检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]军事医学科学院毒物药物研究所,北京100850
出 处:《中国临床药理学与治疗学》2005年第6期633-636,共4页Chinese Journal of Clinical Pharmacology and Therapeutics
基 金:国家863计划重大专项(№2002AA2Z3137)
摘 要:目的:研究新结构类型的ATP敏感性钾通道(KATP)开放剂(KCO)、抗高血压新药埃他卡林(iptakalim,Ipt)对胃、回肠和膀胱等非血管平滑肌舒张作用的影响,并比较Ipt与其结构完全不同的KCO、氰胍类的吡那地尔(pinacidil,Pin)和苯并噻二嗪类的二氮嗪(diazoxide,Dia)舒张作用的差异,为进一步明确Ipt舒张作用的选择性特征提供一定的依据。方法:采用大鼠离体胃底、回肠和膀胱肌条3种组织,以10-5mol·L-1乙酰胆碱预收缩,观察不同浓度的药物对它们的舒张作用。结果:Ipt在10-8~10-4mol·L-1范围内对3种组织均无显著的舒张作用;Pin在10-8~10-4mol·L-1范围内对胃底条和膀胱平滑肌等均无显著的舒张作用,但在10-5和10-4mol·L-1时对回肠的舒张率分为28.8%和51.9%,诱发显著的舒张作用;Dia对3种组织的作用与Ipt相似,均不引起明显的舒张作用。结论:Ipt不影响胃、回肠和膀胱的舒张作用,选择性优于Pin,与Dia相似;化学结构类型不同的KCO对回肠、胃和膀胱的作用既相似也有不同。AIM: To investigate the relaxation effects of iptakalim (Ipt), a novel structural ATP-sensitive potassium channel opener (KCO), compare the relaxation characteristics of Ipt to the other structurally diverse KCOs, pinacidil (Pin) and diazoxide (Dia), and further understand the relaxation selectivity of Ipt. METHODS: Strips of stomach, ileum, and bladder isolated from rats were prepared and treated with different concentrations of drugs after contraction of 10 -5 mol·L -1 acetylcholine. RESULTS: Ipt at the concentrations of 10 -8-10 -4 mol·L -1 caused no relaxation effects on strips of stomach, ileum and bladder. The same results as Ipt were detected in diazoxide-treated tissue strips. Pin showed no effects on strips of stomach and bladder, however, Pin at concentrations of 10 -5 and 10 -4 mol·L -1 induced significant relaxations in ileum strips compared with the former concentration, and the relaxation rates were 28.8% and 51.9%, respectively. CONCLUSION: Ipt shows no effect on the relaxation of stomach, ileum and bladder, which is different from Pin, but the same as Dia. Moreover, similarities and differences in relaxation are also found among the structurally diverse KCOs.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222