Natural sodium sesquicarbonate fed for an entire lactation: influence on performance and acid-base status of dairy cows.

Forty-eight multiparous Holstein cows were blocked according to month of parturition, age, and previous milk yield and arranged in a randomized complete block design to evaluate the effect of a naturally occurring sodium sesquicarbonate on DMI, milk yield, milk composition, milk value, and systemic acid-base status. Cows were assigned at parturition to diets containing sorghum silage, alfalfa hay, concentrate, and 0 or 1% naturally occurring sodium sesquicarbonate (DM basis); cows were fed these diets for 308 d postpartum. Blood was collected every 4 wk via jugular venipuncture for analysis of pH, HCO3, partial pressure of O2, and partial pressure of CO2. Sesquicarbonate exhibited alkalogenic properties by increasing blood HCO3, partial pressure of CO2, and total CO2 for the 308-d lactation. Buffer tended to increase DMI and increased milk protein throughout lactation. During 0 to 56 d postpartum, sodium sesquicarbonate did not affect milk yield or composition. In midlactation (56 to 252 d postpartum), buffer increased milk protein content only. During 252 to 308 d postpartum, milk fat and protein contents increased with buffer supplementation. Hence, the value of milk yielded daily was similar for all cows. Effects of dietary buffer on all variables were more pronounced during late lactation.

Influence of dietary buffer value index on the ruminal milieu of lactating dairy cows fed sorghum silage and grain.

The objective of this study was to evaluate the influence of dietary buffer value index on ruminal fluid pH, buffering capacity, and buffer value index in lactating cows. Three Holstein cows averaging 18 +/- 10 DIM were used in a 3 x 3 Latin square with 3-wk experimental periods. Diets contained grain:sorghum silage DM ratios of 50:50, 60:40, and 70:30. By analysis, these diets had buffer value indexes of -74, -41, and -7. The analyzed dietary buffer value index of the total diets was higher than the index that was calculated from the buffer value index of individual ingredients. Although milk fat content tended to be highest for milk from cows fed the 50:50 concentrate to forage diet and although milk protein production was highest for cows fed the 70:30 concentrate to forage diet, milk yield, 4% FCM, milk fat yield, protein content, and milk fat content were not significantly affected by dietary buffer value index. Dietary buffer equivalents were calculated to be 11% of total buffering equivalents available to the cow, and dietary acid equivalents were 15% of total acid production in the rumen. Compared with ruminal acid production and salivary buffering in the rumen, dietary acid and dietary buffer contributions to the acid-base balance of the cow are minor quantitatively. Ruminal fluid pH, hydrogen ion concentration, buffer value index, buffering capacity, and total VFA were not affected significantly by dietary buffer value index. Hence, dietary acid-base status alone is inadequate as a predictor of the need for buffers in the diet of lactating cows.

Effects of inert fat on energy balance, plasma concentrations of hormones, and reproduction in dairy cows.

The objective was to determine the effects of dietary inert fat on estimated energy balance, hormones in plasma, and reproduction during early lactation. From wk 0 to 12 postpartum, 14 pluriparous Holstein cows were fed individually a TMR, and blood samples were taken twice weekly for quantification of IGF-I, progesterone, and cholesterol. During wk 5 to 12, one-half of the cows remained on the TMR, and the other half were fed the TMR containing inert fat at 1.8% of dietary DM. Estrous behavior was monitored twice daily, and body condition scores were recorded every 4 wk. Cows fed inert fat between wk 5 and 12 postpartum had similar concentrations of IGF-I in plasma but greater luteal phase progesterone secretions than cows fed the control diet. Total cholesterol in plasma also was greater in cows fed inert fat than in cows fed the control diet. Intervals to first, second, and third ovulation or estrus did not differ among cows fed control or inert fat diets. Body condition scores, daily DMI, and milk production were not affected by dietary inert fat. Inert fat fed to cows between wk 5 and 12 postpartum did not affect ovulatory activity but may enhance luteal activity.

Controlled ruminal infusion of sodium bicarbonate. 3. Influence of infusion dose on systemic acid-base status, minerals, and ruminal milieu.

