“…The results demonstrate that EE was statistically able to inhibit the pain induced by PGE 2 suggesting their participation in acute pain. In the model of nociception induced by BK, it was observed that only the dose of 500 mg/kg decreased pain threshold (Mattos et al, 2006). The anti-nociceptive effect of the extract was also observed in the model of pain induced by CAP.…”
Section: Discussionmentioning
confidence: 76%
“…The procedure for producing phgogen-induced nociception in mice was similar to that described previously (Mattos et al, 2006). Twenty microlitres of PGE 2 (3 nmol/paw), formalin (FORM, 2.5%), BK (10 nmol/paw), or CAP (1 nmol/paw), diluted in PBS solution, were injected intra-plantarly (i.pl.)…”
Section: Algogen-induced Nociception In Micementioning
The results, including the inhibition of mediators (BK, NO, SP, PGE(2) and TNF-á) and enzyme (MPO and ADA) activity, validate the use of the plant under study for therapeutic treatment of anti-inflammatory, painful and wound healing processes.
“…The results demonstrate that EE was statistically able to inhibit the pain induced by PGE 2 suggesting their participation in acute pain. In the model of nociception induced by BK, it was observed that only the dose of 500 mg/kg decreased pain threshold (Mattos et al, 2006). The anti-nociceptive effect of the extract was also observed in the model of pain induced by CAP.…”
Section: Discussionmentioning
confidence: 76%
“…The procedure for producing phgogen-induced nociception in mice was similar to that described previously (Mattos et al, 2006). Twenty microlitres of PGE 2 (3 nmol/paw), formalin (FORM, 2.5%), BK (10 nmol/paw), or CAP (1 nmol/paw), diluted in PBS solution, were injected intra-plantarly (i.pl.)…”
Section: Algogen-induced Nociception In Micementioning
The results, including the inhibition of mediators (BK, NO, SP, PGE(2) and TNF-á) and enzyme (MPO and ADA) activity, validate the use of the plant under study for therapeutic treatment of anti-inflammatory, painful and wound healing processes.
“…[5] Further pharmacological studies showed that 1 has potent anti-inflammatory activity and behaves as a selective antagonist for the B1R subtype. [6] To the best of our knowledge, 1 is the first and only B1R antagonist among nonpeptide natural products to be published to date. A complex structural model of velutinol A bound to B1R was generated with the homology module by using a model of metarhodopsin photointermediates in the bovine rhodopsin photocascade as the template.…”
A concise route to the bradykinin B1 receptor antagonist velutinol A, a natural product isolated from the rhizomatous of mandevilla velutina (Apocynaceae), has been developed. This synthesis features the highly regioselective construction of Δ 14 silyl enol ether 13 from diol 8a followed by stereoselective introduction of a sterically hindered β-hydroxy group at the C14 position by Rubottom oxidation. A prolonged reaction time and the presence of an excess amount of mCPBA
“…8,9 A investigação fitoquímica de plantas deste gênero levou ao isolamento de glicosídeos cardíacos, pregnanos e triterpenos e à caracterização de substância com importante propriedade anti--inflamatória e antinociceptiva. 10 No gênero Macrosiphonia, a planta medicinal mais conhecida e estudada, para a qual são atribuídas diversas propriedades, destacando-se a atividade anti-inflamatória, é a M. velame, popularmente designada como velame-branco. 11 A espécie Macrosiphonia petraea, também designada pelas sinonímias Macrosiphonia petrea, Macrosiphonia verticillata var.…”
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