Portal Flux Research Articles

Absorption and metabolism of benzoic acid in growing pigs1

Dietary benzoic acid (BA) supplementation causes a pronounced reduction in urinary pH but only small changes in blood pH. The present study aimed to investigate the portal absorption profile, hepatic metabolism of BA, and renal excretion of hippuric acid (HA) underlying the relatively small impact of BA on systemic acid-base status. Eight growing pigs (BW = 63 +/- 1 kg at sampling) fitted with permanent indwelling catheters in the abdominal aorta, hepatic portal vein, hepatic vein, and mesenteric vein were allocated to 4 sampling blocks and randomly assigned to control (CON; nonsupplemented diet) or BA supplementation (B; control diet + 1% BA top-dressed). Feed intake was restricted to 3.6% of BW and the ration divided into 3 equally sized meals offered at 8-h intervals. Blood pH (7.465 and 7.486 +/- 0.004) and urinary pH (4.99 and 7.01 +/- 0.09) were less (P = 0.03 and P < 0.01) in B compared with CON. The arterial concentration, net portal flux, and net hepatic uptake of BA increased (P < 0.01) in B compared with CON. The net portal flux of BA increased (P < 0.01) after feeding with B, but remained positive (P < 0.01) at all sampling times (n = 8). Recovery of dietary BA as increased net portal flux and hepatic uptake of BA was 87 +/- 5% and 89 +/- 15%, respectively. The recovery of dietary BA as urinary excretion of BA and HA was 0.08 +/- 0.02% and 85 +/- 7%, respectively. It is concluded that the small impact of BA supplementation on systemic acid-base status was caused by a protracted BA absorption and efficient hepatic extraction and glycine conjugation in combination with efficient renal clearance of HA. Together, these physiological mechanisms prevented major BA and HA accumulation in body fluids.

Fluxo portal e visceral líquido de metabólitos em ovinos alimentados com feno de capim-arroz cortado com diferentes idades de rebrota

Foram conduzidos dois ensaios para medir os fluxos portal e visceral total de metabólitos em ovinos (peso vivo (PV) médio de 35 ± 3 kg) recebendo feno de capim-arroz (Echinochloa sp.) cortado aos 32, 46, 72 ou 90 dias de rebrota. Um dos ensaios foi realizado em quadrado latino 4 × 4 (ensaio 1) para avaliação dos quatro fenos e outro em quadrado latino 3 × 3 (ensaio 2), sem o feno do capim cortado aos 32 dias de rebrota. Os animais foram implantados com cateteres permanentes nas veias mesentérica e hepática. Sangue arterial foi acessado através de cateteres temporários na carótida. O fluxo de sangue portal e visceral foi estimado com base na diluição de paraminohipurato infundido continuamente em uma veia mesentérica. Na refeição prévia às amostragens, o consumo de matéria orgânica (MO) total e digestível não foi afetado, mas o consumo de nitrogênio total e digestível diminuiu linearmente com o aumento da idade de rebrota do capim-arroz em ambos os ensaios. Os fluxos de sangue portal e visceral, o fluxo visceral líquido de glicose, uréia e aminoácidos e o fluxo portal líquido de glicose e uréia não foram afetados pela idade de rebrota da forrageira. Os fluxos portais de aminoácidos e amônia foram maiores nos animais que consumiram o feno de 46 dias e maior quantidade de nitrogênio digestível. A maior parte dos nutrientes absorvidos pelos ovinos consumindo feno de capim-arroz foi metabolizada pelo sistema visceral, de modo que a disponibilidade de aminoácidos e de glicose aos tecidos periféricos representou somente pequena proporção do nitrogênio ou da matéria orgânica ingerida. Em geral, o metabolismo visceral dos animais não foi afetado pela idade de rebrota da forrageira.

