Navegando por Assunto "Atividade antinociceptiva"
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Item Acesso aberto (Open Access) Análise nutricional e atividade antinociceptiva do óleo Plukenetia polyadenia(Universidade Federal do Pará, 2013-05-27) ALBUQUERQUE, Thayana Lucy Freitas; BASTOS, Gilmara de Nazareth Tavares; http://lattes.cnpq.br/2487879058181806; NASCIMENTO, José Luiz Martins do; http://lattes.cnpq.br/7216249286784978This study investigated the nutritional effects resulting from chronic oral administration of oil Plukenetia polyadenia in rats on weight, feed intake, blood lipid composition, and histology of the organs, and to investigate the toxicity and antinociceptive activity after administration of different dosages orally in mice. The nutritional analysis of food intake and weight showed that chronic administration of this oil did not interfere nutritionally in the homeostasis of these variables, regardless of the dosages used (100 and 200mg.kg/weight). The lipid fractions of blood as total cholesterol, LDL, HDL and triglycerides also are unchanged in the supplemented animals. Not found edema, cell death or cell inflammatory response in the liver, heart, lung, stomach, intestines, pancreas and chronic renal after supplementation in both dosages. In the writhing test induced by acetic acid, the oil administered orally (25, 50 and 100mg.kg/ weight) significantly reduced the number of writhes compared to the control. In the hot plate test, the treatment with oil at a dosage of 200mg.kg/weight induced no change in latency to thermal stimulus compared to the control. In the formalin test, oral treatment at doses of 50 and 100mg.kg/ weight showed a significant antinociceptive effect, reducing the time to lick only in the second phase (inflammatory). The oil in 200mg.kg/ weight dosage did not affect the behavioral activity of rats submitted to the open field test and showed no toxic effects. Our results demonstrated that Plukenetia polyadenia present antinociceptive activity without toxicicity.Item Acesso aberto (Open Access) Avaliação das atividades antinociceptiva e anti-inflamatória do extrato hidroetanólico de partes aéreas de Portulaca pilosa L. (Portulacaceae)(Universidade Federal do Pará, 2012-08-30) FERREIRA, Fabrício Alexopulos; DOLABELA, Maria Fâni; http://lattes.cnpq.br/0458080121943649; SOUSA, Pergentino José da Cunha; http://lattes.cnpq.br/9909053957915090This study investigated the acute oral toxicity, the antinociceptive effect in chemical and thermal nociception models as such as the anti-inflammatory activity in carrageenan and croton oil models of the hydroethanolic extract from aerial parts of Portulaca pilosa (HEEPp). Also identified some possible mechanism involved in antinociception of the extract as such as the effects of HEEPp on central nervous system of rats. In the oral acute toxicity test, the treatment with HEEPp ( 2000 mg/kg) caused no deaths. In the acetic acid-induced writhing test, the HEEPp (100, 200, 400 and 600 mg/kg) administered by oral route (p.o.) significantly reduced the number of contortions acetic acid-induced in 18.18, 33.25, 47.27, 65.81 e 73.94%, respectively. In the hot plate test, the treatment with HEEPp (200, 400 e 600 mg/kg, p.o.) did not alter the latency to the thermal stimuli of 50 ± 0,5 ºC. In the formalin test, the treatment with HEEPp (200, 400 e 600 mg/kg, p.o.) significantly reduced the licking-time in neurogenic phase (first phase) in 38.79, 60.61 and 75.18 %, and inflammatory phase (second phase) in 49.23, 53.03 e 87.53 %, respectively. The previous naloxone administration, significantly reversed the effect of HEEPp (600 mg/kg, p.o.) in both phases of the formalin test. The pre-treatment with L-NAME and methylene blue significantly reversed the effect of HEEPp (600 mg/kg, p.o.) in both phases of the formalin test. The pre-treatment with glibenclamide also significantly reversed the effect of HEEPp (600 mg/kg, p.o.) in both phases of the formalin test. HEEPp (600 mg/kg, p.o.) did not affect the locomotor activity of rats in the open field test. In the carrageenan-induced paw edema and croton-induced ear edema, the HEEPp (400 and 600 mg/kg, p.o.) did not inhibit significantly the edema formation in both the tests. The results of this study showed that HEEPp, when administered by oral route, presented low toxicity and its antinociceptive actuation observed in neurogenic phase involves peripherals interaction with opioids receptors and activation of the in the NO/GCs/GMPc/ KATP pathway. Already the antinociceptive activity observed in the inflammatory phase does not seem to depend of the inhibition on via phospholipase A2/cyclooxygenases, but interaction with peripheral opioid receptors and the NO/sGC /cGMP/ KATP pathway.Item Acesso aberto (Open Access) Caracterização química, avaliação da toxicidade oral aguda e da atividade antinociceptiva do