Four ruminally cannulated, lactating Holstein cows were assigned to a 4 x 4 Latin square to monitor effects of intraruminal NaHCO3 infusion on temporal changes in ruminal and systemic acid-base status and mineral metabolism. Twice daily from 2 to 4 h postfeeding, cows were infused with 0, 110, 220, or 330 g of NaHCO3 dissolved in 3.8 L of water. All cows had access to their TMR of sorghum silage and concentrate (35: 65, DM basis) for 2 h twice daily. Ruminal fluid, blood, and urine were collected at feeding and every 30 min postfeeding for 12 h on the last day of each 14-d period. Total urine volume also was measured during this interval. Infusion of buffer increased ruminal fluid buffering capacity transiently at 4.5 h postfeeding but otherwise did not markedly affect ruminal fluid acid-base status. Systemic acid-base status was unaffected by the buffer primarily because renal excretion of base successfully reduced systemic base load. Urine volume increased in response to NaHCO3 infusion. Buffer infusion increased urinary excretion of Na, Mg, and K but decreased Ca excretion for 12 h postfeeding; Cl excretion was not affected. Buffer infusion tended to increase total VFA in ruminal fluid. Our data indicate that homeostatic mechanisms can eliminate exogenous base via the kidneys; hence, acid-base status was not perturbed by infusion of NaHCO3. The increased excretion of Mg and K with buffer infusion indicates that the dietary requirements for these minerals may be increased by NaHCO3. Although loss of Ca through the urine was reduced by buffer infusion, this reduction may indicate reduced availability of Ca to the cow. The diuresis accompanying large doses of NaHCO3 may increase dietary requirements for some minerals.

Influence of dietary fiber and buffer value index on the ruminal milieu of lactating dairy cows.

The influence of dietary buffer value index and dietary ADF content on ruminal fluid pH, buffering capacity, and buffer value index was measured. Four lactating Holstein cows (two primiparous) averaging 72 +/- 60 DIM were used in a 4 x 4 Latin square with 3-wk experimental periods. Treatments were a 2 x 2 factorial arrangement of TMR containing two ADF concentrations (16 and 21% of DM) and two buffer value indexes (calculated from analysis of individual dietary ingredients to be -200 and 0). Milk fat content and milk fat yield tended to be increased by high ADF, and protein yield tended to increase with low buffer value index and low ADF. Although the high ADF diets increased ruminal fluid pH, they reduced buffering capacity; because the magnitude of the pH increase was greater than the reduction in buffering capacity, ruminal fluid buffer value index was increased by added ADF. The high buffer value index diets reduced ruminal fluid pH and increased ruminal fluid buffering capacity; effects on pH outweighed those on buffering capacity so that the ruminal fluid index paradoxically decreased as the dietary index increased. Ruminal fluid acetate increased and propionate decreased as ADF increased. We conclude that ruminal fluid buffer value index increases with dietary ADF, likely because of reduced ruminal concentrations of fermentation acids. Because diets with the highest index produced the lowest ruminal indexes, dietary buffer value index must be studied further before it can be included in any model purporting to predict the need for supplemental dietary buffers.

Sodium bicarbonate or multielement buffer via diet or rumen: effects on performance and acid-base status of lactating cows.

