摘要
目的:观察多塞平(doxepin,Dox)对兔脑血管的作用.方法:采用离体兔基底动脉和隐动脉动脉环离体实验方法.结果:多塞平抑制KCl45.6mmol·L-1和5羟色胺10μmol·L-1诱发的兔基底动脉环和隐动脉环收缩,其拮抗CaCl2量效反应的pD2值分别为5.28±0.40和4.76±0.14(n=6,P<001).多塞平5.8μmol·L-1抑制在无Ca2+液中去甲肾上腺素引起的隐动脉环收缩,多塞平30μmol·L-1对无Ca2+液中去甲肾上腺素和恢复正常Ca2+液(1.25mmol·L-1)引起的隐动脉环收缩均有抑制作用.结论:与隐动脉环相比较。
AIM: To study the effects of doxepin (Dox) on cerebral artery. METHODS: The effects of Dox were observed using the isolated basilar and saphenous artery rings of rabbits. RESULTS: Dox inhibited the constriction of the basilar and saphenous artery rings evoked by KCl with IC50 5.75 mu mol . L-1 (95% confidence limits were 2.3 - 14 mu mol . L-1, n = 8) and 34.6 mu mol . L-1 (95% confidence limits were 3.8 - 316 mu mol L-1, n = 8), respectively. Dox also inhibited the constriction of the basilar and saphenous artery rings of the rabbits stimulated by 5-hydroxytryptamine (5-HT), IC50 were 6.3 mu mol . L-1 (95% confidence limits were 1.7 - 23.3 mu mol . L-1, n = 7) and 8.0 (mu mol . L-1(95% confidence limits were 6.3 - 10.3 mu mol . L-1, n = 6), respectively. In both samples (basilar and saphenous artery rings) CaCl2 evoked, the pD(2) of Dox was 5.28 +/- 0.40 and 4.76 +/- 0.14, respectively (n = 6, P < 0.01). Dox 5.8 mu mol L-1 inhibited the constriction of the saphenous artery evoked by norepinephrine (NE) in Ca2+-free medium. Dox 30 mu mol . L-1 inhibited the constriction of the saphenous artery evoked both by NE and by readmission of CaCl2 (1.25 mmol L-1). CONCLUSION: As compared with its effect on the saphenous artery, Dox selectively inhibited the basilar artery.
出处
《中国药理学报》
CSCD
1998年第6期572-574,共3页
Acta Pharmacologica Sinica