Davis W M, Hatoum N S
Toxicology. 1979 Oct;14(2):141-51. doi: 10.1016/0300-483x(79)90060-x.
Interactions of (+/-)-propranolol HCl with various narcotics were determined in albino rats. The 24-h intraperitoneal (i.p.) LD50 of morphine sulfate + saline was 15--16 times greater than for morphine + propranolol in both sexes although morphine was nearly twice as toxic to males as to females. The potency ratios for LD50's with saline vs. with propranolol were: codeine, 1.9, (+/-)-methadone, 6.0; (-)-alpha-acetylmethadol, 2.8 (72 h). The toxicity of levorphanol also was greatly increased with propranolol, but the dose-effect relationship showed non-parallelism vs. levorphanol + saline. Albino mice and mongrel dogs also showed synergism between morphine and propranolol. Mortality after morphine and propranolol was antagonized by naloxone or naltrexone in rats and mice. The potency ratio in rats for morphine + saline vs. morphine + practolol was 3.5. However, the synergism between propranolol and the narcotics probably was unrelated to beta-adrenergic blocking effects of propranolol because of the apparent equivalence of (+)-, (-)- and (+/-)-propranolol in rats for synergism with morphine.
在白化大鼠中测定了盐酸(±)-普萘洛尔与各种麻醉剂的相互作用。硫酸吗啡+生理盐水的24小时腹腔内(i.p.)半数致死剂量(LD50)在两性中均比吗啡+普萘洛尔高15 - 16倍,尽管吗啡对雄性的毒性几乎是雌性的两倍。生理盐水与普萘洛尔存在时LD50的效价比为:可待因,1.9;(±)-美沙酮,6.0;(-)-α-乙酰美沙醇,2.8(72小时)。普萘洛尔也极大地增加了左啡诺的毒性,但剂量-效应关系与左啡诺+生理盐水相比显示出非平行性。白化小鼠和杂种狗中吗啡与普萘洛尔之间也表现出协同作用。在大鼠和小鼠中,纳洛酮或纳曲酮可拮抗吗啡和普萘洛尔联合用药后的死亡率。大鼠中吗啡+生理盐水与吗啡+醋氨心安的效价比为3.5。然而,普萘洛尔与麻醉剂之间的协同作用可能与普萘洛尔的β-肾上腺素能阻断作用无关,因为在大鼠中,(+)-、(-)-和(±)-普萘洛尔与吗啡协同作用时表现出明显的等效性。