Portal-drained visceral metabolism of 3-hydroxybutyrate in sheep

The present experiment was conducted to study the impact of portal-drained visceral (PDV) metabolism of arterial 3-OH-butyrate on estimates of the portal recovery of intraruminally infused butyrate. Three multicatheterized and rumen-fistulated Leicester ewes were subjected to three intraruminal infusion protocols in a Latin square design: control (C; water), butyrate (B; 20 mmol x h(-1)), and butyrate (20 mmol x h(-1)) + propionate (40 mmol x h(-1)) (BP). During the experiments, the sheep were infused with 1,2,3,4-13C4-D-3-OH-butyrate in a mesenteric vein. Portal recoveries of intraruminally infused butyrate and propionate were obtained by comparing Treatments B and BP, respectively, with Treatment C. The portal net appearance of butyrate and the portal net appearance of butyrate + 3-OH-butyrate accounted for 20 +/- 2% and 48 +/- 14% of intraruminally infused butyrate, respectively. Metabolism by the PDV tissues accounted for 32 to 44% of the whole-body irreversible loss rate of 3-OH-butyrate (12.0 to 24.7 +/- 0.5 mmol x h(-1)). The portal net appearance of butyrate plus the unidirectional PDV output of 3-OH-butyrate accounted for 62 +/- 5% of the intraruminally infused butyrate, and this estimate was comparable to the portal recovery of intraruminally infused propionate (62 +/- 7%). The results from the present study show that the extent of epithelial butyrate oxidation is overestimated and the portal recovery of butyrate carbon underestimated if only portal net appearance rates of butyrate and 3-OH-butyrate are considered.     

Effect of increasing ruminal butyrate absorption on splanchnic metabolism of volatile fatty acids absorbed from the washed reticulorumen of steers

Four steers fitted with a ruminal cannula and chronic indwelling catheters in the mesenteric artery, mesenteric vein, hepatic portal vein, hepatic vein, and the right ruminal vein were used to study the absorption and metabolism of VFA from bicarbonate buffers incubated in the temporarily emptied and washed reticulorumen. Portal and hepatic vein blood flows were determined by infusion of p-aminohippurate into the mesenteric vein, and portal VFA fluxes were calibrated by infusion of isovalerate into the ruminal vein. The steers were subjected to four experimental treatments in a Latin square design with four periods within 1 d. The treatments were Control (bicarbonate buffer) and VFA buffers containing 4, 12, or 36 mmol butyrate/kg of buffer, respectively. The acetate content of the buffers was decreased with increasing butyrate to balance the acidity. The butyrate absorption from the rumen was 39, 111, and 300 +/- 4 mmol/h for the three VFA buffers, respectively. The ruminal absorption rates of propionate (260 +/- 12 mmol/h), isobutyrate (11.4 +/- 0.7 mmol/h), and valerate (17.3 +/- 0.7 mmol/h) were not affected by VFA buffers. The portal recovery of butyrate and valerate absorbed from the rumen increased (P < 0.01) with increasing butyrate absorption and reached 52 to 54 +/- 4% with the greatest butyrate absorption. The liver responded to the increased butyrate absorption with a decreasing fractional extraction of propionate and butyrate, and with the greatest butyrate absorption, the splanchnic flux was 22 +/- 1% and 18 +/- 1% of the absorbed propionate and butyrate, respectively. The increased propionate and butyrate release to peripheral tissues was followed by increased (P < 0.05) arterial concentrations of propionate (0.08 +/- 0.01 mmol/kg) and butyrate (0.07 +/- 0.01 mmol/kg). Arterial insulin concentration increased (P = 0.01) with incubation of VFA buffers compared with Control and was numerically greatest with the greatest level of butyrate absorption. We conclude that the capacity to metabolize butyrate by the ruminal epithelium and liver is limited. If butyrate absorption exceeds the metabolic capacity, it affects rumen epithelial and hepatic nutrient metabolism and affects the nutrient supply of peripheral tissues.     

Effects of adding valerate, caproate, and heptanoate to ruminal buffers on splanchnic metabolism in steers under washed-rumen conditions

