Holzer-Petsche U
Department of Experimental and Clinical Pharmacology, Karl-Franzens-University, Graz, Austria.
Regul Pept. 1995 May 4;57(1):19-42. doi: 10.1016/0167-0115(95)00019-8.
For a long time research on the action of TKs on gastrointestinal tissue has been demonstrating the importance of the TKs as non-cholinergic stimulators of motility in most parts of the mammalian gastrointestinal tract. The past years witnessed the development of TK agonists and antagonists selective for the various receptor types, which prompted a wealth of new insight into the pharmacology and molecular biology of the TK receptors. This knowledge now allows a more specific elucidation of the role of TKs and their receptors in the various aspects of gastrointestinal motility, not only in normal tissue but also under pathological conditions.
长期以来,关于酪氨酸激酶(TKs)对胃肠道组织作用的研究一直表明,在哺乳动物胃肠道的大部分区域,TKs作为非胆碱能运动刺激物具有重要意义。过去几年见证了针对各种受体类型的TK激动剂和拮抗剂的开发,这促使人们对TK受体的药理学和分子生物学有了大量新的认识。现在,这些知识使我们能够更具体地阐明TKs及其受体在胃肠道运动各个方面的作用,不仅在正常组织中,而且在病理条件下也是如此。