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1.
J Anim Sci ; 83(6): 1267-73, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15890804

RESUMEN

An experiment was conducted to determine the effect of feeding blends of grains naturally contaminated with Fusarium mycotoxins to mature, exercised horses, and to test the efficacy of a polymeric glucomannan mycotoxin adsorbent (GM polymer) in preventing Fusarium mycotoxicoses. Six mature, mixed-breed mares with an average BW of 530 kg were assigned to one of three dietary treatments for 21 d in a replicated 3 x 3 Latin square design. Feed consumed each day was a combination of up to 3.5 kg of concentrates and 5.0 kg of mixed timothy/alfalfa hay (as-fed basis). The concentrates fed included 1) manage; 2) blend of contaminated grains; and 3) contaminated grains + 0.2% GM polymer (MTB-100, Alltech Inc., Nicholasville, KY). Concentrates containing contaminated grains averaged 11.0 ppm deoxynivalenol, 0.7 ppm 15-acetyldeoxynivalenol, and 0.8 ppm zearalenone (as-fed basis). Feed intake and BW were monitored over a 21-d period. Horses were maintained on a fixed exercise schedule throughout the experiment. At the end of the experiment, each horse completed a time-to-fatigue treadmill step test. Variables measured during pretest, each step of the test, and 5 and 10 min posttest were as follows: 1) time-to-fatigue, 2) heart rate, 3) hematological variables, and 4) serum lactate concentration. Each step consisted of 2 min of fast trot with a 2% increase in incline after each 2 min. Feed intake by horses fed contaminated grains was decreased compared with controls throughout the experiment (P < 0.05). Supplementation of 0.2% GM polymer to the contaminated diet did not alter feed intake by horses compared with those fed the unsupplemented contaminated diet. All hay was consumed regardless of concentrate fed. Weight loss from 0 to 21 d was observed in horses fed contaminated grains compared with controls (P < 0.05). No effect of diet was seen on variables used to measure athletic ability, although the results showed an expected response to exercise for a fit horse. We conclude that exercised horses are susceptible to Fusarium mycotoxicoses as indicated by appetite suppression and weight loss.


Asunto(s)
Fenómenos Fisiológicos Nutricionales de los Animales , Ingestión de Alimentos/efectos de los fármacos , Caballos/fisiología , Micotoxicosis/veterinaria , Micotoxinas/farmacología , Condicionamiento Físico Animal/fisiología , Alimentación Animal/análisis , Animales , Prueba de Esfuerzo/veterinaria , Femenino , Contaminación de Alimentos , Fusarium , Caballos/metabolismo , Micotoxicosis/prevención & control , Micotoxinas/análisis , Polímeros/administración & dosificación , Polímeros/farmacología , Distribución Aleatoria , Factores de Tiempo , Pérdida de Peso/efectos de los fármacos
2.
J Anim Sci ; 81(9): 2123-30, 2003 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12968685

RESUMEN

The feeding of Fusarium mycotoxin-contaminated grains adversely affects the performance of swine and poultry. Very little information is available, however, on adverse effects associated with feeding these mycotoxin-contaminated grains on the performance of horses. An experiment was conducted to investigate the effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on feed intake, serum immunoglobulin (Ig) concentrations, serum chemistry, and hematology of horses. A polymeric glucomannan mycotoxin adsorbent (GM polymer) was also tested for efficacy in preventing Fusarium mycotoxicoses. Nine mature, nonexercising, light, mixed-breed mares were assigned randomly to one of three dietary treatments for 21 d. The horses were randomly reassigned and the experiment was subsequently replicated in time following a 14-d washout interval. Feed consumed each day was a combination of up to 2.8 kg of concentrates and 5 kg of mixed timothy/alfalfa hay. The concentrates fed included the following: 1) control, 2) blend of contaminated grains (36% contaminated wheat and 53% contaminated corn), and 3) blend of contaminated grains + 0.2% GM polymer. Diets containing contaminated grains averaged 15.0 ppm of deoxynivalenol, 0.8 ppm of 15-acetyldeoxynivalenol, 9.7 ppm of fusaric acid, and 2.0 ppm of zearalenone. Feed intake by all horses fed contaminated grains was reduced (P < 0.001) compared with controls throughout the experiment. Supplementation of 0.2% GM polymer to the contaminated diet increased (P = 0.004) feed intake of horses compared with those fed the unsupplemented contaminated diet. Serum activities of gamma-glutamyltransferase were higher (P = 0.047 and 0.027) in horses fed the diet containing contaminated grain compared with those fed the control diet on d 7 and 14, but not on d 21 (P = 0.273). Supplementation of GM polymer to the contaminated diet decreased (P < 0.05) serum gamma-glutamyltransferase activities of horses compared with those fed unsupplemented contaminated diet on d 7 and 14. Other hematology and serum chemistry measurements including serum IgM, IgG, and IgA, were not affected by diet. It was concluded that the feeding of grains naturally contaminated with Fusarium mycotoxins caused a decrease in feed intake and altered serum gamma glutamyltransferase activities. The supplementation of GM polymer prevented these mycotoxin-induced adverse effects.


