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Influencia Del Biacarbonato de Sodio
Influencia Del Biacarbonato de Sodio
R. A. E R D M A N , R. L. BOTTS, 2
R, W. H E M K E N , and L. S. B U L L ~
Department of Animal Sciences
University of Kentucky
Lexington 4 0 5 4 6
TABLE 1. Ingredient and chemical composition of complete mixed rations (% dry matter basis).
Ration
.8% MgO +
Component Control 1.5% NaHCO3 .8% MgO 1.5% NaHCO3
Corn silage 40 40 40 40
Ground corn 38.6 36.6 37.2 35.2
Soybean meal (44%) 20.2 20.7 20.8 21.3
Trace mineral salt .6 .6 .6 .6
Limestone .6 .6 .6 .6
NaHCO3 .... 1.5 .... 1.5
MgO . . . . . . . . . 8 .8
Chemical analysis
Prote~n 15.9 16.0 15.9 16.1
Starch 41.5 41.3 41.6 40.0
ADF 15.2 15.3 15.3 15.4
Ca .58 .58 .59 .55
P .51 .48 .51 .46
Mg .15 .15 .61 .61
measured on wet samples by Kjeldahl procedure Figure 1) than those fed control rations (P< .05).
and acid detergent fiber (ADF) by the method Differences in voluntary intake were mainly in
of Goering and VanSoest (10). wk 4 to 7 where cows receiving NaHCO3
Analysis of variance was factorial in a peaked in intake earlier (P<.05) (Figure 1).
randomized complete block design (1). Milk Other studies where NaHCO3 and MgO have
production was analyzed by analysis of covari- been used to maintain fat test have reported
ance with 305-day mature equivalent records slight decreases in total intake from addition of
for adjustment (1). Rumen, blood, fecal, and either of these buffers (6, 7, 23). In most
urinary data were analyzed as a split-plot design studies of milk fat depression a m i n i m u m of
with treatments and blocks whole-plots and forage was fed, and grain and forage were fed
weeks subplots (1). Individual differences separately. These differences in ration content
between treatment means were tested for might be related to difference in response to
significance by Fisher's least significant differ- buffers. Earlier peak intakes of feed in Figure 1
ence (1) where tests were only after a significant suggest benefits from improved adjustment to
F-test. ration similar to those for beef cattle and sheep
in feedlots (2, 13, 21).
Actual milk production was increased (P<.I)
RESULTS AND DISCUSSION
by addition of NaHCO3 (Table 2), with the
Incidence of metabolic problems was low, greatest response in the groups receiving both
possibly because diets were fed as completely sodium bicarbonate and magnesium oxide
mixed rations which maintained a constant (Figure 2). One study of early lactation (16)
fiber content and prevented overconsumption reported similar increases in milk production,
of concentrate. One cow, receiving the ration while most midlactation fat-depression studies
containing both NaHCO~ and MgO, had a have reported no effect on milk production (6,
displaced abomasum 10 days after calving and 7, 19) with added NaHCO3 in the diet. A study
was removed. The next cow to calve replaced (16) of cows in a similar stage of lactation
her in that block. From the small incidence of and with similar diets also reported increased
metabolic problems, statements cannot be intake from dietary NaHCO3.
conclusive as to positive or negative effects of Sodium bicarbonate and MgO did not affect
treatment on incidence. milk fat test significantly, although cows
Cows fed the NaHCO 3 rations had 2.1 kg receiving MgO alone had slightly lower fat tests
per day greater total intakes (Table 2 and than all other treatment groups (Table 2).
TABLE 2. Effect of treatment on feed intake, milk production, fat test, and body weight change.
Ration
.8% MgO +
Parameter Control 1.5% NaHCO3 .8% MgO 1.5% NaHCO3 SE
a'bMeans in the same row with different superscripts are different (P<.05).
BNaHCO3 treatment effect (P<.I).
BBNaHCO3 treatment effect (P<.05).
BBBNaHCO3 treatment effect (P<.O1).
*Adjusted by covariance for previous 305-day mature-equivalent lactation average.