Four steers fitted with a ruminal cannula and chronic indwelling catheters in the mesenteric artery, mesenteric vein, hepatic portal vein, hepatic vein, and the right ruminal vein were used to study VFA absorption from bicarbonate buffers incubated in the washed reticulorumen, and metabolism by splanchnic tissues. Portal and hepatic vein blood flows were determined by infusion of p-aminohippurate into the mesenteric vein. The steers were subjected to four experimental treatments in a Latin square design. The treatments were Control (ruminal bicarbonate buffer with [mmol/kg]: acetate = 72; propionate = 30; isobutyrate = 2.1; butyrate = 12; valerate = 1.2; caproate = 0; and heptanoate = 0); Val (same as control except for valerate = 8 mmol/kg); Cap (same as control except for caproate = 3.5 mmol/kg); and Hep (same as control except for heptanoate = 3 mmol/kg). All buffers were incubated for 90 min in the rumen, and ruminal VFA absorption rates were maintained by continuous intraruminal infusion of VFA. The arterial concentrations of valerate and heptanoate showed a small increase (< or = 1 micromol/L; P < 0.05) with inclusion of the respective acid in the ruminal buffer, but no change (P = 0.57) in arterial concentration of caproate was detected. Valerate increased (P < 0.05) the net portal flux of butyrate and valerate, as well as the net splanchnic flux of propionate, butyrate, and valerate. With Cap and Hep, the net portal flux of caproate and heptanoate accounted for 54 and 45% of ruminal disappearance rates, respectively, indicating that these acids were extensively metabolized by the ruminal epithelium. Caproate was ketogenic both in the ruminal epithelium and in the liver, and Cap increased (P < 0.05) the arterial concentration, ruminal vein minus arterial concentration difference, net hepatic flux, and net splanchnic flux of 3-hydroxybutyrate. The net hepatic flux of glucose decreased (P = 0.02) with Cap and Hep compared with Control and Val; however, no effect (P = 0.14) on the net splanchnic flux of glucose could be detected. We conclude that the strong biological activity of valerate, caproate, and heptanoate warrant increased emphasis on monitoring their ruminal presence and their potential systemic effects on ruminant metabolism.     

Splanchnic metabolism of volatile fatty acids absorbed from the washed reticulorumen of steers

Six steers fitted with a ruminal cannula and chronic indwelling catheters in the mesenteric artery, mesenteric vein, hepatic portal vein, hepatic vein, as well as in the right ruminal vein were used to study metabolism of VFA absorbed from buffers in the emptied and washed reticulorumen. [2-(13)C]Acetate was infused into a jugular vein to study portal-drained visceral (PDV) uptake of arterial acetate, hepatic unidirectional uptake of acetate, and whole-body irreversible loss rate (ILR). Isobutyrate was infused into the right ruminal vein to calibrate VFA fluxes measured in the portal vein. On sampling days, the rumen was emptied and incubated in sequence with a 0-buffer (bicarbonate buffer without VFA), a VFA-buffer plus continuous intraruminal infusion of VFA, and finally another 0-buffer. Ruminal VFA absorption was determined as VFA uptake from the VFA-buffer and metabolic effects determined as the difference between metabolite fluxes with VFA-buffer and 0-buffers. Steady absorption rates of VFA were maintained during VFA-buffer incubations (4 h; 592+/-16, 257+/-5, 127+/-2, 17+/-<1, 20+/-<1 mmol/h, respectively, of acetate, propionate, butyrate, isovalerate, and valerate). The portal flux of acetate corrected for PDV uptake of arterial acetate accounted for 105+/-3% of the acetate absorption from the rumen, and the net portal flux of propionate accounted for 91+/-2% of propionate absorption. Considerably less butyrate (27+/-3%) and valerate (30+/-3%) could be accounted for in the portal vein. The sum of portal VFA and 3-hydroxybutyrate as well as lactate represented 99+/-3% of total VFA acetyl units and 103+/-2% of VFA propionyl units. Estimates are maximum because no accounting was made for lactate derived from glycolysis in the PDV. The net splanchnic flux of VFA, lactate, 3-hydroxybutyrate, and glucose accounted for 64+/-2% of VFA acetyl units and 34+/-5% of VFA propionyl units. Results indicate that there is a low "first-pass" uptake of acetate and propionate in the ruminal epithelium of cattle, whereas butyrate and valerate are extensively metabolized, though seemingly not oxidized to carbon dioxide in the epithelium but repackaged into acetate, 3-hydroxybutyrate, and perhaps other metabolites. When PDV "second-pass" uptake of arterial nutrients is accounted for, PDV fluxes of VFA, lactate, and 3-hydroxybutyrate represent VFA production in the gastrointestinal tract and thereby VFA availability to the ruminant animal.     

Determination of volatile fatty acids in the blood plasma of cattle before and after an infusion of propionate and butyrate

Before and after infusion of propionate and butyrate the concentrations of volatile fatty acids (VFA) in the blood of heifers were determined by gas chromatography, in order to indicate activity and regulation of the carbohydrate metabolism. 14 heifers were loaded after food deprivation with intravenous infusions of propionate and butyrate. Concentrations of acetate, propionate, isobutyrate, butyrate, and valerate were measured in blood samples which were taken later on. The methods used for clearance and extraction as well as for gas chromatographic analysis are described. Retention times and blood concentrations are given for each VFA. Concentrations prior to infusion were for: acetate 10.14 +/- 2.51 microliters/ml; propionate 0.42 +/- 0.35 microliters/ml; iso-butyrate 3.72 +/- 1.37 microliters/ml; butyrate 3.44 +/- 0.68 microliters/ml blood plasma. The concentrations of the infused VFA showed a 100 (butyrate) to 1000 (propionate) fold increase followed by a subsequent decrease to the initial values. These investigations on the profile of VFA elucidated criteria of the energy metabolism.     

