Kikuchi M, Oh-ishi S
Jpn J Pharmacol. 1985 Dec;39(4):467-73. doi: 10.1254/jjp.39.467.
Rat pleurisy was induced by an intrapleural injection of 1 nmol (0.1 ml) of phorbol myristate acetate (PMA). Accumulation of pleural fluid peaked at a volume of 1 ml at 1 hr, and exudation rate peaked at 30 min when measured by the amount of dye leaked into the pleural cavity during 20 min. Histamine contents decreased in the pleural cell pellets markedly at 30 min and increased in the supernatant fluid simultaneously, reflecting histamine release that occurred in 30 min after PMA. Pretreatment with mepyramine maleate or methysergide 30 min prior to the PMA-injection suppressed the fluid volume significantly. The result indicates that there are involvements of 5-hydroxytryptamine and the H1-receptor of histamine in the vascular permeability increase at the early stage of PMA-pleurisy.
通过向大鼠胸膜腔内注射1 nmol(0.1 ml)的佛波酯(PMA)诱导大鼠胸膜炎。胸膜液的积聚在1小时时达到1 ml的峰值,当通过20分钟内漏入胸膜腔的染料量测量时,渗出率在30分钟时达到峰值。在30分钟时,胸膜细胞沉淀中的组胺含量显著降低,同时上清液中的组胺含量增加,这反映了PMA后30分钟发生的组胺释放。在注射PMA前30分钟用马来酸氯苯那敏或甲基麦角新碱预处理可显著抑制液体量。结果表明,5-羟色胺和组胺的H1受体参与了PMA胸膜炎早期血管通透性的增加。