Ono N, Kushiku K, Morishita H, Nakagami K, Nakahara T
Nihon Yakurigaku Zasshi. 1975 Oct;71(7):739-52. doi: 10.1254/fpj.71.739.
The actions on the bronchial smooth muscle and cardiovascular system S-1540 (Bitolterol) (Shionogi Pharmaceuticals), a new bronchodilator which is chemically related to isoprenaline, and S-1541 which is the active metabolite of S-1540 were studied in comparison with the action of isoprenaline (isoproterenol) and orciprenaline (metaproterenol). 1) The relaxing effect on isolated guinea-pig tracheal muscle constricted previously with histamine BaCl2 or acetylcholine was highest with S-1541, followed by isoprenaline and orciprenaline, in that order, and lowest with S-1540. The relaxing effect of S-1541 on acetylcholine-induced tracheal constriction was reduced and that of S-1540 was completely abolished by a previous treatment with propranolol. The relaxing actions of those drugs on bronchial spasms induced by histamine in vivo were highest with S-1541, followed by isoprenaline, and lowest with S-1540. 2) All these drugs exhibited the depressor and positive chronotropic actions in guinea-pigs. The potencies of the actions were found to be in the following order; isoprenaline was most potent, followed by S-1541 with a little less intensity, orciprenaline much weaker, and S-1540 still weaker with a positive chronotropic action of about 1/1000 of S-1541 and depressor action about 1/500. In the open chest guinea-pig, positive inotropic and chronotropic actions of S-1541 were about the same or slightly more potent than those of isoprenaline; S-1540 had a very weak action, being only about 1/1000 as active as S-1541. These actions of S-1540 were completely eliminated by propranolol pretreatment. S-1540 induced to remarkable changes in the electrocardiogram wave forms even in high doses. 3) Those drugs elicited the depressor, positive chronotropic and inotropic actions in rabbits and dogs. In rabbits, isoprenaline was most potent; S-1541 was similar to or a little weaker than isoprenaline; and S-1540 was extremely weak. In the dog, isoprenaline showed the highest of the above effect, followed by S-1541, orciprenaline and S-1540 in that order, with S-1540 having an extremely low activity. 4) The actions of S-1541 and isoprenaline appeared very rapidly but were of short duration, the duration of orciprenaline was moderate, and the actions of S-1540 rapidly appeared and were of an extremely long duration. It is suggested that S-1540 itself has pharmacological activities in vivo and the active metabolites such as S-1541 also have the activities. S-1540 can be administered by the oral route, is of long duration, and is thus considered to be a bronchodilator with a relative high specificity.
研究了新型支气管扩张剂S - 1540(双甲苯喘定)(盐野义制药公司)及其活性代谢产物S - 1541对支气管平滑肌和心血管系统的作用,并与异丙肾上腺素(异丙基去甲肾上腺素)和奥西那林(间羟异丙肾上腺素)进行了比较。1)对先前用组胺、氯化钡或乙酰胆碱收缩的豚鼠离体气管平滑肌的松弛作用,以S - 1541最强,其次是异丙肾上腺素和奥西那林,S - 1540最弱。普萘洛尔预处理可降低S - 1541对乙酰胆碱诱导的气管收缩的松弛作用,而S - 1540的松弛作用则完全消失。这些药物对组胺诱导的体内支气管痉挛的松弛作用,以S - 1541最强,其次是异丙肾上腺素,S - 1540最弱。2)所有这些药物在豚鼠中均表现出降压和正性变时作用。作用强度顺序如下:异丙肾上腺素最强,其次是S - 1541,强度稍低,奥西那林弱得多,S - 1540更弱,其正性变时作用约为S - 1541的1/1000,降压作用约为1/500。在开胸豚鼠中,S - 1541的正性变力和变时作用与异丙肾上腺素大致相同或稍强;S - 1540作用非常弱,仅为S - 1541活性的约1/1000。普萘洛尔预处理可完全消除S - 1540的这些作用。即使大剂量使用,S - 1540也会引起心电图波形的显著变化。3)这些药物在兔和狗中引起降压、正性变时和变力作用。在兔中,异丙肾上腺素最强;S - 1541与异丙肾上腺素相似或稍弱;S - 1540极弱。在狗中,异丙肾上腺素上述作用最强,其次是S - 1541、奥西那林和S - 1540,S - 1540活性极低。4)S - 1541和异丙肾上腺素的作用出现非常迅速,但持续时间短,奥西那林的持续时间适中,S - 1540的作用迅速出现且持续时间极长。提示S - 1540本身在体内具有药理活性,其活性代谢产物如S - 1541也具有活性。S - 1540可口服给药,作用持续时间长,因此被认为是一种相对高特异性的支气管扩张剂。