外周阿片类受体在炎症性疼痛的调节:一个叙述性审查
Nader-Mugurel Jafal1,2, Smaranda Stoleru1, Carmen Orban1,2
1"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Maedica
|July 18, 2025
概括
外周阿片类受体提供局部疼痛缓解和抗炎功效,没有中央副作用. 针对这些受体显示出有效的疼痛管理策略的希望.
科学领域:
- 药理学 药理学是指药理学的学科.
- 免疫学 免疫学 免疫学
- 疼痛管理 疼痛管理
背景情况:
- 阿片类受体调节中心和外围的疼痛.
- 神经终端和免疫细胞上的外周阿片类受体提供局部效应.
- 中央阿片类受体研究广泛,但外围受体正在获得关注.
研究的目的:
- 审查外围阿片类受体的分类,定位和激活.
- 为了强调它们在调节炎性疼痛中的作用.
- 探索它们在疼痛管理中的治疗潜力.
主要方法:
- 现有文献的叙述性审查.
- 关于炎症组织中受体上调的讨论.
- 对参与 nociception 和免疫调节的信号通路的分析.
主要成果:
- 周围阿片类受体在炎症中受到上调,增强了疼痛缓解.
- 激活通过神经递质抑制和免疫调节调节疼痛信号.
- 边缘作用的激动剂提供有针对性的缓解;对抗剂减少副作用.
结论:
- 外周阿片类受体向提供局部疼痛缓解,减少中央副作用.
- 临床前模型支持它们在炎症性疼痛治疗中的潜力.
- 未来的研究应该优化代理商,交付和整合到多式联络战略中.
相关概念视频
Analgesia and Pain Management
809
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...
809
Opioid Receptors: Overview
1.9K
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,...
1.9K
Nociception
29.5K
Nociception—the ability to feel pain—is essential for an organism’s survival and overall well-being. Noxious stimuli such as piercing pain from a sharp object, heat from an open flame, or contact with corrosive chemicals are first detected by sensory receptors, called nociceptors, located on nerve endings. Nociceptors express ion channels that convert noxious stimuli into electrical signals. When these signals reach the brain via sensory neurons, they are perceived as pain.
29.5K
Opioid Analgesics: Synthetic and Semisynthetic Opioids
437
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...
437
Opioid Analgesics: Morphine and Other Natural Cogeners
370
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...
370
Pain
632
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...
632


