Morice A H, Schofield P, Keal E E, Sever P S
Br J Clin Pharmacol. 1986 Aug;22(2):149-53. doi: 10.1111/j.1365-2125.1986.tb05242.x.
Intravenous infusion of placebo for 30 min followed by either salbutamol 10 micrograms min-1, aminophylline 0.2 mg kg-1 min-1 or vasoactive intestinal peptide (VIP) 6 pmol kg-1 min-1 for 30 min was performed in a single blind fashion in six normal volunteers. Both salbutamol and aminophylline increased minute ventilation, (P less than 0.05) the mean increase being 26% and 19% respectively. Aminophylline also increased the ventilatory response to carbon dioxide by 47% (P less than 0.05) when measured by hyperoxic rebreathing, whereas salbutamol and VIP were without significant effect. All three drugs caused a tachycardia, mean increase in the pulse being 16, 8 and 2 beats min-1 for salbutamol, aminophylline and VIP respectively, and aminophylline also increased both systolic and diastolic blood pressure, mean arterial pressure increasing by 14 mmHg. VIP caused haemoconcentration and salbutamol the expected changes in plasma biochemistry. Plasma catecholamines increased slightly during drug infusion, although this effect is unlikely to be important.
对6名正常志愿者采用单盲法进行静脉输注安慰剂30分钟,随后分别以10微克/分钟的沙丁胺醇、0.2毫克/千克/分钟的氨茶碱或6皮摩尔/千克/分钟的血管活性肠肽(VIP)输注30分钟。沙丁胺醇和氨茶碱均增加了分钟通气量(P<0.05),平均增加分别为26%和19%。通过高氧重复呼吸测量时,氨茶碱还使对二氧化碳的通气反应增加了47%(P<0.05),而沙丁胺醇和VIP无显著影响。所有三种药物均引起心动过速,沙丁胺醇、氨茶碱和VIP使脉搏平均增加分别为16次/分钟、8次/分钟和2次/分钟,氨茶碱还增加了收缩压和舒张压,平均动脉压升高14 mmHg。VIP导致血液浓缩,沙丁胺醇引起血浆生化指标的预期变化。药物输注期间血浆儿茶酚胺略有增加,尽管这种作用可能并不重要。