Rumen microbial sequestration of [2-(13)C]acetate in cattle

To investigate the impact of rumen microbial sequestration of VFA carbon on estimates of acetate availability based on intraruminal infusion of [2-(13)C] acetate, three nonlactating or low-yielding dairy cows were continuously intraruminally infused with [2-(13)C]acetate for 26 h. The 13C content of ruminal VFA, duodenal carbon, and fatty acids (FA) and AA isolated from liquid-associated ruminal microbes and duodenal DM was measured by an isotope ratio mass spectrometer interfaced to an elemental analyzer or a gas-liquid chromatograph. The ruminal gross production of acetate was 38 +/- 4 mol/d and could account for about 38% of the DE intake. Of the intraruminally infused 13C in [2-(13)C]acetate, 7.6 +/- 0.9% was recovered at the duodenum. The 13C content of ruminal propionate, butyrate, and valerate increased (P < 0.05) with intraruminal infusion of [2-(13)C]acetate. It was estimated that about 28% of the 13C intraruminally infused in [2-(13)C]acetate could be accounted for by duodenal 13C flow and absorption of non-acetate VFA. A number of FA isolated from liquid-associated ruminal microbes (C6, C12, C14, anteiso C15, and iso C15) were enriched with 13C (P < 0.05) at a level comparable to the enrichment of ruminal butyrate. Any absorption of these FA from the rumen would further contribute to non-acetate 13C uptake. A maximum of 72% of the ruminal gross production of acetate represented acetate absorption from the rumen in the present study. Consequently, previously used models using intraruminal isotope dilution techniques seem not to be appropriate for measuring acetate availability in ruminants. The number of metabolites exchanging carbon with acetate was found to be so high that assessments of the entire range of inter conversions seem to be practically impossible. Portal absorption studies are discussed as an alternative method of estimating VFA availability to the metabolism in ruminants.     

Effects of volatile fatty acid supply on their absorption and on water kinetics in the rumen of sheep sustained by intragastric infusions

Three sheep fitted with a ruminal cannula and an abomasal catheter were used to study water kinetics and absorption of VFA infused continuously into the rumen. The effects of changing VFA concentrations in the rumen by shifting VFA infusion rates were investigated in an experiment with a 3 x 3 Latin square design. On experimental days, the animals received the basal infusion rate of VFA (271 mmol/h) during the first 2 h. Each animal then received VFA at a different rate (135, 394, or 511 mmol/h) for the next 7.5 h. Using soluble markers (polyethylene glycol and Cr-EDTA), ruminal volume, liquid outflow, apparent water absorption, and VFA absorption rates were estimated. There were no significant effects of VFA infusion rate on ruminal volume and water kinetics. As the VFA infusion rate was increased, VFA concentration and osmolality in the rumen were increased and pH was decreased. There was a biphasic response of liquid outflow to changes in the total VFA concentration in the rumen, as both variables increased together up to a total VFA concentration of 80.1 mM, whereas, beyond that concentration, liquid outflow remained stable at an average rate of 407 mL/h. There were significant linear (P = 0.003) and quadratic (P = 0.001) effects of VFA infusion rate on the VFA absorption rate, confirming that VFA absorption in the rumen is mainly a concentration-dependent process. The proportion of total VFA supplied that was absorbed in the rumen was 0.845 (0.822, 0.877, and 0.910 for acetate, propionate, and butyrate, respectively). The molar proportions of acetate, propionate, and butyrate absorbed were affected by the level of VFA infusion in the rumen, indicating that this level affected to a different extent the absorption of the different acids.     

