212 research outputs found

    Balancing Rations for Milk Components

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    ABSTRACT: Yields of protein and fat are positively correlated with yield of milk but increased milk yield can dilute the percentages of protein and fat in milk. Milk components can be altered through ration formulation. Fat is easier to change than protein which is easier to change than lactose. Substrates for mammary synthesis of milk components are provided by fermentation in the rumen and by digestion in the small intestine. Substrates like trans octadecenoic acids can inhibit mammary synthesis of fat. Imbalances of amino acids can lower mammary synthesis of protein. Carbohydrates affect milk yield through the supply of glucose to the mammary gland and milk protein through growth of ruminal bacteria. Fibre is needed to maintain normal rumen function. Through altered carbohydrate fermentation and decreased bacterial growth, subclinical rumen acidosis can decrease yields of milk, protein and fat. Buffers affect milk fat by increasing acetate:propionate and by decreasing ruminal synthesis and mammary uptake of trans octadecenoic acids. Rumen bacteria need degradable protein. Escape protein should contain amino acids that promote synthesis of milk protein. Balancing rations for amino acids increases mammary synthesis of protein and milk yield is increased in early lactation cows. Rations with added fat need to contain more rumen escape protein. Ionophores provide a means of increasing the ratio of protein:fat in milk

    A revised CNCPS feed carbohydrate fractionation scheme for formulating rations for ruminants

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    Balancing ruminant diets for appropriate levels and types of dietary carbohydrates (CHO) is necessary to maximize production while assuring the health of the animals. Several feed fractions (i.e., volatile fatty acids (VFA), lactate, sugars, starch) are now being measured in some commercial feed laboratories and this information may assist in better formulating diets. A CHO fractionation scheme based on ruminal degradation characteristics needed for nutritional models is described and its impact on predictions with the Cornell Net Carbohydrate and Protein System (CNCPS) is assessed. Dietary CHO are divided into eight fractions: the CA1 is volatile fatty acids (VFA), CA2 is lactic acid, CA3 is other organic acids, CA4 is sugars, CB1 is starch, CB2 is soluble fiber, CB3 is available neutral detergent fiber (NDF), and CC is unavailable NDF. A Monte Carlo analysis was conducted with an example lactating dairy cow ration to compare the original CNCPS CHO scheme (CA=sugars and organic acids, CB1=starch and soluble fiber, CB2=available NDF, CC=unavailable NDF) with the developed CHO scheme. A database was used to obtain distributions and correlations of the feed inputs used in the schemes for the ingredients of the ration (corn and grass silages, high moisture corn, soybean meal, and distillers\u27 grains). The CHO fractions varied in a decreasing order as VFAs, soluble fiber, lactic acid, sugar, NDF, starch, and total non-fiber carbohydrates (NFC). Use of the expanded scheme in the CNCPS decreased the microbial CP production, which was sensitive (standard regression coefficient in parenthesis) to corn silage starch (0.55), grass silage NDF rate (0.46), high moisture corn grain starch rate (0.44), and corn silage NDF rate (0.33). Predicted ruminal NFC digestibility remained similar. The expanded CHO scheme provides a more appropriate feed description to account for variation in changes in silage quality and diet NFC composition. However, to fully account for differences in feed CHO utilization, further improvements in the methodology used to estimate the fractions and their corresponding degradation rates, inclusion of dietary factors in dry matter intake predictions, and prediction of ruminal VFA production and pH are necessary

    In vitro evaluation of sugar digestibility in molasses

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    Beet and cane molasses mainly contain mono- di-, and tri-saccharides, composed by hexoses, as well as pentoses in traces. However, rationing software consider sugars as only one entity, with a rate of digestion ∼20% h−1. The aim of this initial study was to investigate and evaluate the in vitro digestion dynamics and rates of the sugar fraction in molasses. Three beet and three cane molasses were randomly selected from a variety of samples collected world-wide and digested via in vitro rumen fermentation, at 1, 2, 3, 4, 6, 8, and 24 h. Samples were then analysed with a specific enzymatic kit to quantify residual sucrose, glucose, fructose, raffinose, galactose, and arabinose. Complete disappearance of sucrose happened within 3 hours of incubation. Glucose and fructose were completely digested within 4-6 h, showing variability among samples. Even if not so representative, galactose showed a similar trend of digestion (97% digestion within 3-4 h). Raffinose was quite slower in cane molasses, while it was completely digested within 1 h in beet molasses. Arabinose, a pentose, never reached a complete digestion, and its fermentation dynamic was different compared to other sugars. Calculated rates of digestion for sucrose, glucose and fructose, most representative sugars in molasses, were higher than 50% h−1 in both cane and beet. Obtained results showed that sugar fraction in molasses may vary, and different sugars are rapidly fermented by rumen microbes. Modern rationing models should consider a modification of sugar rates of digestion, since the actual one appears too slow than those observed in vitro.Highlights Molasses are unique blends of several sugars Major sugars are digested in few hours Rationing software should consider a faster rate of digestion for different sugars

