Anti-nociceptive, anti-hyperalgesic and anti-arthritic activity of amides and extract obtained from Piper amalago in rodents
Autor: | Ubirajara Lanza Junior, Jucicléia da Silva Arrigo, Jonas da Silva Mota, Andersson Barison, Eloise Balen, Mario Mateus Sugizaki, Cândida Aparecida Leite Kassuya, Renan Donomae Iwamoto |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Analgesic Motor Activity Anti arthritic 03 medical and health sciences Mice 0302 clinical medicine Drug Discovery Piper amalago medicine Animals Edema Anti nociceptive Rats Wistar Swimming Pain Measurement Pharmacology Folk medicine Piper Analgesics Traditional medicine biology Chemistry Plant Extracts Piperaceae biology.organism_classification Amides Arthritis Experimental Antidepressive Agents Rats Cold Temperature Plant Leaves 030104 developmental biology Hyperalgesia Anesthesia medicine.symptom Sciatic Neuropathy 030217 neurology & neurosurgery |
Zdroj: | Journal of ethnopharmacology. 179 |
ISSN: | 1872-7573 |
Popis: | Piper amalago (Piperaceae) has been used in folk medicine as an analgesic. This study aimed to evaluate the pharmacological effects of extract and pure amides obtained from P. amalago on pain to provide a pharmacological basis for their use in traditional medicine.This study evaluated the anti-nociceptive, anti-hyperalgesic, anti-arthritic and anti-depressive activities of the ethanolic extract of P. amalago (EEPA) and the amides N-[7-(3',4'-methylenedioxyphenyl)-2(Z),4(Z)-heptadienoyl] pyrrolidine (1) and N-[7-(3',4'-methylenedioxyphenyl)-2(E),4(E)-heptadienoyl] pyrrolidine (2) obtained from P. amalago in animal models.Mice treated daily with EEPA (100mg/kg, p.o.) were assayed for 20 days for knee edema (micrometer measurement), mechanical hyperalgesia (analgesiometer analysis), heat sensitivity and immobility (forced swim test) in the Complete Freund's Adjuvant (CFA) model. Cold (acetone test) and mechanical hyperalgesia (electronic von Frey analysis) responses were evaluated for 15 days in rats treated with oral EEPA (100mg/kg) in the spared nerve injury (SNI) model. Meanwhile, mice were evaluated for carrageenan-induced edema and mechanical hyperalgesia and for nociception using the formalin model after a single administration of EEPA (100mg/kg) or amides 1 and 2 (1mg/kg).Amides (1) and (2) were detected and isolated from the EEPA. The EEPA inhibited mechanical hyperalgesia, knee edema, and heat hyperalgesia, but not depressive-like behavior, induced by the intraplantar injection of CFA. When evaluated in the SNI model, the EEPA inhibited mechanical and cold hyperalgesia. The EEPA, 1 and 2 prevented the mechanical hyperalgesia induced by carrageenan and the anti-nociceptive effects in both phases of formalin nociception. The EEPA did not induce alterations in the open field test.The EEPA was effective for inhibition of pain and arthritic parameters but was not effective against depressive-like behavior; additionally, it did not alter locomotor activity. The amides obtained seemed to be the active component(s) present in the EEPA because they proved to be anti-nociceptive and anti-hyperalgesic in models of acute pain. Considering that few drugs are currently available for the treatment of chronic pain, especially neuropathic pain, the present results may have clinical relevance and open new possibilities for the development of new anti-hyperalgesic and anti-arthritic agents from P. amalago. |
Databáze: | OpenAIRE |
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