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α2肾上腺素能受体拮抗剂氟哌沙明对可乐定作用的拮抗作用。

Antagonism of the effects of clonidine by the alpha 2-adrenoceptor antagonist, fluparoxan.

作者信息

Johnson M A, Blackwell C P, Smith J

机构信息

Clinical Pharmacology Division, Glaxo Research and Development Limited, Greenford, Middlesex, UK.

出版信息

Br J Clin Pharmacol. 1995 May;39(5):477-83. doi: 10.1111/j.1365-2125.1995.tb04483.x.

Abstract
  1. The effects of fluparoxan, an alpha 2-adrenoceptor antagonist, on the pharmacodynamic changes induced by clonidine were investigated in this placebo-controlled, double-blind, two-period, cross-over study in 16 healthy male volunteers (aged 19 to 44 years). 2. Subjects received either fluparoxan or placebo, twice-daily for 5 1/2 days (11 doses). One hour after the first and last dose of each treatment period, clonidine (200 micrograms) was infused intravenously over 5 min. 3. Indices of clonidine-mediated pharmacodynamic responses (growth hormone secretion, bradycardia, hypotension, xerostomia and sedation) were taken before and after clonidine infusion. Growth hormone secretion was assessed by quantifying serum growth hormone concentrations; sedation was assessed by both visual analogue scales (VAS) and by a visual psychomotor response meter, measuring critical flicker fusion (CFF). 4. The majority of subjects reported minor adverse events such as lethargy, headache and dry mouth following clonidine infusion. All adverse events were likely to be related to clonidine, as they occurred consistently between treatment groups. Fluparoxan has, however, in previous studies been reported to cause headache and light-headedness. 5. Prior to the clonidine infusion, fluparoxan caused small but statistically significant increases in systolic blood pressure (4 mm Hg) and salivary flow (approximately 30%) after both single and repeated doses. A small increase in heart rate (2 beats min-1) was seen after a single dose which was also statistically significant.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在这项安慰剂对照、双盲、两阶段、交叉研究中,对16名健康男性志愿者(年龄19至44岁)研究了α2肾上腺素能受体拮抗剂氟哌罗生对可乐定诱导的药效学变化的影响。2. 受试者每日两次接受氟哌罗生或安慰剂治疗,持续5.5天(11剂)。在每个治疗阶段的首剂和末剂后1小时,静脉输注可乐定(200微克),持续5分钟。3. 在可乐定输注前后测定可乐定介导的药效学反应指标(生长激素分泌、心动过缓、低血压、口干和镇静)。通过定量血清生长激素浓度评估生长激素分泌;通过视觉模拟量表(VAS)和视觉心理运动反应仪测量临界闪烁融合频率(CFF)评估镇静。4. 大多数受试者在可乐定输注后报告了嗜睡、头痛和口干等轻微不良事件。所有不良事件可能与可乐定有关,因为它们在各治疗组中一致出现。然而,在先前的研究中,氟哌罗生据报道可引起头痛和头晕。5. 在可乐定输注前,氟哌罗生单次和重复给药后均可使收缩压小幅但有统计学意义地升高(4毫米汞柱),唾液流量增加(约30%)。单次给药后心率小幅增加(每分钟2次),也具有统计学意义。(摘要截断于250字)

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