Effect of abomasal glucose infusion on splanchnic and whole-body glucose metabolism in periparturient dairy cows

Six periparturient Holstein cows fitted with ruminal cannulas and permanent indwelling catheters in the hepatic portal vein, hepatic vein, mesenteric vein, and an artery were used to study the effects of abomasal glucose infusion on splanchnic and whole-body glucose metabolism. The experimental design was a split plot, with cow as the whole plot, treatment as the whole-plot factor, and days in milk (DIM) as the subplot factor. Cows were assigned to 1 of 2 treatments: the control (no infusion) or infusion (1,500g/d of glucose infused into the abomasum from the day of calving). Cows were sampled at 12 d prepartum and at 4, 15, and 29 DIM. To study portal-drained visceral uptake of arterial glucose, [U-13C]glucose was continuously infused into the jugular vein on sampling days. Postpartum, voluntary dry matter intake and milk yield increased at a lower rate with the infusion compared with the control. The net portal flux of glucose increased with the infusion compared with the control, and 67±5% of the infused glucose was recovered as increased portal flux of glucose. The net hepatic flux of glucose was lower with the infusion compared with the control; however, the net hepatic flux of glucose per kilogram of dry matter intake was not affected by treatment. The arterial concentrations of glucose and insulin decreased and concentrations of nonesterified fatty acids increased from prepartum to 4 DIM with the control, but these effects were not observed with the infusion. The arterial concentration of β-hydroxybutyrate decreased more from prepartum to 4 DIM with the infusion, compared with the control. Uptake of arterial [U-13C]glucose in the portal-drained viscera was affected neither by the infusion nor by the DIM and averaged 2.5±0.2%. The whole-body glucose supply changed to be less dependent on the recycling of lactate (Cori cycle) with the infusion. It was concluded that small intestinal glucose absorption is an efficient source of glucose to the peripheral tissues of dairy cows in very early lactation. At least 67% of the available glucose was recovered in the portal vein without affecting hepatic gluconeogenesis. Infused cows produced less milk and had a lower feed intake, indicating that an improved glucogenic status in very early lactation impaired metabolic adaptations to lactation.

Urea and short-chain fatty acids metabolism in Holstein cows fed a low-nitrogen grass-based diet

Three ruminally cannulated and multicatheterised lactating dairy cows were used to investigate the effect of different supplement strategies to fresh clover grass on urea and short-chain fatty acid (SCFA) metabolism in a zero-grazing experiment with 24-h blood and ruminal samplings. Fresh clover grass was cut every morning and offered from 0800 to 1500 h. Maize silage was fed at 1530 h. The three treatments, arranged in a Latin square, differed by timing of feeding rolled barley and soya-bean hulls relative to fresh clover grass. All diets had the same overall composition. Treatments were soya-bean hulls fed at 0700 h and barley fed at 1530 h (SAM), barley fed at 0700 h and soya-bean hulls fed at 1530 h (BAM), and both soya-bean hulls and barley fed at 1530 h (SBPM). The grass had an unexpectedly low content of crude protein (12.7%) and the cows were severely undersupplied with rumen degradable protein. The treatment effects were numerically small; greater arterial ammonia concentration, net portal flux of ammonia and net hepatic flux of urea during part of the day were observed when no supplementary carbohydrate was fed before grass feeding. A marked diurnal variation in ruminal fermentation was observed and grass feeding increased ruminal concentrations of propionate and butyrate. The net portal fluxes of propionate, butyrate, isovalerate and valerate as well as the net hepatic uptake of propionate, butyrate, valerate and caproate increased after feeding at 0700 h. The hepatic extraction of butyrate showed a relatively large depression with grass feeding with nadir at 1200 to 1330 h. The increased net portal absorption and the decreased hepatic extraction resulted in an approximately six-fold increase in the arterial blood concentration of butyrate. The gut entry rate of urea accounted for 70 ± 10% of the net hepatic production of urea. Saliva contributed to 14% of the total amount of urea recycled to the gut. Urea recycling to the gut was equivalent to 58% of the dietary nitrogen intake. Despite the severe undersupply of rumen degradable protein, the portal-drained viscera did not extract more than 4.3% of the urea supplied with arterial blood. This value is in line with the literature values for cows fed diets only moderately deficient in rumen degradable protein and indicates that cows maximise urea transfer across gut epithelia even when the diet is moderately deficient in rumen degradable protein.