    Short communication: Characterization of molasses chemical composition

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    Beet and cane molasses are produced worldwide as a by-product of sugar extraction and are widely used in animal nutrition. Due to their composition, they are fed to ruminants as an energy source. However, molasses has not been properly characterized in the literature; its description has been limited to the type (sugarcane or beet) or to the amount of dry matter (DM), total or water-soluble sugars, crude protein, and ash. Our objective was to better characterize the composition of cane and beet molasses, examine possible differences, and obtain a proper definition of such feeds. For this purpose, 16 cane and 16 beet molasses samples were sourced worldwide and analyzed for chemical composition. The chemical analysis used in this trial characterized 97.4 and 98.3% of the compounds in the DM of cane and beet molasses, respectively. Cane molasses contained less DM compared with beet molasses (76.8 ± 1.02 vs. 78.3 ± 1.61%) as well as crude protein content (6.7 ± 1.8 vs. 13.5 ± 1.4% of DM), with a minimum value of 2.2% of DM in cane molasses and a maximum of 15.6% of DM in beet molasses. The amount of sucrose differed between beet and cane molasses (60.9 ± 4.4 vs. 48.8 ± 6.4% of DM), but variability was high even within cane molasses (39.2–67.3% of DM) and beet molasses. Glucose and fructose were detected in cane molasses (5.3 ± 2.7 and 8.1 ± 2.8% of DM, respectively), showing high variability. Organic acid composition differed as well. Lactic acid was more concentrated in cane molasses than in beet molasses (6.1 ± 2.8 vs. 4.5 ± 1.8% of DM), varying from 1.6 to 12.8% of DM in cane molasses. Dietary cation-anion difference showed numerical differences among cane and beet molasses (7 ± 53 vs. 66 ± 45 mEq/100 g of DM, on average). It varied from −76 to +155 mEq/100 g of DM in the cane group and from +0 to +162 mEq/100 g of DM in the beet group. Data obtained in this study detailed differences in composition between sources of molasses and suggested that a more complete characterization could improve the use of molasses in ration formulation

    In vitro evaluation of sugar digestibility in molasses

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    Beet and cane molasses mainly contain mono- di-, and tri-saccharides, composed by hexoses, as well as pentoses in traces. However, rationing software consider sugars as only one entity, with a rate of digestion similar to 20% h(-1). The aim of this initial study was to investigate and evaluate the in vitro digestion dynamics and rates of the sugar fraction in molasses. Three beet and three cane molasses were randomly selected from a variety of samples collected world-wide and digested via in vitro rumen fermentation, at 1, 2, 3, 4, 6, 8, and 24 h. Samples were then analysed with a specific enzymatic kit to quantify residual sucrose, glucose, fructose, raffinose, galactose, and arabinose. Complete disappearance of sucrose happened within 3 hours of incubation. Glucose and fructose were completely digested within 4-6 h, showing variability among samples. Even if not so representative, galactose showed a similar trend of digestion (97% digestion within 3-4 h). Raffinose was quite slower in cane molasses, while it was completely digested within 1 h in beet molasses. Arabinose, a pentose, never reached a complete digestion, and its fermentation dynamic was different compared to other sugars. Calculated rates of digestion for sucrose, glucose and fructose, most representative sugars in molasses, were higher than 50% h(-1) in both cane and beet. Obtained results showed that sugar fraction in molasses may vary, and different sugars are rapidly fermented by rumen microbes. Modern rationing models should consider a modification of sugar rates of digestion, since the actual one appears too slow than those observed in vitro

    Low cost feeding strategies for dual purpose cattle in Venezuela

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    This simulation study was to evaluate low cost feeding strategies in response to higher cost of commercial concentrates to maintain current milk sales from dual purpose cattle herds in the humid lowlands of western Venezuela. Data were from farm surveys in 1987 and 1988. Baseline net margins from milk and beef per cow per year were 132and132 and 99 for two farm cases with average dally milk of 10 and 7 kg/cow and grazing mature forage supplemented with commercial concentrate. Alternative diets were 1) improving forage quality by more intensive grazing; 2) replacing commercial concentrate with a mixture of cassava tuber (Manihot esculenta), urea, and molasses and 3) supplementing grazing with a mixture of molasses and urea. Alternatively priced feeding strategies were compared by partial budgeting. Using less mature forage was .always more profitable than mature grass. Feeding molasses and urea with mature forage increased profits at least 64/cowonthehighmilkyieldfarmand64/cow on the high milk yield farm and 44/cow on the low milk yield farm compared with feeding commercial concentrate. The most costly cassava mixture with mature forage increased annual profit over the baseline diet at least 11/cowonthehighmilkyieldfarmandby11/ cow on the high milk yield farm and by 22/cow on the low yield farm. Efficient use of existing feed resources may enhance economical livestock production in the humid lowlands of Venezuela

    A Pair of Dopamine Neurons Target the D1-Like Dopamine Receptor DopR in the Central Complex to Promote Ethanol-Stimulated Locomotion in Drosophila

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    Dopamine is a mediator of the stimulant properties of drugs of abuse, including ethanol, in mammals and in the fruit fly Drosophila. The neural substrates for the stimulant actions of ethanol in flies are not known. We show that a subset of dopamine neurons and their targets, through the action of the D1-like dopamine receptor DopR, promote locomotor activation in response to acute ethanol exposure. A bilateral pair of dopaminergic neurons in the fly brain mediates the enhanced locomotor activity induced by ethanol exposure, and promotes locomotion when directly activated. These neurons project to the central complex ellipsoid body, a structure implicated in regulating motor behaviors. Ellipsoid body neurons are required for ethanol-induced locomotor activity and they express DopR. Elimination of DopR blunts the locomotor activating effects of ethanol, and this behavior can be restored by selective expression of DopR in the ellipsoid body. These data tie the activity of defined dopamine neurons to D1-like DopR-expressing neurons to form a neural circuit that governs acute responding to ethanol
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