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Chemical composition and evaluation of the anti-inflammatory and antinociceptive activities of Duguetia furfuracea essential oil: Effect on edema, leukocyte recruitment, tumor necrosis factor alpha production, iNOS expression, and adenosinergic and opioidergic systems.

AbstractETHNOPHARMACOLOGICAL RELEVANCE:
Duguetia furfuracea (A. St. -Hil.) Saff. (Annonaceae) is commonly known in Brazil as "araticum-seco," and its root is used in folk medicine to treat inflammatory and painful disorders. However, no studies have been performed to evaluate these therapeutic activities.
AIM OF THE STUDY:
Investigate the chemical composition, anti-inflammatory and antinociceptive effects, and elucidate the possible antinociceptive mechanisms of action from the essential oil of D. furfuracea (EODf) underground stem bark.
MATERIALS AND METHODS:
Chemical composition was determined by gas chromatography and mass spectrometry (GC/MS). The paw edema induced by LPS, formalin-induced nociception, LPS-induced thermal hyperalgesia and rota-rod tests in vivo were used to evaluate the anti-inflammatory and antinociceptive effects in addition to the alteration on motor coordination. Histological analyses and an immunohistochemistry assay for iNOS were performed on mouse footpads of naive, control, 10 mg/kg EODf, and 10 mg/kg indomethacin (Ind) groups. The samples were removed at 1, 3, and 6 h after subplantar injection of LPS. In addition, the involvement of the adenosinergic, opioidergic, serotonergic, and cholinergic systems were investigated, in order to elucidate possible antinociceptive mechanisms.
RESULTS:
Twenty-four volatile constituents were detected and identified. (E)-asarone (21.9%), bicyclogermacrene (16.7%), 2,4,5-trimethoxystyrene (16.1%), α-gurjunene (15%), cyperene (7.8%), and (E)-caryophyllene (4.6%) were major compounds found in EODf. Oral treatment (p.o.) with EODf (1, 3, and 10 mg/kg) significantly inhibited the paw edema induced by LPS. At 10 mg/kg EODf promoted inhibition of tumor necrosis factor alpha (TNF-α) production, recruitment of polymorphonuclear (PMN) leukocytes and inducible nitric oxide synthase (iNOS) expression in paw tissue. EODf (10 and 30 mg/kg, p.o.) also reduced licking time in both phases of the formalin test and it had a significant effect on the LPS-induced thermal hyperalgesia model. The administration of caffeine (Caf) and naloxone (Nal) reversed the antinociceptive activity of EODf, in the first phase of the formalin test and in the LPS-induced thermal hyperalgesia model. Moreover, Nal was also able to abolish the antinociception caused by EODf, in the second phase of formalin test. In the rota-rod test, EODf-treated animals did not show any alteration of motor coordination.
CONCLUSIONS:
Our findings indicate that EODf underground stem bark produces anti-inflammatory and both central and peripheral antinociceptive effects. Furthermore, the antinociceptive activity of EODf underground stem bark is possibly mediated by adenosinergic and opioidergic pathways, and its properties do not induce effects on motor coordination. These results support the use of the folk medicine, D. furfuracea root, to treat inflammation and painful conditions.
AuthorsAline Aparecida Saldanha, Letícia Vieira, Rosy Iara Maciel de Azambuja Ribeiro, Ralph Gruppi Thomé, Hélio Batista Dos Santos, Denise Brentan Silva, Carlos Alexandre Carollo, Flávio Martins de Oliveira, Débora de Oliveira Lopes, João Máximo de Siqueira, Adriana Cristina Soares
JournalJournal of ethnopharmacology (J Ethnopharmacol) Vol. 231 Pg. 325-336 (Mar 01 2019) ISSN: 1872-7573 [Electronic] Ireland
PMID30445104 (Publication Type: Journal Article)
CopyrightCopyright © 2018 Elsevier B.V. All rights reserved.
Chemical References
  • Analgesics
  • Anti-Inflammatory Agents
  • Narcotic Antagonists
  • Oils, Volatile
  • Phytochemicals
  • Purinergic P1 Receptor Antagonists
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse
Topics
  • Analgesics (chemistry, pharmacology, therapeutic use)
  • Animals
  • Annonaceae (chemistry)
  • Anti-Inflammatory Agents (chemistry, pharmacology, therapeutic use)
  • Edema (drug therapy, immunology)
  • Leukocytes (drug effects, immunology)
  • Male
  • Mice
  • Narcotic Antagonists (pharmacology)
  • Nitric Oxide Synthase Type II (immunology)
  • Oils, Volatile (chemistry, pharmacology, therapeutic use)
  • Pain (drug therapy)
  • Pain Measurement
  • Phytochemicals (analysis, pharmacology, therapeutic use)
  • Plant Roots (chemistry)
  • Purinergic P1 Receptor Antagonists (pharmacology)
  • Tumor Necrosis Factor-alpha (immunology)

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