M. Gomes
University of São Paulo
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Featured researches published by M. Gomes.
Nuclear Physics | 2000
Horacio Oscar Girotti; M. Gomes; Victor O. Rivelles; A. J. da Silva
Abstract We show that the noncommutative Wess–Zumino model is renormalizable to all orders of perturbation theory. The noncommutative scalar potential by itself is non-renormalizable but the Yukawa terms demanded by supersymmetry improve the situation turning the theory into a renormalizable one. As in the commutative case, there are neither quadratic nor linear divergences. Hence, the IR/UV mixing does not give rise to quadratic infrared poles.
Journal of Applied Physiology | 2010
Marcelo Pires-Oliveira; Ana Leticia G.C. Maragno; Lucas T. Parreiras-e-Silva; Tiago Chiavegatti; M. Gomes; Rosely Oliveira Godinho
Skeletal muscle atrophy induced by denervation and metabolic diseases has been associated with increased ubiquitin ligase expression. In the present study, we evaluate the influence of androgens on muscle ubiquitin ligases atrogin-1/MAFbx/FBXO32 and Murf-1/Trim63 expression and its correlation with maintenance of muscle mass by using the testosterone-dependent fast-twitch levator ani muscle (LA) from normal or castrated adult male Wistar rats. Gene expression was determined by qRT-PCR and/or immunoblotting. Castration induced progressive loss of LA mass (30% of control, 90 days) and an exponential decrease of LA cytoplasm-to-nucleus ratio (nuclear domain; 22% of control after 60 days). Testosterone deprivation induced a 31-fold increase in LA atrogin-1 mRNA and an 18-fold increase in Murf-1 mRNA detected after 2 and 7 days of castration, respectively. Acute (24 h) testosterone administration fully repressed atrogin-1 and Murf-1 mRNA expression to control levels. Atrogin-1 protein was also increased by castration up to 170% after 30 days. Testosterone administration for 7 days restored atrogin-1 protein to control levels. In addition to the well known stimulus of protein synthesis, our results show that testosterone maintains muscle mass by repressing ubiquitin ligases, indicating that inhibition of ubiquitin-proteasome catabolic system is critical for trophic action of androgens in skeletal muscle. Besides, since neither castration nor androgen treatment had any effect on weight or ubiquitin ligases mRNA levels of extensor digitorum longus muscle, a fast-twitch muscle with low androgen sensitivity, our study shows that perineal muscle LA is a suitable in vivo model to evaluate regulation of muscle proteolysis, closely resembling human muscle responsiveness to androgens.
Muscle & Nerve | 2010
Flávia Alessandra Guarnier; Alessandra Lourenço Cecchini; Andréia Akemi Suzukawa; Ana Leticia G.C. Maragno; Andréa Name Colado Simão; M. Gomes; Rubens Cecchini
Reactive oxygen species oxidize proteins and modulate the proteasomal system in muscle‐wasting cancer cachexia. On day 5 (D5), day 10 (D10), and day 14 (D14) after tumor implantation, skeletal muscle was evaluated. Carbonylated proteins and thiobarbituric acid reactive substances were measured. Chemiluminescence was employed for lipid hydroperoxide estimation. Glutathione, superoxide dismutase, and total radical antioxidant capacity were evaluated. The proteasomal system was assessed by mRNA atrogin‐1 expression. Increased muscle wasting, lipid hydroperoxide, and superoxide dismutase, and decreased glutathione levels and total radical antioxidant capacity, were found on D5 in accordance with increased mRNA atrogin‐1 expression. All parameters were significantly modified in animals treated with α‐tocopherol. The elevation in aldehylde levels and carbonylated proteins observed on D10 were reversed by α‐tocopherol treatment. Oxidative stress may trigger signal transduction of the proteasomal system and cause protein oxidation. These pathways may be associated with the mechanism of muscle wasting that occurs in cancer cachexia. Muscle Nerve 42: 950–958, 2010
Physical Review D | 2009
M. Gomes; V. G. Kupriyanov
The model of the position-dependent noncommutativity in quantum mechanics is proposed. We start with given commutation relations between the operators of coordinates
Physics Letters B | 2007
A. F. Ferrari; M. Gomes; J. R. Nascimento; E. Passos; A. Yu. Petrov; A. J. da Silva
[{\stackrel{^}{x}}^{i},{\stackrel{^}{x}}^{j}]={\ensuremath{\omega}}^{ij}(\stackrel{^}{x})
Protein and Peptide Letters | 2004
Emer S. Ferro; Flávia Regina Carreño; Camila N. Goñi; Paula Amaral Gurgel Garrido; Alessander O. Guimaraes; Leandro M. Castro; Vitor Oliveira; Maurício de Campos Araújo; Vanessa Rioli; M. Gomes; José Domingues Fontenele‐Neto; Stephen Hyslop
, and construct the complete algebra of commutation relations, including the operators of momenta. The constructed algebra is a deformation of a standard Heisenberg algebra and obeys the Jacobi identity. The key point of our construction is a proposed first-order Lagrangian, which after quantization reproduces the desired commutation relations. Also we study the possibility to localize the noncommutativity.
