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Dive into the research topics where Paulo Cesar Lock Silveira is active.

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Featured researches published by Paulo Cesar Lock Silveira.


Cell Biology International | 2006

Imbalance in SOD/CAT activities in rat skeletal muscles submitted to treadmill training exercise

Ricardo A. Pinho; Michael Everton Andrades; Marcos Roberto de Oliveira; Aline C. Pirola; Morgana S. Zago; Paulo Cesar Lock Silveira; Felipe Dal-Pizzol; José Cláudio Fonseca Moreira

The association between physical exercise and oxidative damage in the skeletal musculature has been the focus of many studies in literature, but the balance between superoxide dismutase and catalase activities and its relation to oxidative damage is not well established. Thus, the aim of the present study was to investigate the association between regular treadmill physical exercise, oxidative damage and antioxidant defenses in skeletal muscle of rats. Fifteen male Wistar rats (8–12 months) were randomly separated into two groups (trained n = 9 and untrained n = 6). Trained rats were treadmill‐trained for 12 weeks in progressive exercise (velocity, time, and inclination). Training program consisted in a progressive exercise (10 m/min without inclination for 10 min/day). After 1 week the speed, time and inclination were gradually increased until 17 m/min at 10% for 50 min/day. After the training period animals were killed, and gastrocnemius and quadriceps were surgically removed to the determination of biochemical parameters. Lipid peroxidation, protein oxidative damage, catalase, superoxide dismutase and citrate synthase activities, and muscular glycogen content were measured in the isolated muscles. We demonstrated that there is a different modulation of CAT and SOD in skeletal muscle in trained rats when compared to untrained rats (increased SOD/CAT ratio). TBARS levels were significantly decreased and, in contrast, a significant increase in protein carbonylation was observed. These results suggest a non‐described adaptation of skeletal muscle against exercise‐induced oxidative stress.


Cell Biochemistry and Function | 2011

Taurine supplementation decreases oxidative stress in skeletal muscle after eccentric exercise

Luciano A. Silva; Paulo Cesar Lock Silveira; Merieli M. Ronsani; Priscila S. Souza; Débora da Luz Scheffer; Lílian C. Vieira; Magnus Benetti; Cláudio T. De Souza; Ricardo A. Pinho

Infrequent exercise, typically involving eccentric actions, has been shown to cause oxidative stress and to damage muscle tissue. High taurine levels are present in skeletal muscle and may play a role in cellular defences against free radical‐mediated damage. This study investigates the effects of taurine supplementation on oxidative stress biomarkers after eccentric exercise (EE). Twenty‐four male rats were divided into the following groups (n = 6): control; EE; EE plus taurine (EE + Taurine); EE plus saline (EE + Saline). Taurine was administered as a 1‐ml 300 mg kg−1 per body weight (BW) day−1 solution in water by gavage, for 15 consecutive days. Starting on the 14th day of supplementation, the animals were submitted to one 90‐min downhill run session and constant velocity of 1·0 km h−1. Forty‐eight hours after the exercise session, the animals were killed and the quadriceps muscles were surgically removed. Production of superoxide anion, creatine kinase (CK) levels, lipoperoxidation, carbonylation, total thiol content and antioxidant enzyme were analysed. Taurine supplementation was found to decrease superoxide radical production, CK, lipoperoxidation and carbonylation levels and increased total thiol content in skeletal muscle, but it did not affect antioxidant enzyme activity after EE. The present study suggests that taurine affects skeletal muscle contraction by decreasing oxidative stress, in association with decreased superoxide radical production. Copyright


Pulmonary Pharmacology & Therapeutics | 2009

The effects of physical exercise on the cigarette smoke-induced pulmonary oxidative response

Renata Tiscoski Nesi; Priscila S. Souza; Luciano A. Silva; Paulo Cesar Lock Silveira; Samuel Santos Valença; Ricardo A. Pinho

