Thesis (M.Sc.)--Memorial University of Newfoundland, 2003. / Bibliography: leaves 110-138. Also available online.

Thesis (Ph. D.)--University of Washington, 2006. / Vita. Includes bibliographical references (leaves 126-139).

Esta tese de doutorado está dividida em três capítulos. O primeiro capítulo teve sua fundamentação em resultados da literatura, que mostraram que a aplicação de trens de alta freqüência de estimulação elétrica na perna pode gerar forças maiores do que seria esperado pela estimulação direta de axônios motores, por um mecanismo central gerado em motoneurônios por ativação de sinapses de aferências sensoriais. O objetivo foi investigar se estímulos vibratórios aplicados ao tendão de Aquiles são também capazes de gerar torques extras de grande magnitude no grupo muscular do tríceps sural. Para tanto, o torque isométrico gerado pelo tornozelo foi medido em resposta a diferentes padrões de associação entre estímulos elétricos e mecânicos aplicados ao grupo muscular do tríceps sural. As salvas de estímulos vibratórios puderam gerar torques extras substanciais, que eram acompanhados por um aumento da excitabilidade motoneuronal, visto que foi observado um concomitante aumento na amplitude pico a pico das ondas F captadas no músculo sóleo. Esses resultados mostraram que estímulos vibratórios aplicados juntamente a uma estimulação elétrica basal podem gerar níveis de força consideráveis, devido ao recrutamento de motoneurônios na medula espinhal. Os resultados indicam que a associação entre vibração e estimulação elétrica pode ser benéfica para diversas intervenções terapêuticas e programas de exercícios baseados em vibração. O comando para a geração de torques extras pela vibração provavelmente ativa motoneurônios na medula espinhal seguindo o princípio do tamanho, o que é uma característica desejável para paradigmas de estimulação. O segundo capítulo teve como ponto de partida o fato de que, quando indivíduos exercem um leve toque com a ponta dedo indicador sobre uma superfície estacionária, observa-se uma melhora na estabilidade postural. Nosso estudo investigou se uma melhora adicional na estabilidade postural pode ser atingida pela aplicação de um baixo nível de ruído mecânico (ruído vibratório) à superfície de contato com o dedo. Tal hipótese foi baseada na teoria da ressonância estocástica, que consiste na idéia de que a detecção e transmissão de um sinal fraco ou subliminar podem ser otimizadas pela presença de um nível particular de ruído. Os sujeitos permaneceram em postura ortostática sobre uma plataforma de força, enquanto tocavam com a ponta do dedo indicador direito um aparato usado para produzir oscilações vibratórias na superfície de contato do dedo. Parâmetros caracterizando as oscilações posturais foram computados a partir de medidas provenientes dos sinais do centro de pressão (adquiridos por uma plataforma de força). Os resultados mostraram que a aplicação de um ruído vibratório à superfície de contato do dedo causou uma melhora significativa na estabilidade postural quando comparada à condição em que a superfície de contado permanecia estacionária. Os resultados podem ter implicações clínicas relevantes em relação ao projeto de dispositivos de auxílio a pessoas com déficits sensório-motores, como bengalas, visando aumentar a estabilidade postural. Por fim, o terceiro capítulo investigou os efeitos da aplicação de ruído elétrico nos músculos da perna sobre o controle neuromuscular (i.e. variabilidade da força de flexão plantar exercida isometricamente) e sobre o controle postural humano (i.e. medida das oscilações posturais por uma plataforma de força). Os resultados mostraram pela primeira vez que um ruído elétrico abaixo do limiar sensorial pode causar uma melhora no controle neuromuscular durante uma tarefa de manter um determinado nível de força isométrica o mais constante possível, por mecanismo provavelmente associado à ressonância estocástica. Além disso, foi encontrada uma correlação significativa entre as reduções obtidas na variabilidade do torque e as reduções observadas em algumas medidas do centro de pressão, indicando que a variabilidade do torque de flexão plantar obtida com os sujeitos sentados pode ser um bom indicativo da amplitude das oscilações posturais para certas intervenções. Em conjunto, os resultados indicam um potencial de uso clínico de estimulações com ruído elétrico para a melhora do controle neuromuscular de pessoas com diferentes acometimentos sensório-motores. / This doctorate thesis is divided into three chapters. The first chapter was inspired on previous results from the literature which showed that high-frequency trains of electrical stimulation applied over the lower limb muscles can generate forces higher than would be expected by direct activation of motor axons, by a mechanism generated within the central nervous system by synaptic input from sensory afferents to motoneurons. The objective was to investigate if vibration applied to the Achilles tendon is also able to generate large magnitude extra torques in the triceps surae muscle group. The isometric ankle torque was measured in response to different patterns of coupled electrical and mechanical stimuli applied to the triceps surae muscle group. The vibratory bursts could generate substantial extra torques that were accompanied by increased motoneuron excitability, since a parallel increase in the peak-to-peak amplitude of soleus F waves was observed. These results showed that vibratory stimuli applied with a background electrical stimulation generate considerable force levels due to the spinal recruitment of motoneurons. So, the association of vibration and electrical stimulation could be beneficial for many therapeutic interventions and vibration-based exercise programs. The command for the vibration-induced extra torques presumably activates spinal motoneurons following the size principle, which is a desirable feature for stimulation paradigms. The second chapter was based on the knowledge that when a subjects index fingertip touches lightly a rigid and stationary surface there is an improvement of his/her postural stability. Our study investigated whether a further increase in postural steadiness may be achieved by applying a low level mechanical noise (vibratory noise) to the fingertip contact surface. Such a hypothesis is based on the stochastic resonance theory, which says that the detection and transmission of a weak or sub-threshold input signal may be enhanced by the presence of a particular level of noise. The subjects stood as quietly as possible over a force plate while touching with their right index fingertip a surface that could be either quiescent or vibrated. Body sway parameters were computed from measurements of the center of pressure (acquired from the force plate). The results showed that the delivery of the vibratory noise to the fingertips contact surface caused a significant improvement on postural stability when compared with the condition in which the surface was stationary. The results could be helpful for the design of rehabilitation aids such as canes commonly used to improve stability in people with sensory deficits. Finally, in the third chapter, the effects of electrical noise applied to the leg muscles on neuromuscular control (i.e. isometric plantar flexion force variability) and on human postural control (i.e. measures of postural sway) were investigated. The results showed for the first time that a sub-threshold electrical noise may improve neuromuscular control during a task in which an isometric force level is maintained as constant as possible, presumably by a stochastic resonance mechanism. Furthermore, a significant correlation was found between the reductions in torque variability and the improvements in postural sway, indicating that plantarflexion torque variability acquired while subjects are in a seated position may provide a good estimate of their postural sway under the same intervention. Taken together, the results indicate the potential for the clinical usage of noise-based stimulations to enhance neuromuscular control in a population with sensory-motor impairments.

