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Arquivo Brasileiro de Medicina Veterinária e Zootecnia

Print version ISSN 0102-0935On-line version ISSN 1678-4162

Arq. Bras. Med. Vet. Zootec. vol.61 no.3 Belo Horizonte June 2009

http://dx.doi.org/10.1590/S0102-09352009000300024 

ANIMAL SCIENCE AND TECHNOLOGY AND INSPECTION OF ANIMAL PRODUCTS

 

A model on biological flow of phosphorus in growing pigs

 

Modelo do fluxo do fósforo em suínos na fase de crescimento

 

 

J.B. LopesI; J.A. MoreiraII, *; E. KebreabII, III; D.M.S.S. VittiIV; A.L. AbdallaIV; L.A. CromptonIII; J. FranceIII

ICentro de Ciências Agrárias - UFPI - Teresina, PI
IIDepartment of Animal and Plant Science - University of Manitoba - Winnipeg - Manitoba, Canada
IIIDepartment of Animal & Poutry Science - University of Guelph - Guelph - Ontário, Canada
IV Centro de Energia Nuclear na Agricultura - Piracicaba, SP

 

 


ABSTRACT

Ten crossbred barrows weighting 20kg were allocated in five groups fed and on diets consisted of different total phosphorus (P) levels: 0.30%, 0.40%, 0.51%, 0.65%, and 0.73%. The animals were intravenously injected 7.4MBq of radioactive P (32P) and after seven days they were slaughtered for further analysis. The evaluated parameters were intake, excretion, specific activities, and flow of P in compartments (1-gut, 2-blood, 3-bone, and 4-soft tissue). Besides fecal losses, the kidneys played an import role in P regulation. The flows of P from tissue and gut to the blood were affected by P intake.

Keywords: pig, metabolism, balance, true absorption, radio-phosphorus, kinetic


RESUMO

Foram usados 10 leitões machos castrados com média de peso vivo de 20kg, alojados em gaiolas metabólicas. O delineamento experimental foi inteiramente ao acaso e os tratamentos consistiram em níveis de fósforo (P) nas dietas: 0,30; 0,40; 0,51; 0,65 e 0,73%. Os animais receberam injeção de 7,4 MBq de radiofósforo (32P) e após sete dias foram abatidos para posteriores análises. As variáveis avaliadas foram: ingestão, excreção, atividades específicas e fluxo de P nos compartimentos (1-trato digestivo, 2-corrente sanguínea, 3-tecidos moles e 4-ossos). Além das excreções fecais, os rins também representaram uma rota importante para a excreção do P. O fluxo de P dos tecidos e trato digestivo para o sangue não foi afetado pelo consumo de P. O modelo proposto foi eficiente para avaliar o fluxo de P.

Palavras-chave: suíno, metabolismo, balanço, absorção verdadeira, radiofósforo, cinética


 

 

INTRODUCTION

Phosphorus (P) is the second most abundant mineral in the animal body. It is present as structural component (Symonds and Forbes, 1993) and it is involved in a wide variety of biochemical reactions (Ternouth, 1990).

Secretory and absorptive processes of P along the gastrointestinal tract substantially differ in ruminant and non-ruminant animals (Breves and Schroder, 1991). In ruminants, large amount of P is secreted into gut by salivary glands and this endogenous secretion is balanced by net P absorption in the small intestine. However, urinary P excretion is low and does not contribute to P homeostasis. In contrast, in non- ruminants, salivary P concentration is lower but renal excretion plays an important function in P homeostasis.

A variety of techniques have been used to study P metabolism in domestic animals. These techniques differ from simple balance studies to more complex experiments involving cannulated animals or isolated organs. Fernandez (1995c), using combined results of balance studies and radioisotope kinetics, formulated and resolved a model of P metabolism for pigs to evaluate the nutritional implications of increasing P intake by pigs.

Experiments have been carried out using radioactive tracers to study the distribution of P by means of compartimental models (Grace, 1981; Schneider et al., 1987; Teixeira et al., 2004; Dias, 2006; Vitti et al., 2006). Kinetics of 32P, following intravenous injection, was studied using a compartment analysis supported by a computer program (Boston et al., 1981).

