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1.
Sci Rep ; 7(1): 13112, 2017 10 13.
Artículo en Inglés | MEDLINE | ID: mdl-29030642

RESUMEN

Urea cycle enzyme deficiency (UCED) patients with hyperammonemia are treated with sodium benzoate (SB) and sodium phenylacetate (SPA) to induce alternative pathways of nitrogen excretion. The suggested guidelines supporting their use in the management of hyperammonemia are primarily based on non-analytic studies such as case reports and case series. Canine congenital portosystemic shunting (CPSS) is a naturally occurring model for hyperammonemia. Here, we performed cross-over, randomized, placebo-controlled studies in healthy dogs to assess safety and pharmacokinetics of SB and SPA (phase I). As follow-up safety and efficacy of SB was evaluated in CPSS-dogs with hyperammonemia (phase II). Pharmacokinetics of SB and SPA were comparable to those reported in humans. Treatment with SB and SPA was safe and both nitrogen scavengers were converted into their respective metabolites hippuric acid and phenylacetylglutamine or phenylacetylglycine, with a preference for phenylacetylglycine. In CPSS-dogs, treatment with SB resulted in the same effect on plasma ammonia as the control treatment (i.e. saline infusion) suggesting that the decrease is a result of volume expansion and/or forced diuresis rather than increased production of nitrogenous waste. Consequentially, treatment of hyperammonemia justifies additional/placebo-controlled trials in human medicine.


Asunto(s)
Hiperamonemia/tratamiento farmacológico , Nitrógeno/sangre , Aguas Salinas/uso terapéutico , Animales , Perros , Femenino , Hiperamonemia/sangre , Masculino , Fenilacetatos/efectos adversos , Fenilacetatos/farmacocinética , Fenilacetatos/uso terapéutico , Distribución Aleatoria , Benzoato de Sodio/efectos adversos , Benzoato de Sodio/farmacocinética , Benzoato de Sodio/uso terapéutico
2.
Vet Rec ; 173(2): 41, 2013 Jul 13.
Artículo en Inglés | MEDLINE | ID: mdl-23784060

RESUMEN

Nineteen dogs with vesico-urethral reflex dyssynergia (VURD) were treated with prazosin or terazosin 0.5 mg/kg twice daily to compare efficacy and side effects. Dogs were referred because of signs of (partial) urethral obstruction. Physical examination, abdominal ultrasonography, urinalysis and a radiographic contrast study of bladder and urethra (urethrocystography) were routinely performed. If no mechanical causes of obstruction or disease of the distal urinary tract were observed, the diagnosis VURD was presumed and the dogs were included in our study. Follow-up information was obtained from owners or referring veterinarians. Significantly more side effects were seen in the dogs treated with terazosin (n=14; 93 per cent) compared with the dogs treated with prazosin (n=5; 20 per cent; P=0.002). Effects of the treatment were comparable between prazosin and terazosin. Labradors and dogs that were castrated surgically had a significant better survival (P<0.01) compared with other breeds and animals that were castrated chemically. There was a moderate to good effect in 60 per cent of the dogs treated with prazosin, and in 64 per cent of the dogs treated with terazosin.


Asunto(s)
Antagonistas de Receptores Adrenérgicos alfa 1/uso terapéutico , Enfermedades de los Perros/tratamiento farmacológico , Prazosina/análogos & derivados , Prazosina/uso terapéutico , Retención Urinaria/veterinaria , Antagonistas de Receptores Adrenérgicos alfa 1/efectos adversos , Animales , Perros , Masculino , Prazosina/efectos adversos , Resultado del Tratamiento , Vejiga Urinaria/patología , Retención Urinaria/tratamiento farmacológico , Agentes Urológicos/efectos adversos , Agentes Urológicos/uso terapéutico
3.
J Vet Intern Med ; 23(5): 957-63, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19627473

RESUMEN

BACKGROUND: Copper-associated chronic hepatitis (CACH) recently has been recognized in the Labrador Retriever as an inherited disorder with a late onset of clinical signs. No studies have investigated dietary management for the long-term treatment of this disease or for its potential in delaying the onset of clinical signs in subclinical cases. OBJECTIVES: To investigate the effects of a low-copper diet and zinc gluconate on hepatic copper concentrations in Labrador Retrievers with abnormal hepatic copper concentrations. ANIMALS: Twenty-four client-owned Labradors that were related to patients affected with CACH and that had been diagnosed with increased hepatic copper concentrations. METHODS: Hepatic copper concentrations were assessed before and after an average of 8 and 16 months of treatment. During this time, all dogs were fed exclusively a low-copper diet. In addition, dogs were assigned to 1 of 2 groups in a randomized double-blind manner to receive a supplement of zinc gluconate or placebo. RESULTS: Twenty-one dogs completed the study. Hepatic copper concentrations decreased in both groups at recheck 1 (n = 21; group 1, P < .001; group 2, P= .001) and at recheck 2 (n= 16; group 1, P= .03; group 2, P= .04). No difference in hepatic copper concentrations was found between the 2 groups before treatment (P= .65), at recheck 1 or at recheck 2 (P= .52-.79). CONCLUSIONS AND CLINICAL RELEVANCE: Feeding low-copper diets to Labradors is effective in decreasing hepatic copper concentrations. Adjunctive treatment with zinc does not appear to increase the copper-lowering effects of dietary management.


Asunto(s)
Enfermedad Hepática Crónica Inducida por Sustancias y Drogas/veterinaria , Cobre/metabolismo , Enfermedades de los Perros/dietoterapia , Enfermedades de los Perros/metabolismo , Gluconatos/administración & dosificación , Hepatitis Animal/inducido químicamente , Animales , Biopsia/veterinaria , Enfermedad Hepática Crónica Inducida por Sustancias y Drogas/dietoterapia , Enfermedad Hepática Crónica Inducida por Sustancias y Drogas/metabolismo , Cobre/administración & dosificación , Perros , Método Doble Ciego , Femenino , Predisposición Genética a la Enfermedad , Gluconatos/farmacocinética , Hepatitis Animal/dietoterapia , Histocitoquímica , Hígado/efectos de los fármacos , Hígado/metabolismo , Masculino
7.
Tijdschr Diergeneeskd ; 121(5): 126-30, 1996 Mar 01.
Artículo en Holandés | MEDLINE | ID: mdl-8685885

RESUMEN

Before a veterinary drug is licensed for the Dutch market it has to comply to basic pharmaceutical standards. From the results of this study, carried out in the Spring of 1995, it appeared that many amoxicillin-containing tablets marketed in Holland do not fulfil these requirements. Only one third of the preparations complied with all criteria set by us. The preparations investigated originated from eight licence holders. The preparations from two licence holders satisfied our criteria. When choosing a veterinary drug, veterinarians should be aware of the considerable differences in pharmaceutical quality.


Asunto(s)
Amoxicilina/normas , Legislación de Medicamentos , Legislación Veterinaria , Comprimidos/normas , Animales , Países Bajos
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