Our objective was to compare the influence of dietary NaHCO3 and a multielement buffer on ruminal acid-base status and lactation performance of dairy cows. Five ruminally fistulated, primiparous and multiparous lactating Holstein cows averaging 123 +/- 21 d postpartum were assigned randomly to treatments in a 5 x 5 Latin square with 3-wk experimental periods. Treatments were a basal diet without supplemental buffers, with 1.5% NaHCO3 or 1.5% multielement buffer, or with NaHCO3 or multielement buffer solutions poured into the rumen via cannula at 2 h postfeeding. Addition of either buffer to the diet reduced ruminal fluid hydrogen ion concentration from 0 to 6 h postfeeding; only NaHCO3 reduced ruminal fluid acidity when dosed via the cannula. Addition of buffers via ruminal cannula appeared to retard the reduction in ruminal fluid acidity that normally occurs from 6 to 12 h postfeeding; this may have been related to a feedback mechanism inhibiting salivary buffer secretion. Buffering capacity of ruminal fluid tended to increase with buffer addition; the increase was greatest during infusion of NaHCO3. The ruminal fluid buffer value index increased by 4 units for control cows from early (0 to 6 h) to late (6 to 12) postfeeding; smaller increases were noted for addition of multielement buffer. This index was not different for NaHCO3 during these two intervals. Milk yield and DMI were not affected by buffer addition. Although milk fat content tended to be higher with the multielement buffer than with NaHCO3, it was not accompanied by the expected alterations in ruminal acid-base status. Therefore, this increase may be related to systemic effects of specific minerals in the multielement buffer rather than to a more stable ruminal environment. Based on the ruminal fluid buffer value index, NaHCO3 tended to maintain the most stable ruminal acid-base status.

Influence of dietary cation-anion balance during the dry period on the occurrence of parturient paresis in cows fed excess calcium.

Our objective was to evaluate the effectiveness of a low dietary cation-anion balance (DCAB) in preventing milk fever and udder edema in dry cows consuming a high-Ca diet and to evaluate the effect of this diet on calves delivered by these cows. Seventy primiparous or multiparous cows and 50 pregnant heifers were offered alfalfa hay-based diets beginning 4 wk before their projected calving date. Diets contained 1.6% Ca and a DCAB of -3 or +9 mEq/100 g of diet DM. Blood and urine samples were collected weekly from 3 wk prepartum until 3 wk postpartum. Blood samples were collected from calves at parturition and weekly thereafter for 3 wk. Feeding a low vs high DCAB in a high-Ca diet for 3 wk prepartum did not reduce the incidence of milk fever; this lack of response may have been attributable to the relatively low DCAB of each diet and the small difference in DCAB between the two diets. Udder edema seemed to regress more rapidly postpartum for cows that had consumed the low DCAB during the dry period. Test diets fed to prepartum cows did not affect systemic acid-base status or plasma mineral content of their calves, although plasma Ca was somewhat lower for calves from cows consuming a low DCAB and was higher for calves from primigravid cows. Correlations of plasma mineral concentration of the cows with those of their calves were highest for plasma Ca (r = .75; P less than .001). We conclude that the prophylactic effects on the occurrence of milk fever of feeding a low DCAB during the dry period may be absent when diets contain greater than 1.6% Ca and DCAB is greater than or equal to -3. The cation-anion balance of the diet consumed by dry cows did not affect the acid-based status or plasma mineral content of their calves.

A buffer value index to evaluate effects of buffers on ruminal milieu in cows fed high or low concentrate, silage, or hay diets.

Our objective was to develop a buffer value index that would incorporate alterations in both ruminal fluid pH and buffering capacity as indicators of the influence of dietary buffering and alkalinizing agents on ruminal acid-base status. This index was evaluated using ruminal fluid from four lactating Holstein cows fed either sorghum silage or alfalfa hay in high or low concentrate diets. Ruminal fluid was incubated in vitro for 1, 2, 3, 4, or 5 h with no buffer or with 7.1 g of either NaHCO3, sodium sesquicarbonate, or a multielement buffer added per liter of ruminal fluid. Ruminal fluid pH was lower for diets based on high concentrate or alfalfa; buffering capacity between pH 5 and 7 was greater for high concentrate diets but was not affected by forage type. Ruminal fluid pH was higher for sesquicarbonate than for NaHCO3, the multielement buffer, or the control; however, ruminal fluid H+ concentration was similar between sesquicarbonate and NaHCO3, and both were lower than for the multielement buffer. Hydrogen ion concentration for the multielement buffer was lower than for the control. Buffering capacity was highest for NaHCO3, followed by sesquicarbonate, the multielement buffer, and the control. The buffer value index, which accounted for alterations in both H+ concentration and buffering capacity, was highest for NaCHO3, followed by sesquicarbonate, the multielement buffer, and the control. The poor response to the multielement buffer may be attributable to our relatively short incubation interval (less than 5 h). Dietary buffers increase both ruminal fluid pH and buffering capacity; both of these responses are beneficial.(ABSTRACT TRUNCATED AT 250 WORDS)

Controlled ruminal infusion of sodium bicarbonate. 2. Effects of dietary and infused buffer on ruminal milieu.

