RESUMEN
In a captive Macaca mulatta breeding colony, a single family group with 39 animals showed 19 individuals being born with dramatic tail shortening. Through clinical, genealogical, radiographic, and cytogenetic evaluation, it was related to a probable dominant autosomal inheritance of the reduction in the number of distal caudal vertebrae.
Asunto(s)
Macaca mulatta/anomalías , Enfermedades de los Monos/congénito , Cola (estructura animal)/anomalías , Animales , Animales de Laboratorio/anomalías , Femenino , Masculino , Cola (estructura animal)/anatomía & histologíaRESUMEN
BACKGROUND: The high consumption of medicines by the population and their storage at home might cause an increase in the number of pharmaceutical substances that may be inappropriately discarded in the sanitary sewage, reaching an environmental aquatic. Thus, the effects of these emerging contaminants need more studies. OBJECTIVES: To identify the profile of most medicines that are discarded by users of community pharmacy and evaluate the toxicity of the most disposed drugs. METHODS: This was a translational study. A descriptive observational study was carried out for convenience of community pharmacy users using a standardized questionnaire. Subsequently, the lethal concentration 50 (LC50) for medicine that is most frequently discarded was determined. After LC50, the embryos (n = 144) were exposed to sublethal concentrations for most discarded drug at 24, 48, and 72 h. Mortality, heartbeat, and embryo deformities were used as parameters of toxicity. RESULTS: Most respondents (96%) had a "home pharmacy." The primary forms of disposal were in the common household waste, kitchen sink, and/or bathroom. The medicines that were most incorrectly discarded by the interviewees were nimesulide (17.1%), dipyrone (10.7%), and paracetamol (5.2%). LC50 of nimesulide was calculated (0.92 µgmL-1). The toxicological test revealed that embryos exposed to nimesulide showed several abnormalities, such as defects in the spinal cord, tail, yolk sac, as well as pericardial edema. Furthermore, the heartbeat decreased by 30% at a concentration of 0.4 µgmL-1 as compared with control group. The yolk sac and pericardial areas increased to >100% in all treatment groups when compared with the control group. CONCLUSION: Respondents disposed medicines in an inappropriate manner primarily in household waste and in the toilet. Nimesulide was the most discarded drug according to study population. Moreover, teratogenic effects such as spinal cord defects, decreasing heartbeats, and increasing pericardial and yolk sac area in embryos were observed after exposure to nimesulide. These results show that nimesulide may promote risk to aquatic organisms and to human health if it is discarded in an unsafe manner.
Asunto(s)
Sulfonamidas/toxicidad , Administración de Residuos/métodos , Contaminantes Químicos del Agua/toxicidad , Adolescente , Adulto , Anciano , Animales , Embrión no Mamífero/anomalías , Embrión no Mamífero/efectos de los fármacos , Embrión no Mamífero/fisiología , Femenino , Corazón/efectos de los fármacos , Corazón/embriología , Corazón/fisiología , Cardiopatías Congénitas/inducido químicamente , Frecuencia Cardíaca/efectos de los fármacos , Humanos , Masculino , Persona de Mediana Edad , Preparaciones Farmacéuticas , Medición de Riesgo , Médula Espinal/anomalías , Médula Espinal/efectos de los fármacos , Cola (estructura animal)/anomalías , Cola (estructura animal)/efectos de los fármacos , Residuos , Saco Vitelino/efectos de los fármacos , Adulto Joven , Pez Cebra/anomalías , Pez Cebra/fisiologíaRESUMEN
