Mense S S
Institut für Anatomie und Zellbiologie III, Universität Heidelberg.
Schmerz. 2004 Jun;18(3):225-37. doi: 10.1007/s00482-003-0297-8.
This short overview presents some of the current neuroanatomical knowledge concerning pathways and nuclei mediating pain sensations. The axonal membrane of the nociceptor is equipped with a multitude of receptor molecules that specifically bind pain-producing and sensitizing substances. Recently, adenosine triphosphate and protons have attracted much interest. The different nociceptor types are probably characterized by different sets of receptor molecules in the membrane of the nociceptive ending. Nociceptive cells are present in the superficial laminae and the neck of the dorsal horn. The cells in the former region include nociceptive-specific ones that receive input from nociceptors exclusively, whereas in the neck of the dorsal horn a convergent input from nociceptive and non-nociceptive afferent fibers prevails. At the spinal level, neuroplastic sensitizing processes take place that are assumed to underlie the allodynia and hyperalgesia of pain patients. In addition to the lateral spinothalamic tract, the spinoreticular and spinomesencephalic tracts are involved in pain sensations. The medial and lateral thalamus contains several nociceptive nuclei, the medial ones mediating the affective-emotional component of pain, the lateral ones the sensory-discriminative component. In contrast to other sensory modalities, the modality of pain does not have a specific cortical center. The cortical areas that are activated by painful stimuli are distributed over large parts of the cortex surface. During chronic painful conditions, at all levels massive neuroplastic changes take place that lead to rewiring of connections and structural alterations in the nuclei of the nociceptive pathways. In chronic pain patients the neuroanatomy of pain probably differs from that of healthy people.
本简短综述介绍了一些当前有关介导痛觉的神经通路和神经核的神经解剖学知识。伤害感受器的轴突膜配备有多种受体分子,这些分子能特异性结合产生疼痛和使痛觉敏感的物质。最近,三磷酸腺苷和质子引起了广泛关注。不同类型的伤害感受器可能以伤害性末梢膜中不同的受体分子组合为特征。伤害性感受细胞存在于脊髓背角的浅层和颈部。前一区域的细胞包括仅从伤害感受器接收输入的伤害性感受特异性细胞,而在背角颈部,伤害性和非伤害性传入纤维的汇聚输入占主导。在脊髓水平,会发生神经可塑性敏感化过程,据认为这是疼痛患者出现痛觉过敏和异常性疼痛的基础。除了脊髓丘脑侧束外,脊髓网状束和脊髓中脑束也参与痛觉感受。丘脑内侧和外侧包含几个伤害性感受神经核,内侧神经核介导疼痛的情感 - 情绪成分,外侧神经核介导感觉辨别成分。与其他感觉模态不同,痛觉模态没有特定的皮质中枢。被疼痛刺激激活的皮质区域分布在皮质表面的大部分区域。在慢性疼痛状态下,在所有层面都会发生大量神经可塑性变化,导致伤害性感受通路神经核中的连接重新布线和结构改变。慢性疼痛患者的痛觉神经解剖结构可能与健康人不同。