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Highlights • Supplementation of branched-chain VFA with or without rumen protected folic acid was evaluated. • Milk yield, true protein content and yield as well as feed efficiency increased with both supplements. • Ruminal fermentation characteristics, cellulolytic bacteria and enzyme activities were improved. • Serum GHRH, GH, IGF-1 and total protein increased with both supplements. • There was no interaction detected between branched-chain VFA and rumen protected folic acid. Abstract This study evaluated the effects of branched-chain volatile fatty acids (BCVFA) and rumen protected folic acid (RPFA) supplementation on lactation performance, ruminal fermentation, nutrient digestion and blood metabolites in dairy cows. Fifty-six multiparous Chinese Holstein cows (3.2 ± 1.1 of parity, 631 ± 16.4 kg of body weight [BW], 65 ± 2.6 days in milk [DIM] and 30.2 ± 2.1 kg of milk yield per day, mean ± SD) were blocked by lactation number, milk yield per day and DIM and were arranged into one of four groups in a randomized block design with a 2 × 2 factorial arrangement. Supplemental BCVFA (0 g/d [BCVFA-] or 80 g/d [BCVFA+]) and RPFA (0 mg/d [RPFA-] or 128 mg/d [RPFA+]) were hand-mixed into the top one-third of total mixed ration. Dietary concentrate to forage ratio was 50:50 based on a dry matter (DM) basis. Experimental periods comprised 105 days with 15 d of adaptation followed by 90 d of data collection. DM intake was increased with BCVFA supplementation, but was unaffected by RPFA. The BW changes were similar among treatments. Yields of milk, milk fat and lactose were increased, and milk true protein yield tended to increase with BCVFA or RPFA supplementation. Milk fat percentage was increased with BCVFA supplementation, but was unaffected by RPFA. Percentage of milk true protein was increased, lactose was unaltered and feed conversion ratio was decreased with BCVFA or RPFA supplementation. Ruminal pH and ammonia N concentration were decreased, but total volatile fatty acids concentration was increased with BCVFA or RPFA supplementation. Molar proportion of acetate was increased and propionate was decreased, resulting in an increased ratio of acetate to propionate with BCVFA supplementation. Acetate and propionate molar proportion and the ratio of acetate to propionate were not affected by RPFA. Digestibilities of DM, organic matter, crude protein, non-fiber carbohydrates, neutral detergent fibre and acid detergent fibre were increased with BCVFA or RPFA supplementation. Similarly, activities of caboxymethyl-cellulase, cellobiase, xylanase, pectinase, α-amylase and protease and abundance of R. albus, R. flavefaciens , F. succinogenes , B. fibrisolvens and P. ruminicola were increased. However, R. amylophilus abundance was not affected by BCVFA and increased with RPFA supplementation. Serum concentrations of glucose and non-esterified fatty acids (NEFA) were unaltered and total protein was increased with BCVFA or RPFA supplementation. Serum acetoacetate (ACAC) and BHBA were increased by BCVFA, but were decreased by RPFA. Supplementation of BCVFA or RPFA increased serum growth hormone releasing hormone, growth hormone and insulin-like growth factor-1. These results indicated that lactation performance, ruminal fermentation, nutrient digestion and hormone secretion improved due to the stimulated ruminal bacteria growth and enzyme activity with BCVFA or RPFA supplementation, but no BCVFA × RPFA interaction was detected during the trial. [ABSTRACT FROM AUTHOR]

