Hargreaves K M, Bowles W R, Garry M G
University of Minnesota School of Dentistry, Minneapolis.
J Endod. 1992 Dec;18(12):597-600. doi: 10.1016/S0099-2399(06)81329-4.
Although pulpal neuropeptides such as calcitonin gene-related peptide and substance P may mediate neurogenic inflammation, little is known about the regulation of neuropeptide release from dental pulp. This article describes an in vitro method for superfusing dental pulp which permits the study of mechanisms regulating the release of immunoreactive CGRP (iCGRP). Tissue extracts from bovine dental pulp dilute in parallel to authentic calcitonin gene-related peptide and substance P peptide standards when assayed by radioimmunoassay. Pulpal levels of iCGRP were 17-fold greater than levels of immunoreactive substance P. Administration of a potassium pulse evoked a significant release of iCGRP from dental pulp (155 +/- 21 fmol/g/9 min) as compared with iCGRP spontaneously released from concurrent control chambers (18 +/- 11 fmol/g/9 min). The in vitro superfusion of pulp tissue may serve as a useful method for identifying peripherally acting drugs which modulate nociceptor secretory activity and for determining their mechanisms of action.
尽管牙髓中的神经肽如降钙素基因相关肽和P物质可能介导神经源性炎症,但关于牙髓中神经肽释放的调节却知之甚少。本文描述了一种体外灌注牙髓的方法,该方法可用于研究调节免疫反应性降钙素基因相关肽(iCGRP)释放的机制。通过放射免疫测定法检测时,牛牙髓组织提取物与真实的降钙素基因相关肽和P物质肽标准品呈平行稀释。牙髓中iCGRP的水平比免疫反应性P物质的水平高17倍。给予钾脉冲可引起牙髓中iCGRP的显著释放(155±21 fmol/g/9分钟),而同期对照室中iCGRP的自发释放量为(18±11 fmol/g/9分钟)。牙髓组织的体外灌注可能是一种有用的方法,可用于鉴定调节伤害感受器分泌活性的外周作用药物,并确定其作用机制。