Morice A H, Sever P S
Peptides. 1986;7 Suppl 1:279-80. doi: 10.1016/0196-9781(86)90202-0.
In two studies vasoactive intestinal peptide (VIP) was administered intravenously to two groups of eight in-patient volunteers recovering from severe acute asthma. VIP (6 pmol/kg/min) infusion caused significant (p less than 0.01) increase in peak expiratory flow rate (PEFR) of 26 +/- 9 (SEM) l/min after 30 minutes infusion compared with a bronchodilation of 39 +/- 19 l/min seen with salbutamol (5 mcg/min). Following pretreatment with nebulized ipratropium bromide, VIP infusion caused a significant (p less than 0.02) bronchodilation of 25 l/min. VIP is a bronchodilator in severe asthma, although its effects are less than conventional medication. Reflex mechanisms are unlikely to explain the bronchodilatory effect of intravenous VIP.
在两项研究中,对两组共16名正在从严重急性哮喘中康复的住院志愿者静脉注射血管活性肠肽(VIP)。VIP(6皮摩尔/千克/分钟)输注30分钟后,呼气峰值流速(PEFR)显著(p<0.01)增加26±9(标准误)升/分钟,而沙丁胺醇(5微克/分钟)引起的支气管扩张为39±19升/分钟。雾化吸入异丙托溴铵预处理后,VIP输注引起显著(p<0.02)的25升/分钟的支气管扩张。VIP是重症哮喘的支气管扩张剂,尽管其效果不如传统药物。反射机制不太可能解释静脉注射VIP的支气管扩张作用。