The present study reported the mutation C189G in the T gene (Brachyury gene) as the cause of malformation in the tail of the Labrador dog. One litter of Labradors, from a mating between a female with short tail and a male with normal tail admitted at the Veterinary Teaching Hospital of Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil, was evaluated in this study. Blood samples were collected from the female and her puppies. After DNA extraction, sequencing and PCR-RFLP were carried out. The C189G mutation was identified through both techniques only in dogs with short tail.(AU)
No presente trabalho relata-se a mutação C189G no gene T (Brachyury gene) como causa da malformação da cauda em cães da raça Labrador. Uma ninhada de labradores, provenientes do acasalamento entre uma fêmea com a cauda curta e um macho com a cauda normal, encaminhados ao Hospital Veterinário da Universidade Federal de Mato Grosso do Sul, Campo Grande, Brasil, foi avaliada nesse estudo. Amostras de sangue da cadela e filhotes foram coletadas. Após extração de DNA, sequenciamento e PCR-RFLP foram realizados. A mutação C189G foi identificada por meio de ambas as técnicas apenas nos cães com a cauda malformada.(AU)
Asunto(s)
Animales , Perros , Cola (estructura animal)/anomalías , Perros/anomalías , Técnicas de Genotipaje/veterinariaRESUMEN
The present study reported the mutation C189G in the T gene (Brachyury gene) as the cause of malformation in the tail of the Labrador dog. One litter of Labradors, from a mating between a female with short tail and a male with normal tail admitted at the Veterinary Teaching Hospital of Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil, was evaluated in this study. Blood samples were collected from the female and her puppies. After DNA extraction, sequencing and PCR-RFLP were carried out. The C189G mutation was identified through both techniques only in dogs with short tail.(AU)
No presente trabalho relata-se a mutação C189G no gene T (Brachyury gene) como causa da malformação da cauda em cães da raça Labrador. Uma ninhada de labradores, provenientes do acasalamento entre uma fêmea com a cauda curta e um macho com a cauda normal, encaminhados ao Hospital Veterinário da Universidade Federal de Mato Grosso do Sul, Campo Grande, Brasil, foi avaliada nesse estudo. Amostras de sangue da cadela e filhotes foram coletadas. Após extração de DNA, sequenciamento e PCR-RFLP foram realizados. A mutação C189G foi identificada por meio de ambas as técnicas apenas nos cães com a cauda malformada.(AU)
Asunto(s)
Animales , Perros , Cola (estructura animal)/anomalías , Perros/anomalías , Técnicas de Genotipaje/veterinariaRESUMEN
In the face of mosquito-borne disease outbreaks, effective mosquito control is a primary goal for public health. Insect repellents, containing active compounds such as DEET and picaridin, are a first defence against biting insects. Owing to widespread use and incomplete sewage treatment, these compounds are frequently detected in surface waters, but their effects on aquatic taxa such as mosquito larvae or their naturally occurring aquatic predators are poorly understood. We investigated the effects of environmentally realistic concentrations of commercial products containing DEET and picaridin on survivorship of mosquito larvae, and their potential indirect effects on survival of larval salamanders, a major predator of mosquito larvae. Larval mosquitos were not affected by exposure to repellents containing DEET or picaridin. We found no larval salamander mortality in control and DEET treatments, but mortality rates in picaridin treatments ranged from 45 to 65% after 25 days of exposure. Salamander larvae exposed to repellents containing picaridin began to display tail deformities and impaired development four days after the experiment began. Our findings suggest the possibility that environmentally realistic concentrations of picaridin-containing repellents in surface waters may increase the abundance of adult mosquitos owing to decreased predation pressure.
