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1.
J Agric Food Chem ; 66(31): 8262-8271, 2018 Aug 08.
Artículo en Inglés | MEDLINE | ID: mdl-29984998

RESUMEN

Reducing dietary crude protein (CP) intake effectively decreases nitrogen excretion in growing-finishing pigs but at the expense of poor growth when dietary CP content is reduced by ≥3%. In this study, we investigated the main disadvantages of low-protein diets supplemented with lysine, methionine, threonine, and tryptophan in pigs. First, changes in the nitrogen balance in response to differences in dietary CP content (18%, 15%, and 13.5%) were investigated in barrows (40 kg). Then, barrows (40 kg) surgically fitted with catheters in the mesenteric vein, portal vein, hepatic vein, and carotid artery were used to investigate changes in amino acid (AA) metabolism in the portal-drained viscera and liver in response to differences in dietary CP content. The results showed that low-protein diets reduced fecal and urinary nitrogen excretion ( P < 0.05) meanwhile resulted in significant decreases in nitrogen retention ( P < 0.05). Moreover, a reduction in the dietary CP content from 18% to 13.5% resulted in decreases in the net portal fluxes of NH3, glycine, and alanine as well as in the urea production in the liver ( P < 0.05), whereas their values as a percentage of nitrogen intake did not decline ( P > 0.05). The net portal fluxes of nonessential AA (NEAA) were reduced in the low-protein diet groups ( P < 0.05), while essential AA consumption in the liver increased ( P < 0.05). Thus, low-protein diets result in reductions in both nitrogen excretion and retention, and NEAA deficiency may be a major disadvantage of low-protein diets.


Asunto(s)
Aminoácidos/metabolismo , Dieta con Restricción de Proteínas/veterinaria , Nitrógeno/metabolismo , Sus scrofa/metabolismo , Aminoácidos/administración & dosificación , Animales , Dieta/veterinaria , Dieta con Restricción de Proteínas/efectos adversos , Suplementos Dietéticos , Heces/química , Hígado/metabolismo , Lisina/administración & dosificación , Masculino , Metionina/administración & dosificación , Nitrógeno/administración & dosificación , Nitrógeno/orina , Treonina/administración & dosificación , Triptófano/administración & dosificación , Urea/metabolismo , Vísceras/metabolismo
2.
J Anim Sci ; 96(9): 3804-3814, 2018 Sep 07.
Artículo en Inglés | MEDLINE | ID: mdl-30059979

RESUMEN

This study was performed to determine if pyruvate, which acts as a critical intermediate in energy metabolism, can substitute the role of glutamate as a metabolic fuel and effectively reduce nitrogen excretion in pigs. First, the experiment in vitro was carried out to investigate the effects of culturing porcine small intestinal epithelial cell line with pyruvate on the oxidation. Then, barrows weighing 40 kg were used in the experiment investigating the changes of nitrogen balance in response to addition of pyruvate to low-protein diets. Last, barrows (40 kg), which were surgically fitted with permanent catheters in the mesenteric vein, portal vein, hepatic vein, and carotid artery, were used to investigate the effects of supplementing low-protein diets with calcium pyruvate on the net portal fluxes of amino acids (AAs) and the consumption of AAs in the liver. The results showed that culturing cells with sodium pyruvate significantly reduced the number of glutamate oxidation (P < 0.05). Addition of calcium pyruvate to low-protein diets significantly reduced urinary nitrogen excretion from 13.2 g/d (18.0% crude protein, CP) to 10.3 g/d (15.0% CP) or 7.80 g/d (13.5% CP) and total nitrogen excretion from 22.5 g/d (18.0% CP) to 17.8 g/d (15.0% CP) or 14.2 g/d (13.5% CP) (P < 0.05), without obviously negative effects on the nitrogen retention (P > 0.05). Addition of calcium pyruvate to low-protein diets significantly decreased essential AA consumption rate in the liver (P < 0.05). This diet modification reduced the net portal fluxes of NH3, glycine, and alanine, as well as urea production rate in the liver (P < 0.05). The results indicated that pyruvate is an effective substitute for glutamate as a supplement in low-protein diets, reducing porcine nitrogen excretion and nitrogen consumption.


Asunto(s)
Alimentación Animal/análisis , Ácido Glutámico/farmacología , Nitrógeno/metabolismo , Ácido Pirúvico/farmacología , Porcinos/metabolismo , Alanina/metabolismo , Aminoácidos/metabolismo , Fenómenos Fisiológicos Nutricionales de los Animales , Animales , Línea Celular , Dieta/veterinaria , Dieta con Restricción de Proteínas , Proteínas en la Dieta/metabolismo , Suplementos Dietéticos , Metabolismo Energético/fisiología , Células Epiteliales/efectos de los fármacos , Células Epiteliales/metabolismo , Ácido Glutámico/metabolismo , Mucosa Intestinal/citología , Masculino , Oxidación-Reducción , Urea/metabolismo
3.
J Agric Food Chem ; 66(15): 3793-3800, 2018 Apr 18.
Artículo en Inglés | MEDLINE | ID: mdl-29471628

RESUMEN

The extensive metabolism of amino acids (AA) as fuel is an important reason for the low use efficiency of protein in pigs. In this study, we investigated whether regulation of the pyruvate dehydrogenase kinase (PDK)/pyruvate dehydrogenase alpha 1 (PDHA1) pathway affected AA consumption by porcine intestinal epithelial (IPEC-J2) cells and intestinal bacteria in pigs. The effects of knockdown of PDHA1 and PDK1 with small interfering RNA (siRNA) on nutrient consumption by IPEC-J2 cells were evaluated. IPEC-J2 cells were then cultured with sodium dichloroacetate (DCA) to quantify AA and glucose consumption and nutrient oxidative metabolism. The results showed that knockdown of PDHA1 using siRNA decreased glucose consumption but increased total AA (TAA) and glutamate (Glu) consumption by IPEC-J2 cells ( P < 0.05). Opposite effects were observed using siRNA targeting PDK1 ( P < 0.05). Additionally, culturing IPEC-J2 cells in the presence of 5 mM DCA markedly increased the phosphorylation of PDHA1 and PDH phosphatase 1, but inhibited PDK1 phosphorylation ( P < 0.05). DCA treatment also reduced TAA and Glu consumption and increased glucose depletion ( P < 0.05). These results indicated that PDH was the regulatory target for shifting from AA metabolism to glucose metabolism and that culturing cells with DCA decreased the consumption of AAs by increasing the depletion of glucose through PDH activation.


Asunto(s)
Aminoácidos/metabolismo , Ácido Dicloroacético/farmacología , Glucosa/metabolismo , Mucosa Intestinal/metabolismo , Complejo Piruvato Deshidrogenasa/metabolismo , Porcinos/metabolismo , Animales , Bacterias/metabolismo , Línea Celular , Suplementos Dietéticos/análisis , Intestinos/efectos de los fármacos , Intestinos/microbiología , Piruvatos/metabolismo
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