Yasue H, Omote S, Takizawa A, Nagao M, Miwa K, Kato H, Tanaka S, Akiyama F
Jpn Circ J. 1978 Jan;42(1):1-10. doi: 10.1253/jcj.42.1.
To twenty six patients with angina at rest (including 13 patients with Prinzmetal's variant angina), propranolol 40--50 mg, dilitiazem 60--90 mg, dipyridamole 50 mg, atropine sulfate 0.6 mg and phenoxybenzamine 10--20 mg were given at 9:00 p.m. and 2:00 a.m. (except phenoxybenzamine which was given only at 9:00 p.m.) to examine the effect of these drugs on the attack. Propranolol was not only ineffective in suppressing the attack but rather tended to aggravate it in all the cases of Prinzmetal's variant angina. It was effective to some degree in 5 of 13 cases of angina at rest other than Prinzmetal's variant angina. Diltiazem suppressed the attack completely and dramatically in all the cases of angina at rest (including Prinzmetal's variant angina). Dipyridamole was ineffective in all the cases except one in suppressing the attack. Atropine sulfate and phenoxybenzamine suppressed the attack in 13 of 21 cases and in 6 of 12 cases respectively. Coronary arteriography was done before and after the intravenous administration of 10 mg of diltiazem in 8 patients and it was demonstrated that diltiazem dilates large coronary arteries in all these patients. It is concluded that diltiazem, a calcium antagonistic drug, is specifically effective in suppressing the attack of angina at rest by dilating large coronary arteries and that the autonomic nervous system plays a role in the genesis of the attack probably by constricting large coronary arteries by way of alpha adrenergic receptors.
对26例静息性心绞痛患者(包括13例变异型心绞痛患者),于晚上9点和凌晨2点给予普萘洛尔40 - 50毫克、地尔硫䓬60 - 90毫克、双嘧达莫50毫克、硫酸阿托品0.6毫克和酚苄明10 - 20毫克(酚苄明仅在晚上9点给药),以检查这些药物对发作的影响。普萘洛尔不仅对变异型心绞痛的发作抑制无效,反而在所有变异型心绞痛病例中均有加重发作的倾向。在13例非变异型静息性心绞痛病例中,有5例有一定程度的效果。地尔硫䓬在所有静息性心绞痛病例(包括变异型心绞痛)中均能完全且显著地抑制发作。双嘧达莫除1例之外,对所有病例的发作抑制均无效。硫酸阿托品和酚苄明分别在21例中的13例和12例中的6例中抑制了发作。对8例患者静脉注射10毫克地尔硫䓬前后进行了冠状动脉造影,结果表明地尔硫䓬能使所有这些患者的大冠状动脉扩张。结论是,钙拮抗药地尔硫䓬通过扩张大冠状动脉对抑制静息性心绞痛发作具有特效,自主神经系统可能通过α肾上腺素能受体使大冠状动脉收缩,从而在发作的发生中起作用。