Hypertension affects one in two adults in the United States and contributes to more than 10% of deaths worldwide. The salt sensitivity of blood pressure, a clinical phenomenon present in one half of hypertensive patients and one quarter of normotensive individuals, predicts the development of hypertension. The prevalence of hypertension rises with age, and age-related increases in salt sensitivity and sympathetic nervous system activity, which promotes renal sodium reabsorption and plays a pathophysiological role in salt sensitivity and hypertension, have been documented. Increased mechanistic insight into the integrated renal and neural mechanisms influencing sodium homeostasis and blood pressure, particularly in aging, could yield valuable information for the phenotypically targeted treatment of hypertension. The renal nerves, comprised of the sensory afferent renal nerves (ARN) and the efferent renal sympathetic nerves, influence sodium homeostasis and blood pressure. The ARN, which include mechanosensitive and chemosensitive fibers, mediate a sympathoinhibitory reno-renal reflex that suppresses renal sympathetic nerve activity. The renal sympathetic nerves release norepinephrine, which can promote salt-sensitive hypertension in part by activating the sodium chloride cotransporter (NCC). In this thesis, Sprague Dawley rats were used as a model of normal aging to demonstrate that 1) the ARN are critical to the sympathoinhibitory and natriuretic responses to alterations in sodium homeostasis and protect against salt sensitivity of blood pressure, 2) the paraventricular nucleus of the hypothalamus may be a site of central integration of the mechanosensitive sympathoinhibitory reno-renal reflex, 3) norepinephrine promotes NCC activity through an α1-adrenoceptor-gated WNK1-OxSR1-dependent signaling pathway, driving salt-sensitive hypertension, and 4) impairments in the sympathoinhibitory reno-renal reflex may promote sympathoexcitation and NCC-mediated sodium retention, driving salt-sensitive hypertension in aging rats. Finally, data from the Genetic Epidemiology of Salt Sensitivity study were used to demonstrate that variance in the gene encoding Gαi2 proteins, which are upregulated in the paraventricular nucleus during high salt intake in salt-resistant animal models and are required for dietary sodium-evoked suppression of renal sympathetic outflow, may be a biomarker for the salt sensitivity of blood pressure in humans. Together, these findings highlight the integrated renal and neural mechanisms contributing to salt sensitivity and age-related hypertension.

