下降疼痛调节系统的自上而下的控制驱动着安慰剂镇痛
Giulia Livrizzi1,2, Jingzhu Liao1, Desiree A Johnson1
1Department of Neurobiology, School of Biological Sciences, University of California San Diego, La Jolla, CA, USA.
bioRxiv : the preprint server for biology
|February 24, 2025
概括
安慰剂止痛,一种止痛效应,由小鼠的下降疼痛调节系统 (DPMS) 介导. 这涉及到由大脑皮层活动影响的近水道灰色 (PAG) 中的阿片类信号传递.
科学领域:
- 神经科学是一个神经科学.
- 疼痛研究 疼痛研究
- 行为科学 行为科学
背景情况:
- 使用安慰剂镇痛,通过惰性物质抑制疼痛,缺乏明确的神经证据.
- 之前的经验和预期影响着安慰剂效应.
- 了解安慰剂的神经回路对于疼痛管理至关重要.
研究的目的:
- 为了识别用于安慰剂止痛的神经回路.
- 为了建立安慰剂效应神经基础的因果证据.
- 弥合疼痛调节的临床和临床前研究.
主要方法:
- 从人类向小鼠逆转翻译一个有条件的安慰剂协议.
- 调查围水管灰色 (PAG) 中下降疼痛调节神经元的作用.
- 分析皮质输入 (中间前额,前带皮层,前岛皮层) 对PAG的影响.
主要成果:
- 发现安慰剂效应可以抑制小鼠的感觉和情绪-动机性疼痛行为.
- 在PAG中的下降疼痛调节神经元对于安慰剂和吗啡反感觉都至关重要.
- 安慰剂疼痛缓解取决于来自中间前额外和前带皮层的PAG输入,但不是前岛皮层.
- 条件化增强PAG中的内源性阿片类药物释放,导致疼痛缓解.
结论:
- 下降疼痛调节系统 (DPMS) 的皮质控制是通过在安慰剂给药期间在PAG中快速内源性阿片类药物信号传递的门.
- 该DPMS在安慰剂止痛中发挥着核心作用.
- 这项研究在疼痛研究中提供了临床观察和临床前发现之间的关键联系.
相关概念视频
Analgesia and Pain Management
422
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...
422
Pain
439
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...
439
Opioid Analgesics: Synthetic and Semisynthetic Opioids
205
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...
205
Nociception
27.6K
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.
27.6K
Opioid Analgesics: Morphine and Other Natural Cogeners
163
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...
163
Blind Procedures
10.6K
Ideally, the people who observe and record the children’s behavior are unaware of who was assigned to the experimental or control group, in order to control for experimenter bias. Experimenter bias refers to the possibility that a researcher’s expectations might skew the results of the study. Remember, conducting an experiment requires a lot of planning, and the people involved in the research project have a vested interest in supporting their hypotheses. If the observers knew which...
10.6K