Asunto(s)
Ambystoma/crecimiento & desarrollo , Culicidae/efectos de los fármacos , DEET/toxicidad , Piperidinas/toxicidad , Ambystoma/anomalías , Animales , Cadena Alimentaria , Repelentes de Insectos/toxicidad , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Cola (estructura animal)/anomalías , Contaminantes Químicos del Agua/efectos adversosRESUMEN
Tadpoles of two sympatric anurans, Bufo gargarizans Cantor, 1842 and Rana zhenhaiensis Ye, Fei & Matsui, 1995, were used as model organisms to examine the effects of different levels of tail loss on swimming performance and survival. On average, B. gargarizans tadpoles were shorter and had smaller tails and body mass than R. zhenhaiensis. After 75% tail loss, the survival rate of experimental and control B. gargarizans tadpoles, and of experimental tadpoles of the two species, differed significantly; the number of tadpoles surviving a complete impairment of their swimming ability did not differ between B. gargarizans and R. zhenhaiensis. After 50% tail loss, the swimming performance (swimming speed, maximum distance and number of stops) of the two species was significantly affected. However, the adverse influence of tail loss on the swimming speed of B. gargarizans tadpoles was greater compared to R. zhenhaiensis tadpoles. Our data indicates that a 50% tail loss results in swimming costs for B. gargarizans and R. zhenhaiensis tadpoles, and that 75% tail loss decreases the survival rate of B. gargarizans tadpoles. Therefore, we conclude that tadpoles of different species and with the same degree of tail loss use distinctive strategies to improve individual fitness in the face of predator pressure.(AU)
Asunto(s)
Animales , Bufonidae/anomalías , Ranidae/anomalías , Análisis de Supervivencia , Locomoción , Cola (estructura animal)/anomalíasRESUMEN
Tadpoles of two sympatric anurans, Bufo gargarizans Cantor, 1842 and Rana zhenhaiensis Ye, Fei & Matsui, 1995, were used as model organisms to examine the effects of different levels of tail loss on swimming performance and survival. On average, B. gargarizans tadpoles were shorter and had smaller tails and body mass than R. zhenhaiensis. After 75% tail loss, the survival rate of experimental and control B. gargarizans tadpoles, and of experimental tadpoles of the two species, differed significantly; the number of tadpoles surviving a complete impairment of their swimming ability did not differ between B. gargarizans and R. zhenhaiensis. After 50% tail loss, the swimming performance (swimming speed, maximum distance and number of stops) of the two species was significantly affected. However, the adverse influence of tail loss on the swimming speed of B. gargarizans tadpoles was greater compared to R. zhenhaiensis tadpoles. Our data indicates that a 50% tail loss results in swimming costs for B. gargarizans and R. zhenhaiensis tadpoles, and that 75% tail loss decreases the survival rate of B. gargarizans tadpoles. Therefore, we conclude that tadpoles of different species and with the same degree of tail loss use distinctive strategies to improve individual fitness in the face of predator pressure.
Asunto(s)
Animales , Análisis de Supervivencia , Bufonidae/anomalías , Cola (estructura animal)/anomalías , Locomoción , Ranidae/anomalíasRESUMEN
Lithium has been the paradigmatic treatment for bipolar disorder since 1950s, offering prophylactic and acute efficacy against maniac and depressive episodes. Its use during early pregnancy and the perinatal period remains controversial due to reports of negative consequences on the newborn including teratogenic and neurobehavioral effects generally referred as Floppy baby syndrome. The mechanisms underlying lithium therapeutic action are still elusive but exacerbation of Wnt signaling pathway due to GSK-3 inhibition is believed to represent its main effect. In this study we evaluated the impact of lithium exposure during zebrafish embryonic and early development including behavioral and molecular characterization of Wnt-ß-catenin pathway components. Wild-type zebrafish embryos were individually treated for 72 hpf with LiCl at 0.05, 0.5 and 5mM. No significant teratogenic and embryotoxic effects were observed. At the end of treatment period western blot analysis of selected Wnt-ß-catenin system components showed increased ß-catenin and decreased N-cadherin protein levels, without significant changes in Wnt3a, supporting GSK-3 inhibition as lithium's main target. At 10 dpf 0.5 and 5mM lithium-treated larvae showed a dose-dependent decrease in locomotion among other exploratory parameters, resembling lithium-induced Floppy baby syndrome neurobehavioral symptoms in humans. At this later period previously altered proteins returned to control levels in treated groups, suggesting that the neurobehavioral effects are a lasting consequence of lithium exposure during early development. RT-qPCR analysis of ß-catenin and N-cadherin gene expression showed no effects of lithium at 3 or 10 dpf, suggesting that protein fluctuations were likely due to post-transcriptional events. Other Wnt target genes were evaluated and only discrete alterations were observed. These results suggest that zebrafish may be a valuable model for investigation of early effects of lithium that may be mediated by effects on the Wnt signaling pathway.
