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Métodos Terapêuticos e Terapias MTCI
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1.
Eur J Pharmacol ; 575(1-3): 75-81, 2007 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-17826764

RESUMO

In spite of prominent progress in basic pain research, neuropathic pain remains a significant medical problem, because it is often poorly relieved by conventional analgesics. Thus this situation encourages us to make more sophisticated efforts toward the discovery of new analgesics. We previously showed that i.t. administration of acromelic acid-A (ACRO-A), a Japanese mushroom poison, provoked prominent tactile pain (allodynia) at an extremely low dose of 1 fg/mouse. In the present study we synthesized ACRO-A analogues (2S,3R,4R)-3-carboxymethyl-4-phenoxypyrrolidine-2-carboxylic acid (POPA-2) and (2S,3R,4R)-3-carboxymethyl-4-(phenylthio)pyrrolidine-2-carboxylic acid (PSPA-1) chemically and examined their ability to induce allodynia in conscious mice. Whereas POPA-2 induced allodynia at extremely low doses from 1 to 100 fg/mouse, similar to ACRO-A, PSPA-1 did not induce allodynia; rather, it inhibited the ACRO-A-induced allodynia with an ID(50) value (95% confidence limits) of 2.19 fg/mouse (0.04-31.8 fg/mouse). Furthermore, PSPA-1 relieved neuropathic pain produced by L5 spinal nerve transection on day 7 after the operation in a dose-dependent manner from 1 to 100 pg/mouse. In contrast, it did not affect thermal or mechanical nociception or inflammatory pain. PSPA-1 reduced the increase in neuronal nitric oxide synthase activity in the spinal cord of neuropathic pain mice assessed by NADPH-diaphorase histochemistry and blocked the allodynia induced by N-methyl-d-aspartate. These results demonstrate that PSPA-1 may represent a novel class of anti-allodynic agents for neuropathic pain acting by blocking the glutamate-nitric oxide pathway.


Assuntos
Analgésicos/uso terapêutico , Ácido Caínico/análogos & derivados , Mononeuropatias/tratamento farmacológico , Dor/tratamento farmacológico , Medula Espinal/efeitos dos fármacos , Analgésicos/síntese química , Analgésicos/farmacologia , Animais , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Ácido Glutâmico/metabolismo , Hiperalgesia/tratamento farmacológico , Hiperalgesia/patologia , Imuno-Histoquímica , Inflamação/tratamento farmacológico , Inflamação/patologia , Ácido Caínico/síntese química , Ácido Caínico/farmacologia , Ácido Caínico/uso terapêutico , Camundongos , Mononeuropatias/patologia , N-Metilaspartato/farmacologia , NADPH Desidrogenase/metabolismo , Óxido Nítrico/metabolismo , Óxido Nítrico Sintase/metabolismo , Nociceptores/metabolismo , Dor/patologia , Medula Espinal/enzimologia , Fatores de Tempo
2.
Neurosci Lett ; 370(2-3): 130-4, 2004 Nov 11.
Artigo em Inglês | MEDLINE | ID: mdl-15488309

RESUMO

Neuropathic pain arising from peripheral nerve injury is a clinical disorder characterized by a combination of spontaneous pain, hyperalgesia and tactile pain (allodynia), and remains a significant clinical problem since it is often poorly relieved by conventional analgesics. To seek an analgesic compound(s) in Chinese herbs, we examined the effect of seven Chinese herbs that are routinely prescribed for pain management in two neuropathic pain models: allodynia induced by intrathecal administration of prostaglandin F2alpha (PGF2alpha) and by selective L5 spinal nerve transection. The extracts of Moutan cortex and Coicis semen dose-dependently alleviated the PGF2alpha-induced allodynia by oral administration 1 h before intrathecal injection of PGF2alpha. When orally administrated every day for 7 days, these extracts attenuated neuropathic pain in the ipsilateral side, but not in the contralateral side, day 7 after L5 spinal nerve transection. The increase in NADPH diaphorase activity in the spinal cord associated with neuropathic pain was also blocked by these extracts. These results suggest that Moutan cortex and Coicis semen contain substances effective in neuropathic pain.


Assuntos
Medicamentos de Ervas Chinesas/uso terapêutico , Neuralgia/tratamento farmacológico , Anestesia , Animais , Dinoprosta/metabolismo , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Masculino , Camundongos , NADPH Desidrogenase , Neuralgia/induzido quimicamente , Paeonia , Medição da Dor/efeitos dos fármacos , Medula Espinal/efeitos dos fármacos , Medula Espinal/patologia , Traumatismos da Medula Espinal/complicações , Traumatismos da Medula Espinal/tratamento farmacológico , Fatores de Tempo
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