The anti-inflammatory and antinociceptive effects of NF-κB inhibitory guanidine derivative ME10092

2010 ◽  
Vol 10 (4) ◽  
pp. 455-460 ◽  
Author(s):  
Maija Dambrova ◽  
Liga Zvejniece ◽  
Elina Skapare ◽  
Reinis Vilskersts ◽  
Baiba Svalbe ◽  
...  
Biomedicines ◽  
2020 ◽  
Vol 8 (5) ◽  
pp. 111
Author(s):  
Dayana da Costa Salomé ◽  
Natália de Morais Cordeiro ◽  
Tayná Sequeira Valério ◽  
Darlisson de Alexandria Santos ◽  
Péricles Barreto Alves ◽  
...  

Aristolochia trilobata, popularly known as “mil-homens,” is widely used for treatment of stomach aches, colic, asthma, pulmonary diseases, diabetes, and skin affection. We evaluated the antinociceptive and anti-inflammatory activities of the essential oil (EO) and the main constituent, 6-methyl-5-hepten-2-yl acetate (sulcatyl acetate, SA). EO and SA (1, 10, and 100 mg/kg, p.o.) were evaluated using chemical (formalin-induced licking) and thermal (hot-plate) models of nociception or inflammation (carrageenan-induced cell migration into the subcutaneous air pouch, SAP). The mechanism of antinociceptive activity was evaluated using opioid, cholinergic receptor antagonists (naloxone and atropine), or nitric oxide synthase inhibitor (L-NAME). EO and SA presented a central antinociceptive effect (the hot-plate model). In formalin-induced licking response, higher doses of EO and SA also reduced 1st and 2nd phases. None of the antagonists and enzyme inhibitor reversed antinociceptive effects. EO and SA reduced the leukocyte migration into the SAP, and the cytokines tumor necrosis factor and interleukin-1 (TNF-α and IL-1β, respectively) produced in the exudate. Our results are indicative that EO and SA present peripheral and central antinociceptive and anti-inflammatory effects.


Molecules ◽  
2021 ◽  
Vol 26 (10) ◽  
pp. 3054
Author(s):  
Bruna Araujo Sousa ◽  
Osmar Nascimento Silva ◽  
William Farias Porto ◽  
Thales Lima Rocha ◽  
Luciano Paulino Silva ◽  
...  

Early plants began colonizing earth about 450 million years ago. During the process of coevolution, their metabolic cellular pathways produced a myriad of natural chemicals, many of which remain uncharacterized biologically. Popular preparations containing some of these molecules have been used medicinally for thousands of years. In Brazilian folk medicine, plant extracts from the bamboo plant Guadua paniculata Munro have been used for the treatment of infections and pain. However, the chemical basis of these therapeutic effects has not yet been identified. Here, we performed protein biochemistry and downstream pharmacological assays to determine the mechanisms underlying the anti-inflammatory and antinociceptive effects of an aqueous extract of the G. paniculata rhizome, which we termed AqGP. The anti-inflammatory and antinociceptive effects of AqGP were assessed in mice. We identified and purified a protein (AgGP), with an amino acid sequence similar to that of thaumatins (~20 kDa), capable of repressing inflammation through downregulation of neutrophil recruitment and of decreasing hyperalgesia in mice. In conclusion, we have identified the molecule and the molecular mechanism responsible for the anti-inflammatory and antinociceptive properties of a plant commonly used in Brazilian folk medicine.


Author(s):  
Gabriela Mastrangelo Gonçalves ◽  
Víctor de Carvalho Martins ◽  
André Romero Henrique da Costa ◽  
Thayane Ferreira da Costa Fernandes ◽  
Sidney Pacheco ◽  
...  

2021 ◽  
Vol 93 (suppl 4) ◽  
Author(s):  
RENATA F. MENDES ◽  
PAULA M.Q. BELLOZI ◽  
JÉSSICA L. MOTA CONEGUNDES ◽  
MARIA F. FERNANDES ◽  
NÍCOLAS C.C. PINTO ◽  
...  

