75 research outputs found

    Three-Dimensional Printed Custom-Made Prostheses after Partial Scapulectomy: A Case Report

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    Abstract: This case study focuses on scapula reconstruction using three-dimensional printing in a patient with low-grade osteosarcoma. Malignant tumors originating from the scapula often lead to destructive surgery, with poor functional status and quality of life for the patients. Using custom prosthetic technology through three-dimensional printing could be a possible solution for reconstruction with greater long-term functional outcomes. This study aims to assess the functional outcomes of the reconstruction. A 39-year-old patient with low-grade central osteosarcoma involving the lateral two-thirds of the scapula underwent a custom prosthetic reconstruction. The patient subsequently followed a rehabilitation protocol for 12 months. The results indicate that even though there was a slight decrease in the range of movement, and an increase in the disabilities of the arm, shoulder, and hand (DASH) score, no relevant increase in activities of daily living (ADL) disability was present at follow-up. The patient returned to carry out his daily activities without pain and with a minimal functional reduction in movement. In conclusion, three-dimensional prosthetic reconstruction is a valid alternative for scapula reconstruction, allowing excellent functional and aesthetic results in oncological cases

    The Relationship between Gait Velocity and Walking Pattern in Hemiplegic Patients

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    Abstract: Background Gait speed represents a functional predictor and an impairment severity index in stroke survivors; gait analysis parameters are descriptors of walking strategies used to compensate for the muscle impairment such as vaulting, circumduction and hip hiking. The aim of this study was to assess if there is a relationship between the gait compensatory strategy and gait speed of progression. Methods A sample of 30 patients with post-stroke hemiparesis was assessed for gait compensatory patterns through gait analysis and videorecording. BMI, pain-VAS, Barthel Index, Nottingham Extended ADL Scale, Motricity Index, lower limb muscles strength and aROMs were also included in the assessment. Results In 19 patients it was possible to identify one or more compensatory strategies; in 11 patients no specific gait pattern was found. The vaulting and hip hiking combined gait strategy had an effect on gait speed. Gait speed was directly related to Barthel Index, Nottingham Extended ADL Scale, Motricity Index of the paretic side and in particular with quadriceps and iliopsoas strength and hip extension aROM. Gender, age and paretic side did not influence gait speed. Conclusion Compensatory gait strategies influence gait speed but studies with larger sample size are needed to better highlight their impact

    Polyamine supplementation reduces DNA damage in adipose stem cells cultured in 3-D

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    According to previous research, natural polyamines exert a role in regulating cell committment and differentiation from stemness during skeletal development. In order to assess whether distinct polyamine patterns are associated with different skeletal cell types, primary cultures of stem cells, chondrocytes or osteoblasts were dedicated for HPLC analysis of intracellular polyamines. Spermine (SPM) and Spermidine (SPD) levels were higher in adipose derived stem cells (ASC) compared to mature skeletal cells, i.e. chondrocytes and osteoblasts, confirming the connection of polyamine content with stemness. To establish whether polyamines can protect ASC against oxidative DNA damage in a 3-D differentiation model, the level of gamma H2AX was measured by western blot, and found to correlate with age and BMI of patients. Addition of either polyamine to ASC was able to hinder DNA damage in the low micromolecular range, with marked reduction of gamma H2AX level at 10 mu M SPM and 5 mu M SPD. Molecular analysis of the mechanisms that might underlie the protective effect of polyamine supplementation evidences a possible involvement of autophagy. Altogether, these results support the idea that polyamines are able to manage both stem cell differentiation and cell oxidative damage, and therefore represent appealing tools for regenerative and cell based applications

    The expression of hyperpolarization activated cyclic nucleotide gated (HCN) channels in the rat ovary are dependent on the type of cell and the reproductive age of the animal: a laboratory investigation

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    <p>Abstract</p> <p>Background</p> <p>Aim of this study was to test the hypothesis that levels of hyperpolarization activated cyclic nucleotide gated channels 1 to 4 (HCN1-4) are linked to the reproductive age of the ovary.</p> <p>Methods</p> <p>Young, adult, and reproductively aged ovaries were collected from Sprague-Dawley rats. RT-PCR and western blot analysis of ovaries was performed to investigate the presence of mRNA and total protein for HCN1-4. Immunohistochemistry with semiquantitative H score analysis was performed using whole ovarian histologic sections.</p> <p>Results</p> <p>RT-PCR analysis showed the presence of mRNA for HCN1-4. Western blot analysis revealed HCN1-3 proteins in all ages of ovarian tissues. Immunohistochemistry with H score analysis demonstrated distinct age-related changes in patterns of HCN1-3 in the oocytes, granulosa cells, theca cells, and corpora lutea. HCN4 was present only in the oocytes, with declining levels during the reproduction lifespan.</p> <p>Conclusion</p> <p>The evidence presented here demonstrates cell-type and developmental age patterns of HCN1-4 channel expression in rat ovaries. Based on this, we hypothesize that HCN channels have functional significance in rat ovaries and may have changing roles in reproductive aging.</p