Intravenous injection of 3-33 nmol/kg of substance P (SP) caused pressor and tachycardic responses in anesthetized rats. The responses were not blocked by a ganglion nicotinic receptor antagonist or by pithing. Pretreatment with reserpine blocked both responses. β-Adrenoceptor blockade attenuated only the tachycardic response, and α-adrenoceptor blockade attenuated only the pressor response. These findings indicated that the effects of SP to increase blood pressure and heart rate are due to sympathetic ganglion stimulation. Studies with adrenalectomized rats showed that stimulation of the adrenals by SP contributes to both responses but makes a greater contribution to the tachycardic response. These observations raise the possibility that the tachykinin innervation of sympathetic ganglia and the adrenal medulla may be involved in the local regulation of blood pressure and heart rate.

The anterograde horseradish peroxidase method was used to determine if prenatal exposure to ethanol affected the development of the characteristic afferent lamination pattern of the commissural projection to the dentate gyrus. Mean ethanol consumption for the ethanol-consuming dams was 12.7 g/kg ± 0.3 g per day. Adult offspring of rats that consumed a liquid diet containing 35% ethanol-derived calories during days 1-21 of gestation, and both pair-fed and normal controls were examined. Brain weights and volumes of the ethanol and pair-fed control rats did not differ significantly from normal controls. However, body weights of ethanol-exposed rats were significantly reduced compared to normal controls. Computer-assisted image analysis of the HRP-labeling revealed that in spite of the heavy ethanol exposure there was no evidence of alterations in the spatial distribution of the commissural terminal field.

This study compared whether activation of muscle ergoreceptor afferents caused by isometric muscle contraction, activation of baroreceptor afferents induced by i.v. infusion of phenylephrine, or baroreceptor afferent inactivation, caused by carotid artery occlusion, elicit similar patterns of c-Fos induction in brainstem areas. Adult cats were anesthetized with α-chloralose, and in each case, the experimental intervention caused an increase in the arterial blood pressure. There were two sets of control experiments: in both, animals underwent the same surgical procedures but then either remained at rest for the entire study, or the tibial nerve was stimulated, as in the contraction group, following muscle paralysis with tubocurarine. Following the procedures, animals rested for 90 min to allow neuronal expression of c-Fos. Control cats showed very little c-Fos immunoreactivity (c-Fos-ir) in the brainstem. Muscle contraction induced c-Fos-ir expression mainly in the nucleus tractus solitarius, lateral reticular nucleus, lateral tegmental field, vestibular nucleus, subretrofacial nucleus, spinal trigeminal tract and in a lateral region of the periaqueductal grey (P 0.5-1.0). The majority of the c-Fos-ir was found in brainstem areas contralateral to the contracted muscle. In addition, muscle contraction induced c-Fos-ir in the dorsal horns of spinal segments L6-S1 on the ipsilateral side of the spinal cord. Phenylephrine infusion caused c-Fos-ir expression in the nucleus tractus solitarius, spinal trigeminal tract, solitary tract, and dorsal motor nucleus of the vagus. No c-Fos-ir was apparent in the periaqueductal grey. Carotid occlusions induced c-Fos-ir expression in the area postrema, nucleus tractus solitarius, solitary tract, and spinal trigeminal tract. Expression was bilateral. Areas that exhibited c-Fos-ir correspond to sites previously reported to release various neuropeptides in response to muscle contraction or carotid occlusions. These results indicate that the exercise pressor reflex and baroreflex activate similar, but not completely identical, sites in the brainstem.

