摘要
目的 研究四逆汤对高钾和去氧肾上腺素 (Phe)收缩大鼠离体主动脉血管环效应的影响。方法 观察四逆汤在主动脉环上拮抗 KCl (60 mmol/ L )和 Phe (1× 10 - 9~ 1× 10 - 4mmol/ L )的收缩血管作用 ,分别用普萘洛尔(Pro,3× 10 - 6 m mol/ L)和 Bay K8644(BK,1× 10 - 5 mm ol/ L)干预探讨其机制。结果 四逆汤减弱累积浓度的Phe收缩血管的效应 ,最大值 (Tmax)减小 ,Pro不影响四逆汤的拮抗作用 ;四逆汤减小高钾刺激血管的最大收缩效应 ,BK不能恢复这种效应。结论 四逆汤使 Phe的量效曲线右移 ,并减小其最大效应值 ,表现为非竞争性拮抗作用 ;减小高钾收缩血管的作用 ,Ca2 +开放剂 BK不能恢复四逆汤的抑制作用。四逆汤能阻断 α1受体 。
Object To study the effects of SINI TANG (SNT) on the rat aortic rings pre-contracted by high K + and phenylephrine (Phe). Methods The effects of SNT on the aortic rings in the presence of 60 mmol/L KCl and Phe (1×10 -9 -1×10 -4 mmol/L) were observed and t heir me chanisms were studied after treatment with Propranolol (Pro, 3×10 -6 mmol/ L) and Bay K8644 (BK, 1×10 -5 mmol/L) as tool drugs. Results SNT inhibited the contraction induced by cumulative Phe and decreased the maximum tension (T max ); Pro couldn't influe nce the effects of SNT. SNT attenuated the amplitude of contractile effect of hi gh K +; BK couldn't reverse the effects of SNT. Conclusion SNT can shift the dose-response curve to the right and decrease the T max . It shows that SNT is a kind of noncompe titive antagonism. SNT decreases the effect of high K + against contraction of the artery. BK, a L-type Ca 2+ channels activator, couldn't recover the inhibition induced by SNT. The results suggest that SNT inhibit α 1 recep tor, while calcium channel may not be involved in attenuating the effect of SNT on high K +-induced contraction.
出处
《中草药》
CAS
CSCD
北大核心
2003年第9期819-821,共3页
Chinese Traditional and Herbal Drugs
基金
北京市自然科学基金项目 ( 70 1 1 0 0 2 )
关键词
四逆汤
去氧肾上腺素
普萘洛尔
BayK8644
SINI TANG (SNT)
phenylephrine (Phe)
Propranolol (Pro)
Bay K8644 (BK) SINI TANG is a decoction with Chinese prescription of R adix Aconi ti Lateralis Preparata, Rhizoma Zingiberis and Radix Glycyrrhizae. It is used in the treatment of