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1.
Cerebellum ; 23(2): 401-417, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36943575

RESUMEN

Spinocerebellar ataxias (SCAs) are a large and diverse group of autosomal-dominant neurodegenerative diseases. No drugs have been approved for these relentlessly progressive and fatal SCAs. Our previous studies indicate that oxidative stress, neuroinflammation, and neuronal apoptosis are elevated in the SCA17 mice, which are the main therapeutic targets of hyperbaric oxygen treatment (HBOT). HBOT is considered to be an alternative and less invasive therapy for SCAs. In this study, we evaluated the HBOT (2.2 ATA for 14 days) effect and the persistence for the management of SCA17 mice and their wild-type littermates. We found HBOT attenuated the motor coordination and cognitive impairment of SCA17 mice and which persisted for about 1 month after the treatment. The results of several biochemistry and liver/kidney hematoxylin and eosin staining show the HBOT condition has no obvious toxicity in the mice. Immunostaining analyses show that the neuroprotective effect of HBOT could be through the promotion of BDNF production and the amelioration of neuroinflammation. Surprisingly, HBOT executes different effects on the male and female SCA17 mice, including the reduction of neuroinflammation and activation of CaMKII and ERK. This study suggests HBOT is a potential alternative therapeutic treatment for SCA17. Accumulated findings have revealed the similarity in disease pathomechanisms and possible therapeutic strategies in polyQ diseases; therefore, HBOT could be an optional treatment as well as the other polyQ diseases.


Asunto(s)
Disfunción Cognitiva , Oxigenoterapia Hiperbárica , Péptidos , Ataxias Espinocerebelosas , Ratones , Masculino , Femenino , Animales , Oxigenoterapia Hiperbárica/métodos , Enfermedades Neuroinflamatorias , Disfunción Cognitiva/terapia , Ataxias Espinocerebelosas/terapia , Ataxias Espinocerebelosas/tratamiento farmacológico
2.
Vet Q ; 44(1): 1-10, 2024 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-39028259

RESUMEN

Fibrinogen-fibrin degradation products (DR-70) are derived from tumor cells or metastases. Our previous study reported the diagnostic values in dogs with tumors, but no research has yet to be conducted to establish DR-70 as a prognostic marker. Herein, we investigated changes in DR-70 concentrations and disease courses in dogs with tumors. Overall survival time (OST) analysis was performed in 195 dogs with tumors, stratified with a recommended cut-off (1.514 µg/mL). Continual DR-70 measurements were performed during the medical interventions of 27 dogs with neoplasms. Clinical conditions and medical records were retrospectively reviewed. According to a cut-off value, dogs with plasma DR-70 concentrations above 1.514 µg/mL had shorter survival rates than those with concentrations below this threshold. In cases with complete or partial remission in response to treatment, the DR-70 concentration was decreased compared with that at the first visit, whereas it was increased in patients with disease progression. Our study suggested that changes in DR-70 concentration can be used as a prognostic biomarker for canine neoplasms. Furthermore, increased plasma DR-70 levels might be associated with shorter survival, and DR-70 concentrations may reflect responses to medical intervention.


Asunto(s)
Biomarcadores de Tumor , Enfermedades de los Perros , Productos de Degradación de Fibrina-Fibrinógeno , Neoplasias , Perros , Animales , Enfermedades de los Perros/sangre , Enfermedades de los Perros/mortalidad , Enfermedades de los Perros/diagnóstico , Neoplasias/veterinaria , Neoplasias/sangre , Neoplasias/mortalidad , Neoplasias/diagnóstico , Pronóstico , Estudios Retrospectivos , Masculino , Femenino , Biomarcadores de Tumor/sangre , Productos de Degradación de Fibrina-Fibrinógeno/análisis , Productos de Degradación de Fibrina-Fibrinógeno/metabolismo , Análisis de Supervivencia , Fibrinógeno/análisis
3.
J Vet Intern Med ; 37(6): 2391-2401, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37837297

RESUMEN

BACKGROUND: Tumor biomarkers have used widely in clinical oncology in human medicine. Only a few studies have evaluated the clinical utility of tumor biomarkers for veterinary medicine. A test for fibrinogen and fibrin degradation products (DR-70) has been proposed as an ideal biomarker for tumors in humans. The clinical value of DR-70 for veterinary medicine however has yet to be determined. OBJECTIVES: Investigate the diagnostic value of DR-70 concentrations by comparing them between healthy dogs and dogs with tumors. ANIMALS: Two hundred sixty-three dogs with different types of tumors were included. Sixty healthy dogs also were recruited for comparison. METHODS: The DR-70 concentrations were measured in all recruited individuals by ELISA. Clinical conditions were categorized based on histopathology, cytology, ultrasound examination, radiology, clinical findings, and a combination of these tests. RESULTS: The median concentration of DR-70 was 2.130 ± 0.868 µg/mL in dogs with tumors, which was significantly higher than in healthy dogs (1.202 ± 0.610 µg/mL; P < .0001). With a cut-off of 1.514 µg/mL, the sensitivity and specificity of DR-70 were 84.03% and 78.33%, respectively. The area under curve was 0.883. The DR-70 concentration can be an effective tumor biomarker in veterinary medicine. CONCLUSIONS AND CLINICAL IMPORTANCE: Increased DR-70 concentrations were not affected by tumor type, sex, age, or body weight. However, in dogs with metastatic mast cell tumors and oral malignant melanoma, DR-70 concentrations were significantly increased. Additional studies, including more dogs with nonneoplastic diseases, are needed to further evaluate the usefulness of DR-70 as a tumor biomarker.


Asunto(s)
Biomarcadores de Tumor , Enfermedades de los Perros , Productos de Degradación de Fibrina-Fibrinógeno , Neoplasias , Animales , Perros , Humanos , Biomarcadores de Tumor/sangre , Enfermedades de los Perros/sangre , Enfermedades de los Perros/diagnóstico , Productos de Degradación de Fibrina-Fibrinógeno/análisis , Fibrinógeno/metabolismo , Neoplasias/sangre , Neoplasias/diagnóstico , Neoplasias/veterinaria , Sensibilidad y Especificidad
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