Substance P and neurokinin A are tachykinins that are co-localized with calcitonin gene-related peptide (CGRP) in a unique subpopulation of cardiac afferent nerve fibers. These neurons are activated by nociceptive stimuli and exhibit both sensory and motor functions that are mediated by the tachykinins and/or CGRP. Sensory signals (e.g., cardiac pain) are transmitted by peptides released at central processes of these neurons, whereas motor functions are produced by the same peptides released from peripheral nerve processes. This review summarizes our current understanding of intracardiac actions of the tachykinins. The major targets for the tachykinins within the heart are the intrinsic cardiac ganglia and coronary arteries. Intrinsic cardiac ganglia contain cholinergic neurons that innervate the heart and coronary vasculature. Tachykinins can stimulate NK3 receptors on these neurons to increase their excitability and evoke spontaneous firing of action potentials. This action provides a mechanism whereby tachykinins can indirectly influence cardiac function and coronary tone. Tachykinins also have direct effects on coronary arteries to decrease or increase tone. Stimulation of NK1 receptors on the endothelium causes vasodilation mediated by nitric oxide. This effect is normally dominant, but NK2 receptor-mediated vasoconstriction can also occur and is augmented when NK1 receptors are blocked. It is proposed that these ganglion stimulant and vascular actions are manifest by endogenous tachykinins during myocardial ischemia.

Using vagus nerve stimulation (VNS), we sought to determine the contribution of vagal afferents to efferent control of cardiac function. In anesthetized dogs, the right and left cervical vagosympathetic trunks were stimulated in the intact state, following ipsilateral or contralateral vagus nerve transection (VNTx), and then following bilateral VNTx. Stimulations were performed at currents from 0.25 to 4.0 mA, frequencies from 2 to 30 Hz, and a 500-μs pulse width. Right or left VNS evoked significantly greater current-and frequency-dependent suppression of chronotropic, inotropic, and lusitropic function subsequent to sequential VNTx. Bradycardia threshold was defined as the current first required for a 5% decrease in heart rate. The threshold for the right vs. left vagus-induced bradycardia in the intact state (2.91 ± 0.18 and 3.47 ± 0.20 mA, respectively) decreased significantly with right VNTx (1.69 ± 0.17 mA for right and 3.04 ± 0.27 mA for left) and decreased further following bilateral VNTx (1.29 ± 0.16 mA for right and 1.74 ± 0.19 mA for left). Similar effects were observed following left VNTx. The thresholds for afferent-mediated effects on cardiac parameters were 0.62 ± 0.04 and 0.65 ± 0.06 mA with right and left VNS, respectively, and were reflected primarily as augmentation. Afferent-mediated tachycardias were maintained following β-blockade but were eliminated by VNTx. The increased effectiveness and decrease in bradycardia threshold with sequential VNTx suggest that 1) vagal afferents inhibit centrally mediated parasympathetic efferent outflow and 2) the ipsilateral and contralateral vagi exert a substantial buffering capacity. The intact threshold reflects the interaction between multiple levels of the cardiac neural hierarchy.

Previously, we have shown that chronic intermittent hypoxia (CIH) impairs baroreflex control of heart rate and augments aortic baroreceptor afferent function. In the present study, we examined whether CIH induces structural changes of aortic afferent axons and terminals. Young-adult Fischer 344 (F344, 4 months old) rats were exposed to room air (RA) or CIH for 35-45 days. After 14-24 days of exposure, they received tracer DiI injection into the left nodose ganglion to anterogradely label vagal afferent nerves. After surgery, animals were returned to their cages to continue RA or CIH exposure. Twenty-one days after DiI injection, the animals were sacrificed and the aortic arch was examined using confocal microscopy. In both RA and CIH rats, we found that DiI-labeled vagal afferent axons entered the wall of the aortic arch, then fanned out and branched into large receptive fields with numerous terminals (flower-sprays, end-nets and free endings). Vagal afferent axons projected much more to the anterior wall than to the posterior wall. In general, the flower-sprays, end-nets and free endings were widely and similarly distributed in the aortic arch of both groups. However, several salient differences between RA and CIH rats were found. Compared to RA control, CIH rats appeared to have larger vagal afferent receptive fields. The CIH rats had many abnormal flower-sprays, end-nets, and free endings which were intermingled and diffused into "bush-like" structures. However, the total number of flower-sprays was comparable (P>0.05). Since there was a large variance of the size of flower-sprays, we only sampled the 10 largest flower-sprays from each animal. CIH substantially increased the size of large flower-sprays (P<0.01). Numerous free endings with enlarged varicosities were identified, resembling axonal sprouting structures. Taken together, our data indicate that CIH induces significant remodeling of afferent terminal structures in the aortic arch of F344 rats. We suggest that such an enlargement of vagal afferent terminals may contribute to altered aortic baroreceptor function following CIH.