Metabolic Changes and Net Portal Flux in Dairy Cows Fed a Ration Containing Rumen-Protected Fat as Compared to a Control Diet

Feeding rumen-protected fat (RPF) is an alternative to increase energy density of the diet and therefore energy intake in dairy cows. To investigate metabolic and endocrine changes in dairy cows fed either a diet containing RPF (FD) or a control diet with an increased amount of cornstarch (SD), 3 Holstein cows (83±1 d in milk) were fitted with catheters in the portal vein, a mesenteric artery, and 2 mesenteric veins. Cows were fed consecutively SD and FD for 3 wk, respectively. In FD, cornstarch [92 g/kg of dry matter (DM)] was replaced by 50g of RPF/kg of DM (mainly C16:0 and C18:1). Tracer infusions of NaH13CO3 and d-[U-13C6]glucose were performed into a jugular vein to measure rate of appearance and oxidation of glucose. Arterial and portal blood samples were collected to measure concentrations of glucose, lactate, volatile fatty acids, nonesterified fatty acids, β-hydroxybutyrate, triglycerides, AA, insulin, and glucagon. Concomitantly, para-aminohippurate was infused into a mesenteric vein for measurement of portal plasma flow. Although DM intake was slightly lower in FD, protein and energy intakes were unaffected by diets. Milk and lactose yields were higher in FD than SD. Arterial plasma glucose concentration was lower with FD than SD, whereas nonesterified fatty acid and triglyceride concentrations were higher in FD. Glucagon concentration and glucagon-to-insulin ratio were both augmented by FD feeding. When feeding FD, greater milk and lactose yields, but not energy-corrected milk, were associated with elevated lipid status and higher glucagon concentrations but occurred despite lower plasma glucose concentration and were not linked with changes in whole body glucose rate of appearance. This study suggests a glucose-sparing effect allowing an enhanced lactose synthesis when feeding RPF.

Ruminal and Intermediary Metabolism of Propylene Glycol in Lactating Holstein Cows

Four lactating Holstein cows fitted with ruminal cannulas and permanent indwelling catheters in the mesenteric artery, mesenteric vein, hepatic portal vein, and hepatic vein were used in a cross-over design to study the metabolism of propylene glycol (PG). Each cow received 2 treatments: control (no infusion) and infusion of 650g of PG into the rumen at the time of the morning feeding. Propylene glycol was infused on the day of sampling only. Samples of arterial, portal, and hepatic blood as well as ruminal fluid were obtained at 0.5h before feeding and at 0.5, 1.5, 2.5, 3.5, 5, 7, 9, and 11h after feeding. Infusion of PG did not affect ruminal pH or the total concentration of ruminal volatile fatty acids, but did decrease the molar proportion of ruminal acetate. The ruminal concentrations of PG, propanol, and propanal as well as the molar proportion of propionate increased with PG infusion. The plasma concentrations of PG, ethanol, propanol, propanal, glucose, l-lactate, propionate, and insulin increased with PG and the plasma concentrations of acetate and β-hydroxybutyrate decreased. The net portal flux of PG, propanol, and propanal increased with PG. The hepatic uptake of PG was equivalent to 19% of the intraruminal dose. When cows were dosed with PG, the hepatic extraction of PG was between 0 and 10% depending on the plasma concentration of PG, explaining the slow decrease in arterial PG. The increased net hepatic flux of l-lactate with PG could account for the entire hepatic uptake of PG, which suggests that the primary hepatic pathway for PG is oxidation to l-lactate. The hepatic uptake of propanol increased with PG, but no effects of PG on the net hepatic and net splanchnic flux of glucose were observed. Despite no effect of PG on net portal flux and net hepatic flux of propionate, the net splanchnic flux of propionate increased and the data suggest that propionate produced from hepatic metabolism of propanol is partly released to the blood. The data suggest that PG affects metabolism of the cows by 2 modes of action: 1) increased supply of l-lactate and propionate to gluconeogenesis and 2) insulin resistance of peripheral tissues induced by increased concentrations of PG and propanol as well as a decreased ratio of ketogenic to glucogenic metabolites in arterial blood plasma.

