Navegando por Autor "GARCEZ, Daniela Rosa"

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Acesso aberto (Open Access)
Ajustes posturais antecipatórios e compensatórios em idosos com e sem lombalgia
(Universidade Federal do Pará, 2021-03) GARCEZ, Daniela Rosa; CALLEGARI, Bianca; http://lattes.cnpq.br/0881363487176703; https://orcid.org/0000-0001-9151-3896; YAMADA, Elizabeth Sumi; http://lattes.cnpq.br/7240314827308306
Chronic low back pain (DLC) is associated with changes in postural control and is highly prevalent in the elderly. Research shows that aging and DLC are described as important factors that affect postural control. The postural control impairments increase the risk of falls. Researches evaluating the postural control in elderly people with DLC are still necessary for greater effectiveness in balance rehabilitation programs to prevention falls in this population. The objective of this study is to verify whether anticipatory postural adjustments (APAs) and compensatory postural adjustments (CPAs) are affected by DLC in elderly people by assessing their postural control during a self-initiated perturbation paradigm induced by rapid upper arm movement when pointing to a target. Elderly people were divided into: Group with DLC (GDLC) (n = 15) and Control Group (CG) (n = 15). The participants’ lower limb muscle onset and center of pressure (COP) displacements were assessed prior to perturbation and throughout the entire movement. T0 moment (i.e., the beginning of the movement) was defined as the anterior deltoid (DEL) onset, and all parameters were calculated with respect to it. The rectus femoris (RT), semitendinosus (ST), and soleous (SOL) showed delayed onset in the GDLC group compared with the control group: RF (control: -0.094 ± 0.017 s; GDLC: -0.026 ± 0.012 s, t = 12, p < 0.0001); ST (control: - 0.093 ± 0.013 s; GDL: -0.018 ± 0.019 s, t = 12, p < 0.0001); and SOL (control: -0.086± 0.018 s; GDL: -0.029 ± 0.015 s, t = 8.98, p < 0.0001). In addition, COP displacement was delayed in the GDLC group (control: -0.035 ± 0.021 s; GDL: -0.015 ± 0.009 s, t = 3; p = 0.003) and presented a smaller amplitude during APA COPAPA [control: 0.444 cm (0.187; 0.648); GDLC: 0.228 cm (0.096; 0.310), U = 53, p = 0.012]. The GDLC group required a longer time to reach the maximum displacement after the perturbation (control: 0.211 ± 0.047 s; GDLC 0.296 ± 0.078 s, t = 3.582, p = 0.0013). This indicates that GDLC elderly patients have impairments to recover their postural control and less efficient anticipatory adjustments during the compensatory phase. Our results suggest that people with GDL have altered feedforward hip and ankle muscle control, as shown from the SOL, ST, and RT muscle onset. This study is the first study in the field of aging that investigates the postural adjustments of an elderly population with GDLC. Clinical assessment of this population should consider postural stability as part of a rehabilitation program.
Acesso aberto (Open Access)
Análise comportamental e histológica de um modelo animal da doença de Parkinson em camundongos suíços
(Universidade Federal do Pará, 2011-12-29) GARCEZ, Daniela Rosa; YAMADA, Elizabeth Sumi; http://lattes.cnpq.br/7240314827308306
Parkinson’s disease (PD) is one of the most common aging-related neurodegenerative diseases, having a clinical presentation featuring classic motor symptoms related to the degeneration of dopaminergic neurons of the substantia nigra pars compacta (SNpc) and dopamine decr ease in the striatum. Animal models of PD are important tools employed by researcher aiming a better understading of pathophysiologic disease mechanisms and for evaluation of potential therapeutic interventions. Such models must mimic some aspect of the disease as for instances, the degeneration of nigral dopaminergic neurons. In this context, the PD model induced by the injection of the neurotoxina 6-hydroxydopamine (6-OHDA) has been widely established in rats but a better characterization in diferent mice strain is lacking, concerning both behavioral changes and the lesion in nigrostriatal system. Such characterization is important so that this model can be reliably used for investigations of therapeutic interventions. The goal of the present study was to improve the characterization of the unilateral 6-OHDA PD model using Swiss mice, through the evaluation of behavioral changes and the effects on the SNpc dopaminergic neurons. In this investigation we have used a single unilateral intraestriatal injection of 6-OHDA, in two different toxin concentrations: 10 µg/2µl e 20 µg/2 µl. Our results have demonstrated that both 6-OHDA concentrations used provoked severe loss of nigral dopaminergic neurons, amounting to 74,5% e 89,5% respectively. This neuronal loss was highly correlated to the apomorphine-induced rotational behavior but not to the ambulation assessed in the open field test. Therefore, intraestriatal injection of 10 µg/2µl or 20 µg/2µl of 6-OHDA, using Swiss mice, reproduce an effective unilateral 6-OHDA PD model that can be reliably employed in experiments aiming to investigate neuroprotective, cellular and/or pharmacological therapies for PD.