

[29]  C. Krehbiel,et al.  Evaluation of models of acute and subacute acidosis on dry matter intake, ruminal fermentation, blood chemistry, and endocrine profiles of beef steers. , 2000, Journal of animal science.

[30]  K. Schwartzkopf-Genswein,et al.  Effect of a trainer cow on health, behavior, and performance of newly weaned beef calves. , 2000, Journal of animal science.

[31]  N. Kristensen,et al.  Feed-induced Changes in the Transport of Butyrate, Sodium and Chloride Ions Across the Isolated Bovine Rumen Epithelium , 2000 .

[32]  Y. Beckers,et al.  Effects of level of intake and of available volatile fatty acids on the absorptive capacity of sheep rumen , 1997 .

[33]  J. L. Albright,et al.  Feeding behavior and management factors during the transition period in dairy cattle. , 1995, Journal of animal science.

[34]  Pekka Huhtanen,et al.  The use of internal markers to predict total digestibility and duodenal flow of nutrients in cattle given six different diets. , 1994 .

[35]  M. Doreau,et al.  Effect of undernutrition on the ability of the sheep rumen to absorb volatile fatty acids. , 1994, Reproduction, nutrition, development.

[36]  H. Martens,et al.  Influence of food deprivation on SCFA and electrolyte transport across sheep reticulorumen. , 1993, Zentralblatt fur Veterinarmedizin. Reihe A.

[37]  C. Krehbiel,et al.  Influence of dietary forage and energy intake on metabolism and acyl-CoA synthetase activity in bovine ruminal epithelial tissue. , 1991, Journal of Animal Science.

[38]  P. V. Soest,et al.  Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. , 1991, Journal of dairy science.

[39]  R. Grummer,et al.  Response of lactating dairy cows to fat supplementation during heat stress. , 1991, Journal of dairy science.

[40]  D. Hutcheson,et al.  Management of Transit-Stress Syndrome in Cattle: Nutritional and Environmental Effects , 1986 .

[41]  R. Brown,et al.  Magnesium absorption from the digestive tract of sheep. , 1984, Quarterly journal of experimental physiology.

[42]  W. Horwitz Official Methods of Analysis , 1980 .