The relationships between intake and net portal fluxes of energy metabolites in ruminants: A meta-analysis

In a research programme aiming at characterising the energy value of ruminant diets by the net portal energy fluxes in ruminants, the present work focused on the relationships between intakes of both dry matter (DMI) and digestible organic matter (DOMI) and the portal blood flow and the net portal fluxes of oxygen (O 2), volatile fatty acids, β-hydroxybutyrate, glucose and lactate in sheep and growing cattle. Response equations were generated, expressed as a function of liveweight (LW), using meta-analysis on published that were compiled into the FLORA (FLux of nutrients through the Organs and tissues of Ruminant Animals) database and that investigated changes in intake at constant dietary metabolisable energy (ME) contents within experimental groups. The experimental groups in the selected data set were predominantly adult sheep ( n = 17), with nine experimental groups on growing cattle and only one experimental group on lactating dairy cows. Intake range was larger in sheep than in growing cattle (0–35 g/d/kg LW versus 0–23 g/d/kg LW, respectively), and the types of diets fed also differed, with sheep predominantly being fed forage-rich diets (60% of experimental groups). Blood flow and portal O 2 consumption showed curvilinear relationships; however the response equations generated for nutrients were best described by linear relationships. With the exception of glucose net portal flux, 70–95% of variation was explained by the models generated. The magnitude of the response equations was largely different between species, and this may also include differences in diets and/or physiological state between the datasets. Both DMI and DOMI were good predictors of the influence of a change in intake level on net portal fluxes of energy metabolites. Subsequent work needs to focus on the influence of diet composition ( i.e., dietary ME content).

Metabolism of Silage Alcohols in Lactating Dairy Cows

Dairy cows fed silage are subjected to various alcohols and low molecular weight esters. Four lactating Holstein cows fitted with ruminal cannulas and permanent indwelling catheters in the hepatic portal vein, hepatic vein, mesenteric vein, and mesenteric artery were used to study the absorption of alcohols into portal blood and the metabolism of feed alcohols in the rumen and splanchnic tissues. The cows were allocated to 4 experimental treatments in a Latin square design. All treatments were formulated as total mixed rations with the same overall nutrient composition, differing by the source of corn silage. Treatments were a control silage and 3 qualities of problematic corn silage (silage with Fusarium toxin, Penicillium-infected silage, and silage with a high propanol content). Feeding was followed by a decreasing ruminal pH, as well as decreasing molar proportions of ruminal acetate and isobutyrate. The ruminal concentrations of total VFA, ethanol, propanol, 2-butanol, ethyl acetate, propyl acetate, glucose, and l-lactate, and molar proportions of propionate, butyrate, isovalerate, valerate, and caproate increased after feeding. Treatments affected ruminal concentrations of propanol, propyl acetate, and butyrate and a strong correlation was observed between ruminal propyl acetate and the molar proportion of butyrate (r=−0.79). Arterial concentrations of ethanol, propanol, propanal, acetone (sum of acetone and acetoacetate), 3-hydroxybutyrate, l-lactate, glutamate, and glutamine increased, and the arterial concentration of glucose decreased after feeding, but no effects of treatment were observed for arterial variables. The postprandial increase in arterial ethanol was maintained for 5h. The net portal release of ethanol tended to decrease with the treatment with the lowest ethanol content, and the net splanchnic release of ethanol increased after feeding, but overall, the net splanchnic flux of ethanol was not different from zero, in agreement with the liver being the major organ for alcohol metabolism. The net portal flux and net hepatic flux of propanol were affected by treatment. All dietary ethanol and propanol were accounted for by absorption of the respective alcohol into the portal blood. The hepatic extraction ratios of ethanol and propanol were, on average, 63 to 66%, and no indications of saturation of hepatic alcohol metabolism were observed at any time. We concluded that typical amounts of alcohols in corn silage do not interfere with splanchnic metabolism of any of the measured variables and do not saturate hepatic pathways for alcohol metabolism. However, even low concentrations of alcohols in feed might affect ruminal metabolism and are followed by hours of elevated peripheral blood concentrations of alcohols.

Changes in Net Portal Nutrient Flux in Response to Weaning Transition and Ionophore Supplementation in Dairy Calves