Asunto(s)
Catárticos/farmacología , Grano Comestible/microbiología , Contaminación de Alimentos , Caballos/fisiología , Mananos/farmacología , Micotoxinas/administración & dosificación , Adsorción , Alimentación Animal/efectos adversos , Alimentación Animal/microbiología , Animales , Análisis Químico de la Sangre/veterinaria , Catárticos/administración & dosificación , Ingestión de Alimentos/efectos de los fármacos , Grano Comestible/química , Femenino , Fusarium/metabolismo , Caballos/sangre , Caballos/crecimiento & desarrollo , Inmunoglobulina A/sangre , Inmunoglobulina G/sangre , Inmunoglobulina M/sangre , Mananos/administración & dosificación , Micotoxinas/antagonistas & inhibidores , Micotoxinas/metabolismo , Distribución Aleatoria , gamma-Glutamiltransferasa/metabolismo
3.
Blood ; 67(6): 1568-77, 1986 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-3011147

RESUMEN

A unique, intrinsic, hereditary canine platelet disorder attributable to abnormal fibrinogen receptor availability is described. Thrombopathic platelets from 13 severely affected basset hounds failed to aggregate in response to all agonists tested except thrombin. Normal platelet interaction with the various stimuli was inferred on the basis of their ability to elicit unimpaired shape change in thrombopathic platelets. No quantitative differences in major platelet membrane glycoproteins, intraplatelet fibrinogen, adenine nucleotides, or serotonin uptake were detected. Dense granule secretion was impaired. The ultrastructural appearance of thrombopathic platelets was normal. Fibrinogen-platelet interaction was evaluated by reacting platelet-rich plasma (PRP) with fibrinogen coupled to polymeric acrylonitrile beads and scoring the extent of stimulus-induced agglutination. The aggregatory responses of normal and thrombopathic platelets were closely correlated with fibrinogen receptor availability. In contrast to human platelets, epinephrine-stimulated canine platelets did not interact with immobilized fibrinogen, and arachidonate generally induced only weak agglutination. Thrombopathic platelets agglutinated fibrinogen beads at reduced rates when stimulated with physiologic doses of thrombin and high-dose calcium ionophore, A23187. Our data suggest that thrombin-mediated induction of canine platelet fibrinogen receptors may proceed by pathway(s) alternate to those shared by other platelet agonists, and/or that secreted granule constituents may act synergistically with thrombin to overcome inhibition of signal-response-coupled reactions mediating the interaction of fibrinogen with its receptor. This congenital platelet defect provides further evidence, in a species other than human, for the pivotal role of fibrinogen receptor induction in platelet aggregation.


Asunto(s)
Plaquetas/metabolismo , Enfermedades de los Perros/fisiopatología , Fibrinógeno/metabolismo , Trombosis/veterinaria , Nucleótidos de Adenina/metabolismo , Animales , Plaquetas/ultraestructura , Calcimicina/farmacología , Adhesión Celular , Enfermedades de los Perros/genética , Perros , Relación Dosis-Respuesta a Droga , Epinefrina/farmacología , Femenino , Glicoproteínas/análisis , Inmunoelectroforesis , Masculino , Proteínas de la Membrana/análisis , Microscopía Electrónica , Agregación Plaquetaria , Glicoproteínas de Membrana Plaquetaria , Receptores de Superficie Celular/biosíntesis , Receptores de Superficie Celular/genética , Serotonina/metabolismo , Trombosis/genética , Trombosis/fisiopatología
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