不同精粗比日粮对奶山羊瘤胃液pH值、VFA及血液VFA含量的影响

本试验旨在探讨不同精粗比日粮对奶山羊瘤胃液pH值、VFA以及血液中VFA含量的影响。选择8只安装永久性瘤胃瘘管的奶山羊作为试验动物,采用完全随机分组试验设计随机分为2组,分别饲喂精粗比为6∶4和4∶6的日粮,预饲期15 d,采样期3 d。结果表明,高精料组(HC组)瘤胃液pH值显著低于低精料组(HR组)(P<0.05);在采食后3 h,HC组与HR组瘤胃液pH值均下降至最低值,分别为5.71和6.08。除了乙酸含量外,HC组瘤胃液丙酸、异丁酸、丁酸、异戊酸、戊酸以及总挥发性脂肪酸(TVFA)含量分别比HR组提高4.99%、5.58%、21.81%、17.95%、18.27%、1.66%。HC组血浆中各种VFA的含量均高于HR组,其中丙酸、丁酸含量两组间差异达到显著水平(P<0.05)。HC组瘤胃液以及血浆中乙酸与丙酸比值均低于HR组,但两组间差异均不显著(P>0.05)。HC组瘤胃液乙酸、丙酸、TVFA浓度在采食后2 h达到最大值,HR组在采食后3 h达到最大值,两组日粮血浆中VFA浓度均在采食后2 h达到最大值,然后逐渐恢复到采食前水平。结论:高精料日粮导致瘤胃液pH值显著降低,瘤胃液和血浆中VFA含量增加;瘤胃液VFA生成速率HC组高于HR组。     

Portal-drained visceral flux of nutrients in lambs fed alfalfa or maintained by total intragastric infusion

An experiment was performed using lambs fitted with chronic indwelling catheters in appropriate blood vessels for portal-drained visceral (PDV) flux measurements. The objective of the experiment was to evaluate PDV nutrient flux in alfalfa-fed and intragastrically infused lambs and to evaluate the effects of amount of energy and N infused on PDV nutrient metabolism. Lambs were fed alfalfa or infused with 1.64 and 10.9; 1.82 and 12.3; or 2.37 and 15.0 Mcal GE and g N/d, respectively. Arterial concentrations and PDV fluxes of glucose, L-lactate, acetate and portal blood flow were not different (P greater than .10) between alfalfa-fed and infused lambs. Net flux of alpha-amino N, ammonia N and branched-chain VFA were lower (P less than .05) and net flux of propionate, butyrate and total VFA were higher for intragastric infusion vs alfalfa. No consistent differences in PDV fluxes were noted among the three levels of energy and N infused, although the energy and N levels tested were near maintenance requirements. Nitrogen retention increased as level of energy and N infusion increased. Approximately 47, 70 and 22% of ruminally infused acetate, propionate and butyrate, respectively, were found on a net basis in portal blood as VFA. Measurements of net nutrient utilization by the PDV that eliminate the influence of ruminal fermentation are possible. How the changes in PDV tissues due to intragastric infusion influence these estimates is unknown.     

Metabolism of propionate and 1,2-propanediol absorbed from the washed reticulorumen of lactating cows

To investigate the metabolism of 1,2-propanediol (PPD) in lactating cows independently of normal rumen microbial metabolism, three ruminally cannulated lactating Holstein cows were subjected to three experimental infusion protocols under washed reticulo-ruminal conditions in a Latin square design. Reticulo-ruminal absorption rates were maintained for 420 min by continuous intraruminal infusion of VFA and PPD. With the control treatment, 1,246 +/- 39 mmol/ h of acetate and 213 +/- 5 mmol/h of butyrate were absorbed from the reticulorumen. With the propionate treatment, 1,148 +/- 39 mmo/h of acetate, 730 +/- 23 mmol/h of propionate and 196 +/- 5 mmol/h of butyrate were absorbed from the reticulorumen. With PPD treatment, 1,264 +/- 39 mmol/h of acetate, 220 +/- 5 mmol/h of butyrate and 721 +/- 17 mmol/h of PPD were absorbed from the reticulorumen. Glucose irreversible loss rate (ILR), as well as the relative enrichment of plasma lactate and alanine, were determined by primed continuous infusion of [U-13C]glucose in a jugular vein. Treatments did not affect (P > 0.10) the plasma concentrations of glucose (4.2 +/- 0.1 mmoVL), alanine (0.14 +/- 0.01 mmol/L), or insulin (80 +/- 25 pmol/L). The plasma concentration of lactate was higher (P < 0.05) with both propionate (0.84 +/- 5 mmol/L) and PPD treatment (0.81 +/- 5 mmol/ L) compared with the control treatment (0.29 +/- 0.5 mmol/L). The plasma concentration of pyruvate was higher (P < 0.05) with the propionate treatment (0.09 +/- 0.01 mmol/L) compared with the control treatment (0.03 +/- 0.01 mmol/L). The plasma concentration of 3-hydroxybutyrate was lower (P < 0.05) with the propionate treatment (0.15 +/- 0.03 mmol/L) compared with the control treatment (0.40 +/- 0.03). With the PPD treatment, the plasma concentrations of pyruvate and 3-hydroxybutyrate were in between the other treatments and tended (P < 0.10) to be different from both. The plasma concentration of PPD increased throughout the infusion period with the PPD treatment and reached a concentration of 4.9 +/- 0.6 mmol/L at 420 min. The ILR of glucose was not affected (P > 0.10) by treatments (441 +/- 35 mmol/h). The relative 13C enrichment of plasma lactate compared with that of glucose decreased (P < 0.05) with the PPD treatment compared with the control treatment (44 to 21 +/- 3%). It was concluded that PPD has a low rate of metabolism in cows without a normal functioning rumen, although about 10% of the absorbed PPD was metabolized into lactate.     

