Publications by authors named "Claudia Cervantes-Duran"

Article Synopsis
  • - Psoriasis pain is often overlooked in clinical studies, prompting research to explore how certain anti-inflammatory agents and a compound called C48/80 affect allodynia and hyperalgesia in a mouse model of psoriasis induced by imiquimod (IMQ).
  • - The study assessed pain responses in mice treated with IMQ and found that nociceptive behaviors improved with treatments like ketorolac, adalimumab, and C48/80, indicating that inflammation contributes to increased pain sensitivity.
  • - Additionally, the study highlighted changes in serotonin levels in psoriasis-affected mice, suggesting the serotonergic system, particularly the 5-HT1A receptor, could be a promising target for developing new pain treatments in
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Psoriasis is an incurable cutaneous illness characterized by the presence of well-delimited reddish plaques and silvery-white dry scales. So far, there is a limited understanding of its pathogenesis, though recent discoveries on the immunological, genetic and molecular aspects of this disease have significantly contributed to the identification of new targets and the development of novel drugs. Despite these advances, many patients are still dissatisfied, so to improve patient satisfaction, reliability, and clinical outcomes, the individualization of the treatments for this disease becomes a necessity.

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The purpose of this study was to evaluate the effect of acute toluene exposure on formalin (0.5% and 1%)-induced acute and long-lasting nociceptive hypersensitivity in rats. In addition, we sought to investigate the role of peripheral 5-HT receptors in the pronociceptive effect of toluene.

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Background: The purpose of this study was to determine the role of spinal 5-HT2A, 5-HT2B and 5-HT2C receptors in the development and maintenance of formalin-induced long-lasting secondary allodynia and hyperalgesia in rats, as well as their expression in the dorsal root ganglia (DRG) during this process.

Methods: 0.5-1% formalin was used to produce long-lasting secondary allodynia and hyperalgesia in rats.

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The role of P2X2/3, P2X3, P2X4 or P2X7 and P2Y2, P2Y6, and P2Y12 receptors in neuropathic pain has been widely studied. In contrast, the role of P2Y1 receptors is scarcely studied. In this study we assessed the role of P2Y1 receptors in several neuropathic pain models in the rat.

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Preclinical Research This work was performed to assess the effects of intrathecal serotonin 2B (5-HT ) receptor antagonists in rats with neuropathic pain. With RS-127445, its effect was also determined on 5-HT receptor expression. Neuropathic pain was induced by L5/L6 spinal nerve ligation.

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Background: The participation of spinal P2X receptors in neuropathic pain is well recognized. However, the role of P2Y receptors has been less studied. The purpose of this study was to investigate the contribution of spinal P2Y6,11 receptors following peripheral nerve damage induced by spinal nerve ligation.

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The activation of GABAA receptor by γ-amino butyric acid (GABA) in primary afferent fibers produces depolarization. In normal conditions this depolarization causes a reduction in the release of neurotransmitters. Therefore, this depolarization remains inhibitory.

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The antinociceptive role of spinal 5-HT5A receptors in rat models of pain along with their expression was evaluated in the spinal cord and dorsal root ganglion (DRG). Nociception was assessed in the formalin, capsaicin, and acetic acid writhing tests. The expression of 5-HT5A receptors was determined by Western blot analysis.

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Aims: The purpose of this study was to investigate the antinociceptive effect of epicatechin as well as the possible mechanisms of action in diabetic rats.

Main Methods: Rats were injected with streptozotocin to produce hyperglycemia. The formalin test was used to assess the nociceptive activity.

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The purpose of this study was to investigate the possible antinociceptive effect of mangiferin, a glucosylxanthone present in Mangifera indica L., in inflammatory pain. Furthermore, we sought to investigate the possible mechanisms action that contributes to these effects.

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In this study we assessed the role of local peripheral and spinal serotonin 2B (5-HT(2B)) receptors in rats submitted to the formalin test. For this, local peripheral ipsilateral, but not contralateral, administration of the highly selective 5-HT(2B) receptor antagonist 2-amino-4-(4-fluoronaphth-1-yl)-6-isopropylpyridine (RS-127445, 0.01-1 nmol/paw) significantly prevented 1% formalin-induced flinching behavior.

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The role of peripheral and spinal 5-HT(3) receptors in formalin-induced secondary allodynia and hyperalgesia in rats was assessed. Formalin produced acute nociceptive behaviors (flinching and licking/lifting) followed by long-term secondary mechanical allodynia and hyperalgesia in both paws. In experiments where the test drug was anticipated to augment or antagonize the response, 0.

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