Chakrin L W, Krell R D
J Pharmacol Exp Ther. 1978 Dec;207(3):756-66.
SK&F 78729-A, one of a series of pyranenamine compounds, was studied in several laboratory models of immediate-type hypersensitivity reactions. In vivo, SK&F 78729-A, i.v./p.o., inhibited the antigen-induced rat 48-hr passive cutaneous anaphylaxis by a mechanism other than end-organ antagonism to either histamine or serotonin. In vitro, the compound produced a concentration-related inhibition of the immunologic release of histamine and slow-reacting substance of anaphylaxis from passively sensitized fragmented rhesus monkey and canine lung, and modest inhibition of histamine release from passively sensitized fragmented rhesus monkey skin. Similarly, SK&F 78729-A inhibited the antigen-induced release of histamine from passively sensitized fragmented rat lung. Under certain conditions, SK&F 78729-A inhibited antigen-induced pathophysiologic pulmonary responses in in vivo canine and rhesus monkey models of allergic asthma. The results of these studies suggest that clinically, SK&F 78729-A should exhibit a pharmacologic profile consistent with that of a prophylactic antiallergic agent.
SK&F 78729 - A是吡喃烯胺化合物系列之一,在几种速发型超敏反应的实验室模型中进行了研究。在体内,静脉注射/口服SK&F 78729 - A,通过一种不同于对组胺或5 - 羟色胺的终末器官拮抗作用的机制,抑制抗原诱导的大鼠48小时被动皮肤过敏反应。在体外,该化合物对来自被动致敏的恒河猴和犬肺碎片的组胺和过敏反应慢反应物质的免疫释放产生浓度相关的抑制作用,并对来自被动致敏的恒河猴皮肤碎片的组胺释放有适度抑制作用。同样,SK&F 78729 - A抑制抗原诱导的来自被动致敏的大鼠肺碎片的组胺释放。在某些条件下,SK&F 78729 - A在体内犬类和恒河猴过敏性哮喘模型中抑制抗原诱导的病理生理肺部反应。这些研究结果表明,在临床上,SK&F 78729 - A应表现出与预防性抗过敏药物一致的药理学特征。