Gasthuys F, Parmentier D, Goossens L, De Moor A
Large Animal Surgical Clinic, Faculty of Veterinary Medicine, State University of Gent, Belgium.
Vet Res Commun. 1990;14(6):489-502. doi: 10.1007/BF00367061.
Romifidine (STH 2130-Cl or Sedivet) is an alpha 2-agonistic imino-imidazol sedative for intravenous use in horses recently developed by Boehringer Ingelheim, Vetmedica GmbH. An exploratory study was done in nine warm-blood horses, randomly divided into three groups, which received different dosages of romifidine (0.04, 0.08 and 0.12 mg/kg of body weight (BWT) intravenously (i.v.)) with at least one week's interval between tests. Romifidine induced a marked bradycardia accompanied by second degree atrioventricular (AV) block and some sinus blocks at all tested dosages. A placebo (NaCl 0.9% i.v.) given 5 min before and after romifidine did not affect the cardiac disturbances induced by romifidine. A low dose of atropine sulphate (0.005 mg/kg of BWT i.v.) given 5 min before romifidine counteracted the bradycardia and caused a normal to increased heart rhythm at all romifidine dosages. A higher dose of atropine sulphate (0.01 mg/kg of BWT i.v.) administered 5 min before sedation induced a tachycardia (average 70 beats/min) at all romifidine dosages and completely prevented the bradycardia and the heart blocks. The positive chronotrope effects of atropine sulphate were attenuated by increasing doses of romifidine. The effects of atropine sulphate (low or high doses) given 5 min after romifidine only appeared after 5 min. Both dosages counteracted the bradycardia and suppressed the heart blocks. No atropine-dependent side effects were observed in non-fasted horses. The degree of the romifidine induced sedation was not affected by the use of atropine sulphate given before or after romifidine.
罗米非定(STH 2130-Cl或Sedivet)是勃林格殷格翰动物药业有限公司最近研制的一种用于马匹静脉注射的α2激动剂亚氨基咪唑镇静剂。对9匹温血马进行了一项探索性研究,随机分为三组,分别静脉注射不同剂量的罗米非定(0.04、0.08和0.12毫克/千克体重,静脉注射),两次试验之间至少间隔一周。在所有测试剂量下,罗米非定均引起明显的心动过缓,并伴有二度房室传导阻滞和一些窦性阻滞。在罗米非定给药前后5分钟静脉注射安慰剂(0.9%氯化钠),对罗米非定引起的心脏紊乱没有影响。在罗米非定给药前5分钟静脉注射低剂量硫酸阿托品(0.005毫克/千克体重)可抵消心动过缓,并使所有罗米非定剂量下的心律正常或加快。在镇静前5分钟静脉注射较高剂量的硫酸阿托品(0.01毫克/千克体重),在所有罗米非定剂量下均引起心动过速(平均70次/分钟),并完全预防了心动过缓和心脏传导阻滞。硫酸阿托品的正性变时作用随着罗米非定剂量的增加而减弱。罗米非定给药后5分钟给予硫酸阿托品(低剂量或高剂量),其作用仅在5分钟后出现。两种剂量均抵消了心动过缓并抑制了心脏传导阻滞。在未禁食的马匹中未观察到阿托品依赖性副作用。罗米非定诱导的镇静程度不受罗米非定给药前后使用硫酸阿托品的影响。