In Brazil, P metabolism has been studied in pigs using the model proposed by Fernandez (1995c) and modified by Lopes (Lopes et al., 2001; Moreira, 2002; Moreira et al., 2004). However, there are information related to P metabolism in pigs using the model of Vitti et al. (2000).

In the present study, the hypothesis that P intake regulates P utilization and P flow in gut, blood, soft tissues, and bone was assumed. The isotopic technique by using labeled P allows the formulation of a model showing the biological flows of phosphorus.

The aim of this study was to evaluate the effects of P intake on P metabolism in pigs, by using isotope and balance techniques. A mathematical model for P metabolism in pigs is proposed.

 

MATERIAL AND METHODS

The research was performed at the Center for Nuclear Energy in Agriculture, at the Universidade de São Paulo, in Piracicaba, SP. Ten crossbred barrows, mean live weight 20 kg, were housed in metabolic cages for a period of seven days for adaptation and another seven days for sampling (faeces, urine, and blood). Treatments consisted of: basal diet - treatment A - corn, soybean meal, and vitamin and mineral supplementation (except supplemental P), with 0.30% of total P. Adjustment of the total P in the other treatments was obtained by adding dicalcium phosphate to obtain the following total P levels: treatment B - 0.40%; C - 0.51%; D - 0.65%, and E - 0.73% (Table 1). Phosphorus levels in the experimental diets were deficient in treatments A and B, adequate in treatment C, and in excess in treatments D and E, according to NRC (Nutrient..., 1998). Feed was given twice a day.

After seven days, pre-experimental period, each animal was intravenously injected with 7.4MBq of 32P in 1mL of sterile isotonic saline solution (9g/L sodium chloride). Blood samples (10mL) were taken at 24 hours intervals, after isotope administration, for seven days. Blood samples were centrifuged and plasm removed for analysis. Nine mL trichloroacetic acid (100g/L) was added to 1mL plasm for protein precipitation. After centrifugation (1,100g) inorganic P was determined by colorimetric analysis (Fiske and Subbarow, 1925).

Phosphorus intake, total faeces excretion weight, and urine volume were daily recorded and sub-samples (10% of total outputs) were stored for further analysis. Faecal samples (1g) were overnight dried (105°C) and ashed (500°C for 8h). The ash was dissolved in concentrated HCl and the P concentration was determined by colorimetric method (Sarruge and Haag, 1974). Similar procedure was followed to determine the P concentration in food. Urine samples (30mL) were dissolved in 12N HCl, dried (55°C), and ashed (500°C). Ashes samples were diluted (3N HCl) and volume was made up to 10mL. Inorganic P was determined using vanadate-molybdate reagents (Sarruge and Haag, 1974).

For radioactivity measurements, 1mL plasma and 1mL urine samples were added to 19mL distilled water into counting vials. Ashed faecal samples (1g) were dissolved in 18N H2SO4 and placed into counting vials. Radioactivity of 32P was measured in a Packard Liquid Scintillation Spectrometer (model 2450B) using Cerenkov radiation. Specific activities in plasma (Psap) and feces (Psaf) were determined as follows (Lofgreen and Kleiber, 1953; Salviano and Vitti, 1998):

being Rcpm the radioactivity count per minute measured by the equipment in 1mL of plasma. Equation (1) also applies to specific activity measurement in 1g of faeces.

At the end of the experimental period, pigs were slaughtered by intravenous injection of pentobarbital (200mg/mL) and soft tissues (liver, heart, kidney, and longissimus dorsi muscle) and bone samples (13th and 14th ribs) were collected. Organs, muscle, and bone material were cleaned, weighed, and autoclaved. Samples were ground and dissolved in 18N H2SO4. The extract was transferred to vials for radioactivity determination. For mineral determination, bone samples were dissolved in concentrated HCl (Sarruge and Haag, 1974). Bone specific activity (Psab) in 1g dry matter and 32P incorporation (Pinc) in bone were calculated as follows:

being Pinj and Pt the total dose injected and the total inorganic P in bone (mg/g DM), respectively.

An isotope kinetics model based in Vitti et al. (2000) was used to describe P metabolism in pigs (Fig. 1). Data were analyzed using multiple regression system by SAS/2000.