Effect of increasing ruminal butyrate on portal and hepatic nutrient flux in steers.

Six Holstein steers (mean +/- SE BW = 344 +/- 10 kg) fitted with hepatic, portal, and mesenteric vein and mesenteric artery catheters and a ruminal cannula were used in a 6 x 6 Latin square design to evaluate the effects of increasing ruminal butyrate on net portal-drained visceral and hepatic nutrient flux. Steers were fed a 40% brome hay, 60% concentrate diet in 12 portions daily at 1.25 x NEm. Water (control) or butyrate at 50, 100, 150, 200, or 250 mmol/h was supplied continuously via the ruminal cannula. Simultaneous arterial, portal, and hepatic blood samples were taken at hourly intervals from 15 to 20 h of ruminal infusion. Portal and hepatic blood flow was determined by continuous infusion of P-aminohippurate, and net nutrient flux was calculated as the difference between venous and arterial concentrations times blood flow. Ruminal and arterial concentrations and total splanchnic flux of butyrate increased (P less than .01) with increased butyrate infusion. Arterial concentrations of acetate (P less than .10), alpha-amino-N (P less than .05), and glucose (P less than .01) decreased with increased butyrate, whereas arterial beta-hydroxybutyrate (P less than .01) and acetoacetate (P less than .05) increased. Increased butyrate produced an increased portal-drained visceral flux of acetoacetate and an increased net hepatic flux of beta-hydroxybutyrate. Urea N and glucose net portal and hepatic fluxes were not affected by ruminal butyrate. Alpha-amino-N uptake by the liver decreased with increased butyrate (P less than .10). Simple linear regression (r2 = .985) indicated that 25.8% of ruminally infused butyrate appeared in portal blood as butyrate. Only 14% could be accounted for as net portal-drained visceral flux of acetoacetate plus beta-hydroxybutyrate.     

Using a novel macro in vitro technique to estimate differences in absorption rates of volatile fatty acids in the rumen

A novel macro in vitro system was used to test the theory that rumen proportions of acetate, propionate and butyrate are not representative of their respective net production rates. Whole rumen content (10–16 kg) from two cows was mixed with a bicarbonate buffer and incubated separately in two 40‐l in vitro vessels for 3 h. A total of six experimental periods were used. In this study, a total of six cows were used and fed 1/8 of the daily ration by hand every 3 h. To obtain differences in rumen volatile fatty acids (VFA) composition, 1 l of acetate (416 mm ), propionate (108 mm ), butyrate (79 mm ), lactic acid (300 mm ) or nothing was infused during 24 h into the rumen before collection of representative samples of rumen contents. Infusions of acids were then continued during the in vitro incubations in exact proportion to the digesta removed from the rumen. In Periods 1 and 2, the cows were alternatively infused with acetate or nothing. In Periods 3 and 4, the infusions consisted of propionate or butyrate and in Periods 5 and 6 of lactate or nothing. Nine liquid samples were obtained between 3 and 180 min after the start of incubation and analysed for concentrations of VFA. Changes in proportions of individual VFA were estimated by linear regression. No differences in VFA proportions were observed in the absence of infusion (p > 0.5) over time, but when individual VFA were infused, their respective proportions increased. This was interpreted as the result of a decreased in vitro fermentation rate of digesta substrates compared with that in the rumen. Lactate infusion increased butyrate proportion in vitro. It is concluded that this study could not provide any evidence that ruminal VFA proportions are unrepresentative of the proportions of net production.     

Effects of isoenergetic infusions of propionate and glucose on portal-drained visceral nutrient flux and concentrations of hormones in lambs maintained by total intragastric infusion