Highlights • Ruminal fermentation was improved with coated folic acid (CFA) supplementation, but depressed by soybean oil (SO) supplementation. • Microbial cellulolytic enzyme activities and ruminal NDF degradability increased with supplementary CFA, but decreased with SO supplementation. • The growth of cellulolytic bacteria was promoted by supplementary CFA, but depressed by SO supplementation. • Urinary excretion of purine derivatives increased with CFA, but decreased with SO supplementation. • CFA + SO interacted: CFA reduced the negative effects of SO on ruminal fermentation. Abstract This study was conducted to evaluate the effects of dietary soybean oil (SO) and coated folic acid (CFA) supplementation on ruminal digestion kinetics, fermentation, microbial enzyme activity and bacterial abundance in Jinnan beef steers. Eight ruminally cannulated Jinnan beef steers, averaging 15 months of age and 415 ± 5.6 kg of body weight (BW; Mean ± S.E.), were used in a replicated 4 × 4 Latin square design by a 2 × 2 factorial arrangement. Two levels of CFA (0 mg [FA-] or 115 mg per kg dietary DM [FA + ]) were supplemented to the diets without or with SO supplementation (0 g [SO−] or 30 g per kg dietary dry matter [DM] [SO + ]). Steers were fed a total mixed ration with ensiled corn forage to concentrate ratio of 50:50 on a DM basis. The SO × CFA interaction was observed for ruminal pH, total VFA concentration, molar proportions of acetate and propionate, the ratio of acetate to propionate and ammonia N content. Ruminal pH increased with SO supplementation, but decreased with CFA supplementation. Ruminal total VFA concentration, acetate molar proportion and acetate to propionate ratio decreased with SO supplementation, but increased with CFA supplementation. Ruminal ammonia-N content decreased with SO or CFA supplementation. No SO × CFA interaction was observed for nutrient degradability and digestibility. Degradability of neutral detergent fibre (NDF) and digestibility of DM, organic matter, NDF and acid detergent fibre decreased with SO supplementation, but increased with CFA supplementation. Degradability and digestibility of crude protein was not affected by SO supplementation, but increased with CFA supplementation. Pectinase activity was unaltered, whereas, other microbial enzyme activity, bacterial abundance and total PD excretion were affected by SO × CFA interaction. Activities of carboxymethyl-cellulase, cellobiase and xylanase and abundance of R. albus, R. flavefaciens, F. succinogenes and B. fibrisolvens decreased with SO supplementation, but increased with CFA supplementation. Activities of pectinase, α-amylase and protease as well as total bacterial abundance were not affected by SO supplementation, but increased with CFA supplementation. Total protozoal abundance decreased with SO supplementation, but was not affected by CFA supplementation. Abundance of P. ruminicola and R. amylophilus increased with SO or CFA supplementation. Total PD excretion increased with CFA supplementation, but decreased with SO supplementation. The results suggested that ruminal fermentation, NDF degradability, protozoal abundance, cellulolytic bacterial abundance and enzyme activity decreased with dietary SO supplementation, but increased with CFA supplementation. The supplementation of CFA in the SO diet could relieve the negative effects of SO on ruminal fermentation. [ABSTRACT FROM AUTHOR]

This study evaluated the effects of branched-chain volatile fatty acids (BCVFA) supplementation on growth performance, ruminal fermentation, nutrient digestibility, hepatic lipid content and gene expression of dairy calves. Forty-eight Chinese Holstein male calves (10 months of age; 345 ± 6.4 kg of body weight [BW]) were assigned randomly to four treatments with 0, 60, 120 and 180 mg BCVFA per kg BW per day for each calf. Supplemental BCVFA was hand-mixed into the top third of the daily ration and fed to calves for 100 days to the experimental treatments. Supplementation of BCVFA in calves ration increased ADG and feed conversion linearly. Dry matter (DM) intake was unaffected, but digestibilitiy of DM, organic matter, crude protein, ether extract, neutral detergent fibre and acid detergent fibre increased linearly with increasing levels of BCFVA supplementation. Similarly, Supplementation of BCVFA linearly decreased ruminal pH and ammonia-N but increased total VFAs. Molar proportion of acetate linearly increased, whereas propionate linearly decreased and the ratio of acetate to propionate increased linearly with increasing BCVFA in rations. Relative mRNA expressions of peroxisome-proliferator-activated receptor α and carnitine palmitoyl transferase-1 linearly increased with BCVFA levels. The results suggested that BCVFA supplementation improved ruminal fermentation, nutrient digestibility and growth of calves with promoted hepatic lipid oxidation. Due to the unsignificant difference between 120 and 180 mg groups for all parameters, the optimum supplementary dose of BCVFA was 120 mg per kg BW per day. [ABSTRACT FROM AUTHOR]

This experiment was to evaluate the effects of rumen-protected pantothenate (RPP) on ruminal fermentation, microbial enzyme activity, bacteria population and urinary excretion of purine derivatives in growing beef steers. Eight ruminally cannulated first-generation crossbred (Blonde d′Aquitaine × Simmental) beef steers, averaging 12 months of age and 363 ± 7 kg of body weight (BW), were allocated into a replicated 4 × 4 Latin square design. Four treatments were control, low-RPP (LRPP), medium-RPP (MRPP) and high-RPP (HRPP) with 0, 0.32, 0.48 and 0.64 g RPP per kg dietary DM, respectively. Steers were fed a total mixed ration and dietary concentrate to corn silage ratio was 50:50 based on a dry matter (DM) basis. The experiment included four periods and lasted for 96 days, each period contained 14 days of adaptation and 10 days of data collection. Ruminal pH decreased linearly with increasing RPP supplementation and was lower for MRPP than for control. Ruminal total VFA concentration increased linearly with increasing RPP supplementation and was higher for MRPP than for control. The acetate to propionate ratio increased linearly due to the unchanged acetate molar proportion and the tendency towards decreased propionate proportion. Ruminal DM and neutral detergent fibre degradability of corn silage increased quadratically, whereas DM and crude protein degradability of concentrate mix increased linearly with increasing RPP supplementation. Activities of carboxymethyl-cellulase, cellobiase, xylanase and α-amylase increased linearly and was higher for MRPP than for control. Populations of R. albus, R. flavefaciens, F. succinogenes, B. fibrisolvens, P. ruminicola and R. amylophilus increased linearly and quadratically with increasing RPP supplementation. Urinary excretion of purine derivatives increased linearly with increasing RPP supplementation and was higher for HRPP and MRPP than for LRPP and control. The results indicated that dietary supplementary RPP improved ruminal fermentation, in situ ruminal degradation and urinary excretion of purine derivatives by stimulating bacteria growth and microbial enzymes secretion. It is suggested that supplementary RPP regulated bacteria growth and microbial enzymes secretion in a dose-dependent manner. Under the current experimental condition, the appropriate dose of RPP was at 0.48 g per dietary DM for growing crossbred beef steer. [ABSTRACT FROM AUTHOR]