Asunto(s)
Antimaníacos/toxicidad , Cloruro de Litio/toxicidad , Proteína Wnt3A/metabolismo , Proteínas de Pez Cebra/metabolismo , Pez Cebra/crecimiento & desarrollo , beta Catenina/metabolismo , Animales , Western Blotting , Cadherinas/metabolismo , Relación Dosis-Respuesta a Droga , Cardiopatías Congénitas/inducido químicamente , Estimación de Kaplan-Meier , Actividad Motora/fisiología , ARN Mensajero , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Cola (estructura animal)/anomalías , Pez Cebra/fisiologíaRESUMEN
Endosulfan is a widely used pesticide despite its extreme toxicity to a variety of taxa and its worldwide ban. The aim of the present study was to evaluate the acute and chronic toxicity of endosulfan on the embryonic-larval development of the common South American toad Rhinella arenarum. The results showed that lethal and sublethal effects increased with concentration and exposure time. The sensitivity to endosulfan increased during the larval period, the complete operculum stage (S.25) being the most sensitive (504-h median lethal concentration [LC50] = 0.01 mg endosulfan/L; 10% lethal concentration [LC10] = 0.004 mg endosulfan/L). Endosulfan exposure caused morphological abnormalities such as general underdevelopment, edema, gill malformations, and cellular dissociation as well as neurotoxicity. Our results also showed that larvae exposed to concentrations of 0.005 mg endosulfan/L and 0.01 mg endosulfan/L completed metamorphosis earlier than controls, but with underdevelopment. The 240-h teratogenic index was 6.13, implying a high risk for embryos to be malformed in the absence of significant embryonic lethality. Because the hazard quotients for chronic exposure were over 1, the level of concern value and toxicity endpoints obtained in the present study for R. arenarum occurred at concentrations lower than the levels of endosulfan reported in the environment, this pesticide should be considered a potential risk for this species.
Asunto(s)
Bufonidae/anomalías , Embrión no Mamífero/efectos de los fármacos , Endosulfano/toxicidad , Plaguicidas/toxicidad , Teratógenos/toxicidad , Animales , Embrión no Mamífero/anomalías , Branquias/anomalías , Branquias/efectos de los fármacos , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Metamorfosis Biológica/efectos de los fármacos , Microcefalia/inducido químicamente , Medición de Riesgo , Cola (estructura animal)/anomalías , Cola (estructura animal)/efectos de los fármacosRESUMEN
STUDY DESIGN: To inhibit ß-catenin specifically signaling in chondrocytes Col2-ICAT transgenic mice were generated. Anomalies in caudal vertebrae were detected during embryonic and postnatal stages of Col2-ICAT transgenic mice. OBJECTIVE: To determine the role of canonical ß-catenin signaling in caudal vertebral development. SUMMARY OF BACKGROUND DATA: ß-catenin signaling plays a critical role in skeletal development. Col2-ICAT transgenic mice were generated to selectively block ß-catenin signaling by overexpression of the ICAT gene in chondrocytes. METHODS: Tails of E16.5 transgenic embryos and adult Col2-ICAT transgenic mice and their wild-type littermates were collected and analyzed. Skeletal preparation, 3-dimensional micro-computed tomographic and histological analyses were performed to evaluate changes in the structure of caudal vertebrae. Bromodeoxyuridine labeling was performed to evaluate changes in chondrocyte proliferation in caudal vertebrae. RESULTS: Skeletal preparation and 3-dimensional micro-computed tomographic analyses revealed bone deformation and angulated deformities in tail tissue in Col2-ICAT transgenic mice. Histological studies revealed abnormal bone development and dysplastic caudal vertebrae in Col2-ICAT transgenic mice. Inhibition of ß-catenin signaling in cartilage resulted in vertebral dysplasia leading to aberrant resegmenting process. Thus, 2 poorly developed sclerotomes failed to fuse to form a complete vertebrae. BrdU labeling revealed a decreased chondrocyte proliferation in both cartilageous templates of transgenic embryos and the growth plate of adult Col2-ICAT transgenic mice. CONCLUSION: Wnt/ß-catenin signaling plays an important role in vertebral development. Inhibition of ß-catenin signaling in chondrocytes results in caudal vertebra deformity in mice, which may occur as early as in the stage of sclerotome formation. LEVEL OF EVIDENCE: N/A.
