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1.
Nature ; 485(7398): 368-71, 2012 May 17.
Artigo em Inglês | MEDLINE | ID: mdl-22522928

RESUMO

Patients with spinal cord injury lack the connections between brain and spinal cord circuits that are essential for voluntary movement. Clinical systems that achieve muscle contraction through functional electrical stimulation (FES) have proven to be effective in allowing patients with tetraplegia to regain control of hand movements and to achieve a greater measure of independence in daily activities. In existing clinical systems, the patient uses residual proximal limb movements to trigger pre-programmed stimulation that causes the paralysed muscles to contract, allowing use of one or two basic grasps. Instead, we have developed an FES system in primates that is controlled by recordings made from microelectrodes permanently implanted in the brain. We simulated some of the effects of the paralysis caused by C5 or C6 spinal cord injury by injecting rhesus monkeys with a local anaesthetic to block the median and ulnar nerves at the elbow. Then, using recordings from approximately 100 neurons in the motor cortex, we predicted the intended activity of several of the paralysed muscles, and used these predictions to control the intensity of stimulation of the same muscles. This process essentially bypassed the spinal cord, restoring to the monkeys voluntary control of their paralysed muscles. This achievement is a major advance towards similar restoration of hand function in human patients through brain-controlled FES. We anticipate that in human patients, this neuroprosthesis would allow much more flexible and dexterous use of the hand than is possible with existing FES systems.


Assuntos
Força da Mão/fisiologia , Músculos/fisiologia , Paralisia/fisiopatologia , Paralisia/reabilitação , Próteses e Implantes , Traumatismos da Medula Espinal/reabilitação , Animais , Estimulação Elétrica , Eletrodos Implantados , Mãos/fisiologia , Mãos/fisiopatologia , Macaca mulatta , Microeletrodos , Córtex Motor/citologia , Córtex Motor/fisiologia , Movimento/fisiologia , Bloqueio Nervoso , Quadriplegia/fisiopatologia , Quadriplegia/reabilitação , Traumatismos da Medula Espinal/fisiopatologia
2.
Eur J Appl Physiol ; 81(1-2): 132-9, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10552278

RESUMO

In this study we determined the influence of improving aerobic power (VO(2max)) on basal plasma levels of insulin and glucose of 11- to 14-year-old children, while accounting for body fat, gender, pubertal status, and leisure-time physical activity (LTPA) levels. Blood samples were obtained from 349 children after an overnight fast and analyzed for plasma insulin and glucose. Height, mass, body mass index (BMI), and sum of skinfolds (Sigma triceps + subscapular sites) were measured. LTPA levels and pubertal status were estimated from questionnaires, and VO(2max) was predicted from a cycle ergometry test. Regardless of gender, insulin levels were significantly correlated (P = 0.0001) to BMI, skinfolds, pubertal stage, and predicted VO(2max), but were not related to LTPA levels. Fasting glucose levels were not correlated to measures of adiposity or exercise (LTPA score, VO(2max)) for females; however, BMI and skinfolds were correlated for males (P < 0.006). The children then took part in an 8-week aerobic exercise program. The 60 children whose VO(2max) improved (>/=3 ml x kg(-1) x min(-1)) had a greater reduction in circulating insulin than the 204 children whose VO(2max) did not increase -16 (41) vs -1 (63) pmol x l(-1); P = 0.028. The greatest change occurred in those children with the highest initial resting insulin levels. Plasma glucose levels were slightly reduced only in those children with the highest insulin levels whose VO(2max) improved (P < 0.0506). The results of this study indicate that in children, adiposity has the most significant influence on fasting insulin levels; however, increasing VO(2max) via exercise can lower insulin levels in those children with initially high levels of the hormone. In addition, LTPA does not appear to be associated with fasting insulin status, unless it is sufficient to increase VO(2max).


Assuntos
Glicemia/análise , Insulina/sangue , Consumo de Oxigênio/fisiologia , Adolescente , Antropometria , Índice de Massa Corporal , Criança , Humanos , Concentração Osmolar , Educação Física e Treinamento , Descanso , Caracteres Sexuais , Dobras Cutâneas
3.
Otolaryngol Head Neck Surg ; 103(6): 981-5, 1990 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-1980534

RESUMO

Controversy prevails regarding the accuracy of the clinical diagnosis of perilymphatic fistula (PLF). The diagnosis of PLF has been based on the subjective evaluation of vestibular function tests and the intraoperative macroscopic visualization of "clear fluid" from the oval/round windows at the time of exploratory tympanotomy. However, the subjective visual characterization of PLF varies among observing surgeons. Furthermore, perilymph can be "contaminated" with serum, blood, cerebrospinal fluid (CSF), and local anesthesia. This article presents a scientific biochemical microassay for the free amino acid profile of perilymph. Microaliquots of uncontaminated perilymph were sampled from the bilateral round windows (scala tympani) of 20 guinea pigs and analyzed for 19 free amino acid concentrations (FAAC) by high-performance liquid chromatography (HPLC). These samples were compared with the FAAC of guinea pig serum samples. Perfect predictor value ranges were nonoverlapping for 12 of 19 free amino acids in perilymph vs. plasma. Amino acid microassay of middle ear fluid for verification of "true" perilymph vs. nonperilymph fluids by the identification of nonoverlapping FAA markers may allow scientific verification of the existence of PLF in "suspected" patients.


Assuntos
Aminoácidos/análise , Fístula/diagnóstico , Doenças do Labirinto/diagnóstico , Perilinfa/química , Aminoácidos/sangue , Animais , Arginina/análise , Arginina/sangue , Asparagina/análise , Asparagina/sangue , Biomarcadores/química , Cromatografia , Cromatografia Líquida de Alta Pressão , Glutamatos/análise , Glutamatos/sangue , Ácido Glutâmico , Glutamina/análise , Glutamina/sangue , Cobaias , Histidina/análise , Histidina/sangue , Isoleucina/análise , Isoleucina/sangue , Leucina/análise , Leucina/sangue , Lisina/análise , Lisina/sangue , Fenilalanina/análise , Fenilalanina/sangue , Espectrometria de Fluorescência , Treonina/análise , Treonina/sangue , Tirosina/análise , Tirosina/sangue , Valina/análise , Valina/sangue
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