Three lambs were used in a repeated Latin square design to determine the influence of isoenergetic infusions of propionate or glucose on portal-drained visceral flux (PDV) of nutrients and concentrations of insulin, glucagon, growth hormone and prolactin. Lambs were fitted with appropriate catheters for blood sampling and maintained on total intragastric infusion of nutrients. Basal VFA, casein, mineral and vitamin infusions (isocaloric and isonitrogenous) were supplemented with an additional 22 +/- .5 kcal/h from propionate, glucose or a combination of propionate plus glucose. Ruminal fluid proportion and arterial blood concentration and PDV flux of propionate increased (P less than .10) by 17 mol/100 mol, .02 mM and 40 mmol/h, respectively, with infusion of an additional 61 mmol/h of propionate. Regression equations predicted that, on a net basis, 67% of ruminally infused propionate and 43% of abomasally infused glucose appeared in portal blood. Arterial L-lactate, beta-hydroxybutyrate and acetate concentrations, and beta-hydroxybutyrate flux were increased (P less than .10) by .34 mM, .20 mM, .50 mM and 4.2 mmol/h, respectively, with infusion of 33 mmol/h of added glucose. Net utilization of glucose by the PDV was approximately 4.4 mmol/h when no glucose was infused. Increased infusion of propionate resulted in a 22.2-micrograms/h increase in PDV flux of insulin (P less than .08) but had no effect on arterial insulin, glucagon and prolactin concentrations (P greater than .10). Arterial growth hormone increased by 3.8 ng/ml with increasing glucose infusion (P less than .08).(ABSTRACT TRUNCATED AT 250 WORDS)     

Diurnal Patterns of Ruminal Concentrations and Portal Appearance Rates of Short-chain Fatty Acids in Sheep Fed a Hay or a Concentrate/Straw Diet in Two Meals Daily

Abstract

Three rumen fistulated and catheterized sheep were meal-fed and used to study ruminal and arterial concentrations of short-chain fatty acids (SCFA) as well as portal appearance rates of SCFA and irreversible loss rate (ILR) of acetate in 24 h periods on a hay and a concentrate/straw diet, respectively.

Ruminal and arterial concentrations as well as portal appearance rates of SCFA and ILR of acetate were significantly affected by the intake of feed. Generally, the highest concentrations and appearance rates were obtained 2 h after feeding. The portal recovery of arterial acetate was not affected by feeding or diet. The 24 h means were 0.68 ± 0.01 and 0.67 ± 0.01 on the hay and the concentrate/straw diet, respectively. Partial correlation coefficients corrected for the effects of time, sheep, and diet were calculated for the relationships evaluated. The portal appearance rate of acetate (r = 0.52, P <0.001) and the portal net appearance rate of propionate (r = 0.68, P <0.001) were linearly related to the ruminal concentrations of the two SCFA. The logarithm of the portal net appearance rate of butyrate seemed to be linearly related to the logarithm of the ruminal concentration of undissociated butyric acid (r = 0.70, P <0.001) when the effect of time was omitted from the model. The portal appearance rate of acetate (r = 0.22, P <0.05) and the portal net appearance rate of propionate (r = 0.63, P <0.001) as well as butyrate (r = 0.55, P <0.001) were linearly related to the arterial concentration of the respective SCFA. The results show that within animal and diet the ruminal as well as arterial concentrations are good predictors of SCFA portal appearance rates in sheep fed roughage at maintenance. Ruminal and arterial concentrations of SCFA seem less reliable predictors of portal appearance rates of SCFA between diets and sheep. The portal appearance of SCFA, 5.6 ± 0.5 and 7.0 ± 0.3 mol d^?1, accounted for 44 ± 4 and 43 ± 2% of the calculated metabolizable energy intake on the hay and the concentrate/straw diets, respectively.     

高精料日粮下添加阿卡波糖对奶牛瘤胃及后肠发酵的影响研究

本试验旨在探讨高精料日粮下添加阿卡波糖对奶牛瘤胃和后肠发酵的影响。试验选用3头干奶期荷斯坦奶牛,采用3×3拉丁方试验设计,阿卡波糖添加剂量为0,0.5和1.0 g/d,试验分3期进行,每期21 d。结果表明,与对照组比较,添加阿卡波糖显著降低了奶牛瘤胃液中丙酸浓度(P<0.05),提高了乙丙比(P<0.05),但对瘤胃pH值、乳酸、乙酸、异丁酸、丁酸、异戊酸、戊酸、总挥发性脂肪酸和氨氮浓度无显著影响(P>0.05);与对照组比较,添加阿卡波糖显著降低了粪便pH值和氨氮浓度(P<0.05),提高了乳酸、丁酸和异戊酸浓度(P<0.05),但对乙酸、丙酸、异丁酸、戊酸、总挥发性脂肪酸和乙丙比无显著影响(P>0.05)。结果说明,高精料日粮下长期添加阿卡波糖虽可影响瘤胃液中个别挥发性脂肪酸的浓度,但对瘤胃整体发酵和瘤胃pH值无显著影响,此外,添加阿卡波糖可增加后肠发酵,并可能对后肠健康带来潜在危害。     

Net portal absorption of lactate and volatile fatty acids in steers experiencing glucose-induced acidosis or fed a 70% concentrate diet ad libitum