Studies have shown that the oxidative power of cigarettes is related to the pathogenesis of several pulmonary diseases and that regular physical exercise contributes significantly to reducing the deleterious effects of cigarettes. The objective of the present study was to investigate the therapeutic effects of physical exercise on histological and oxidative stress markers in animals exposed to cigarette smoke. Thirty-six male, eight-week-old C57BL-6 mice were divided into four groups (n = 9 for each group): control, exercise, cigarette smoke, and cigarette smoke plus exercise. The cigarette smoke (CS) groups were exposed to cigarette smoke 3 times/day (4 cigarettes/session) for 60 consecutive days. The exercise groups were submitted to swimming physical training 5 days/week for eight weeks. Forty-eight hours after the last exercise and cigarette exposure, the animals were sacrificed using cervical traction. The right lung was removed, processed, and stored for future analysis. In addition to the analysis of collagen content (hydroxyproline), oxidant production (anion superoxide), antioxidant enzyme activity (SOD and CAT), and lipid and protein oxidative damage (TBARS and Carbonylation), histological and morphological studies were performed. The results revealed that the animals exposed to cigarette smoke showed enlargement and destruction of the alveolar septum and increases in the numbers of macrophages and neutrophils, as well as in the amount of collagen. Our results also showed a decrease in the volume density of elastic fibers and an increase in the volume density of airspaces. However, physical exercise partially improved these markers. Additionally, physical exercise decreased oxidant production and increased the activity of the enzymatic antioxidant defense system, but did not reverse lipid and protein oxidative damage induced by cigarette smoke. These results suggest that physical training partially improves histological and oxidative stress parameters in the lungs of animals chronically exposed to cigarette smoke and that other therapies can contribute to potentiate these effects.


Cell Biology International | 2007

Effect of therapeutic pulsed ultrasound on parameters of oxidative stress in skeletal muscle after injury

Luciana Sperb de Freitas; Tiago P. Freitas; Paulo Cesar Lock Silveira; Luís G.C. Rocha; Ricardo A. Pinho; Emilio L. Streck

Contusion injuries are a very common form of both athletic and non‐athletic injury, that effect muscle function. Treatments to augment the normal repair and regeneration processes are important for a wide variety of patients. Therapeutic ultrasound has been claimed to promote tissue repair, especially by enhancing cell proliferation and protein synthesis. The present study aimed to investigate the effect of therapeutic pulsed ultrasound (TPU) on parameters of oxidative stress, namely thiobarbituric acid‐reactive substances (TBARS), protein carbonyl content and the activities of antioxidant enzymes, catalase and superoxide dismutase (SOD), in skeletal muscle after injury. Wistar rats were submitted to an animal model of muscle (gastrocnemius) laceration. TPU was used once a day. One, three or five days after muscle laceration, the animals were killed by decapitation and oxidative stress parameters were evaluated. Serum CK levels were increased in muscle‐injured animals, indicating that the laceration animal model was successful. TBARS were not altered after muscle injury, when compared to the sham group. Protein carbonyl content was increased after muscle laceration. Catalase and SOD activities were increased 1 day after muscle injury and not altered at days 3 and 5. TPU decreased TBARS levels after muscle laceration when compared to injured muscle animals without treatment. Protein carbonyl content evaluation presented similar results. It is tempting to speculate that TPU seems to protect the tissue from oxidative injury. TPU diminished catalase and SOD activities, especially on the first day following muscle laceration.


Life Sciences | 2012

Effects of different physical training protocols on ventricular oxidative stress parameters in infarction-induced rats

Cleber A. Pinho; Camila B. Tromm; Angela Maria Vicente Tavares; Luciano A. Silva; Paulo Cesar Lock Silveira; Cláudio T. De Souza; Magnus Benetti; Ricardo A. Pinho

AIM Physical exercise is important in the prevention and treatment of cardiovascular diseases. Nevertheless, controversy remains around type and intensity of effort required for significant biochemical protective changes. This study investigates two exercise protocols on ventricular oxidative parameters in rats post-infarction. MAIN METHODS Thirty-six 2-month-old male Wistar rats were divided in two groups (n=18): Sham and acute myocardial infarction (AMI) conducted by blocking the coronary artery. Thirty days after AMI, animals were divided in 6 subgroups (n=6): sham, sham+continuous training (60 min), sham+interval training, AMI, AMI+continuous training, and AMI+interval training. Training was conducted in water (30-32°C) 5 times a week for 6 weeks. Animals were sacrificed 48 h after the last exercise routine. Left ventricles were used for oxidative stress analyses (antioxidant enzyme activity and level, oxidative damage) and HIF1α and cit c oxidase expression. KEY FINDINGS After AMI, both exercise models decreased superoxide levels significantly. Training routines did not alter SOD expression and activity, though CAT expression increased with continuous training and GPX level diminished in both training groups, which coincided with the increase in GPX activity. Lipid damage decreased only in the continuous training group, while protein damage decreased only in the interval training group. Cytochrome C increased in both groups, while HIF-1 α dropped significantly after both exercise protocols. SIGNIFICANCE Significant improvement occurred in myocardium redox status in rats challenged with AMI after different training routines. However, continuous training seems to be more efficient in improving the parameters analyzed.