25
rumen pH (Table 3), although NaHCOa and
23 BO I'll MgO tended to increase urine pH. Changes in
I . 5~ NalIC0
.8"o ~XlgO 3
urinary pH probably do not reflect true changes
~, 21 CONI ROI, in acid excretion. Most acid in urine is thought
to be excreted in the form of the a m m o n i u m
ion in ruminants consuming high concentrate
diets (22). Therefore, differences in pH probably
do not reflect the magnitude of differences in
acid secretion. Some workers have reported
increased ruminal pH with addition (7) of
~T l
T T f -[~ T T
2 3 "~ 5 b 7 S
NaHCO3 while others have not (7, 19). One
I~o t ' k I ' o s I p~l i't tanl
factor which increases variability of rumen pH
Figure 1. Feed intake by week. B) N a H C O a t r e a t - was use of a stomach tube for sampling.
ment effect (P<.05); BB) NaHCOa treatment effect Acetate to propionate molar ratio was
(P<.01). increased by addition of NaHCO3 (P<.05).
Other studies have shown similar shifts toward
acetate with the use of NaHCO3 (5, 6, 19, 23).
Magnesium oxide did not have a significant
Because of low ADF content (15.3%) of the effect on acetate to propionate ratio, although
rations, differences in percentage milk fat might there was a trend toward less acetate. Shifts in
have been expected. Differences in fat test and acetate to propionate ratios from addition of
milk yield contributed to a significant increase buffers or artificial saliva to the rumen have
in fat-corrected milk (FCM) and total fat
production (Table 2, Figure 2) for cows receiv-
~
ing NaHCO3 (P<.O1). Differences, however,
were largest for cows receiving both NaHCO3
and MgO. These differences were greatest -g BOTH
during 3 to 4 wk postpartum (Figure 2), where
cows receiving NaHCO 3 alone or in combination
with MgO had significantly higher FCM produc- CONTROL
Treatment
.8% MgO +
Parameter Control 1.5% NaHCO 3 .8% MgO 1.5% NaHCO 3 SE
a'bMeans in the same row with different superscripts are different (P<.05).
C'dMeans in the same row with different superscripts are different (P<.O1).
BNaHCO3 treatment effect (P<.05).
MMgO treatment effect (P<.01).
b e e n related t o increased rates o f liquid t u r n o v e r pH (8, 27, 28). Wheeler and Noller (27, 28)
in the r u m e n (11, 25). In evaluating e f f e c t s o f s h o w e d a s t r o n g negative c o r r e l a t i o n b e t w e e n
b u f f e r s on r u m e n f e r m e n t a t i o n , t h e i r e f f e c t o n fecal pH and fecal starch w h i l e o t h e r s have
dilution rate o f r u m e n liquid n e e d s to be r e p o r t e d o n l y casual r e l a t i o n s h i p (26). A l t h o u g h
considered. c o w s fed MgO had l o w e r fecal starch d u r i n g w k
A d d i t i o n o f MgO significantly increased 1 and 4, this d i f f e r e n c e was n o t significant.
fecal pH ( P < . 0 1 ) (Table 4). A d d i t i o n o f d i e t a r y D i f f e r e n c e s in fecal starch did n o t c o n t i n u e
l i m e s t o n e resulted in significantly higher fecal t h r o u g h t h e 8th wk, w h i c h suggests a d a p t a t i o n
TABLE 4. Means by week and treatment for fecal pH and fecal starch content.
Treatment
.8% MgO +
Parameter Week Control 1,5% NaHCO 3 .8% MgO 1.5% NaHCO 3 ,X SE
% Fecal starch
(dry matter basis) 1 15.6 11.1 8.4 7.2 10.6 4.5
4 12.2 8.2 3.3 c 9.6 8.3 5.1
8 7.5 6.2 5.3 6.7 6.4 4.5
a'bMeans in the same row with different superscripts are different (P<.01).
CMean of three (3) observations due to missed sampling time.
MMgO treatment effect (P<.01).
40
conducted.
There were no significant effects o f t r e a t m e n t
3C Y = 40.59 - 5.03 x or time on plasma sodium, phosphorus, and
m
12, = ,34 (P .05) L-lactate (Table 3). A d d i t i o n of MgO did
increase plasma potassium ( P < . 0 1 ) (Table 3),
28
although reasons for this are not k n o w n . There
were significant effects o f t i m e and t r e a t m e n t
on plasma magnesium and calcium (Table 5).
A d d i t i o n o f dietary magnesium w o u l d be
e x p e c t e d to increase plasma magnesium. Effects
5,2 514 5,6 5,8 6',0 " ' ,,o of t i m e on calcium and magnesium could be
FECAL Pll interpreted to be f r o m increased intake o f b o t h
Figure 3. Relationship between fecal starch (dry minerals. However, the effect of MgO o n p l a s m a
matter percent) and fecal p H for cows receiving rations calcium c a n n o t be explained because o f simi-
with (n) or without (A) MgO. larity in absorptive mechanisms.
Average daily intakes o f NaHCO3 and MgO
were 310 and 159 g. These a m o u n t s are com-
in the control diet. Regression analysis o f the parable to the largest a m o u n t s in studies o f
data (Figure 3) showed only a slight relationship milk fat depression. Most studies have r e p o r t e d
(r = - . 3 4 ) between fecal starch and fecal pH. that addition of NaHCO3 and MgO alone
F u r t h e r m o r e , although fecal starch remained a n d / o r in c o m b i n a t i o n had a depressing effect
below 10% o f fecal dry m a t t e r at fecal pH on intake o f concentrates (6, 7, 19, 23, 24).
above 6.0, low pH was not associated necessarily E m e r y (4) r e p o r t e d in a review t h a t intakes of
with high c o n c e n t r a t i o n o f fecal starch. It is grcatcr than 272 and 136 g pcr head per day of
still possible that milk p r o d u c t i o n responses in NaHCO3 and MgO, respectively, did not result
cows receiving b o t h buffers could be due to in further i m p r o v e m e n t of milk fat percentage.
both increased intake and digestibility of the In those studies, the dietary buffer was included
rations although digestion trials were not in the c o n c e n t r a t e only, and hay and concen-
TABLE 5. Effect of treatment and time postpartum on plasma calcium and magnesium.
Treatment
.8% MgO +
Parameter Week Control 1.5% NaHCO 3 .8% MgO 1.5% NaHCO 3 X SE
Plasma Ca
(mg/lO0 ml) 1 9.3 8.8 10.7 10.4 9.8 .4 M
4 10.6 10.1 11.7 9.9 10.6 d .4
Plasma Mg
(mg/100 ml) 1 2.09 2.35 2.85 2.58 2.47 c .06 M
4 2.46 2.66 3.26 3.03 2.85 d .06
a'bMeans in the same row with different superscripts are different (P<.OI).
C'dMeans in the same column with different superscripts are different (P<.O1).
MMgO treatment effect (P<.01).
TTime effect (P<.01).
t r a t e s were fed s e p a r a t e l y . ed. Church and Dwight Co., Inc., New York, NY.
It is u n c e r t a i n w h e t h e r t h e r e s p o n s e w o u l d 5 Emery, R. A., and L. D. Brown. 1961. Effect of
feeding sodium and potassium bicarbonate on milk
have b e e n similar if alfalfa h a y or even haylage
fat, tureen pH and volatile fatty acid production. J.
h a d b e e n used as t h e forage in this e x p e r i m e n t . Dairy Sci. 44:1899.
B e n e f i t s in i n t a k e f r o m a d d i t i o n o f N a H C O 3 6 Emery, R. S., L. D. Brown, and J. W. Bell. 1965.
m a y have b e e n f r o m t h e n e u t r a l i z i n g e f f e c t Correlation of milk fat with dietary and metabo-
o n t h e acid in c o r n silage (18). A d d i t i o n o f lism factors in cows fed restricted-roughage rations
supplemented with magnesium oxide or sodium
2.5% NaHCO3 to ryegrass silage increased bicarbonate. J. Dairy Sci. 48:1647.
i n t a k e in sheep a n d dairy calves (18). K e l l a w a y 7 Emery, R. S., L. D. Brown, and J. W. Thomas.
