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Featured researches published by Arine Pellegrino.


Journal of Zoo and Wildlife Medicine | 2012

ELECTROCARDIOGRAPHIC PARAMETERS OF CAPTIVE TUFTED CAPUCHINS (CEBUS APELLA) UNDER CHEMICAL IMMOBILIZATION

Maria Helena Matiko Akao Larsson; Arine Pellegrino; V.M.C. Oliveira; Cristiana Sanctis Prada; José Daniel Luzes Fedullo; Carlos Eduardo Larsson Junior

This study presents the electrocardiogram findings from 97 captive tufted capuchin monkeys (Cebus apella) at the São Paulo Zoo (São Paulo, Brazil) while under ketamine anesthesia. The results did not differ greatly from data of domestic carnivores or other studied primate species. The most common rhythm recorded was normal sinus rhythm, followed by normal sinus rhythm with wandering pacemaker. Electrical axis varied from 0 degrees to -150 degrees but was most commonly between +60 degrees and +90 degrees. QRS complexes were predominantly positive in leads DI, DII, DIII, and AVF. These findings allow for the recognition of abnormal rhythms in these primate species and can contribute to future investigations into the cardiovascular diseases routinely diagnosed in primates and humans.


Ciencia Rural | 2007

Padronização de parâmetros ecocardiográficos de cães da raça Golden Retriever clinicamente sadios

Arine Pellegrino; Lilian Caram Petrus; Guilherme G. Pereira; Elaine Cristina Soares; Ronaldo Jun Yamato; Eduardo Lipparelli Fernandez; Maria Helena Matiko Akao Larsson

The Duchennes muscular dystrophy (DMD) in humans is a recessive X-linked neuromuscular disease, caused either by the absence or dysfunction of the dystrophin. Clinically it is characterized by severe alteration in the skeletal musculature, resulting in precocious death of the affected patient. In Golden Retriever dogs, the mutation that determines the muscular dystrophy occurs spontaneously and the extensive homology among the pathogenesis of DMD and of Golden Retriever muscular dystrophy allows to qualify the dog as the main substitute of humans in the clinical tests of new therapies. The deficient myocardium in dystrophin is more vulnerable to the pressure overload, and the patients with DMD can develop dilated cardiomyopathy as well as arterial hypertension; in echocardiography, diastolic function abnormalities are verified and systolic inadequacy can be observed in some old patients. In the present study, 41 healthy Golden Retriever dogs were evaluated by echocardiographic exam with the purpose to obtain parameters for the standardization of these cardiovascular characteristics in the refered breed, what hereafter can be used as reference in the identification of bearer or affected dogs by muscular dystrophy.


Pesquisa Veterinaria Brasileira | 2010

Padronização de parâmetros eletrocardiográficos de cães da raça Golden Retriever clinicamente sadios

Arine Pellegrino; Fernanda Lie Yamaki; Roberto Carvalho e Pereira; V.M.C. Oliveira; Maria Helena Matiko Akao Larsson

The Duchennes muscular dystrophy (DMD) in humans is a X-linked neuromuscular disease, of recessive character, caused either by the absence or dysfunction of the dystrophin. Clinically, it is characterized by severe alteration in the skeletal musculature, resulting in precocious death. In Golden Retriever dogs, the mutation that takes to the muscular dystrophy happens spontaneously and the extensive homology among the pathogenesis of DMD and of Golden Retriever muscular dystrophy allows to qualify the dog as the main substitute of humans in the clinical tests of new therapies. The deficient myocardium in distrofin is more vulnerable to the pressure overload and the patients with DMD can develop dilated cardiomyopathy, arterial hypertension and the electrocardiogram can come distinctly abnormal. In the present study, 38 healthy Golden Retriever dogs were evaluated by electrocardiographic exam with the purpose to obtain parameters for the standardization of the electrocardiogram in the referred breed, what hereafter can serve as reference in the identification of bearer or affected dogs. Electrocardiographic values obtained were within normal values and reference for the various breeds of dogs, and the variables weight and age significantly altered heart rate and amplitude of the QRS complex.


Journal of Feline Medicine and Surgery | 2018

Age-based ultrasonographic criteria for diagnosis of autosomal dominant polycystic kidney disease in Persian cats:

J. G. M. Guerra; Mariana F. Freitas; Alexandre Gt Daniel; Arine Pellegrino; N. C. Cardoso; Isac de Castro; Luiz F. Onuchic; Bruno Cogliati

Objectives The aim of this study was to establish ultrasound criteria for the diagnosis of autosomal dominant polycystic kidney disease (ADPKD) in Persian cats. Methods Eighty-two Persian cats were assessed using renal ultrasound and genotyped for the C→A transversion in exon 29 of PKD1. The animals were also submitted to hematological characterization, serum biochemistry analyses and urinalysis. Results Age, sex and neutering status did not differ between ADPKD (n = 12) and non-ADPKD (n = 70) cats. After integrated molecular genetics/ultrasonographic analysis, the presence of at least one renal cyst was sufficient to establish a diagnosis of ADPKD in animals up to 15 months of age. Two or more cysts were required for diagnosis in cats aged 16–32 months, and at least three cysts warranted diagnosis of ADPKD in animals aged 33–49 months. Finally, four or more cysts led to diagnosis in cats aged 50–66 months. Although cats with ADPKD exhibited higher serum calcium levels than non-affected cats, hematological, urinalysis and other biochemical parameters did not differ between the two groups. Conclusions and relevance Integrated analyses of imaging and molecular genetics data enabled, for the first time, the establishment of age-based ultrasonographic criteria for the diagnosis of ADPKD in Persian cats. The development of imaging criteria is particularly relevant and useful in the clinical setting given the current limitations to access and the cost of molecular genetics-based diagnostic tests.