Asunto(s)
Condrocitos/metabolismo , Transducción de Señal , Columna Vertebral/metabolismo , beta Catenina/metabolismo , Proteínas Adaptadoras Transductoras de Señales , Animales , Proteínas de Ciclo Celular/genética , Proteínas de Ciclo Celular/metabolismo , Proliferación Celular , Condrocitos/citología , Colágeno Tipo II/genética , Embrión de Mamíferos/anomalías , Embrión de Mamíferos/metabolismo , Elementos de Facilitación Genéticos/genética , Inmunohistoquímica , Ratones , Ratones Endogámicos C57BL , Ratones Transgénicos , Regiones Promotoras Genéticas/genética , Proteínas Represoras , Columna Vertebral/anomalías , Columna Vertebral/diagnóstico por imagen , Cola (estructura animal)/anomalías , Cola (estructura animal)/diagnóstico por imagen , Cola (estructura animal)/metabolismo , Factores de Transcripción/genética , Factores de Transcripción/metabolismo , Microtomografía por Rayos X , beta Catenina/genéticaRESUMEN
A 2-day-old poodle puppy was seen to have hypoplastic and arthrogrypotic hindlimbs and no tail. Palpation revealed an absence of lumbar and sacral vertebrae. At necropsy examination, the colon had a blind ending at the umbilical area, there were no urinary system organs, the spinal cord ended at the thoracic level and no genital system organs were found except for a structure similar to a rudimentary penis. The pelvis was abnormal with no articulation with the spine. This congenital anomaly was consistent with perosomus elumbis, a rare condition of unknown aetiology with few reported cases.
Asunto(s)
Anomalías Múltiples/veterinaria , Artrogriposis/veterinaria , Enfermedades de los Perros/patología , Anomalías Múltiples/patología , Animales , Animales Recién Nacidos , Artrogriposis/patología , Perros , Miembro Posterior/anomalías , Vértebras Lumbares/anomalías , Masculino , Sacro/anomalías , Médula Espinal/anomalías , Columna Vertebral/anomalías , Cola (estructura animal)/anomalíasRESUMEN
A new mouse mutant, tail short variable (Tsv) produces a reduction deformity of the tail, growth retardation, and, in adults, a mild anemia. Genetic and embryological studies show that on all genetic backgrounds there is variable viability of Tsv/Tsv and Tsv/+ and phenotypic overlap within these and with +/+. A modifier is located to a short segment of chromosome 7, which alters the tail length of Tsv/+ mice up to 15%. The modifier, Tsv, and a coat texture mutant come from the same wild Peru mouse. The tail deformity is associated with, and may be caused by, a vascular disruption of the caudal aorta starting on day 11 of gestation. Thus Tsv appears to be different from each of the thirty known mouse mutants involving the tail. It is suggested that Tsv could be a mouse model for human conditions involving transverse terminal limb defects such as Moebius and de Lange syndromes.
Asunto(s)
Anemia/veterinaria , Vasos Sanguíneos/anomalías , Modelos Animales de Enfermedad , Genes Dominantes , Genes Letales , Trastornos del Crecimiento/veterinaria , Ratones Mutantes/anatomía & histología , Enfermedades de los Roedores/genética , Cola (estructura animal)/anomalías , Anemia/embriología , Anemia/genética , Animales , Animales Salvajes/genética , Mapeo Cromosómico , Anomalías Congénitas/clasificación , Anomalías Congénitas/genética , Anomalías Congénitas/veterinaria , Cruzamientos Genéticos , Epistasis Genética , Femenino , Ligamiento Genético , Variación Genética/genética , Trastornos del Crecimiento/embriología , Trastornos del Crecimiento/genética , Humanos , Masculino , Ratones , Ratones Endogámicos/genética , Ratones Mutantes/embriología , Ratones Mutantes/genética , Muridae/genética , Perú , Fenotipo , Enfermedades de los Roedores/embriología , Selección Genética , Cola (estructura animal)/irrigación sanguínea , Cola (estructura animal)/embriología , Cola (estructura animal)/patologíaRESUMEN
O nascimento de uma criança com apêndice caudal é evento benigno e raro. De acordo com a literatura, a cauda humana é uma estrutura embrionária näo relacionada ao tubo neural e portanto näo associada a malformaçöes congênitas da coluna e medula espinhal. Nosso trabalho apresenta um novo caso de persistência da cauda e a moderna perspectiva científica sobre o assunto é discutida