Fungal Genetics and Biology | 2012
Ana Cristina Colabardini; Ana Carolina Humanes; Paula Fagundes de Gouvêa; Marcela Savoldi; Maria Helena S. Goldman; Marcia Regina von Zeska Kress; Özgür Bayram; Juliana Velasco de Castro Oliveira; M. Gomes; Gerhard H. Braus; Gustavo H. Goldman
Abstract We study some physical consequences of the introduction of a Lorentz-violating modification term in the linearized gravity, which leads to modified dispersion relations for gravitational waves in the vacuum. We discuss two possible mechanisms for the induction of such a term in the Lagrangian. First, it is generated at the quantum level by a Lorentz-breaking coupling of the gravity field to a spinor field. Second, it appears as consequence of a particular modification of the Poisson algebra of the canonical variables, in the spirit of the so-called “noncommutative fields approach”.
Physics Letters B | 2001
Horacio Oscar Girotti; M. Gomes; A.Yu. Petrov; Victor O. Rivelles; A. J. da Silva
Endopeptidase 24.15 (EC 3.4.24.15; EP24.15) and endopeptidase 24.16 (EC 3.4.24.16; EP24.16) are enzymes involved in general peptide metabolism in mammalian cells and tissues. This review will focus on morphological and biochemical aspects related to the subcellular distribution and secretion of these homologous enzymes in the central nervous system. These are important issues for a better understanding of the functions of EP24.15 and EP24.16 within neuroendocrine systems.
Physical Review D | 2012
Pedro R. S. Gomes; M. Gomes
The filamentous fungus Aspergillus nidulans has been used as a fungal model system to study the regulation of xylanase production. These genes are activated at transcriptional level by the master regulator the transcriptional factor XlnR and repressed by carbon catabolite repression (CCR) mediated by the wide-domain repressor CreA. Here, we screened a collection of 42 A. nidulans F-box deletion mutants grown either in xylose or xylan as the single carbon source in the presence of the glucose analog 2-deoxy-D-glucose, aiming to identify mutants that have deregulated xylanase induction. We were able to recognize a null mutant in a gene (fbxA) that has decreased xylanase activity and reduced xlnA and xlnD mRNA accumulation. The ΔfbxA mutant interacts genetically with creAd-30, creB15, and creC27 mutants. FbxA is a novel protein containing a functional F-box domain that binds to Skp1 from the SCF-type ligase. Blastp analysis suggested that FbxA is a protein exclusive from fungi, without any apparent homologs in higher eukaryotes. Our work emphasizes the importance of the ubiquitination in the A. nidulans xylanase induction and CCR. The identification of FbxA provides another layer of complexity to xylanase induction and CCR phenomena in filamentous fungi.
Physical Review D | 2010
M. Gomes; V. G. Kupriyanov; A. J. da Silva
Abstract We study the superspace formulation of the noncommutative nonlinear supersymmetric O ( N ) invariant sigma-model in 2+1 dimensions. We prove that the model is renormalizable to all orders of 1/ N and explicitly verify that the model is asymptotically free.