This experiment was done to investigate the influences of supplementary rumen-protected folic acid (RPFA) on ruminal fermentation parameters, microbial enzyme activity, cellulolytic bacteria and urinary excretion of purine derivatives in growing beef steers. Eight ruminally fistulated Jinnan beef steers (398.4 ± 1.9 kg) were used in a repeated 4 × 4 Latin square experimental design. The treatments were: control (without RPFA), low RPFA (LRPFA), medium RPFA (MRPFA) and high RPFA (HRPFA) with 0, 0.6, 1.2 and 1.8 g RPFA per steer per day, respectively. The dietary corn silage to concentrate ratio was 50:50 (dry matter [DM] basis). The dry matter intake was confined to 95% of voluntary intake. Mean ruminal pH was quadratically reduced with altering RPFA supplementation, and was the lowest for MRPFA and HRPFA, highest for the control, and intermediate for the LRPFA. Ruminal total VFA concentration was quadratically increased with increasing RPFA supplementation and was higher in MRPFA than in control. The ratio of acetate to propionate was quadratically increased due to the increased acetate concentration and the unchanged propionate concentration. Ruminal degradabilities of DM and neutral detergent fibre of corn silage, and DM and crude protein of concentrate mix increased quadratically with increasing RPFA supplementation. Ruminal enzyme activity of cellobiase, xylanase, pectinase and α-amylase quadratically increased and was higher in MRPFA than in control. The populations of B. fibrisolvens , R. albus, R . flavefaciens and F. succinogenes quadratically increased with altering the supplementary PRFA. Urinary excretion of purine derivatives quadratically increased with altering RPFA supplementation and was higher in HRPFA and MRPFA than in LRPFA and control. The results indicated that dietary supplements of RPFA improved ruminal fermentation, in situ ruminal degradation and urinary excretion of purine derivatives. It was suggested that the RPFA regulated the activity of rumen microbe or enzymes in a concentration-dependent manner. Under this experimental condition, the appropriate dose of RPFA was at 1.2 g/d for steer. [ABSTRACT FROM AUTHOR]

• Dietary addition of laccase did not affect dry matter intake but elevated average daily gain in Holstein bulls. • Apparent nutrient digestibility and neutral detergent fibre degradability of corn silage increased with laccase addition. • Dietary laccase addition increased total volatile fatty acids and altered fermentation mode to more propionate production. • Addition of laccase increased fiber degrading enzyme activity and copies of total bacteria, fungi and fibrolytic bacteria. This study investigated the impacts of dietary laccase addition on performance, nutrient digestion, rumen fermentation and microbiota in bulls. Eight Holstein bulls with rumen cannula were allocated in a repeated 4 × 4 Latin square experiment design into four groups: control, low-laccase (LL), medium-laccase (ML) and high-laccase (HL) with 0, 0.2, 0.4 and 0.6 g/kg dietary dry matter (DM) of laccase addition, respectively. Addition of laccase did not influence DM intake but higher average daily gain and lower feed conversion ratio were found for bulls in ML group. Apparent nutrients digestibility elevated linearly with increasing laccase supplementation. Digestibility of DM and organic matter in ML, crude protein (CP) in ML and HL as well as neutral detergent fibre (NDF) and acid detergent fibre in LL, ML and HL were higher. Increasing laccase addition quadratically decreased ruminal pH, quadratically increased total volatile fatty acids content and changed ruminal fermentation mode to more propionate formation. Ruminal ammonia-N concentration decreased linearly. Ruminal degradability of concentrate CP and corn silage DM were higher for bulls in ML, but degradability of corn silage NDF was higher for bulls in ML and HL groups. Activities of cellobiase, α-amylase and laccase were higher for bulls in ML group. Populations of total bacteria, methanogens, Fibrobacter succinogenes , Ruminococcus albus , Butyrivibrio fibrisolvens , Prevotella ruminicola and Ruminobacter amylophilus increased linearly, but fungi and R. flavefaciens increased quadratically. Urine excretion of total purine derivatives was higher for bulls receiving medium or high level of laccase supplementation. The results suggested that dietary laccase supplementation increased performance and nutrient digestibility, and the appropriate addition level of laccase was 0.4 g/kg DM in bulls. [ABSTRACT FROM AUTHOR]

