Wing L M, Reid J L, Davies D S, Neill E A, Tippett P, Dollery C T
Eur J Clin Pharmacol. 1977 Dec 28;12(6):463-9. doi: 10.1007/BF00561067.
The effect of oral doses of 300 microgram of clonidine hydrochloride on blood pressure, sedation and saliva production in 5 essential hypertensives were qualitatively similar to the effects in normotensive subjects. Peak plasma clonidine concentration (1.34 +/- 0.28 ng/ml) and plasma half-life (10.0 +/- 0.8 h) were similar to normotensives. During chronic oral dosing there was no evidence of drug accumulation. Some tolerance to the sedative and salivary flow effects occurred but no tolerance to the hypotensive effect was observed. There was a linear relationship between reduction in saliva flow and plasma levels of clonidine. The hypotensive effect was also related to plasma level at low concentrations. At plasma levels greater than 1.5 ng/ml the hypotensive effect was diminished. This loss of effect at high plasma concentration may be related to the peripheral, post-synaptic alpha-adrenoceptor agonist action of the drug.
口服300微克盐酸可乐定对5名原发性高血压患者的血压、镇静作用和唾液分泌的影响,在性质上与对血压正常受试者的影响相似。可乐定的血浆峰值浓度(1.34±0.28纳克/毫升)和血浆半衰期(10.0±0.8小时)与血压正常者相似。在长期口服给药期间,没有药物蓄积的证据。对镇静和唾液分泌作用出现了一定程度的耐受性,但未观察到对降压作用的耐受性。唾液分泌减少与可乐定血浆水平之间存在线性关系。降压作用在低浓度时也与血浆水平相关。当血浆水平大于1.5纳克/毫升时,降压作用减弱。高血浆浓度时这种作用丧失可能与该药物的外周突触后α肾上腺素能受体激动剂作用有关。