RESUMO -Avaliou-se o uso de matéria seca indigestível (MSi) e de fibra detergente neutro indigestível (FDNi) como indicadores internos de digestibilidade em ovinos. Utilizaram-se dados e amostras provenientes de seis ensaios independentes de digestibilidade com ovinos mantidos em gaiolas de metabolismo recebendo à vontade diversos tipos de volumoso e/ou concentrado. Os resíduos indigestíveis (MSi e FDNi) foram determinados após 144 horas de incubação in situ de amostras de alimentos e fezes. O grau de recuperação da MSi variou de 64,8 a 108,5% e o da FDNi, de 49,5 a 67,9%. Quando a relação entre a concentração dos indicadores nas fezes e nos alimentos não foi corrigida para a recuperação fecal, a maior parte das estimativas médias de digestibilidade da matéria orgânica dos experimentos foi inferior às médias obtidas in vivo. Quando a relação foi corrigida para a recuperação fecal, as estimativas médias de digestibilidade da matéria orgânica usando os dois indicadores foram similares às obtidas in vivo em todos os experimentos. Quando as estimativas individuais, corrigidas para recuperação fecal do indicador, foram relacionadas às observações in vivo por análise de regressão, o coeficiente de regressão linear foi similar a 1 usando a MSi, mas foi menor que 1 usando a FDNi. Os valores individuais de digestibilidade da matéria orgânica estimados com os dois indicadores, contudo, foram pobremente relacionados às observações in vivo (r 2 variou de 0,60 a 0,63). Corrigindo-se para a recuperação fecal, a matéria seca residual após 144 horas de incubação in situ pode ser utilizada como indicador interno para estimar a digestibilidade média da dieta consumida por um grupo de animais, mas não é precisa para detectar pequenas diferenças na digestibilidade de alimentos impostas pelos tratamentos em um experimento.Palavras-chave: consumo, digestibilidade, fibra em detergente neutro indigestível, matéria seca indigestível, recuperação fecal Evaluation of indigestible feed fractions as internal markers for predicting digestibility in lambsABSTRACT -The use of indigestible dry matter (iDM) and indigestible neutral detergent fiber (iNDF) as internal markers to estimate digestibility in lambs was evaluated. Data and samples were obtained from six independent digestion trials with lambs housed in metabolism cages given ad libitum different forage and concentrate feedstuffs. Indigestible residues were determined after 144 hours of in situ incubation of feed and faeces samples. Recovery rate varied from 64.8 to 108.5% for iDM, and from 49.5 to 67.9% for iNDF. As the marker ratio between marker concentration in the faeces and the feed was not corrected for fecal recovery, the large part of the estimated apparent organic matter digestibility (AOMD) of the experimental means were lower than the in vivo that obtained. As the marker ratio was corrected for fecal recovery of the marker, the AOMD means estimated using both markers were similar to the in vivo data in all experiments. As individual estimates, corrected for fecal recovery of ...
The amount of digesta flowing to the duodenum is a relevant measurement for the evaluation of nutrient supply to ruminants, which is usually estimated in animals fitted with a duodenal T-type cannula using internal or external markers. This study evaluated acid detergent fiber (ADF) compared with external (C32n-alkane) and internal [sulfuric acid lignin (ADL) and n-alkanes C31 and C33] markers for estimating duodenal flow and(or) ruminal digestibility of dry matter (DM) in cattle and sheep. In the first assay, 4 duodenally cannulated Holstein steers housed in metabolism cages, dosed with C32n-alkane, and fed Avena strigosa plus concentrate and increasing levels of tannin extract to reduce ruminal digestibility, were used in a Latin square design. The mobile-bag technique was used to measure the intestinal disappearance of ADL and ADF from forage (Avena strigosa, Pennisetum purpureum, Cynodon dactylon, and Medicago sativa) and concentrate (corn grain, soybean meal, and sunflower meal) samples that were previously incubated in the rumen of additional fistulated steer for 12, 24, 36, or 48 h. The ADF concentration in residues recovered in the feces was strongly related to the ADF concentration in residues at the duodenum (R(2)=0.93, standard deviation=30.0, n=901). This relationship showed a lower precision for ADL fraction (R(2)=0.88, standard deviation=12.6, n=590). In a second assay, duodenal flow and ruminal DM digestibility were calculated from the duodenal and fecal concentration of either marker. We observed a significant effect of marker type on ruminal DM digestibility values, and the effect of tannin treatments was observed only when ADF or ADL was used as the marker. The lowest residual error was obtained for ADF. Ruminal DM digestibility was, on average, higher for C31 and C(33)n-alkanes, and the use of dosed C(32)n-alkane resulted in a negative value. In the third assay, a data set of 235 individual observations was compiled from digestibility trials to compare ADF and ADL as markers for estimating duodenal digesta flow in wethers (n=204) and cattle (n=31). We observed a strong relationship between markers (R(2)=0.84 in sheep and R(2)=0.88 in cattle), but variance analysis within trials indicated that ADF was more precise than ADL. In conclusion, in digestibility trials in which fecal output was measured and spot samples of the duodenal digesta were obtained, duodenal flow and ruminal digestibility of the DM may be estimated from the relationship between the ADF concentration in feces and that in the duodenal digesta of ruminants.
