NEUROGENIC AMPLIFICATION OF PANCREATITIS PAIN

内脏疼痛是非常令人关注的，因为它构成了医学界治疗的疼痛的很大一部分。 疼痛是胰腺炎或胰腺癌患者的主要主诉。 疼痛可能是严重和顽固的，甚至对吗啡有抵抗力。 我们以前的研究已经确定，疼痛的癌症患者涉及盆腔内脏器官是缓解神经外科病变局限于脊髓背柱中线。 在大鼠中，我们确定来自结肠的感觉输入主要作为背柱通路的中线成分传递到更高的大脑感觉处理中心。 这提出了一个主要的内脏疼痛途径在背柱的可能性，我们将考虑作为一个整体的假设。 我们建议进一步研究这种以前未被认识到的内脏疼痛通路相关的传输胰腺输入从胸部水平。 我们的初步数据支持以下关于胰腺伤害性信息传递的假设：来自胰腺的伤害性信息被传递到位于脊髓内侧的细胞。 这些细胞将它们的轴突以先前未描述的薄束和楔束之间的通路向上发送到背柱，以支配髓质中背柱核的边缘。然后信息被传递到丘脑。 提出的研究的一个目的是确定负责传输由电和化学刺激大鼠胰腺传入纤维引起的有害信息的中枢神经元通路。 将绘制通往感觉处理中心的路径。 一个目的是评估通路中断作为消除胰腺伤害性传递的手段。 另一个目的是在胰腺炎模型中研究谷氨酸受体拮抗剂的药理学干预。 该项目采用多学科方法，包括电生理学，行为和解剖学方法，应提供基本信息的伤害性处理的理解，在这些痛苦的情况下，涉及胰腺。

Visceral pain is of great concern since it constitutes a large part of the pain treated by the medical community. Pain is a major complaint in particular of patients with pancreatis or pancreatic cancer. The pain can be severe and intractable, resistant even to morphine. Our previous studies have determined that pain in patients with cancer involving the pelvic visceral organs is relieved by a neurosurgical lesion limited to the midline of the dorsal column of the spinal cord. In rats we determined that sensory input from the colon is primarily transmitted to higher brain sensory processing centers as a midline component of the dorsal column pathways. This raises the possibility of a major visceral pain pathway in the dorsal column which we will consider as an overall hypothesis. We propose further study of this previously unrecognized visceral pain pathway relevant to transmission of pancreatic inputs from thoracic levels. Our preliminary data support the following hypothesis for transmission of pancreatic nociceptive information: Nociceptive information from the pancreas is transmitted to cells located medially in the spinal cord. These cells send their axons up the dorsal columns in a previously undescribed pathway between the gracile and cuneate fasciculi to innervate the edges of the dorsal column nuclei in the medulla. The information is then relayed to the thalamus. One aim of the proposed studies will define the central neuronal pathway responsible for transmission of noxious information evoked by electrical and chemical stimulation of pancreatic afferent fibers in rats. The route of the pathway to sensory processing centers will be mapped. One aim will assess pathway disruption as a means of abrogating pancreatic nociceptive transmission. Another aim will examine pharmacological intervention with glutamate receptor antagonists in pancreatitis models. This project using a multidisciplinary approach including electrophysiological, behavioral and anatomical methods should provide information fundamental to the understanding of nociceptive processing in these devastatingly painful conditions involving the pancreas.