Ultrasound in Medicine and Biology | 2010

Effects of Therapeutic Pulsed Ultrasound and Dimethylsulfoxide (DMSO) Phonophoresis on Parameters of Oxidative Stress in Traumatized Muscle

Paulo Cesar Lock Silveira; Eduardo G. Victor; Débora Schefer; Luciano A. Silva; Emilio L. Streck; Marcos Marques da Silva Paula; Ricardo A. Pinho

Many studies have demonstrated an increase in reactive oxygen species (ROS) and oxidative damage markers after muscle damage. Phonophoresis aims to achieve therapeutically relevant concentrations of the transdermally introduced drug in the tissues subjected to the procedure by the use ultrasound waves. The aim of the study was to evaluate the effects on the therapeutic pulsed ultrasound (TPU) together with gel-dimethylsulfoxide (DMSO) in the parameters of muscular damage and oxidative stress. Male Wistar rats were divided randomly into six groups (n=6): sham (uninjured muscle); muscle injury without treatment; muscle injury and treatment with gel-saline (0.9%); muscle injury and treatment with gel-DMSO (15mg/kg); muscle injury and TPU plus gel-saline; and muscle injury and TPU plus gel-DMSO. Gastrocnemius injury was induced by a single impact blunt trauma. TPU (6min duration, frequency of 1.0MHz, intensity of 0.8W/cm(2)) was used 2, 12, 24, 48, 72, 96 and 120h after muscle trauma. The CK and acid phosphatase activity in serum was used as an indicator of skeletal muscle injury. Superoxide anion, TBARS, protein carbonyls, superoxide dismutase (SOD) and catalase (CAT) activity was used as indicators of stress oxidative. Results showed that TPU and gel-DMSO improved muscle healing. Moreover, superoxide anion production, TBARS level and protein carbonyls levels, superoxide dismutase (SOD) and catalase (CAT) activity were all decreased in the group TPU plus gel-DMSO. Our results show that DMSO is effective in the reduction of the muscular lesion and in the oxidative stress after mechanical trauma only when used with TPU. (E-mail: [email protected]).


Journal of Renal Nutrition | 2010

Physical Exercise Prevents the Exacerbation of Oxidative Stress Parameters in Chronic Kidney Disease

Bárbara L.P. Coelho; Luís G.C. Rocha; Karoline S. Scarabelot; Débora da Luz Scheffer; Merieli M. Ronsani; Paulo Cesar Lock Silveira; Luciano A. Silva; Cláudio T. De Souza; Ricardo A. Pinho

OBJECTIVE Reactive oxygen species play an important role in the pathogenesis of chronic kidney disease (CKD). Physical exercise was suggested as a useful approach to diminish impaired oxidative defense mechanisms. This study sought to observe the effects of physical training before the induction of renal lesions on oxidative stress parameters in animals induced for CKD. METHODS Twenty-four male Wistar rats were divided into four groups (n = 6): sham, sham plus exercise, CKD, and CKD plus exercise. Exercise groups performed physical training on a treadmill for 8 weeks (up to 1 km/h for 50 min/day, 5 days/week). Forty-eight hours after the final exercise session, a surgical reduction of renal mass was performed (5/6 nephrectomized). Thirty days later, blood samples were collected to determine serum creatinine and urea concentrations, and the right kidney was surgically removed and stored at -70 degrees C for later analysis of superoxide production, antioxidant enzymes (superoxide dismutase and catalase), and oxidative damage of lipids (thiobarbituric acid reactive susbstances level) and proteins (carbonyl groups and sulfhydryl content). RESULTS A significant increase occurred in creatinine and urea levels, superoxide production, antioxidant enzymes, and oxidative damage in the CKD group, compared with sham-treated animals (P < .05). Physical training prevented superoxide production, and decreased the oxidative damage in the CKD group (P < .05), but did not increase the effect of antioxidants. CONCLUSION Physical training before induction of a renal lesion is capable of improving oxidative damage parameters and oxidant production, without altering renal function and the antioxidant defense system.


