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1.
Braz. j. med. biol. res ; 54(7): e10865, 2021. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1249318

RESUMO

This study verified the effects of respiratory muscle training (RMT) on hemodynamics, heart rate (HR) variability, and muscle morphology in rats with streptozotocin-induced diabetes mellitus (DM). Thirty-six male Wistar rats were randomized into 4 groups and 34 completed the study: i) sham-sedentary (Sham-ST; n=9); ii) sham-RMT (Sham-RMT; n=9); iii) DM-sedentary (DM-ST; n=8); and iv) DM-RMT (DM-RMT; n=8). Hemodynamics were assessed by central cannulation, and R-R intervals were measured by electrocardiogram. In addition, the effects of RMT on the cross-sectional area of the diaphragm, anterior tibial, and soleus muscles were analyzed. The induction of DM by streptozotocin resulted in weight loss, hyperglycemia, reduced blood pressure, and attenuated left ventricular contraction and relaxation (P<0.05). We also observed a decrease in root mean square of successive differences between adjacent RR intervals (RMSSD) index and in the cross-sectional area of the muscles assessed, specifically the diaphragm, soleus, and anterior tibial muscles in diabetic rats (P<0.05). Interestingly, RMT led to an increase in RMSSD in rats with DM (P<0.05). The induction of DM produced profound deleterious changes in the diaphragmatic and peripheral muscles, as well as impairments in cardiovascular hemodynamics and autonomic control. Nevertheless, RMT may beneficially attenuate autonomic changes and improve parasympathetic modulation.


Assuntos
Animais , Masculino , Ratos , Diabetes Mellitus Experimental , Músculos Respiratórios , Exercícios Respiratórios , Ratos Wistar , Frequência Cardíaca , Hemodinâmica
2.
Genet. mol. res. (Online) ; 3(2): 288-292, jun. 2004.
Artigo em Inglês | LILACS | ID: lil-387946

RESUMO

Trisomy 13 is a clinically severe entity; 85% of the patients do not survive beyond one year, and most children die before completing six months of age. We report a female child, 28 months old, white, the fourth child of a non-consanguineous couple, who presented trisomy 13. The child was born at term, from a vaginal delivery, weighing 2600 g. At birth, she was cyanotic, icteric, spastic, and cried weakly. The initial clinical examination detected polydactyly in the left hand, congenital clubfoot and convex soles, ocular hypertelorism, a low nasal bridge, numerous hemangiomas distributed throughout the body, cardiomegaly, and perimembranous inter-ventricular communication. There was no cleft lip or palate. On physical examination at 18 months old, the child weighed 6,900 g, had a cephalic perimeter of 41 cm, a thoracic perimeter of 43 cm and was 76 cm tall. At 28 months, she weighed 10,760 g and was 88.5 cm tall. Neuropsychomotor development retardation was evident from birth and, according to the psychologist and the social assistant of APAE (Handicapped Parents and Friends Association) in Cangucu, Rio Grande do Sul, there was a noticeable improvement after physiotherapy and recreational sessions.


Assuntos
Humanos , Feminino , Pré-Escolar , Anormalidades Múltiplas , Cromossomos Humanos Par 13 , Trissomia , Anormalidades Múltiplas , Fenótipo , Síndrome
3.
Genet. mol. res. (Online) ; 3(3): 303-308, 2004. tab
Artigo em Inglês | LILACS | ID: lil-482176

RESUMO

From 1986 to 2002, we examined the chromosomal composition of 916 patients attended by two genetic counseling services in the city of Pelotas, in the Brazilian State of Rio Grande do Sul, to determine the genetic causes of their disturbances. Patterns of G-banding using trypsin and Giemsa (GTG) and C-banding using barium and Giemsa (CBG) were studied using phytohemagglutinin M-stimulated lymphocytes cultured from peripheral blood. Among the patients, 110 had Down's syndrome, 7 had Edward's syndrome, 4 had Patau's syndrome, 29 had Turner's syndrome, 5 had Klinefelter's syndrome, and 3 had [quot ]cri-du-chat[quot ] syndrome. Abnormal chromosomes were observed in 29.3% of the patients. Most of these (56.3%) were numerical abnormalities, with the remaining being structural variants.


Assuntos
Feminino , Humanos , Masculino , Bandeamento Cromossômico/métodos , Aberrações Cromossômicas , Aconselhamento Genético , Transtornos Cromossômicos/diagnóstico , Ativação Linfocitária/efeitos dos fármacos , Ativação Linfocitária/genética , Brasil , Cariotipagem/métodos , Fito-Hemaglutininas , Transtornos Cromossômicos/genética
4.
Rev. bras. neurol ; 23(1): 31-4, jan.-fev. 1987. ilus
Artigo em Português | LILACS | ID: lil-39652

RESUMO

Säo apresentados dois casos de hemiparesia atáxica devidos a infarto no território da artéria cerebral média, visualizados por tomografia conputadorizada. Säo feitas revisöes sucintas da literatura sobre as relaçöes cérebro-cerebelares humanas e sobre a hemiparesia atáxica, e é postulado que as vias corticonucleares e as corticoespinhais (piramidais), com origem na regiäo pré-motora do cérebro humano, representam os principais efetores supra-segmentares de contingente quantitativamente preponderante da eferência funcional do cerebelo humano. Nesse sentido, o córtex pré-central e suas vias relacionadas parecem ser a via comum para a passagem da atividade fisiológica gerada nos níveis basonucleares e cerebelares


Assuntos
Idoso , Humanos , Masculino , Feminino , Ataxia Cerebelar/etiologia , Infarto Cerebral/complicações , Hemiplegia/etiologia , Ataxia Cerebelar/diagnóstico , Tomografia Computadorizada por Raios X
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