Four ruminally cannulated, lactating Holstein cows were assigned to a 4 X 4 Latin square to monitor the effects of NaHCO3 infusion on ruminal environment of cows receiving dietary sodium bicarbonate. Sodium bicarbonate (110 g) was mixed with 3.8 L of water and infused at a constant rate into the rumen from 0 to 2, 2 to 4, or 4 to 6 h postfeeding twice daily. All cows were fed sorghum silage and concentrate in a 35:65 DM ratio for 45 min twice daily. Ruminal fluid was collected at feeding and every 30 min postfeeding for 8 h on the last day of each 1-wk experimental period. Dry matter intake was not affected by NaHCO3 infusion. Yields of milk and its components were reduced with 4- to 6-h NaHCO3 infusion. At certain isolated times, especially during infusion, NaHCO3 infusion increased ruminal fluid buffer. Concentrations of ruminal fluid total VFA were not affected by NaHCO3 infusions, whereas acetate to propionate ratio tended to be reduced. Ruminal liquid volume tended to be increased by 0- to 2-h NaHCO3 infusion, and ruminal outflow rate tended to be reduced by the 2- to 4-h infusion. Intraruminal infusion of NaHCO3 into cows receiving supplemental dietary NaHCO3 altered ruminal acid-base status as typically reported for those receiving dietary NaHCO3; however, these alterations were not accompanied by shifts in ruminal VFA patterns or in milk composition that normally result from such feeding regimens. The effects of NaHCO3 infused directly into the rumen may be different from those of dietary NaHCO3 and are possibly related to the different time of entry into the rumen relative to feeding.

Influence of dietary sodium bicarbonate on the potassium metabolism of growing dairy calves.

We evaluated the influence of supplemental dietary NaHCO3 on K metabolism of young dairy calves. Thirty-two Holstein and Jersey male and female calves were blocked at 56 to 70 d after birth according to breed, sex, and age and assigned randomly to a 2 x 2 factorial arrangement of dietary treatments for 8 wk: .4% K with 0% NaHCO3, .4% K with 2% NaHCO3, .6% K with 0% NaHCO3, and .6% K with 2% NaHCO3. Feed intake was not affected by dietary KCl or NaHCO3 supplementation, but average daily gain increased with increased K and tended to be reduced by dietary NaHCO3. Plasma K was elevated by increased dietary K but generally was unaffected by NaHCO3. Urinary Ca excretion appeared to be reduced by NaHCO3; urine pH increased with supplemental NaHCO3. Results indicate 1) the K requirement of the growing calf is between .40 and .55% of diet DM, 2) because urinary K excretion was elevated by dietary NaHCO3, the K requirement may be increased when the diet is supplemented with NaHCO3, and 3) average daily gain and plasma K are sensitive indicators of dietary K in the growing calf.

Controlled ruminal infusion of sodium bicarbonate. 1. Influence of postfeeding infusion interval on ruminal milieu.