Molecular Neurobiology | 2017

Physical Exercise Attenuates Experimental Autoimmune Encephalomyelitis by Inhibiting Peripheral Immune Response and Blood-Brain Barrier Disruption.

Priscila S. Souza; Elaine C. D. Gonçalves; Giulia S. Pedroso; Hemelin Resende Farias; Stella Célio Junqueira; Rodrigo Marcon; Talita Tuon; Maíra Cola; Paulo Cesar Lock Silveira; Adair R.S. Santos; João B. Calixto; Cláudio T. De Souza; Ricardo A. Pinho; Rafael C. Dutra

AbstractMultiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) caused by demyelination, immune cell infiltration, and axonal damage. Herein, we sought to investigate the influence of physical exercise on mice experimental autoimmune encephalomyelitis (EAE), a reported MS model. Data show that both strength and endurance training protocols consistently prevented clinical signs of EAE and decreased oxidative stress, an effect which was likely due to improving genomic antioxidant defense—nuclear factor erythroid 2-related factor (Nrf2)/antioxidant response elements (ARE) pathway—in the CNS. In addition, physical exercise inhibited the production of pro-inflammatory cytokines interferon (IFN)-γ, interleukin (IL)-17, and IL-1β in the spinal cord of mice with EAE. Of note, spleen cells obtained from strength training group incubated with MOG35–55 showed a significant upregulation of CD25 and IL-10 levels, with a decrease of IL-6, MCP-1, and tumor necrosis factor (TNF)-α production, mainly, during acute and chronic phase of EAE. Moreover, these immunomodulatory effects of exercise were associated with reduced expression of adhesion molecules, especially of platelet and endothelial cell adhesion molecule 1 (PECAM-1). Finally, physical exercise also restored the expression of tight junctions in spinal cord. Together, these results demonstrate that mild/moderate physical exercise, when performed regularly in mice, consistently attenuates the progression and pathological hallmarks of EAE, thereby representing an important non-pharmacological intervention for the improvement of immune-mediated diseases such as MS. Graphical AbstractSchematic diagram illustrating the beneficial effects of physical exercise during experimental model of MS. Physical exercise, especially strength (ST) and endurance (ET) training protocols, inhibits the development and progression of disease, measured by the mean maximal clinical score (1.5 and 1.0, respectively), with inhibition of 30 % and 50 %, respectively, based on the AUC, compared with EAEuntreated group. In addition, ST and ET decreased oxidative stress, possibly, through genomic antioxidant defense, Nrf2-Keap1 signaling pathway, in the CNS. Physical exercise inhibited the production of inflammatory cytokines, such as IFN-γ, IL-17 and IL-1β in the spinal cord after EAE induction, as well as spleen cells obtained from ST group showed a significant upregulation of regulatory T cell markers, such as CD25 and IL-10 levels, and blocked IL-6, MCP-1 and TNF-α production, mainly, during acute and chronic phase of EAE. Finally, these immunomodulatory effects of exercise were associated with inhibition of adhesion molecules and reestablishment of tight junctions expression in spinal cord tissue, thereby limiting BBB permeability and transmigration of autoreactive T cells to the CNS. NO, nitric oxide; GPx, glutathione peroxidase, GSH, glutathione; Nrf2, nuclear factor (erythroid-derived 2)-like 2; CNS, central nervous system; BBB, blood–brain barrier; IFN-g, interferon-gamma; IL-17, interleukin 17; IL-1b, interleukin-1beta.