Five crossbred steers (347 kg) were surgically fitted with rumen fistulae, hepatic portal, abdominal aorta and mesenteric catheters to measure organic acid absorption from the gut during acute [intraruminal glucose, 12 g/kg body weight (G)] or subacute [ad libitum 70% concentrate diet (C)] acidosis. Samples were taken at time 0, then every 2 h for 48 h after a switch from an alfalfa diet to C, or dosing with G. Steers receiving C received G 1 wk later so that five steers provided four observations/treatment. Blood flow rates were determined by infusion of para-amino hippuric acid (PAH) and averaged 767.8 and 712.5 liters/h for C and G, respectively. Animals consuming C averaged 13.6 kg dry matter from 0 to 24 h and 1.5 kg from 24 to 48 h. Rumen pH declined to 4.2 for G compared with 6.0 for C. Blood pH and HCO3 showed only slight depressions for G from 16 to 26 h, the period of lowest rumen pH. Rumen L-lactate concentration averaged 53.4 mM (peak 77 mM) and 2.1 mM for G and C, respectively. Rumen D-lactate concentration averaged 30.2 mM (peak 47 mM) for G and 1.2 mM for C. Net portal absorption of L-lactate averaged 96.6 and 164.4 mmol/h, whereas that of D-lactate averaged 10.5 and 71.8 mmol/h for C and G, respectively. Mean net portal volatile fatty acid absorptions were 442.8, 192.1, 53.8, 5.3 and 10.4 mmol/h (C) and 100.0, 47.2, 9.4, .98 and .78 mmol/h (G) for acetate, propionate, butyrate, isobutyrate and isovalerate, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)     

Empirical prediction of net portal appearance of volatile fatty acids, glucose, and their secondary metabolites (beta-hydroxybutyrate, lactate) from dietary characteristics in ruminants: A meta-analysis approach

The current trend in energy feeding systems for ruminants toward a nutrient-based system requires dietary energy supply to be determined in terms of amount and nature of absorbed energy-yielding nutrients. The objective of this study was to establish response equations on the net portal appearance (NPA) of VFA and glucose, and their secondary metabolites beta-hydroxybutyrate (BHBA) and lactate, to changes in intake level and chemical dietary characteristics based on the Institut National de la Recherche Agronomique Feed Evaluation System for Ruminants. Meta-analyses were applied on published data compiled from the FLORA database, which pools the results on net splanchnic nutrient fluxes in multi-catheterized ruminants from international publications. For each nutrient, several prediction variables were tested. We obtained robust models for intakes up to 30 g of DM x d(-1) x kg of BW(-1) and diets containing less than 70 g of concentrate per 100 g of DM. These models were designed to predict the NPA (mmol x h(-1) x kg of BW(-1)) of total VFA based on the amount of ruminally fermented OM (RfOM) intake [adjusted R(2) (R(2)(adj)) = 0.95; residual means square errors (RMSE) = 0.24], to predict VFA profile (mol/100 mol of total VFA) based on type of RfOM intake (acetate: R(2)(adj) = 0.85, RMSE = 2.2; propionate: R(2)(adj) = 0.76, RMSE = 2.2; butyrate: R(2)(adj) = 0.76, RMSE = 1.09), and to predict the NPA (mmol x h(-1) x kg of BW(-1)) of glucose based on the starch digested in the small intestine independent of ruminant species, and while presenting no interfering factors on the residuals and individual slopes. The model predicting the NPA (mmol x h(-1) x kg of BW(-1)) of BHBA based on the amount of RfOM intake (R(2)(adj) = 0.91; RMSE = 0.036) was species-dependent, and the model predicting NPA (mmol x h(-1) x kg of BW(-1)) of lactate based on starch digested in the rumen (R(2)(adj) = 0.77; RMSE = 0.042) presented a wide dispersion. However, the NPA (mmol x h(-1) x kg of BW(-1)) of BHBA was related to the NPA of both butyrate (R(2)(adj) = 0.85; RMSE = 0.054) and acetate (R(2)(adj) = 0.85; RMSE = 0.052), and the NPA (mmol x h(-1) x kg of BW (-1)) of lactate was related to the NPA of propionate (R(2)(adj) = 0.51; RMSE = 0.096). This research showed that it is possible to accurately predict the amount and nature of absorbed nutrient fluxes based on dietary characteristics in both sheep and cattle. This work aims to quantify the consequences of digestion and portal-drained viscera metabolism on nutrient availability. These results can provide deeper insight into biological processes and help develop improved tools for dietary formulation.     

