Wilfong Erin R, Dey Richard D
Department of Neurobiology and Anatomy, West Virginia University, Morgantown, West Virginia 26506-9128, USA.
J Toxicol Environ Health A. 2005 Aug 13;68(15):1337-48. doi: 10.1080/15287390590953590.
Toluene diisocyanate (TDI) produces rhinitis, nasal irritation, and increased synthesis and release of substance P (SP) from airway sensory nerves. Nerve growth factor (NGF) secretion in the nasal cavity is believed to mediate the irritant-induced upregulation of SP, but the cellular source of NGF in the nasal mucosa remains unclear. Studies to localize a source of NGF within the nasal mucosa are complicated by inflammatory-cell influx into the nasal mucosa following TDI, which obscures immunocytochemical identification of endogenous NGF sources. The purpose of this study was to determine the cellular source of NGF within the nasal mucosa following irritant exposure using a combined in vivo and ex vivo approach to reduce or eliminate contribution from inflammatory cells. Both nasal cavities of adult, male Sprague-Dawley rats were instilled with 5 microl of 10% TDI or control vehicle. After 15 min, nasal lavages were performed and the nasal mucosa was removed and placed into culture for 3 or 24 h. NGF was measured in the lavage supernatant and the culture media. Fifteen minutes after TDI exposure, NGF was significantly increased in the nasal lavage fluid. NGF levels in the culture medium of nasal mucosa from rats exposed to TDI ex vivo were significantly increased compared to controls following a 3-h culture. NGF levels in media after 24 h in culture was higher than at the 3-h point, but there was no difference between control and TDI groups. Since the nasal mucosa was removed prior to inflammatory cell influx, these findings suggest that cells in the nasal mucosa release NGF following exposure to TDI.
甲苯二异氰酸酯(TDI)会引发鼻炎、鼻腔刺激,并增加气道感觉神经中P物质(SP)的合成与释放。鼻腔中神经生长因子(NGF)的分泌被认为介导了刺激物诱导的SP上调,但鼻黏膜中NGF的细胞来源仍不清楚。在鼻黏膜中定位NGF来源的研究因TDI后炎症细胞流入鼻黏膜而变得复杂,这模糊了内源性NGF来源的免疫细胞化学鉴定。本研究的目的是使用体内和体外相结合的方法来减少或消除炎症细胞的影响,从而确定刺激物暴露后鼻黏膜中NGF的细胞来源。给成年雄性Sprague-Dawley大鼠的双侧鼻腔滴注5微升10%的TDI或对照载体。15分钟后,进行鼻腔灌洗,取出鼻黏膜并培养3或24小时。在灌洗上清液和培养基中测量NGF。TDI暴露15分钟后,鼻腔灌洗液中的NGF显著增加。与对照组相比,体外暴露于TDI的大鼠鼻黏膜培养基中的NGF水平在培养3小时后显著增加。培养24小时后培养基中的NGF水平高于3小时时,但对照组和TDI组之间没有差异。由于在炎症细胞流入之前就取出了鼻黏膜,这些发现表明鼻黏膜中的细胞在暴露于TDI后会释放NGF。