Journal of Medicinal Food | 2008

Effects of Mikania glomerata Spreng. and Mikania laevigata Schultz Bip. ex Baker (Asteraceae) Extracts on Pulmonary Inflammation and Oxidative Stress Caused by Acute Coal Dust Exposure

Tiago P. Freitas; Paulo Cesar Lock Silveira; Luís G.C. Rocha; Gislaine T. Rezin; João Rocha; Vanilde Citadini-Zanette; Pedro R.T. Romão; Felipe Dal-Pizzol; Ricardo A. Pinho; Vanessa Moraes de Andrade; Emilio L. Streck

Several studies have reported biological effects of Mikania glomerata and Mikania laevigata, used in Brazilian folk medicine for respiratory diseases. Pneumoconiosis is characterized by pulmonary inflammation caused by coal dust exposure. In this work, we evaluated the effect of pretreatment with M. glomerata and M. laevigata extracts (MGE and MLE, respectively) (100 mg/kg, s.c.) on inflammatory and oxidative stress parameters in lung of rats subjected to a single coal dust intratracheal instillation. Rats were pretreated for 2 weeks with saline solution, MGE, or MLE. On day 15, the animals were anesthetized, and gross mineral coal dust or saline solutions were administered directly in the lung by intratracheal instillation. Fifteen days after coal dust instillation, the animals were killed. Bronchoalveolar lavage (BAL) was obtained; total cell count and lactate dehydrogenase (LDH) activity were determined. In the lung, myeloperoxidase activity, thiobarbituric acid-reactive substances (TBARS) level, and protein carbonyl and sulfhydryl contents were evaluated. In BAL of treated animals, we verified an increased total cell count and LDH activity. MGE and MLE prevented the increase in cell count, but only MLE prevented the increase in LDH. Myeloperoxidase and TBARS levels were not affected, protein carbonylation was increased, and the protein thiol levels were decreased by acute coal dust intratracheal administration. The findings also suggest that both extracts present an important protective effect on the oxidation of thiol groups. Moreover, pretreatment with MGE and MLE also diminished lung inflammatory infiltration induced by coal dust, as assessed by histopathologic analyses. The present study indicates that M. glomerata and M. laevigata might become good candidates for the prevention of lung oxidative injury caused by coal dust exposure.


Journal of Surgical Research | 2010

Effect of Therapeutic Pulsed Ultrasound on Lipoperoxidation and Fibrogenesis in an Animal Model of Wound Healing

Tiago P. Freitas; Marcelo Gomes; Daiane B. Fraga; Luciana Sperb de Freitas; Gislaine T. Rezin; Patricia M. Santos; Paulo Cesar Lock Silveira; Marcos Marques da Silva Paula; Ricardo A. Pinho; Emilio L. Streck

Evidence from the literature has shown that the wound healing process is enhanced by ultrasound therapy. In the present study, we measured thiobarbituric acid-reactive substances (TBARS; index of lipoperoxidation) and hydroxyproline (index of collagen synthesis) levels in wounds after therapeutic pulsed ultrasound (TPU) treatment. Male Wistar rats were submitted to skin ulceration, and three doses of TPU (0.4, 0.6, and 0.8W/cm(2)) were used. A circular area of skin was removed with a punch biopsy from the medial dorsal region. After TPU for 10 days, TBARS (Draper and Hadley [21]) and hydroxyproline (Woessner [22]) levels were measured in the tissue around the wound. Results showed that TPU improved wound healing, since the wound size was significantly smaller 5 and 10 days after ulceration in groups submitted to this treatment. Moreover, TBARS levels were decreased in the 0.4, 0.6, and 0.8W/cm(2) TPU groups, and hydroxyproline levels were increased in the 0.6 and 0.8W/cm(2) TPU groups. These findings indicate that TPU presents beneficial effects on the wound healing process, probably by speeding up the inflammatory phase and inducing collagen synthesis.

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Dive into the Paulo Cesar Lock Silveira's collaboration.

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Ricardo A. Pinho

Universidade Federal do Rio Grande do Sul

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Luciano A. Silva

Universidade do Extremo Sul Catarinense

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Cláudio T. De Souza

Universidade do Extremo Sul Catarinense

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Marcos Marques da Silva Paula

Universidade do Extremo Sul Catarinense

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Priscila S. Souza

Universidade do Extremo Sul Catarinense

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Talita Tuon

Universidade do Extremo Sul Catarinense

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Cleber A. Pinho

Universidade do Extremo Sul Catarinense

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Emilio L. Streck

Universidade do Extremo Sul Catarinense

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Felipe Dal-Pizzol

Universidade Federal do Rio Grande do Sul

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Luís G.C. Rocha

Universidade do Extremo Sul Catarinense

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