 

 

 

 

 

 

The model assumes that (a) the gut pool is in both isotopic and non-isotopic steady states (b) and the plasma pool is in non-isotopic steady state.

 

RESULTS

Mean daily intake and daily excretion of P, specific activities, and P concentrations in bone, blood, and soft tissues are summarized in Table 3. Dietary P levels (L) affected P intake (Pint) as expressed by the following equation:

Phosphorus excreted in faeces (PF) and in urine (PU) were related to P intake:

Phosphorus excretion in faeces increased by 46.7% from the lowest to the highest P intake, and P concentration in urine increased by 90.5% from the lowest to the highest P intake.

The specific activity in faeces (SAF) decreased as dietary P increased. Similar response was observed in the specific activity in blood (SAblood):

Specific activity in bone and soft tissues were not affected by treatments, as well P concentrations in bone, tissues, and blood.

Phosphorus outflow of each treatment, obtained according the kinetic model, is shown in Table. 4.

According to the model (Table 4) P flow from to blood to digestive tract (F-12) was increased with P intake exponentially with P intake (P<0.05) (equation 15) as well P from digestive tract to blood (F-21) (equation 16):

Phosphorus bone accretion (F-32) and bone resorption (F-23) were not influenced by P intake. Phosphorus mobilization from the blood to soft tissues (F-42) and P recycling from soft tissues (F-24) to blood increased with P intake, as expressed in the equations 17 and 18:

 

DISCUSSION

The increased P flow across the digestive tract in response to increased P intake shows that the P absorption process was not saturated. According to Reinhardt et al. (1988), two processes are involved in the absorption of P: an active mechanism, which is easily saturated and a passive non-saturated process. The passive mechanism mainly occurs due to the high P concentration in the lumen of the tract which causes a high pressure towards the absorption sites.

The results of the present experiment showed that even at high P intake rates, the passive mechanism play an important role in P homeostasis. The increased P excretion in urine in response to P ingestion shows that, in non-ruminant animals, the kidneys are an important route for regulating P homeostasis, besides P excretion in faeces (Cupák et al., 1972; Vipperman Junior et al., 1974; Georgievskii, 1982; Breves and Schröder 1991; Fernandez, 1995ab).

The decreased values of specific activity feces and blood was due to the dilution process of the radioactive material caused by the high P inorganic concentration in those pools. In bone and soft tissues, inorganic P concentration did not change with P intake level as well as the specific activity in those compartments. The results are in agreement with literature (Fernandez, 1995b), that showed P accretion was constant and independent of the level of P intake. According to Fernandez (1995b), bone resorption is decreased with the increasing levels in P intake.

Bone resorption is dependent of the calcium and phosphorus levels in plasma. If the level of Ca in plasma is decreased, bone resorption is increased, in order to maintain stable the Ca level. Parathyroid hormone is the major regulator of Ca in plasma and its action depends on the presence of 1.25-dihydroxycholecalcipherol. Parathyroid hormone also affects P transport both in kidney and in gut (Furtado, 1991).

In the present study, despite the differences in P intake, the effect in bone resorption was not verified, due to the short experimental period (14 days) and the healthy conditions of the animals at the beginning of the experiment. When P resorption is compared to the total P absorbed (F23/F21), it is observed that for low P intake, higher amount of P is mobilized from bone to the blood. This seems to be a mechanism to maintain P levels in plasma. The increased output of P from soft tissues when low P intake is low also contributes to maintain P levels in the blood for the normal functions of the animal body.

 

CONCLUSIONS

Faecal and urinary losses of phosphorus regulated P homeostasis in growing pigs. Interchanges of phosphorus from the digestive tract and soft tissues to the blood were related to P intake. Phosphorus intake had no influence on phosphorus mobilization in bone in growing pigs. The model formulated based on the use of radioisotopes was coherent with the biological flow of phosphorus in pigs.

 

ACKNOWLEDGEMENTS

We would like to thank Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP Proc. 06/57574-5 and 04/14532-5) for financial support.

 

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Recebido em 25 de novembro de 2008
Aceito em 23 de março de 2009

 

 

* Autor para correspondência (corresponding author)
E-mail: japmoreira@bol.com.br

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