Vysotskaia R A, Loginov A S, Tkachenko E V
Biull Eksp Biol Med. 1990 Aug;110(8):117-9.
Secretion of prostaglandins (Pg) E and F2 alpha in bile in basic condition (without stimulation) and under stimulation with cholecystokinin (CCK) ("Boots", England, 1 unit/kg) in patients with fatty liver with normal (15) and hypokinetic (20) function of gallbladder by radioimmunoassay method was investigated. The mediator role of Pg F2 alpha in the realization of effect of CCK on the contractile function of gallbladder was found. It was concluded, that the disturbance of mediator effect of Pg F2 alpha in the hormone regulation of bile excretion may play an important role in the pathogenesis of biliary dyskinesia. This disturbance of mediator effect of Pg was connected with the reducing of concentration and debit Pg F2 alpha in bile, as well as with the slowing of maximal Pg excretion under stimulation with CCK.
采用放射免疫分析法,对胆囊功能正常(15例)和胆囊运动功能减退(20例)的脂肪肝患者,在基础状态(无刺激)及胆囊收缩素(CCK,英国“Boots”公司生产,1单位/千克)刺激下胆汁中前列腺素E(PgE)和前列腺素F2α(PgF2α)的分泌情况进行了研究。发现PgF2α在CCK对胆囊收缩功能的作用实现过程中起介质作用。得出结论:PgF2α在胆汁排泄激素调节中的介质效应紊乱可能在胆道运动障碍的发病机制中起重要作用。这种Pg介质效应紊乱与胆汁中PgF2α浓度和排出量降低以及CCK刺激下Pg最大排泄量减慢有关。