Pesquisa Veterinaria Brasileira | 2016

Sensibilidade e especificidade do exame eletrocardiográfico na detecção de sobrecargas atriais e/ou ventriculares em gatos da raça Persa com cardiomiopatia hipertrófica

Arine Pellegrino; Alexandre Gonçalves Teixeira Daniel; Rebecca Bastos Pessoa; J. G. M. Guerra; Gabriel Garone de Lucca; Marcelo Demarchi Goissis; Mariana F. Freitas; Bruno Cogliati; Maria Helena Matiko Akao Larsson

Hypertrophic cardiomyopathy (HCM) is the most common feline heart disease and is characterized by increased cardiac mass with a hypertrophied and not dilated left ventricle. The echocardiography is the best noninvasive diagnostic tool for the differentiation of cardiomyopathies and is considered the gold standard for detection of ventricular hypertrophy present in HCM. Electrocardiographic changes are also common in animals with HCM and the electrocardiogram (ECG) is quick, easy and highly available screening test for the detection of ventricular hypertrophy in humans. In cats, few studies have been conducted regarding the sensitivity and specificity of ECG in detecting ventricular hypertrophy. With the intention of evaluating the use of ECG as a screening tool for diagnosis of HCM in cats, Persian cats (n=82) were evaluated by echocardiographic and electrocardiographic examinations. Animals with blocks and/or conduction disturbances were excluded from statistical analysis (n=22). Subsequently the animals included were classified as normal (n=38), suspicious (n=6) and affected by HCM (n=16). Statistical differences were observed in the P-wave amplitude in DII and R-wave amplitude in DII, CV6LL and CV6LU, with higher values in animals with HCM. Velocities and pressure gradient of aortic flow, left atrial diameter (LA) and LA/Ao ratio were higher in cats with HCM. Among the animals with ECG changes suggestive of left atrial enlargement (n=7), only two actually had LA enlargement on echocardiography, and among animals with left atrial enlargement on echocardiogram (n=7), only two had ECG changes suggestive of overload AE (40,4% of sensibility and 90,9% of specificity). Among the animals with ECG changes suggestive of left ventricular hypertrophy (n=6), five actually had ventricular hypertrophy on echocardiography, and among animals with HCM by echocardiography (n=16), only five showed electrocardiographic abnormalities suggestive of LV hypertrophy (31,25% of sensibility and 97,72% of specificity). We observed a positive correlation between diastolic thickness of the interventricular septum and/or left ventricular free wall and R-wave amplitude in DII and CV6LU. The electrocardiogram is quick and easy to perform, has good specificity in detecting ventricular hypertrophy in cats, however, has low sensitivity, with large numbers of false negative animals. Thus, the ECG assists in the diagnosis, but does not replace echocardiography in confirming ventricular hypertrophy.


Brazilian Journal of Veterinary Research and Animal Science | 2010

Valores de pressão arterial de cães da raça Golden Retriever clinicamente sadios

Arine Pellegrino; Lilian Caram Petrus; Fernanda Lie Yamaki; A.L.F. Santos; Maria Helena Matiko Akao Larsson


Brazilian Journal of Veterinary Pathology | 2012

Polycystic liver disease associated with Platynosomum fastosum infection in a cat.

Alexandre Gonçalves Teixeira Daniel; Rodrigo F. Diaz; Luciana O. Camignatto; Nilson K. Kage; Arine Pellegrino; Bruno Cogliati


Medicina Veterinária | 2016

TETRALOGIA DE FALLOT COM HIPOPLASIA DE ARTÉRIA PULMONAR EM UM FELINO: RELATO DE CASO

Ana Cláudia da Fonseca; Alexandre Gonçalves Teixeira Daniel; Arine Pellegrino


Revista de Educação Continuada em Medicina Veterinária e Zootecnia do CRMV-SP | 2015

Definição de critérios ultrassonográficos para o diagnóstico da doença renal policística autossômica dominante em felinos da raça Persa

J. M. Guerra; N. C. Cardoso; A. G. T. Daniel; Arine Pellegrino; Mariana F. Freitas; Luiz F. Onuchic; Bruno Cogliati


Acta Scientiae Veterinariae | 2014

Pimobendan improves clinical signs in short term compared to digoxin or placebo in dogs with heart failure due to chronic degenerative mitral valve disease.

Maria Helena Matiko Akao Larsson; Denise Saretta Schwartz; V.M.C. Oliveira; Paula Hiromi Itikawa; Ariane Marques Mazini; Priscylla Ramos Rosa Melo; Fabrício Lorenzini Aranha Machado; Francisco Ferreira Lima Júnior; Khadine Kazue Kanayama; Arine Pellegrino; Alexandre Gonçalves Teixeira Daniel; Raul Ossada

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Bruno Cogliati

University of São Paulo

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