Dairy calf weaning is associated with ketone concentrations that exceed the levels occurring in adults, and weaning represents a potential energy loss that may be mitigated by ionophore supplementation. To assess the effects of weaning and ionophore supplementation on net nutrient flux across portal-drained viscera (PDV) tissues in dairy calves, concentrations of glucose, acetoacetate (ACAC), β-hydroxybutyrate (BHBA), nonesterified fatty acids, volatile fatty acids, lactate, pyruvate, insulin, and glucagon and PDV flux rates were determined in Jersey bull calves (n=19) at 35, 56, 84, and 112 d of age. Calves were randomly assigned at birth to either a commercial pelleted starter without (CON) or with lasalocid (TRT; 83mg/kg of dry matter). Calves were fed only milk replacer from d 3 to 34 (d 3 to 20=454g/d; d 21 to 34=56g/d). After blood sampling on d 35, calves received replacer (d 35 to 41=45g/d; d 42 to 48=22g/d) and had free access to the CON or TRT starter, and from d 49 to 112 they received CON or TRT ad libitum. Catheters were implanted in the portal vein and in the mesenteric vein and artery between d 21 and 28. Blood flow was measured by continuous infusion of p-aminohippurate into the mesenteric vein. Six serial samples were taken at 30-min intervals from the arterial and portal vein catheters simultaneously. Portal blood flow increased with age but did not differ between CON and TRT calves. Glucose was released preweaning and was extracted postweaning by PDV, but was not affected by ionophore. The portal flux of nonesterified fatty acids was not different from zero during any of the 4 sample ages. Fluxes of ACAC and BHBA in CON and TRT calves went from no measurable flux preweaning to a postweaning PDV release that peaked at d 84, but the d-84 release of ACAC and BHBA was lower in TRT calves. The portal flux of volatile fatty acids increased with age, and PDV release of both butyrate and propionate was lower at d 84 in TRT than in CON calves. However, TRT calves had a greater PDV release of lactate on d 84, partially compensating for the lower release of propionate. Glucagon was greater in CON than in TRT calves at d 84 and could be a response to the elevated ketogenesis observed in CON calves during this period. Changes in the metabolic profile and nutrient flux of transition calves were demonstrated in response to weaning and ionophore supplementation. Inclusion of an ionophore appeared to moderate alimentary output at a postweaning period (d 84) at which ketone concentrations have the potential to exceed the whole animal capacity for utilization.

Physiology, regulation and multifunctional activity of the gut wall: a rationale for multicompartmental modelling

A rationale is given for a modelling approach to identify the mechanisms involved in the functioning and metabolic activity of tissues in the wall of the gastrointestinal tract. Maintenance and productive functions are discussed and related to the distinct compartments of the gastrointestinal tract and the metabolic costs involved. Functions identified are: tissue turnover; tissue proliferation; ion transport; nutrient transport; secretions of digestive enzymes, mucus and immunoglobulins; production of immune cells. The major nutrients involved include glucose, amino acids and volatile fatty acids. In vivo measurements of net portal fluxes of these nutrients in pigs and ruminants are evaluated to illustrate the complexity of physiology and metabolic activity of the gastrointestinal tract. Experimental evidence indicates that high, but variable and specific, nutrient costs are involved in the functioning of the gastrointestinal tract.

Fontes de carboidratos e ionóforo em dietas contendo óleo vegetal para ovinos: digestibilidade, balanço de nitrogênio e fluxo portal de nutrientes

Os objetivos neste trabalho foram avaliar a utilização de duas fontes de carboidratos (casca de soja e milho), com a utilização ou não de monensina em dietas com alta densidade lipídica, e seus efeitos sobre a digestibilidade dos nutrientes, o balanço de nitrogênio e o fluxo portal de nutrientes em ovinos. Adotou-se o método de coleta total de fezes e urina para determinação da digestibilidade e do balanço de nitrogênio. O fluxo líquido de nutrientes foi calculado pelo princípio de Fick. Foram utilizados quatro ovinos (54 kg de PV) da raça Corriedale com três cateteres implantados (veia e artéria mesentérica e veia porta). A ingestão, a excreção fecal, a digestão e a digestibilidade de MS, MO e EE não foram influenciadas pelos tratamentos. A ingestão, a digestão e a digestibilidade da FDN foram maiores para as dietas com casca de soja (757,0; 531,1 g/dia e 70,2%) que para aquelas com milho (392,3; 199,9 g/dia e 51,0%), enquanto a dos carboidratos não-fibrosos (CNF), foram maiores para as dietas com milho (474,6, 416,8 g/dia e 87,8%) que para aquelas com casca de soja (148,0; 97,8 g/dia e 66,1%). A concentração de energia expressa como NDT foi maior nas dietas com milho (80,2%) que naquelas com casca de soja (76,7%). Não houve efeito da utilização da monensina nos parâmetros de digestibilidade e balanço de nitrogênio. A excreção fecal da proteína foi menor e a digestibilidade maior para as dietas com milho. A concentração portal e arterial de nitrogênio alfa amino (N alfa-amino) foi menor para as dietas com monensina (3,161 e 2,922 e 3,530 e 3,218 mM, respectivamente). A concentração portal (0,419 vs 0,516 mM), a diferença venosa-arterial (0,230 vs 0,317 mM) e o fluxo portal de amônia (26,119 vs 37,041 mM/h) foram menores para as dietas com milho.

