scholarly journals Antinociceptive Effects of Artemisia persica Boiss Essential Oil in Male Mice Using Formalin and Tail Immersion Tests

2019 ◽  
Vol 12 (11) ◽  
pp. 23-31 ◽  
Author(s):  
Tayebeh Ebrahimi ◽  
Mahbubeh Setorki ◽  
Nasrollah Dastanpour ◽  
◽  
◽  
...  
Author(s):  
Gabriela Mastrangelo Gonçalves ◽  
Víctor de Carvalho Martins ◽  
André Romero Henrique da Costa ◽  
Thayane Ferreira da Costa Fernandes ◽  
Sidney Pacheco ◽  
...  

2009 ◽  
Vol 22 (3) ◽  
pp. 206 ◽  
Author(s):  
Sun Seek Min ◽  
Seung Ho Han ◽  
Jaeyong Yee ◽  
Chan Kim ◽  
Geun Hee Seol ◽  
...  

2020 ◽  
Vol 24 (10) ◽  
pp. 1990-1998
Author(s):  
Kelly F. Paton ◽  
Rahau Shirazi ◽  
Mikhail Vyssotski ◽  
Bronwyn M. Kivell

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.


2002 ◽  
Vol 35 (10) ◽  
pp. 1215-1219 ◽  
Author(s):  
A.P.V. Abdon ◽  
J.H. Leal-Cardoso ◽  
A.N. Coelho-de-Souza ◽  
S.M. Morais ◽  
C.F. Santos

Author(s):  
Pablinny Moreira Galdino ◽  
Marcus Vinícius Mariano Nascimento ◽  
Iziara Ferreira Florentino ◽  
Roberta Campos Lino ◽  
James Oluwagbamigbe Fajemiroye ◽  
...  
Keyword(s):  

2019 ◽  
Vol 18 (1) ◽  
pp. 25-32
Author(s):  
Daniele C. Fernandes ◽  
Bruna P. Martins P. Martins ◽  
David L. F. Medeiros ◽  
Shirley V. M. Santos ◽  
Carlos R. M. Gayer ◽  
...  

Introduction: Echinodorus macrophyllus (Kunth) Micheli,Alismataceae, commonly known as “chapéu de couro”, isused in the treatment of various inflammatory conditions.The aim of this study was to evaluate the antinociceptiveand anti-inflammatory neurogenic potential and perform thephytochemical analysis of its hexanic extract (HEEm). Materialand methods: The HEEm was obtained by maceration ofdried leaves with hexane (100 g d.w./2 L). Its composition wasdetermined by GC-MS (DB1 column) by comparison of retentionindices in the database and literature. The antinociceptivepotential was evaluated in SW or DBA/1 male mice usingchemical (acetic acid and formalin), thermal (tail immersionand hot plate tests) and topical (xylene) nociception models,all approved by the Ethics Committee (CEA-IBRAG). Results:HEEM presented antinociceptive activity in the model of:acetic acid-induced writhing (52%; 25mg/kg); tail immersion(60 and 90 minutes; 50 mg/kg); hot-plate in 60 minutes (25and 100mg/kg) and 120 minutes (25mg/kg); formalin tests, atthe neurogenic (63.4%, 100mg/kg), and inflammatory (50%;50 and 100mg/kg) phases; and in neurogenic inflammationinduced by xylene (88.3%; 100mg/kg). These activities seem tobe related to the terpene and fatty acid derivatives evidencedby GC-MS. Discussion: HEEm presented antinociceptive, aswell as anti-inflammatory, activity by central and peripheralmechanisms, It consists of terpenic and fatty acid derivatives,described in the literature as antioxidants, anti-inflammatory,and antinociceptives. Conclusions: HEEm showed antinociceptiveactivity in all models, which can be related to thepresence of terpenic and fatty acid derivatives.Keywords: Echinodorus macrophyllus; Nociception;Neurogenic inflammation; Phytochemistry.


2020 ◽  
Vol 22 (4) ◽  
pp. 167-172
Author(s):  
Kosar Asadi ◽  
Saeid Abbasi-Maleki ◽  
Goudarz Sadeghi Hashjin

Background and aims: Several pharmacological and biological activities have been attributed to Cuminum cyminum L. (CC), including analgesic, antioxidant, anti-inflammatory, and anti-epileptic effects. In this regard, the present study evaluated the antidepressant-like effects of the CC essential oil (EO) on the forced swim test (FST) and tail suspension test (TST) in male mice. Materials and Methods: The gas chromatography-mass spectrometry (GC-MS) apparatus was used for detecting the chemical compounds of CC EO. In the present study, 72 male NMRI mice were randomly allocated to 12 groups (each containing 6 animals) including control or vehicle (10 mL/kg, i.p.), fluoxetine (20 mg/kg, i.p.), imipramine (30 mg/kg, i.p), and the CC EO (100, 200, and 300 mg/kg, i.p.). Then, several parameters were measured and recorded, including immobility time, swimming time, and climbing time in FST, along with immobility time in TST, respectively. Results: Cuminaldehyde followed by cymene, γ-terpinene, phenylglycol, 2-caren-10-al, 2-β-pinene, acoradiene, and cuminic acid were the major components of the CC EO. Based on the results, all doses of the CC, fluoxetine, and imipramine reduced immobility time in both FST (P<0.001) and TST (P<0.001). On the other hand, all doses of the CC and fluoxetine increased swimming time (P<0.001) although climbing time was only increased by 200 and 300 mg/kg of the EO (P<0.01 and P<0.001, respectively) and imipramine (P<0.001). Conclusion: Based on the findings of the present study, the components of the CC induced antidepressant-like activity similar to that of fluoxetine and imipramine in both tests. However, further studies are required to confirm the role of different active components and the exact mechanism of action.


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