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3 of 6
Revista Científica, FCV-LUZ / Vol. XXXVI
RESULTS AND DISCUSSION
Trial 2: Gas production kinetics
Chemical analyses
Calculation, chemical and statistical analyses
Each vial received 25 mL of a bicarbonate-buffered solution
containing NaHCO3 and KCl (0.1 M, pH 6.0) and 10 mL of 0.2
M HCl, adjusting the final pH to 1.5. Subsequently, 1 mL of a
pepsin solution containing 25 mg of porcine pepsin (2000 FIP-U/
g, Merck No. 7190) was added to each vial. To prevent bacterial
growth during the enzymatic digestion phases, 0.5 mL of a
gentamicin solution (0.5 g / 100 mL of ethanol) was included.
The vials were sealed with rubber stoppers and incubated at 39
ºC for 1.5 h in a laboratory incubator (Memmert, IN55, Germany).
Intestinal digestion (pH 6.8) was simulated by incubating the
residues obtained from the gastric phase in a buffer solution
containing porcine pancreatin (0.1 g/100 mL; P-7545, Sigma-
Aldrich, St. Louis, MO, USA) at 39 ºC for 3.5 h under the same
incubation conditions.
Samples predigested with pepsin and pancreatin were
filtered and subjected to cecal fermentation to determine
DM digestibility. Fermentation vials were filled with 25 mL of
inoculum mixture, sealed with rubber stoppers, and incubated
at 39 ºC for 19 h under anaerobic conditions maintained by
continuous CO2 flushing. After incubation, the residues were
filtered and washed with cold water for DM determination.
Gas production kinetics were evaluated following the
methodological framework described by Haro et al. [10], with
modifications consisting of the replacement of sheep ruminal
fluid by guinea pig cecal inoculum obtained from soft faeces.
Fermentation vials containing the respective substrates were
filled with 25 mL of inoculum mixture, sealed with rubber
stoppers, and continuously flushed with CO2 to maintain
anaerobic conditions throughout incubation.
Gas production was measured using a pressure transducer
(Delta Ohm HD2304.0 TP705-2BGI, Herter Instruments SL,
Barcelona, Spain) at different time intervals of 2, 4, 8, 16, 24, 48,
72, 96, and 120 h, using four vials per substrate. The potential
degradability of DM was estimated using two vials per substrate,
following the same incubation protocol, the vials were uncovered
at 120 h, filtered, and washed with cold water for DM analysis.
Data were analyzed using a linear mixed model using PROC
MIXED in SAS. Fixed effects included by-product (By-product),
feed type (Feeds), and their interaction (Sub x Feeds), while
the random effect was animal. A difference with P < 0.05 was
considered significant, and values between 0.05 and 0.10 were
interpreted as trends.
The proportion and chemical composition of agro-industrial
by-products (broccoli, cabbage, corn husk, and sugarcane
bagasse) classified as HBP and ABP, as well as the reference
feeds, is shown in TABLE I. By-products had low DM content,
which ranged from 6.20 to 33.3 % and was lower (P = 0.011) in
HBP than in ABP. Compared with ABP, HBP samples had lower (P
< 0.001) OM content but higher (P < 0.001) CP and NSC contents.
In general, broccoli and cabbage showed lower EE, NDF, ADF,
hemicellulose and cellulose contents.
The gross energy and metabolizable energy contents were
similar for all samples (P > 0.05). However, among the by-
products the ME values were lower (P = 0.035, ranging from
2.31 to 2.62 Kcal/g of DM). Significant differences were observed
among the fractions in both groups. Nevertheless, no differences
(P > 0.05) were found in OM, NSC, GE, and ME among feedstuffs.
Additionally, the interaction between by-products and feeds
showed no significant effects (P > 0.05). However, the effect
of by-products varied significantly across different feeds (P <
0.001).
The results of chemical composition align well with the high
CP content (ranging 19.7 to 22.3 %) and GE values (ranging 3.60
to 4.23 Kcal/g of DM), as well as the low NDF, ADF y lignin levels
previously reported for HBP [2, 15]; and the higher fiber content
observed in ABP [2, 16]. However, the cell wall content observed
in cabbage was higher than the value reported by De Evan et al.
[17] for brussels sprouts, white cabbage, savoy cabbage, and red
cabbage, which showed average NDF, ADF and lignin contents
of 23.8, 15.3, and 1.68 %, respectively. It is well established
that factors such as growth stage, seasonality, species, variety,
soil type, and fertilization significantly influence the chemical
composition of plants [8, 18].
The chemical composition of the samples used in the trial was
analyzed in triplicate. Dry matter (934.01), ash (942.05), nitrogen
(984.13), ether extract (920.39), and gross energy (920.87) were
determined according to the procedures outlined by the AOAC
[12]. Cell wall components were analyzed following the methods
described by Van Soest et al. [13].
Gas production values measured at each time were corrected
for the amount of gas produced in the corresponding blanks to
correct for endogenous production. Gas production was fitted
with time using the exponential model:
Where: V is the asymptotic gas production, k is the fractional
rate of gas production, lag is the time before starting gas
production, and t is the time of gas measurement. Data fitting
was performed using the nonlinear regression procedure (PROC
NLIN) of the SAS statistical software (Version 9.4; SAS Institute
Inc., Cary, NC, USA) [14].
The average gas production rate (AV) was defined as the
rate between the incubation start and the time at which half V is
reached, and it was calculated as: