Use of anions and cations in sows
It has been shown that balancing
the diet for anions and cations
plays an important role in preventing
milk fever in dairy cows.
Therefore, why not benefit from this
knowledge and use it in sows too?
Of course sows are not usually
afflicted with milk fever, but delayed
farrowings resulting in increased
numbers of still births are a common
problem in sow herds (see Table I).
The causes include:
- Tedious labour (too weak muscle tones) as a result of too low blood calcium levels.
- Insufficient release of oxytocin, the hormone which elicits labour pains, milk flow and milk let-down.
- Too narrow birth canals due to genetics, constipation and primiparous sows.
- Parity number.
The correlation between too low
blood calcium levels, decreased
muscle tone and increased still births
opens a second area in view of
improving sow performance by
using Biomin
® pHD.
This product line aims to increase
blood calcium levels to decrease still
births.
| Duration of farrowing (hours) |
Litters |
Number of still births (%) |
| < 4 |
376 |
4.0 |
| 4-6 |
161 |
5.8 |
| > 6 |
92 |
9.9 |
Table I. Effect of duration of farrowing on still births (Hiihn 2004).
Beside already published effects on
preventing urinary tract infections
(UTI) and minimising related metritis
problems - reducing the number of
still births could be an additional way
to improve the number of piglets
weaned per sow per year (see Fig. I).

Fig. I. Breeding herd efficiency.
Calcium metabolism
The serum calcium level is regulated
by hormones and has to be kept in
narrow ranges (2.3 -2.8 mm01/1 in
sows).
Hormones involved in the control
mechanism are parathyroid hormone
and calcitonin as well as 1.25- (OH)2-vitamin D (active form of vitamin
D3).
When plasma calcium concentration
declines, parathyroid hormone
and 1.25-(OH)2-vitamin D are activated
and calcium-resorption via the
kidneys, calcium-adsorption from
the digestive tract as well as bone
mobilisation are increaSing.
Since there is a permanent, overconsumption
of calcium during gestation
(because of a low demand)
this mechanism is not trained - the
parathyroid control mechanism is
slowed down and cannot react in
time on the changed/increased calcium
demands peri-farrowing.
Consequences are declining calcium
blood levels which can not be
balanced in time and in the end calcium
is missing for the contraction of
muscles and a deficit in calcium blocks the release of oxytocin,
which is important for muscle contraction
too.
Declining calcium levels delay the
farrowing process and in the end the
livability of the piglets is decreasing
and/or the piglets die prematurely.
Urine acidification
Balancing the acid-base-balance and
regulating the blood pH at around
7.42 (reference value for pigs) is
important for the maintenance of all
vital functions of the body.
The blood pH is regulated via
three mechanisms:
- Binding and release of H+ via puffer systems.
- Regulating the partial pressure of carbon dioxide via respiration.
- Regulating the renal H+ and hydrogen carbonate - excretion.
We now need to have a closer look at regulating the blood pH via
renal excretion, because this mechanism
is relevant for the mode of
action of Biomin
® pHD. Excreta pH is
a function of the acid-base balance
, of the feed and balancing for anions
and cations influences the acid-base
I balance of the body. Increasing
anions in the diet leads to an acidic
stress of the animal.

Urinary Sampling
Depending on the extent of acidic
stress metabolic acidosis is the immediate consequence. The body
tries to compensate acidosis via
increasing H+ excretion and increasl
ing read sorption of hydrogen carbonate,
which acidifies the urine.
Furthermore, it is reported that an
acidic stress of the acid-base balance
lead to a net-excretion of calcium
from the body by increasing renal
calcium excretion.
The body tries to compensate this
lack via an increased mobilisation of
calcium from the bones as the
biggest calcium storage of the body
I and, at the same time, the body tries
, to puffer the blood pH via increasing
calcium resorption (regulated by
parathyroid hormone and 1.25-
(OHh~vitamin D). Resulting in
increasing calcium blood levels. It is
I assumed that by feeding anionic
diets this trains the parathyroid hormone and 1.25-(OH)2-vitamin D
mechanisms to act faster and more
efficiently in times of increased
demands of calcium. particular prefarrowing.
These literature surveys confirm
the already proven effects of feeding
Biomin
® pHD (see Table 2 and 3) and
opens new applications for the
future. Based on these new facts. a
trial was carried out under farm
conditions in Australia and the
results are promising.
| Â |
Control |
Biomin pHD |
P-value |
| Parity |
3.5 |
3.2 |
 |
| pH 1 (day 108 pregnancy) |
6.7 |
6.6 |
0.585 |
| pH 2 (farrowing) |
6.7 |
6.1 |
0.031 |
| pH 3 (day 7 post farrowing) |
7.2 |
6.0 |
<0.001 |
| pH 4 (day 1 post insemination) |
6.7 |
5.7 |
0.001 |
| P < 0.05 |
 |
 |
 |
Table 2. Urine pH in response to feeding Siomin pHD (Cyprus 2006).
Trial results
The trial was conducted in a climate
controlled breeder unit in Southern
Queensland in January 2007.
The control group was fed conventionally and the trial group
received additionally 0.5% Biomin
®
pHD in the feed for 10 days pre-farrowing
until mating. The main focus
was on farrowing performance.
The addition of Biomin
® pHD prefarrowing
had a significant response
in reducing still births from 1.15
down to 0.73 piglets per litter
(P>0.05) + 0.1 piglets/sow/litter.
The number of mummified piglets
was similar in both groups.
The control had numerically less
pre-weaning mortality. however this
fluctuation of 1.0-1.5% is common
on this farm and the difference was
not Significant (see Table 4).
Furthermore. it was suggested that
the addition of Biomin
® pHD eased
farrowing and reduced the number
of farrow assistance as well as
reduced the number of discharges
post lactation.
| Â |
Control |
Biomin® pHD |
P-value |
| Parity |
2.9 |
3.2 |
 |
| pH 1 (day 108 pregnancy) |
6.1 |
6.1 |
0.984 |
| pH 2 (day 112 pregnancy) |
6.3 |
5.8 |
0.148 |
| pH 3 (day 1 post farrowing) |
6.0 |
5.2 |
0.002 |
| pH4 (day 1 post weaning) |
6.3 |
5.5 |
0.002 |
| pH 5 (day 1 post insemination) |
6.1 |
5.3 |
0.027 |
| P < 0.05 |
 |
 |
 |
Table 3. Urine pH in response to feeding Biomin
® pHD (Philippines 2006).
| Â |
Control |
Biomin® pHD |
| Number of sows |
108 |
109 |
| Average parity |
3.3 |
3.0 |
| Average litter size |
10.6 |
10.3 |
| Total born/litter |
12.3 |
11.5 |
| Born alive/litter |
10.8 |
10.4 |
| Still births |
1.15 |
0.73 |
| Mummified |
0.35 |
0.37 |
| Average birth weights |
1.42 |
1.37 |
| Pre-weaning mortality (%) |
12.4 |
13.6 |
| Litter weaning weight |
57.3 |
56.7 |
| Average weaning weight (21 days) |
6.1 |
6.3 |
Table 4. Farrowing performance (Australia 2007).
Conclusion
In consideration of the facts mentioned
above the mode of action of
Biomin
® pHD can be extended in
terms of improving piglets born alive
due to its supposed effect on the
acid -base-balance of the body.
Nevertheless. the main focus is still
on supporting the natural defence
mechanism - via preventing the
invasion. multiplication and adhesion
of pathogenic bacteria to the urogenital
tract of the sow. This effect is based on two strategies:
- Creating unfavourable conditions for the bacteria and inhibiting their, growth by a blend of an inorganic acid and anionic substances.
- Binding pathogenic bacteria and inhibiting their adherence to the urinary tract cell walls by proanthocyanidins (PACs) contained in cranberries.
Consequently. the addition of
Biomin
® pHD increases productivity
of the herd due to its effect against
UTls and related metritis problems
and due to its supposed effect on
piglets born alive.
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