    Up-regulation of L- and non-L, non-N-type Ca2+ channels by basal and stimulated protein kinase C activation in insulin-secreting RINm5F cells

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    AbstractWe studied the effect of protein kinase C (PKC) inhibition and activation on voltage-dependent Ca2+ channels in rat insulinoma RINm5F cells. PKC down-regulation by chronic (24 h) treatment with the PKC activator phorbol 12-myristate 13-acetate (PMA) reduced by about 60% the Ba2+ currents through L- and non-L, non-N-type high-voltage-activated Ca2+ channels, indicating that PKC tonically up-regulates the two main Ca2+ channel subtypes of RINm5F cells under basal conditions. Consistently, PKC activation by acute PMA application caused only a modest increase (average 23%) of Ba2+ currents in a minority of cells (24%). L- and non-L, non-N-type channels were differentially up-regulated by either basal or stimulated PKC activation. Acute up-regulation was predominant on L-type channels and caused an I/V shift of the Ba2+ currents in the hyperpolarizing direction. Non-L, non-N-type channels were less affected by acute PMA application, possibly reflecting a more effective tonic PKC up-regulatory action. Unexpectedly, the increase of Ba2+ currents during acute PMA application was followed by a progressive current decrease, which was also observed in isolation in another 24% of the cells and could be ascribed to PKC-induced ATP depletion, rather than to a direct effect of PKC on Ca2+ channels. We also provide evidence that PKC-mediated phosphorylation is not involved in the G-protein-mediated noradrenergic modulation of Ca2+ channels in RINm5F cells

    Direct interaction of gbetagamma with a C-terminal gbetagamma-binding domain of the Ca2+ channel alpha1 subunit is responsible for channel inhibition by G protein-coupled receptors

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    Several classes of voltage-gated Ca2+ channels (VGCCs) are inhibited by G proteins activated by receptors for neurotransmitters and neuromodulatory peptides, Evidence has accumulated to indicate that for non-L-type Ca2+ channels the executing arm of the activated G protein is its beta gamma dimer (G beta gamma). We report below the existence of two G beta gamma-binding sites on the A-, B-, and E-type alpha(1) subunits that form non-L-type Ca2+ channels. One, reported previously, is in loop 1 connecting transmembrane domains I and Il, The second is located approximately in the middle of the ca, 600-aa-long C-terminal tails, Both G beta gamma-binding regions also bind the Ca2+ channel beta subunit (CC beta), which, when overexpressed, interferes with inhibition by activated G proteins, Replacement in alpha(1E) Of loop 1 with that of the G protein-insensitive and G beta gamma-binding-negative loop 1 of alpha(1C) did not abolish inhibition by G proteins, but the exchange of the alpha(1E) C terminus with that of alpha(1C) did, This and properties of alpha(1E) C-terminal truncations indicated that the G beta gamma-binding site mediating the inhibition of Ca2+ channel activity is the one in the C terminus, Binding of G beta gamma to this site mas inhibited by an alpha(1)-binding domain of CC beta, thus providing an explanation for the functional antagonism existing between CC beta and G protein inhibition. The data do not support proposals that G beta gamma inhibits alpha(1) function by interacting with the site located in the loop I-II linker, These results define the molecular mechanism by which presynaptic G protein-coupled receptors inhibit neurotransmission

    Long-term object recognition memory in aged rats

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    Rats show spontaneous preference for exploring novel rather than familiar objects. Thus, exploratory activity can be used to evaluate recognition memory. To date, the spontaneous novelty-preference test of object recognition has been used to study long-term recognition memory formation in adult rats (Mumby et al., 2002 Behav Brain Res 132:215-26), but not in aged rats. In the present study we used this behavioral test with 25-27 month-old Wistar rats (n=9), but we found that it was not able to elicit recognition memory. Thus, we developed a new experimental protocol and we tested a second group of rats of the same age (n=18). Each animal received 5 training sessions (1 per day on days 1 and 2, and 1 on day 3) lasting 5 min in a small box (48x26,5x21 cm) containing two identical plastic cubes (8 cm high). We found that the time spent in exploring this pair of objects significantly (P&lt;0.01) decreased on the third session. Twenty-four h after the training 8 rats were tested in the same box, in which one of the two cubes (familiar object) was replaced by a plastic pyramid (8 cm high, novel object). The animals displayed a significantly (P&lt;0.05) longer exploration time of the novel object in comparison with the familiar one. When we applied the new protocol to adult animals (4-6 month-old, n=19), we found that the time spent in exploring the pair of familiar objects significantly (P&lt;0.01) decreased on the second training session, and the time spent in exploring the novel object in comparison with the familiar one was significantly (P&lt;0.05, n=10) longer after 24 h. These findings indicate that the new protocol is able to induce long-term recognition memory formation in aged animals, and allows the evaluation of age-related differences in learning ability
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