酸中毒条件下添加阿卡波糖对瘤胃微生物发酵的影响

利用体外培养技术,评估了急性与亚急性酸中毒条件下添加阿卡波糖对瘤胃微生物发酵的影响。设3个实验,实验1和实验2体外摸拟了亚急性酸中毒(5.0P<0.001),乙酸、丙酸、丁酸、总挥发性脂肪酸(total volatile fatty acid, TVFA)、乳酸浓度和累积产气量皆显著降低(P<0.01),但异戊酸浓度变化不显著(P=0.794);实验2中,较对照组相比,添加阿卡波糖提高了4种底物下发酵液的pH值和氨氮浓度(P<0.01),降低了发酵体系中的乙酸、丙酸、异丁酸、丁酸、异戊酸、戊酸和TVFA浓度,提高了乙丙比(P<0.01),除乙酸和TVFA外,对上述其他指标,日粮与阿卡波糖间存在显著的互作效应(P<0.01)。实验3中,与对照相比,添加阿卡波糖显著提高了发酵液pH值、氨氮、丙酸、丁酸和戊酸浓度(P<0.01),降低了乳酸和乙丙比(P<0.05),但对乙酸、异丁酸、异戊酸和TVFA浓度无显著影响(P>0.05)。结果说明阿卡波糖可有效提高发酵体系中的pH值,降低乳酸浓度,预防瘤胃酸中毒。     

Cecal short-chain fatty acids in experimental rabbit mucoid enteropathy

Short-chain fatty acid concentrations were measured in the cecal contents of 9 healthy rabbits and 20 rabbits with experimentally induced mucoid enteropathy. In control rabbits, cecal concentration of acetate was the most abundant, followed by that of butyrate and propionate--a feature distinguishing rabbits from most other mammals. In mucoid enteropathy, cecal acetate and butyrate concentrations were lower, whereas propionate, isobutyrate, valerate, and isovalerate were increased. The results indicated that there were abnormal fermentation and cecal maldigestion in rabbits with mucoid enteropathy.     

体外研究反刍兽新月形单胞菌及与酵母联用对瘤胃微生物发酵的影响

利用体外批次培养技术,分别以羊草、玉米和淀粉为底物,研究了反刍兽新月形单胞菌L9菌株及其与酵母联用对瘤胃微生物发酵的影响。结果显示,以羊草为底物时,添加酵母可显著提高乙酸、丙酸、丁酸、戊酸、异戊酸和TVFA浓度(P<0.05),降低乳酸浓度(P<0.05),有降低乙丙比值的趋势(P=0.082),但对异丁酸及pH值无显著影响(P>0.10),添加L9菌可显著提高pH值、乙酸、丙酸、丁酸、异戊酸和TVFA浓度(P<0.05),降低乳酸浓度和乙丙比值(P<0.05),但对异丁酸及戊酸浓度无显著影响(P>0.10),在影响pH值、丙酸、丁酸、异丁酸、异戊酸、TVFA浓度及乙丙比值方面,酵母与L9菌株间无显著的互作关系(P>0.10);在降低乳酸及戊酸浓度方面,酵母与L9菌株之间有显著的互作作用(P<0.05),在影响pH值及乙酸产量方面,酵母与L9菌之间有互作效应趋势。以玉米为底物时,添加酵母可显著提高pH值、乙酸、丙酸、丁酸、异戊酸和TVFA浓度(P<0.05),降低乳酸浓度和乙丙比值(P<0.05),有提高戊酸浓度的趋势(P=0.082),但对异丁酸无显著影响(P>0.10),添加L9菌可显著提高pH值、乙酸、丙酸、丁酸、戊酸、异戊酸和TVFA浓度(P<0.05),降低乳酸浓度和乙丙比值(P<0.05),但对异丁酸浓度无显著影响(P>0.10),在影响pH值、乳酸、乙酸、丙酸、丁酸、异戊酸、TVFA浓度及乙丙比值方面,酵母与L9菌株间有显著的互作关系(P<0.05);在影响异丁酸及戊酸浓度方面,酵母与L9菌株之间无显著的互作作用(P>0.10)。以淀粉为底物时,添加酵母可显著提高pH值、乙酸、丙酸、丁酸、异戊酸和TVFA浓度(P<0.05),降低乳酸浓度(P<0.05),但对戊酸、异丁酸浓度和乙丙比值无显著影响(P>0.10),添加L9菌可显著提高pH值、乙酸、丙酸、丁酸、戊酸和TVFA浓度(P<0.05),降低乳酸浓度和乙丙比值(P<0.05),但对异丁酸和异戊酸浓度无显著影响(P>0.10),在影响pH值、乳酸、乙酸、丙酸、丁酸、异戊酸、TVFA浓度及乙丙比值方面,酵母与L9菌株间有显著的互作关系(P<0.05);在影响异丁酸及戊酸浓度方面,酵母与L9菌株之间无显著的互作作用(P>0.10)。结果说明,添加酵母与L9菌株均可有效降低乳酸产量,且均可有效提高玉米及淀粉条件下发酵体系中的pH值,酵母与L9菌株联用更有助于发酵前期pH值的稳定。