痛みの細胞および分子メカニズム
Allan I Basbaum1, Diana M Bautista, Grégory Scherrer
1Department of Anatomy, University of California, San Francisco, San Francisco, CA 94158, USA. allan.basbaum@ucsf.edu
Cell
|October 20, 2009
まとめ
神経系は痛みの信号を処理し,神経の可塑性による損傷後に過敏になり得る. これらの分子メカニズムを理解することは,慢性疼痛状態に対処するための鍵です.
科学分野:
- 神経科学は神経科学である.
- 痛みに関する研究 痛みに関する研究
- 分子生物学は分子生物学である.
背景:
- 神経系は,熱的,機械的,化学的刺激を検知する.
- 激しい刺激は,急性痛を引き起こす可能性があります.
- 持続的な傷害は神経の可塑性につながり,疼痛信号を強め,過敏症を引き起こす.
研究 の 目的:
- 痛みの検知,コーディング,および調節の基礎となる分子機構を解明する.
- 神経の可塑性が慢性疼痛にどのように寄与するかを理解する.
主な方法:
- 遺伝子研究 遺伝子研究
- 電気生理学的研究,電気生理学的研究
- 薬理学的な研究は,薬理学的な研究です.
主要な成果:
- 痛みの経路における神経の可塑性は,痛みの信号を強化する.
- プラスチック性は過敏症や慢性疼痛状態につながる可能性があります.
- 分子メカニズムが特定されています.
結論:
- 痛みの処理と可塑性の分子の基礎を理解することは極めて重要です.
- 研究は慢性疼痛メカニズムの理解を進めています.
- この知識は,将来の疼痛管理戦略に役立つかもしれません.
関連する概念動画
Nociception
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. Thus, pain helps the...
Pain
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...
Analgesia and Pain Management
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...
Non-gated Ion Channels
Ion channels are specialized proteins on the plasma membrane that allow charged ions to pass down their electrochemical gradient. Their main function is to maintain the membrane potential which is critical for cell viability. These channels are either gated or non-gated and can transport more than a thousand ions within milliseconds for the cellular event to occur.
Compared to the gated ion channels, the non-gated channels, also known as leakage or passive channels, have no gating mechanism.
Compared to the gated ion channels, the non-gated channels, also known as leakage or passive channels, have no gating mechanism.
Mechanically-gated Ion Channels
Mechanically-gated ion channels are proteins found in eukaryotic and prokaryotic cell membranes that open in response to mechanical stress. Tension, compression, swelling, and shear stress can alter the conformation of the protein, opening a transmembrane channel that allows the passage of ions for signal transmission. In eukaryotes, mechanically-gated channels are distributed in several regions like the neurons, lungs, skin, bladder, and heart, where they play critical roles in numerous...
Opioid Receptors: Overview
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, D-Pen5]-enkephalin or DPDPE for...

