Torphy T J
Department of Inflammation and Respiratory Pharmacology, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406-0939.
Trends Pharmacol Sci. 1994 Oct;15(10):370-4. doi: 10.1016/0165-6147(94)90157-0.
beta-Adrenoceptor agonists are assumed to induce airway smooth muscle relaxation through the cAMP-protein kinase A (PKA) phosphorylation cascade system. This traditional second messenger paradigm of beta-adrenoceptor agonist action is deeply engrained, but in this article Theodore Torphy reviews recent observations that force a re-examination of the dogma. For example, cAMP can activate protein kinase G as well as PKA, and this unanticipated dual action may contribute to the relaxant activity of cAMP. Other studies suggest that beta-adrenoceptor agonists can induce relaxation by a cAMP-independent mechanism involving a direct coupling of the beta-adrenoceptor to Ca(2+)-dependent K+ channels. Consequently, it is possible that multiple cAMP-dependent pathways act in concert with cAMP-independent pathways to mediate bronchodilation in response to beta-adrenoceptor agonists.
β-肾上腺素能受体激动剂被认为是通过环磷酸腺苷-蛋白激酶A(PKA)磷酸化级联系统诱导气道平滑肌舒张。β-肾上腺素能受体激动剂作用的这种传统第二信使范式已深入人心,但在本文中,西奥多·托尔菲回顾了最近的一些观察结果,这些结果迫使人们重新审视这一教条。例如,环磷酸腺苷不仅可以激活蛋白激酶A,还可以激活蛋白激酶G,这种意想不到的双重作用可能有助于环磷酸腺苷的舒张活性。其他研究表明,β-肾上腺素能受体激动剂可以通过一种不依赖环磷酸腺苷的机制诱导舒张,该机制涉及β-肾上腺素能受体与钙依赖性钾通道的直接偶联。因此,多个依赖环磷酸腺苷的途径可能与不依赖环磷酸腺苷的途径协同作用,以介导对β-肾上腺素能受体激动剂的支气管舒张反应。