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醋丁洛尔和美多心安对异丙肾上腺素脂解反应的比较效应。

Comparative effects of acebutolol and practolol on the lipolytic response to isoprenaline.

作者信息

Gibbons D O, Lant A F, Ashford A, Collins R F, Pinder S

出版信息

Br J Clin Pharmacol. 1976 Feb;3(1):177-84. doi: 10.1111/j.1365-2125.1976.tb00586.x.

Abstract

1 The effects of beta-adrenoceptor blockade on the metabolic responses to isoprenaline have been studied in an in vitro system of isolated fat cells and in six normal subjects. 2 The inhibitory effects of varying concentrations of acebutolol, practolol and propranolol on free fatty acid (FFA) release produced by isoprenaline (10(-7) M) were compared in isolated fat cells prepared from rat epididymal adipose tissue. Acebutolol and practolol, at equimolar concentrations, showed a similar inhibitory effect whilst propranolol was approximately 100 times more potent then either drug. At 10(-5)M concentration of propranolol, lipolysis was virtually abolished whilst at the same molar concentration, acebutolol and practolol halved the response. 3 Six healthy volunteers received three successive 15 min intravenous isoprenaline challenges (0.03 mug kg-1 min-1) per individual experiment. The first acted as a control whilst the following two were given either after single oral doses of placebo, acebutolol or practolol. The mean (+/- s.e. mean) basal FFA level was 0.77 +/- 0.06 mE1/1 and subsequent resting values after the administration of placebo or beta-adrenoceptor blocker were not significantly different. 4 Acebutolol inhibited the respective mean rises in FFA, produced by both post-control isoprenaline challenges, by (mean +/- s.e. mean) 70 +/- 4% and 84% +/- 5%. The comparable figures for practolol were 33 +/- 15% and 24 +/- 20%. The higher serum concentration of acebutolol produced greater inhibition but correlation of log serum concentration of the drug with percentage inhibition of FFA rise did not achieve significance. 5 Administration of isoprenaline, acebutolol or practolol did not significantly alter serum glucose, triglyceride or cholesterol levels. 6 Acebutolol and practolol effectively blocked the isoprenaline-induced tachycardia. The degree of blockade produced by practolol was greater than its inhibitory effect on FFA release. The diatolic fall in blood pressure in response to isoprenaline was abolished by acebutolol suggesting that its beta-adrenoceptor blocking action encompasses peripheral vascular sites. The comparable effect with practolol was a partial inhibition of the diastolic fall.

摘要
  1. 已在离体脂肪细胞的体外系统以及六名正常受试者中研究了β - 肾上腺素能受体阻断对异丙肾上腺素代谢反应的影响。2. 在从大鼠附睾脂肪组织制备的离体脂肪细胞中,比较了不同浓度的醋丁洛尔、心得宁和普萘洛尔对异丙肾上腺素(10⁻⁷M)产生的游离脂肪酸(FFA)释放的抑制作用。醋丁洛尔和心得宁在等摩尔浓度时显示出相似的抑制作用,而普萘洛尔的效力约为这两种药物的100倍。在普萘洛尔浓度为10⁻⁵M时,脂解作用几乎完全被消除,而在相同摩尔浓度下,醋丁洛尔和心得宁使反应减半。3. 六名健康志愿者在每个个体实验中接受了三次连续15分钟的静脉注射异丙肾上腺素挑战(0.03μg·kg⁻¹·min⁻¹)。第一次作为对照,而接下来的两次分别在单次口服安慰剂、醋丁洛尔或心得宁后给予。平均(±标准误)基础FFA水平为0.77±0.06mE1/1,给予安慰剂或β - 肾上腺素能受体阻滞剂后的后续静息值无显著差异。4. 醋丁洛尔抑制了由对照后两次异丙肾上腺素挑战产生的FFA各自的平均升高,(平均±标准误)分别为70±4%和84%±5%。心得宁的相应数字为33±15%和24±20%。醋丁洛尔较高的血清浓度产生了更大的抑制作用,但药物的对数血清浓度与FFA升高抑制百分比之间的相关性未达到显著水平。5. 给予异丙肾上腺素、醋丁洛尔或心得宁未显著改变血清葡萄糖、甘油三酯或胆固醇水平。6. 醋丁洛尔和心得宁有效地阻断了异丙肾上腺素引起的心动过速。心得宁产生的阻断程度大于其对FFA释放的抑制作用。醋丁洛尔消除了对异丙肾上腺素反应的舒张压下降,表明其β - 肾上腺素能受体阻断作用包括外周血管部位。心得宁的类似作用是对舒张压下降的部分抑制。

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