Four ruminally cannulated, lactating Holstein cows were assigned to a 4 x 4 Latin square to monitor the effects of intraruminal NaHCO3 infusion on changes in the rumen environment. Sodium bicarbonate (110 g), dissolved in 3.8 L of water, was infused twice daily at a constant rate for 2 h starting at 0, 2, or 4 h postfeeding. All cows had access to their diet containing sorghum silage and concentrate in a 35:65 ration (DM basis) for 45 min twice daily. Ruminal fluid was collected at feeding and every 30 min postfeeding for 12 h on the last day of each 7-d period. Dry matter intake was lower for buffer infusion at 2 to 4 h than for water-infused control but was not affected by the other NaHCO3 infusions. Although total milk yield was not affected, milk fat percentage and fat yield tended to be lower for the NaHCO3 treatments. Compared with the water infusion, the NaHCO3 infusion from 2 to 4 h postfeeding most effectively prevented the postfeeding increase in ruminal free proton concentration. Additionally, volume of ruminal liquid was increased for the NaHCO3 infusions from 0 to 2 h and 4 to 6 h; ruminal liquid turnover time was increased for the NaHCO3 infusion at 4 to 6 h, but ruminal kinetics otherwise were not affected by NaHCO3. Although infusion of NaHCO3 from 2 to 4 h prevented severe alterations in ruminal acid-base status, it did not increase total VFA concentration or the acetate:propionate ratio. Although total VFA concentrations were not affected by NaHCO3 infusion, acetate:propionate ratio was higher for the NaHCO3 infusion from 0 to 2 h than for the control. Based upon alterations in ruminal acid-base status, exogenous buffer ideally should be provided to the rumen from 2 to 4 h postfeeding; however, our results indicate that the effectiveness of this regimen might be improved if buffer is combined with a rapidly released or unprotected dietary buffer.

Role of sulfur and chloride in the dietary cation-anion balance equation for lactating dairy cattle.

Ten Holstein cows averaging 120 d in lactation were arranged in replicated 5 x 5 Latin squares with 3-wk periods to evaluate the role of sulfur (S) in the dietary cation-anion balance equation. Diets were based on corn silage in Exp. 1 and sorghum silage in Exp. 2. Supplemental S and chloride (Cl) from the double sulfate of potassium and magnesium and CaCl2 were used to manipulate dietary cation-anion balance from 0 to +30 meq when expressed as meq [(Na + K)-(Cl + S)]/100 g diet DM and from +19 to +49 meq when expressed as meq [(Na + K)-Cl]/100 g diet DM. Blood pH was not affected by cation-anion balance, although both S and Cl supplementation tended to lower pH. Blood HCO3- and urine pH decreased and plasma calcium (Ca) and urinary Ca excretion increased as anion was added to the diet. Milk fat production tended to be increased by the low S supplementation. Dietary Cl and S had similar effects on acid-base status. Therefore, we suggest that S be included with Cl in the dietary cation-anion balance equation for lactating dairy cows as follows: meq [(Na + K)-(Cl + S)]/100 g diet DM. Although response of acid-base status to S and Cl was similar, as more data comparing the acidogenicity of S vs Cl become available, it may be necessary to include a modifying coefficient for S in the equation to adjust for differences between S and Cl in acid-generating potential. This coefficient may be further dependent on the dietary source of S.

Influence of sodium chloride or potassium chloride on systemic acid-base status, milk yield, and mineral metabolism in lactating dairy cows.

Our objective was to evaluate the response of lactating dairy cows to dietary Na, K, and Cl while holding cation-anion balance constant. Fifteen lactating Holstein cows, blocked according to age and previous milk yield, were assigned randomly to replicated 3 x 3 Latin squares with experimental periods of 3 wk. Diets contained sorghum silage and concentrate in a 40:60 ratio (DM basis) and were formulated to provide +32 meq of [(Na + K) - Cl]/100 g diet DM via one of three variations: 1) basal concentrations of dietary Na, K, and Cl, 2) basal diet with addition of 20 meq of Na and 20 meq of Cl/100 g in the form of 1.17% added NaCl, or 3) basal diet with the addition of 20 meq of K and 20 meq of Cl/100 g in the form of 1.56% added KCl. Free proton concentration in blood was increased by addition of NaCl and KCl; however, this increase did not appear to be physiologically significant, and no other measures of acid-base status were significantly affected. Plasma K was higher and plasma Mg was lower for the diets with supplemental NaCl or KCl than for basal diet. Urine mineral excretion reflected dietary mineral concentration, except Ca and Mg excretion rates were reduced by feeding the KCl diet. Milk yield reflected DM intake, which was lowest with supplemental NaCl. Results of this study indicate that, at a dietary cation-anion balance of +32 meq/100 g of diet DM, the balance of Na and K to Cl in the diet is a more important determinant of dietary impact on systemic acid-base status than actual dietary concentrations of Na, K, and Cl.