extrato metanólico das folhas de Montrichardia linifera (Arruda) Schott(Universidade Federal do Pará, 2024-08) COSTA, Wellington Junior Taisho Nagahama; AMARANTE, Cristine Bastos do; http://lattes.cnpq.br/4101983776191966; https://orcid.org/0000-0002-8602-8180; BASTOS, Gilmara de Nazareth Tavares; http://lattes.cnpq.br/2487879058181806Background: Montrichardia linifera (Arruda) Schott is popularly known as “aninga”, “aningaçu”, “aningaíba” and “aninga-do-igapó”. The compresses and plasters from the leaves of the medicinal plant are used to treat abscesses, tumors and pain caused by stingray stings. Aim of the study: The study aimed to investigate the antinociceptive potential of the methanolic extract of Montrichardia linifera leaves (MEMLL), as well as carry out chemical characterization and acute oral toxicity. Materials and methods: The leaves were collected during the rainy season and the methanolic extract was obtained after gradient extraction in different solvents. The MEMLL was analyzed using high performance liquid chromatography (HPLC) and Nuclear Magnetic Resonance (NMR). The evaluation of the acute oral toxicity test was used to observe the presence of toxic substances. Subsequently, acetic acid, hot plate and formalin tests were used to evaluate the analgesic effects. Results: The HPLC fingerprint analysis allowed the identification of rutin, quercetin and epicatechin. The analysis of NMR spectra identified rutin and quercetin, as well as the flavonoids luteolin and chrysoeriol. The MEMLL did not demonstrate effects considered toxic. In the acetic acid test, the MEMLL inhibited peripheral pain by 51.46% (p < 0.05) at a dose of 50 mg/kg and 75.08% (p < 0.001) at a dose of 100 mg/kg. The hot plate test evaluated the latency time of animals, demonstrating central activity at 30 and 60 min increasing by 164.43% (p < 0.01) and 122.95% (p < 0.05) at a dose of 50 mg /kg and 162.62% (p < 0.01) and 136.68% (p < 0.05) at a dose of 100 mg/kg. The formalin test evaluated the central and peripheral antinociceptive effect of the MEMLL. In the neurogenic phase, a reduction of 35.25% (p < 0.05) at a dose of 50 mg/kg and 52.30% (p < 0.01) at a dose of 100 mg/kg. In inflammatory pain, a reduction of 66.39% (p < 0.0001) and 72.15% (p < 0.0001) was observed. Conclusion: The antinociceptive activity supports its ethnopharmacological use. This analgesic effect is probably associated with the identified flavonoids, all of which have antioxidant, anti-inflammatory and antinociceptive properties. Furthermore, the MEMLL was non-toxic.Item Acesso aberto (Open Access) Poderia um óleo atuar como analgésico opioide? oléo de Plukenetia polyadenia: elucidação do mecanismo de ação(Universidade Federal do Pará, 2016-09-05) MOTA, Amanda Sodré; MAIA, Cristiane do Socorro Ferraz; http://lattes.cnpq.br/4835820645258101; BASTOS, Gilmara de Nazareth Tavares; http://lattes.cnpq.br/2487879058181806The seed oil of Plukenetia polyadenia (Pp-oil) is used by the Amazon people against arthritis and rheumatism, spreading it in the arms and legs. The fatty acid composition, antinociceptive effect and toxicity of Pp-oil were investigated. Materials and methods: The Pp-oil was obtained by pressing and its antinociceptive activity was analyzed in models of nociception (acetic acid-induced abdominal writhing, hot plate and formalin tests) in mice and also mechanism of action was determined using acetic acid- indiced abdominal writing, open field, pole test and rotarod. Results: Pp-oil demonstrated a significant dose dependent antinociceptive effect (p< 0.05) in the chemical stimulation and at the second phase of formalin. However, the result from the hot plate test, open field, pole test and rotarod were not significant (p> 0.05), suggesting that Pp-oil has an analgesic activity, which is putative of peripheral origin. In the writhing test, the oil dosed at 25, 50 and 100 mg/kg reduced the abdominal writhes in a significant manner. In the hot plate test, the oil dosed at 200 mg/kg did not induced alterations in the latency time when compared to the control. At the dose of 100 mg/kg it did not show any difference in motor system proving that Pp-oil does not have any influence at central nervous system. In the formalin test, the oil dosed at 50 and 100 mg/kg reduced in a significant manner the second phase of the algic stimulus. Pp-oil at 100mg/kg did not show any alterations in motor system when analyzed with open field, pole test and rotarod (p>0,05), which corroborates with previous results that affirm Pp-oil has no participation in central nervous system. In addition, its antinociception was reversed by naloxone in evaluation of the mechanism of action. Conclusion: Pp-oil proved to have analgesic properties. Moreover, the results concerning mechanism suggest that opiod receptors are involved in the antinociceptive action of the Pp-oil using a peripheral pathway.