Background: The addition of adsorbents in foods has been the strategy used by nutritionists to reduce the toxic effects of mycotoxins in animals. Mycotoxins are found in a range of foods and commonly they present variations in the chemical structure therefore, it has been appropriate to include adsorbents from different sources in the diet of ruminants. However, few researches were conducted in order to better understand the interaction of adsorbents on ruminal fermentation. Our objective in this study was to investigate the possible effects of two adsorbent products on bovine ruminal fermentation. One consists of 65% of β-glucan (β-glu), originating cell wall of Saccharomyces cerevisiae and used at a concentration of 1% and natural sodium montmorillonite (MMT) at a concentration of 5%. Materials, Methods & Results:The effects of β-glu adsorbents (1%) and MMC (5%) in culture medium that simulated ruminal fermentation were evaluated. Bottles, with a capacity of 120 mL, were used to be filled with substrate such as maize and ryegrass hay ground, nutrient solution (medium of Menke), liquid extracted rumen fistulated bovine and the two adsorbents evaluated, totaling 50 mL. The experiment was conducted with three treatments, named after: control (Cont), β-glu and MMT. In the control treatment adsorbents were not added. Six replicates were used for each treatment and two trials were conducted. One of the tests aimed to determine the fermentation kinetics by means of the gas production after 72 h' incubation and quantifying the production of methane (CH4) at 48h. While another test aimed to quantify the production of short chain fatty acids (SCFA) -acetic, propionic and butyric acid -and the production of ammonia (NH3) in 24 h incubation. All assays were measured by gas chromatography. The highest total SCFA concentration was observed in β-glu treatment (67.71 mM) significantly superior to CONT (57.7 mM) treatment and MMT (53.28 mM), which was significantly lower than the β-glu treatment, but similar to CONT. The average representation (%) of acetic acid for the treatment MMT (62.9%) was significantly higher than the β-glu treatment (61.0%). The average proportions of propionic acid were similar between treatments, while the average representation (%) of butyric acid production was significantly higher for the β-glu treatment (13.1%) compared to CONT treatments (11.3%) and MMT (11.4%). The amount of NH3 was significantly reduced in MMT (9.6 mM) treatment compared to β-glu treatments (12.2 mM) and CONT (11.3 mM). In another test, the greater volume of gas (mL) was produced by β-glu treatment (103.4 mL), which was significantly greater than the treatments CONT (89.0 mL) and MMT (91.6 mL). The lag time, i.e. the time taken by the bacteria inoculum to develop lead-through in the substrate, in the MMT treatment took 6.2 h, slowing significantly compared to CONT treatments (4.8 h) and β Glu (4.33 h). The concentration of CH4 was significantly lower in MMT treatment (33.0%) compared to the CONT treatments (36.3%) and ...
The aim of this study was to evaluate the physicochemical, microbiological, sensory and meat quality characteristics of grumatã fillets after different depuration (0, 48, 72 and 96 h) periods and frozen storage (0, 2, 4 and 6 months). The fish collected in a dam were distributed in tanks at a density of 3.8 kg m3 -1. After depuration periods, all fish were filleted and the fillet samples stored (−18 °C) until analyses. Lower fat content was found in fish submitted to depuration for 48 and 96 h compared to the non-depurated and those depurated for 72 h. Muscle protein was preserved in 48 and 96 h treatments. Coagulase-positive Staphylococcus, coliforms at 45 °C and Salmonella spp. were not observed in the fillets, but aerobic mesophilic microorganisms and coliforms at 35 ºC were detected. Sensory analysis showed no significant differences in appearance, colour, texture, flavour attributes and overall acceptance. During frozen storage, pH, total volatile basic nitrogen (TVB-N), peroxide and thiobarbituric acid reactive substance (TBARS) values were evaluated in fillet samples every two months. The pH values increased up to four months of storage. The TVB-N values ranged in fillets from fish depurated for 48 and 96 h. Peroxide values increased from the fourth month of storage, with the highest values observed in the sixth month. For TBARS values, increased values were found in fillets from non-depurated fish and lower values in other depuration periods. Thus, depuration is more efficient in maintaining the quality of grumatã fillets in frozen storage.
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