Navegando por Autor "Silva, Marco Aurélio Romano"

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Analgesic and side effects of intravenous recombinant Phα1β.
(2020) Rigo, Flavia Karine; Rossato, Mateus Fortes; Borges, Vanessa; Silva, Juliana Figueira da; Pereira, Elizete Maria Rita; Ávila, Ricardo Andrez Machado de; Trevisan, Gabriela; Astoni, Duana Carvalho dos Santos; Diniz, Danuza Montijo; Silva, Marco Aurélio Romano; Castro Junior, Célio José de; Cunha, Thiago Mattar; Ferreira, Juliano; Gomez, Marcus Vinicius
Background: Intrathecal injection of voltage-sensitive calcium channel blocker peptide toxins exerts analgesic effect in several animal models of pain. Upon intrathecal administration, recombinant Phα1β exerts the same analgesic effects as the those of the native toxin. However, from a clinical perspective, the intrathecal administration limits the use of anesthetic drugs in patients. Therefore, this study aimed to investigate the possible antinociceptive effect of intravenous recombinant Phα1β in rat models of neuropathic pain, as well as its side effects on motor, cardiac (heart rate and blood pressure), and biochemical parameters. Methods: Male Wistar rats and male Balb-C mice were used in this study. Giotto Biotech® synthesized the recombinant version of Phα1β using Escherichia coli expression. In rats, neuropathic pain was induced by chronic constriction of the sciatic nerve and paclitaxel-induced acute and chronic pain. Mechanical sensitivity was evaluated using von Frey filaments. A radiotelemeter transmitter (TA11PA-C10; Data Sciences, St. Paul, MN, USA) was placed on the left carotid of mice for investigation of cardiovascular side effects. Locomotor activity data were evaluated using the open-field paradigm, and serum CKMB, TGO, TGP, LDH, lactate, creatinine, and urea levels were examined. Results: Intravenous administration of recombinant Phα1β toxin induced analgesia for up to 4 h, with ED50 of 0.02 (0.01-0.03) mg/kg, and reached the maximal effect (Emax = 100% antinociception) at a dose of 0.2 mg/kg. No significant changes were observed in any of the evaluated motor, cardiac or biochemical parameters. Conclusion: Our data suggest that intravenous administration of recombinant Phα1β may be feasible for drug-induced analgesia, without causing any severe side effects.
Choline oxidase chemiluminéscent assay, after removal of eserine from medium, of acetylcholine released in vitro from brain slices.
(1990) Prado, Marco Antônio Maximo; Santos, T. Moraes; Freitas, Renata Nascimento de; Silva, Marco Aurélio Romano; Gomez, Marcus Vinicius
A chemiluminescent method has been used recently for the determination of acetylcholine with limitations such as the presence of a cholinesterase inhibitor in the incubation medium, which is indispensable for the study of acetylcholine release by various agents. A modified procedure is presented in which the cholinesterase inhibitor eserine (physostigmine) is extracted from the medium. The results showed complete recovery when labelled acetylcholine was used. This modified procedure was used to determine the release of acetylcholine evoked by tityustoxin and ouabain. The results were comparable to those obtained by bioassay using a strip of guinea pig ileum.
Mapping of brain activity in the analgesia induced by Phα1β and morphine.
(2022) Diniz, Danuza Montijo; Malamut, Carlos; Araújo, Marina Rios; Ferreira, Andréa Vidal; Silva, Juliana Figueira; Cordeiro, Marta do Nascimento; Borges, Marcia Helena; Silva, Marco Aurélio Romano; Gomez, Marcus Vinicius; Castro Junior, Célio José de
Preclinical evidence suggests the potential of Phα1β, a toxin obtained from the venom of spider Phoneutria nigriventer, as a new analgesic drug. Molecular brain imaging techniques have afforded exciting opportunities to examine brain processes in clinical pain conditions. This paper aims to study the brain regions involved in the analgesic effects of Phα1β compared with Morphine, in a model of acute pain induced by formalin in Sprague Dawley rats. We used 18F-fluorodeoxyglucose as a metabolic radiotracer to perform brain imaging of rats pretreated with Phα1β or Morphine in a model of acute inflammatory pain caused by intraplantar injection of formalin. The rats’ hind paw’s formalin stimulation resulted in a brain metabolic increase at the bilateral motor cortex, visual cortex, somatosensory cortex, thalamus, and cingulate cortex.In rats treated with Phα1β, selective inhibition of unilateral motor cortex and cingulate cortex was observed. Morphine treatment leads to small and selective inhibition at the bilateral amygdala striatum and accumbens. Our results indicate that the analgesic effect of Phα1β and Morphine possesses a differential profile of central processing in the pain state.
Sociodemographic characteristics, clinical factors, and genetic polymorphisms associated with alzheimer’s disease.
(2013) Bicalho, Maria Aparecida Camargos; Pimenta, Fausto Aloísio Pedrosa; Rodrigues, Luciana Bastos; Hansen, Érika de Oliveira; Neves, Samara Canguçu; Melo, Marina; Rosa, Daniela Valadão; Souza, Renan Pedra de; Miranda, Débora Marques de; Moraes, Edgar Nunes de; Silva, Marco Aurélio Romano; Marco, Luiz de