Genter M B, Llorens J, O'Callaghan J P, Peele D B, Morgan K T, Crofton K M
Department of Toxicology, North Carolina State University, Raleigh.
J Pharmacol Exp Ther. 1992 Dec;263(3):1432-9.
Following a pilot study which revealed olfactory epithelial degeneration induced by beta,beta'-iminodipropionitrile (IDPN), dose-response and time-course analyses were undertaken to further characterize the effects of IDPN on the olfactory system. Male rats were sacrificed at multiple time points ranging from 24 hr after a single dose to 56 days after three consecutive daily doses of IDPN (0-400 mg/kg i.p.). Nasal cavities were fixed, decalcified and embedded in paraffin; 5 microns sections were stained with hematoxylin and eosin, middle neurofilament protein antibody or olfactory marker protein antiserum. Olfactory bulbs were removed for slot blot analyses of glial fibrillary acidic protein, synapsin I and p38. Another group of rats was treated with saline or IDPN and perfused 6 hr or 1, 2, 3, 7, 14 or 28 days after the last dose. Olfactory bulb axonal degeneration was visualized using a modified Gallyas technique. Twenty-four hours after treatment with 200 or 400 mg/kg IDPN, there was severe, highly site-specific mucosal degeneration in the dorsal-medial nasal cavity; regeneration was incomplete 8 weeks later. IDPN increased olfactory bulb glial fibrillary acidic protein, peaking 7 days after three daily 400 mg/kg doses, and remaining significantly elevated 8 weeks after treatment. Olfactory bulbs contained substantial silver deposition in afferent axon bundles in the glomerular layer, beginning 24 hr after the first dose and persisting for 14 days after dosing. Although only a portion of the olfactory epithelium was damaged by IDPN, all axon bundles entering the olfactory bulb were involved, suggesting the lack of a clear topographic arrangement of sensory endings in the olfactory bulb.
在一项初步研究揭示了β,β'-亚氨基二丙腈(IDPN)诱导的嗅上皮变性之后,进行了剂量反应和时间进程分析,以进一步表征IDPN对嗅觉系统的影响。雄性大鼠在单次给药后24小时至连续三天每日给予IDPN(0 - 400 mg/kg腹腔注射)后56天的多个时间点处被处死。鼻腔被固定、脱钙并包埋在石蜡中;5微米切片用苏木精和伊红、中间神经丝蛋白抗体或嗅觉标记蛋白抗血清染色。取出嗅球用于胶质纤维酸性蛋白、突触素I和p38的狭缝印迹分析。另一组大鼠用生理盐水或IDPN处理,并在最后一次给药后6小时或1、2、3、7、14或28天进行灌注。使用改良的Gallyas技术观察嗅球轴突变性。用200或400 mg/kg IDPN处理24小时后,背内侧鼻腔出现严重的、高度位点特异性的黏膜变性;8周后再生不完全。IDPN增加了嗅球胶质纤维酸性蛋白,在每日400 mg/kg剂量连续给药三天后7天达到峰值,并在治疗后8周仍显著升高。嗅球在肾小球层的传入轴突束中含有大量银沉积,在首次给药后24小时开始,并在给药后持续14天。尽管只有一部分嗅上皮被IDPN损伤,但所有进入嗅球的轴突束都受到影响,这表明嗅球中感觉末梢缺乏清晰的拓扑排列。