• Addition of palm fat powder (PFP) and coated folic acid (CFA) increased milk yield and feed efficiency. • Improved energy balance was only observed for PFP addition. • Addition of CFA stimulated nutrient digestibility, ruminal microbial growth, and fermentation. This study investigated the effects of palm fat powder (PFP) and coated folic acid (CFA) supplementation on performance, energy balance, nutrient digestion, ruminal fermentation and blood metabolites in early lactation dairy cows. Thirty-two multiparous Holstein dairy cows were arranged into four treatments in a 2 × 2 factorial randomized block design. Supplemental PFP (0 g/d [PFP−] or 500 g/d [PFP+]) and CFA (0 mg/d [CFA−] or 135 mg/d of folic acid from CFA [CFA+]) were mixed into the top one-third of the daily ration from d 52 prepartum (based on expected calving date) to d 42 postpartum. Dry matter intake was unaltered but milk yield, milk fat content and feed efficiency increased with PFP or CFA supplementation. Milk protein content was not affected by PFP but increased with CFA supplementation. Body weight change was not affected by PFP or CFA supplementation. Energy balance increased with PFP supplementation but decreased with CFA supplementation. Apparent total-tract digestibility of dry matter, organic matter, crude protein, non-fiber carbohydrates, aNDF, ADF and gross energy, ruminal pH and total volatile fatty acids concentration were unchanged with PFP supplementation but increased with CFA supplementation. Ruminal acetate to propionate ratio was decreased by PFP but increased with CFA supplementation. Lower ammonia-N was observed for PFP or CFA supplementation. Activity of α-amylase and population of Butyrivibrio (B.) fibrisolvens and Ruminobacter (Rb.) amylophilu increased but total protozoa decreased with PFP supplementation. Supplementation of CFA increased activity of cellobiase, xylanase, pectinase, α-amylase and protease and population of total bacteria, fungi, protozoa, Ruminococcus (R.) albus , R. flavefaciens , Fibrobacter succinogenes , B. fibrisolvens , Prevotella ruminicola and Rb. amylophilus. Significant PFP × CFA interaction was not observed during the trial. The results indicated that dietary supplementation of PFP or/and CFA had the potential to improve performance of early lactation dairy cows. [ABSTRACT FROM AUTHOR]

• The higher DM and nutrient intake and average daily gain were observed for folic acid (FA) addition. • Nutrient digestibility, total VFA and microbial population increased with FA and sodium selenite (SS) addition. • Urinary purine derivatives (UPD) increased with FAand SS supplementation. • Digestibility, cellulolytic bacteria and UPD induced by SS addition was greater in diet added without FA than with FA. This study evaluated the effects of folic acid (FA) and sodium selenite (SS) supplements on growth performance, nutrient digestion, ruminal fermentation, microbial enzyme activity, microflora and urinary excretion of purine derivatives (PD) in dairy calves. Thirty-six Holstein calves (63 ± 3.4 days of age and 83 ± 2.1 kg of body weight) were randomly assigned to four treatments in a 2 × 2 factorial arrangement. Two levels of FA (0 or 3.0 mg/kg of FA) and SS (0 or 0.3 mg/kg of Se from SS) were added into diets on a dry matter (DM) basis. Nutrient intake and average daily gain increased with FA addition, but were not affected by SS addition. Both supplements increased total tract digestibility of DM, organic matter and neutral detergent fiber. Ruminal pH and ammonia N concentration decreased, but total volatile fatty acids concentration increased with FA or SS addition. Acetate molar proportion and acetate to propionate ratio increased, while propionate molar proportion decreased with FA addition. The unchanged acetate molar proportion, higher propionate molar proportion and lower acetate to propionate ratio were observed with SS addition compared with the control. Activities of xylanase, pectinase, α-amylase and protease as well as populations of total bacteria, protozoa and methanogens were higher for both supplements compared with the control. Carboxymethyl-cellulase activity and Prevotella ruminicola population increased with FA addition. The Ruminobacter amylophilus population decreased with SS addition. The FA×SS interaction was significant for total tract digestibility of crude protein and acid detergent fiber, populations of total fungi, Ruminococcus (R.) albus, R. flavefaciens, Fibrobacter succinogenes and Butyrivibrio fibrisolvens as well as urinary total PD excretion; these variables increased with SS addition and the increase was greater when the diet was not supplemented with FA than with FA supplemented diet. The results indicated that dietary FA and/or SS addition stimulated nutrient digestion, ruminal fermentation, microbial growth and urinary total PD excretion. [ABSTRACT FROM AUTHOR]