Ramage L, Blair A L, Cree I A, Dhillon D P
Department of Pathology, University of Dundee, Ninewells Hospital and Medical School, Scotland.
J Biolumin Chemilumin. 1993 Sep-Oct;8(5):247-52. doi: 10.1002/bio.1170080504.
Although beta-agonists remain an important aspect of the treatment of asthma, their role has recently been questioned. Salmeterol has recently been developed as a beta-agonist with prolonged bronchodilator action. Using lucigenin-enhanced chemiluminescence, we have shown that salmeterol inhibits this aspect of phagocyte function in vitro in a concentration-dependent manner. However, salmeterol differs from classical beta 2-agonists in that at concentrations between 10(-5) and 10(-3) mol/L, its effects on phagocytes cannot be completely reversed by washing the cells or by propranolol. The effects on phagocytes may not therefore be explicable on the basis of beta-adrenergic mechanisms alone.
尽管β-激动剂仍然是哮喘治疗的一个重要方面,但它们的作用最近受到了质疑。沙美特罗最近被开发为一种具有长效支气管扩张作用的β-激动剂。我们使用光泽精增强的化学发光法表明,沙美特罗在体外以浓度依赖的方式抑制吞噬细胞功能的这一方面。然而,沙美特罗与经典的β2-激动剂不同,在10^(-5)至10^(-3)mol/L的浓度之间,其对吞噬细胞的作用不能通过洗涤细胞或使用普萘洛尔完全逆转。因此,对吞噬细胞的作用可能不能仅基于β-肾上腺素能机制来解释。