2019 ◽  
Vol 28 (2) ◽  
pp. 541-549
Author(s):  
Víctor Ermilo Arana-Argáez ◽  
Fabiola Domínguez ◽  
Diego A. Moreno ◽  
Mario Alberto Isiordia-Espinoza ◽  
Julio Cesar Lara-Riegos ◽  
...  

Planta Medica ◽  
2004 ◽  
Vol 70 (11) ◽  
pp. 1027-1032 ◽  
Author(s):  
Jongwon Choi ◽  
Kyoung-Min Shin ◽  
Hee-Juhn Park ◽  
Hyun-Ju Jung ◽  
Hyoung Ja Kim ◽  
...  

2015 ◽  
Vol 87 (2 suppl) ◽  
pp. 1397-1408 ◽  
Author(s):  
GABRIELA L. DA SILVA ◽  
CAROLINA LUFT ◽  
ADROALDO LUNARDELLI ◽  
ROBSON H. AMARAL ◽  
DENIZAR A. DA SILVA MELO ◽  
...  

Several studies have investigated the antinociceptive, immunomodulatory and anti-inflammatory properties of compounds found in the lavender essential oil (LEO), however to date, there is still lack of substantial data. The objective of this study was to assess the antioxidant, anti-inflammatory and antinociceptive effects of lavender essential oil. The 1,1-diphenyl-2-picrylhydrazyl radical decolorization assay was used for antioxidant activity evaluation. The anti-inflammatory activity was tested using two models of acute inflammation: carrageenan-induced pleurisy and croton oil-induced ear edema. The antinociceptive activity was tested using the pain model induced by formalin. LEO has antioxidant activity, which is dose-dependent response. The inflammatory response evoked by carrageenan and by croton oil was reduced through the pre-treatment of animals with LEO. In the pleurisy model, the drug used as positive control, dexamethasone, was more efficacious. However, in the ear swelling, the antiedematogenic effect of the oil was similar to that observed for dexamethasone. In the formalin test, LEO consistently inhibited spontaneous nociception and presented a similar effect to that of tramadol. The results of this study reveal (in vivo) the analgesic and anti-inflammatory activities of LEO and demonstrates its important therapeutic potential.


Molecules ◽  
2019 ◽  
Vol 24 (13) ◽  
pp. 2453 ◽  
Author(s):  
Francesco Maione ◽  
Paola Minosi ◽  
Amalia Di Giannuario ◽  
Federica Raucci ◽  
Maria Giovanna Chini ◽  
...  

The object of the study was to estimate the long-lasting effects induced by ammonium glycyrrhizinate (AG) after a single administration in mice using animal models of pain and inflammation together with biochemical and docking studies. A single intraperitoneal injection of AG was able to produce anti-inflammatory effects in zymosan-induced paw edema and peritonitis. Moreover, in several animal models of pain, such as the writhing test, the formalin test, and hyperalgesia induced by zymosan, AG administered 24 h before the tests was able to induce a strong antinociceptive effect. Molecular docking studies revealed that AG possesses higher affinity for microsomal prostaglandin E synthase type-2 compared to type-1, whereas it seems to locate better in the binding pocket of cyclooxygenase (COX)-2 compared to COX-1. These results demonstrated that AG induced anti-inflammatory and antinociceptive effects until 24–48 h after a single administration thanks to its ability to bind the COX/mPGEs pathway. Taken together, all these findings highlight the potential use of AG for clinical treatment of pain and/or inflammatory-related diseases.


2020 ◽  
pp. 1-6
Author(s):  
Nathalia Lucca Silva ◽  
Aline Aparecida Saldanha ◽  
Letícia Vieira ◽  
Denise Brentan da Silva ◽  
Carlos Alexandre Carollo ◽  
...  

2011 ◽  
Vol 65 (2) ◽  
pp. 330-335 ◽  
Author(s):  
Yazmin Ravelo ◽  
Vivian Molina ◽  
Daisy Carbajal ◽  
Lilia Fernández ◽  
Julio C. Fernández ◽  
...  

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