What is the True Supply of Amino Acids for a Dairy Cow?

Improving the prediction of milk protein yield relies on knowledge of both protein supply and requirement. Definition of protein/amino acid supply in ruminants is a challenging task, due to feedstuff variety and variability and to the remodeling of nutrient intake by the rumen microflora. The questions arise, therefore, how and where should we measure the real supply of AA in the dairy cow? This review will follow the downstream flow of AA from duodenum to peripheral tissue delivery, with a glance at the efficiency of transfer into milk protein. Duodenal AA flow comprises rumen undegrad-able feed, microbial protein, and endogenous secretions. Most attention has been directed toward definition of the first two contributions but the latter fraction can represent as much as 20% of duodenal flow. More information is needed on what factors affect its magnitude and overall impact. Once digested, AA are absorbed into the portal vein. The ratio of portal absorption to small intestinal apparent digestion varies among essential AA, from 0.43 (threonine) to 0.76 (phenylalanine), due to the contributions of preduodenal endogenous secretions to the digestive flow, non-reabsorption of endogenous secretions and gut oxidation of AA. Few data are available on these phenomena in dairy cows but the evidence indicates that they alter the profile of AA available for anabolic purposes. Recent comparisons of estimated duodenal flux and measured portal flux have prompted a revisit of the NRC (2001)approach to estimate AA flows at the duodenum. Changes to the model are proposed that yield predictions that better fit the current knowledge of AA metabolism across the gut. After absorption, AA flow first to the liver where substantial and differential net removal occurs, varying from zero for the branched-chain AA to 50% of portal absorption for phenylalanine. This process alters the pattern of net supply to the mammary gland. Overall, intermediary metabolism of AA between the duodenum and the mammary gland biologically explains the decreased efficiency of the transfer of absorbed AA into milk protein as maximal yield is approached. Therefore, variable, rather than fixed, factors for transfer efficiencies must be incorporated into future predictive models.

Effects of adding valerate, caproate, and heptanoate to ruminal buffers on splanchnic metabolism in steers under washed-rumen conditions1

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.

Effect of increasing ruminal butyrate absorption on splanchnic metabolism of volatile fatty acids absorbed from the washed reticulorumen of steers1

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.

Comparison of predictions of digestible supply and measurements of net portal fluxes of essential amino acids in lactating dairy cows

Comparison of predictions of digestible supply and measurements of net portal fluxes of essential amino acids in lactating dairy cows

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.

Fontes de proteína, ingestão de alimentos e fluxo esplâncnico de nutrientes em ovinos

O objetivo deste trabalho foi avaliar a ingestão de nutrientes e o fluxo esplâncnico de glicose, nitrogênio alfa-amino, amônia e uréia em ovinos alimentados com diferentes fontes de proteína. Foram utilizados três ovinos pesando, em média, 50 kg, implantados com quatro catéteres, sendo um na veia mesentérica, um na artéria mesentérica, um na veia porta e um na veia hepática. O delineamento utilizado foi o quadrado latino 3x3. Os tratamentos consistiram na utilização de três diferentes fontes de proteína: o farelo de soja, a farinha de penas e o farelo de glúten de milho. Não houve efeito dos tratamentos na ingestão de matéria seca (MS), matéria orgânica (MO), proteína bruta (PB) e fibra em detergente neutro (FDN). As concentrações portal, hepática e arterial de glicose, N alfa-amino, amônia e uréia não diferiram com a utilização de diferentes fontes de proteína. Somente o fluxo portal de glicose aumentou e o esplâncnico de N alfa-amino diminuiu com a utilização do farelo de glúten de milho como fonte de proteína. As taxas de extração hepática dos nutrientes foram de -10,51; 4,07; 47,69 e -4,81%, para a glicose, N alfa-amino, amônia e uréia, respectivamente, e não diferiram entre os tratamentos.

Review article: intra-arterial treatments in patients with hepatocellular carcinoma.

