Mundie T G, Cordova-Salinas M, Bray V J, Ainsworth S K
Environ Res. 1983 Oct;32(1):62-71. doi: 10.1016/0013-9351(83)90192-5.
Byssinosis is an occupational respiratory disease contracted by cotton mill workers who inhale cotton mill dust. The acute byssinotic reaction is characterized by a drop in the 1-sec forced expiratory volume (FEV1.0) on Monday following a weekend's absence from work. This physiological reaction is the result of the contraction of bronchial smooth muscle, which causes narrowing of small airways. An isolated tissue bath technique was used to assay smooth muscle contractions induced by cotton dust extract (CDE) and cotton bract extract (CBE). CBE-induced contractions of rat stomach smooth muscle were blocked (82%) by 100 ng/ml methysergide (blocks 5-hydroxytryptamine (5HT) 100%); CDE was not significantly blocked by methysergide (13%). CDE-induced contractions were blocked (100%) by 25 micrograms/ml indomethacin and 100 micrograms/ml salicylic acid (blocks prostaglandin F2 alpha (PGF2 alpha) 100%). The portion of CBE contracting ability not blocked by methysergide was blocked totally by indomethacin. Blocking agents ineffective against CDE or CBE include atropine (acetylcholine blocker), pyrilamine maleate and diphenhydramine (histamine blockers), imidazole and 7-(1-imidazolyl)heptanoic acid (7IHA) (thromboxane blockers), and carboxypeptidase B2 (kinin blocker). The data suggest that cotton bract contains 5HT, which is responsible for a majority of the CBE-induced contraction and a minority of the CDE-induced contraction. The data also suggest that cotton dust and bract contain a substance which causes the release of PGF2 alpha which in turn causes the contraction of smooth muscle. This substance is responsible for a majority of the CDE-induced and a minority of the CBE-induced contractions. Radioimmunoassay (RIA) confirmed PGF2 alpha release from rat fundal smooth muscle when exposed to CDE and CBE. Increased synthesis and release of arachidonic acid metabolites might be a major mechanism in the bronchoconstriction observed in the acute byssinotic reaction.
棉屑沉着病是一种职业性呼吸系统疾病,由吸入棉纺厂粉尘的棉纺厂工人所患。急性棉屑沉着病反应的特征是在周末不上班后的周一,1秒用力呼气量(FEV1.0)下降。这种生理反应是支气管平滑肌收缩的结果,支气管平滑肌收缩会导致小气道变窄。采用离体组织浴技术测定棉尘提取物(CDE)和棉苞叶提取物(CBE)诱导的平滑肌收缩。100 ng/ml麦角新碱(可100%阻断5-羟色胺(5HT))可阻断(82%)CBE诱导的大鼠胃平滑肌收缩;麦角新碱对CDE无明显阻断作用(13%)。25 μg/ml吲哚美辛和100 μg/ml水杨酸(可100%阻断前列腺素F2α(PGF2α))可阻断(100%)CDE诱导的收缩。麦角新碱未阻断的CBE收缩能力部分被吲哚美辛完全阻断。对CDE或CBE无效的阻断剂包括阿托品(乙酰胆碱阻断剂)、马来酸氯苯那敏和苯海拉明(组胺阻断剂)、咪唑和7-(1-咪唑基)庚酸(7IHA)(血栓素阻断剂)以及羧肽酶B2(激肽阻断剂)。数据表明棉苞叶含有5HT,它是CBE诱导收缩的主要原因,也是CDE诱导收缩的次要原因。数据还表明棉尘和棉苞叶含有一种物质,该物质会导致PGF2α释放,进而引起平滑肌收缩。这种物质是CDE诱导收缩的主要原因,也是CBE诱导收缩的次要原因。放射免疫分析(RIA)证实,大鼠胃底平滑肌在暴露于CDE和CBE时会释放PGF2α。花生四烯酸代谢产物合成和释放增加可能是急性棉屑沉着病反应中观察到的支气管收缩的主要机制。