Yanagihara Y, Shida T
Arzneimittelforschung. 1986 Nov;36(11):1627-31.
The effects of 11-oxo-11H-pyrido[2,1-b]-quinazoline-2-carboxylic acid (Sm 857), a new antiallergic drug, on histamine release from human leukocytes and from human and monkey lungs were investigated. Sm 857 dose-dependently inhibited histamine release induced by mite antigen, anti-human IgE, calcium ionophore A23187 (A23187) and protein A from peripheral leukocytes of atopic patients, but had no effect on the levels of cyclic AMP and GMP in human leukocytes. In addition, antigen- or anti-human IgE-induced anaphylactic histamine release from human and monkey lung fragments passively sensitized with human reaginic serum sensitive to mite antigen as well as A23187-induced histamine release from non-sensitized monkey lung fragments, were inhibited dose-dependently by Sm 857. However, no inhibition of spontaneous histamine release from human leukocytes or monkey lung fragments by Sm 857 was observed.
研究了新型抗过敏药物11-氧代-11H-吡啶并[2,1-b]喹唑啉-2-羧酸(Sm 857)对人白细胞以及人肺和猴肺组胺释放的影响。Sm 857剂量依赖性地抑制了螨抗原、抗人IgE、钙离子载体A23187(A23187)和蛋白A诱导的特应性患者外周白细胞组胺释放,但对人白细胞中环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)水平无影响。此外,Sm 857剂量依赖性地抑制了用对螨抗原敏感的人反应素血清被动致敏的人肺和猴肺碎片中抗原或抗人IgE诱导的过敏性组胺释放,以及非致敏猴肺碎片中A23187诱导的组胺释放。然而,未观察到Sm 857对人白细胞或猴肺碎片自发性组胺释放的抑制作用。