In Western countries, most of the patients with hepatocellular carcinoma (HCC) are not eligible for curative treatments. Intra-arterial treatments have a palliative effect that could lead to extensive tumour necrosis and therefore have been widely used. Arterial embolization, Lipiodol-targeted chemoembolization and intra-arterial injection of radioactive iodine mixed with Lipiodol provided promising results in terms of tumoral growth, but were also responsible for severe side-effects, particularly in patients with cirrhosis. Their influence on survival has been assessed by randomized trials with contradictory results. In patients with advanced cases, embolization alone has limited or no influence on survival, and chemoembolization provided a beneficial effect mostly in patients with viral liver diseases, without liver failure, and with an adequate portal flux. The effects of radioactive iodine either in the treatment of advanced cases or the prevention of recurrences after a curative treatment must be investigated further.

Potential nutritional assessment of dwarf elephant grass ( Pennisetum purpureum Schum. cv. Mott) by chemical composition, digestion and net portal flux of oxygen in cattle

This study was conducted to evaluate changes in chemical composition of dwarf elephant grass hay cut at 30, 40, 50 and 60 days of growth, and its effect on apparent digestibility and particle-phase passage through the gastrointestinal tract (Experiment 1) and on oxygen utilization by the portal-drained viscera of cattle (Experiment 2). The experiments were carried out using four Holstein steers in each experiment (mean live weight of 129±17 kg and 139±3 kg in the Experiments 1 and 2, respectively) in a 4×4 Latin square experimental design. The animals of Experiment 2 were implanted surgically with permanent indwelling catheters in portal and mesenteric veins. The experimental diets were chopped hay (10–15 cm length particles) fed two times a day in amounts restricted at 2% of the animal live weight. The content of neutral detergent fiber, acid detergent fiber, acid detergent lignin, titratable cross-ester links and acid detergent insoluble nitrogen increased, but the content of total, non-protein and soluble nitrogen decreased with plant growth. The apparent digestibility of different compounds of hay was not affected ( P>0.05), but retention times in the reticulum-rumen ( P<0.01) and in the caecum-proximal colon ( P<0.05) decreased linearly and, the passage rate of particles through reticulo-rumen ( P<0.01) and through caecum-proximal colon ( P<0.05) increased linearly with plant growth. In addition, oxygen utilization and estimated heat production by the portal-drained viscera, as a proportion on digestible energy intake, increased linearly with dwarf elephant grass growth ( P<0.01 and P<0.05, respectively). In conclusion, if the nutritional value of forage decrease with plant maturity, the results of present study suggest that, at restricted level of intake and within of vegetative stage of dwarf elephant grass this is so due, at least partially, an increase of metabolizable energy use by the gastrointestinal tract. Therefore, energy availability for productive purposes, such as live weight gain or milk synthesis decrease.

Effect of dietary protein degradability on net fluxes of free and peptide amino acids across the portal-drained viscera of steers

Four steers, average body weight 260±15 kg, fitted with portal catheters were used in a 4×4 Latin Square design to evaluate the influence of dietary protein degradability in the rumen on peptide and amino acid fluxes across the gastrointestinal tract. Dietary protein degradability was regulated by using different protein sources and the diets were calculated to contain 130 g CP/kg and 9·62 MJ ME per kg DM. Plasma concentrations of amino acids were analysed before and after acid hydrolysis of samples first subjected to chemical deproteinization and physical ultrafiltration, and peptide amino acids (PAA) were calculated as the difference between total and free amino acids (FAA). Portal blood flow and arterial concentrations of FAA and PAA were not affected by protein degradability or by diet. Venoarterial concentration difference and net portal flux of FAA tended to increase (P &lt; 0·10) with increase of degradable protein intake. Portal-arterial concentration difference (P &lt; 0·05) and net portal flux (P &lt; 0·10) of PAA increased linearly as dietary protein degradability increased. The proportion of PAA in total amino acid (FAA+PAA) net flux was not modified by dietary protein degradability or by diet, and the mean value as a proportion was 0·32. The major PAA absorbed were glutamate, leucine, aspartate and lysine for all diets, accounting in total for 0·50 of PAA flux. The results demonstrate that PAA may contribute significantly to AA flux across the portal-drained viscera (PDV) of steers, and both FAA and PAA net fluxes can be affected by degradable protein intake.