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Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
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Opioid Receptors: Overview01:22

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Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2,...
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Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
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Pain serves as a critical warning signal that alerts the body to potential or actual harm. When mechanical pressure on the skin is intense, such as from a sharp pinch, the sensation transitions from touch to pain. Similarly, extreme temperatures, like a hot pot handle, convert the sensation of heat into pain. Pain can also result from overstimulation of other senses, such as blinding light, loud noise, or the intense heat from habañero peppers. This ability to sense pain is essential for...
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Opioid Analgesics: Morphine and Other Natural Cogeners01:20

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Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
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Updated: Jun 14, 2025

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
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Las neuronas sensibles a la morfina que regulan la antinocicepción mecánica

Michael P Fatt1, Ming-Dong Zhang1, Jussi Kupari1

  • 1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 171 65 Stockholm, Sweden.

Science (New York, N.Y.)
|August 29, 2024
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores identificaron un circuito cerebral específico en ratones que controla la percepción del dolor. Este circuito, que involucra el factor neurotrófico derivado del cerebro (BDNF), explica cómo los opioides como la morfina reducen el dolor mecánico.

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Área de la Ciencia:

  • La neurociencia
  • Farmacología
  • Investigación del dolor

Sus antecedentes:

  • Los opioides son analgésicos eficaces, pero sus mecanismos precisos para el alivio del dolor no se comprenden completamente.
  • El abuso de opiáceos ha alcanzado niveles epidémicos, lo que requiere una comprensión más profunda de su acción.
  • La base neuroanatómica para la analgesia mediada por opioides requiere una mayor aclaración.

Objetivo del estudio:

  • Para identificar los circuitos neuronales específicos en el cerebro responsables del alivio del dolor inducido por los opioides.
  • Para investigar el papel de las neuronas de la médula ventromedial rostral (RVM) en la nocicepción mecánica.
  • Para aclarar los mecanismos moleculares subyacentes a la analgesia de los opioides.

Principales métodos:

  • La transcriptómica de una sola célula se empleó para analizar la expresión génica en las neuronas.
  • Se realizó la manipulación de poblaciones neuronales específicas en el RVM.
  • La antinocicepción inducida por la morfina se evaluó en un modelo de ratón.

Principales resultados:

  • Se identificó un conjunto de neuronas en el RVM como crítico para regular la nocicepción mecánica.
  • La activación o el silenciamiento de las neuronas de proyección RVMBDNF impactaron directamente los efectos analgésicos de la morfina.
  • Una vía del factor neurotrófico derivado del cerebro (BDNF) /receptor de la tromiosina quinasa B (TrkB) y las neuronas de galanina espinal estuvieron implicadas.

Conclusiones:

  • Un circuito espinal RVM específico regula la percepción mecánica del dolor.
  • Este circuito media los efectos antinociceptivos de la morfina.
  • Comprender este circuito ofrece potencial para desarrollar estrategias específicas de manejo del dolor.