et al. (15) r e p o r t e d increased gains and i n t a k e 1964. Effect of sodium and calcium carbonates on
in y o u n g d a i r y calves f r o m a d d i t i o n o f up to milk production and composition of milk, blood
and rumen contents of cows fed grain ad libitum
5.85% NaHCO3 in c o m p l e t e rations. R e s p o n s e s
with restricted roughage. J. Dairy Sci. 47:1325.
in b e e f cattle and s h e e p have b e e n s h o w n w i t h 8 Erdman, R. A. 1977. The effect of dietary potassium
2% or m o r e NaHCOa o n a d r y basis in s t a r t e r and limestone on lactating dairy cows. M.S. thesis,
f e e d l o t r a t i o n s (2, 3, 13). Studies are n e e d e d to University of Kentucky, Lexington.
d e t e r m i n e o p t i m a l a m o u n t s of NaHCO3 n e e d e d 9 Fiske, C. H., and Y. Subbarow. 1925. The colori-
metric determination of phosphorous. J. Biol.
to achieve m a x i m a l response. Such t h i n g s as Chem. 66: 375.
acidity of t h e feed a n d its energy c o n t e n t n e e d 10 Goering, H. K., and P. J. VanSoest. 1970. Forage
t o be considered in e v a l u a t i n g o p t i m a l c o n c e n - fiber analysis. Agric. Handbook No. 379. Agric.
t r a t i o n s o f NaHCO3 a n d MgO. Res. Serv., USDA, Washington, DC.
11 Harrison, D. G., D. E. Beever, D. J. Thomson, and
Up to this time, t h e r e c o m m e n d e d use o f the
D. F. Osborn. 1975. Manipulation of rumen
b u f f e r s in dairy r a t i o n s has b e e n restricted to fermentation in sheep by increasing the role of
i n s t a n c e s of milk fat depression. A d d i t i o n o f flow of water from the rumen. J. Agric. Sci. 85:93.
NaHCO3 m a y be o f b e n e f i t w h e r e d a i r y m e n I2 Huher, ]. T., R. S. Emery, J. W. Thomas, and T. M.
lack the facilities t o adjust p r o p e r l y t h e i r cows Young. 1969. Milk fat synthesis on restricted-
roughage rations containing whey, sodium bicar-
to t h e milking h e r d r a t i o n prior t o calving. bonate and magnesium oxide. J. Dairy Sci. 52:54.
Cows receiving NaHCO3 p e a k e d earlier in 13 Huntington, G. B., R. J. Emerick, and L. B. Embry.
i n t a k e , whereas cows receiving r a t i o n s w i t h o u t 1977. Sodium bentonite or sodium bicarbonate as
NaHCO3 m a y n o t have r e a c h e d t h e i r peak at aids in feeding high-concentrate diets to lambs. J.
Anim. Sci. 45:804.
t h e c o n c l u s i o n o f t h e study. Hopefully, these
14 Hochella, N. J., and S. Weinhouse. 1965. Automated
d i f f e r e n c e s in i n t a k e w o u l d b e t r a n s l a t e d i n t o lactic acid determination in serum and tissue
h i g h e r t o t a l milk p r o d u c t i o n over t h e e n t i r e extracts, Anal. Biochem. 10: 304.
l a c t a t i o n . T h e NaHCO3 a n d MgO b u f f e r s m a y 15 Kellaway, R. C., D. J. Thomson, D. E. Beever, and
be p r o m i s i n g tools for d a i r y m e n t o s t i m u l a t e D. F. Osborn. 1977. Effects of NaCl and NaHCO 3
on food intake, growth rate and acid-base balance
b o t h a p p e t i t e and d i g e s t i o n early in l a c t a t i o n . in calves. Agric. Sci., Camb. 88: 1.
16 Kilmer, L. H., L. D. Muller, and P. J. Wangness.
ACKNOWLEDGMENT 1979. Sodium bicarbonate addition to rations of
pre- and postpartum cows. J. Dairy Sci. 62(Suppl.
This research was s u p p o r t e d in part by 1):231.
C h u r c h a n d D w i g h t Co., Inc. 17 MacRae, J. C., and D. G. Armstrong. 1968. Enzyme
method for determination of c~-linked glucose
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