Institute of Chinese Integrative Medicine, Hebei Medical University, Shijiazhuang 050017, China.
Acta Pharmacol Sin. 2014 Jan;35(1):48-57. doi: 10.1038/aps.2013.154. Epub 2013 Dec 16.
Doxazosin is a racemic mixture of (-)doxazosin and (+)doxazosin that is currently used as an add-on therapy for hypertension. In this study we investigated the contribution of each enantiomer to the hypotensive action of long-term administration of (±)doxazosin in conscious rats.
Blood pressure of conscious SD rats was measured using a volume pressure recording system. The rats were orally administered (-)doxazosin, (+)doxazosin, or (±)doxazosin (8 mg·kg(-1)·d(-1)) for 12 weeks. Plasma concentrations of the agents were analyzed with HPLC. The effect of the agents on α1-adrenoceptor was examined in isolated rat caudal artery preparations.
Treatment of conscious rats with a single dose of (±)doxazosin (8 mg/kg) did not affected DBP and MBP, but significantly decreased SBP by 11.9% 4 h after the administration. Long-term treatment of conscious rats with (±)doxazosin significantly decreased SBP, DBP and MBP with a maximal decrease of SBP by 29.3% 8 h after the last administration. The rank order of the hypotensive actions caused by long-term treatment in conscious rats was (±)doxazosin>(+)doxazosin>>(-)doxazosin. However, the pKB values for inhibiting NA-induced contraction of isolated rat caudal artery were (+)doxazosin (8.995)>(±)doxazosin (8.694)>(-)doxazosin (8.032). The plasma concentrations of (-)doxazosin, (+)doxazosin, and (±)doxazosin were 18.26±3.55, 177.11±20.66, and 113.18±13.21 ng/mL, respectively, 8 h after the last administration of these agents.
Long-term treatment with (±)doxazosin produces potent hypotensive action in conscious rats that seems to result from synergic interaction of the two enantiomers.
多沙唑嗪是(-)多沙唑嗪和(+)多沙唑嗪的外消旋混合物,目前被用作高血压的附加治疗药物。在这项研究中,我们研究了长期给予(±)多沙唑嗪治疗时,每个对映体对清醒大鼠降压作用的贡献。
使用容积压力记录系统测量清醒 SD 大鼠的血压。大鼠口服给予(-)多沙唑嗪、(+)多沙唑嗪或(±)多沙唑嗪(8mg·kg(-1)·d(-1))12 周。用 HPLC 分析药物的血浆浓度。在分离的大鼠尾动脉标本中检查药物对α1-肾上腺素受体的作用。
单次给予(±)多沙唑嗪(8mg/kg)对清醒大鼠的舒张压(DBP)和平均动脉压(MBP)没有影响,但给药后 4 小时可显著降低收缩压(SBP)11.9%。长期给予(±)多沙唑嗪治疗可显著降低清醒大鼠的 SBP、DBP 和 MBP,末次给药后 8 小时 SBP 最大降低 29.3%。长期治疗在清醒大鼠中引起的降压作用的顺序为(±)多沙唑嗪>(+)多沙唑嗪>>(-)多沙唑嗪。然而,抑制去甲肾上腺素诱导的分离大鼠尾动脉收缩的 pKB 值为(+)多沙唑嗪(8.995)>(±)多沙唑嗪(8.694)>(-)多沙唑嗪(8.032)。末次给予这些药物 8 小时后,(-)多沙唑嗪、(+)多沙唑嗪和(±)多沙唑嗪的血浆浓度分别为 18.26±3.55、177.11±20.66和 113.18±13.21ng/mL。
长期给予(±)多沙唑嗪治疗可在清醒大鼠中产生有效的降压作用,这似乎是两种对映体协同作用的结果。