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出 处:《泰山医学院学报》2005年第3期203-205,共3页Journal of Taishan Medical College
摘 要:目的观察钙通道阻滞剂Nifedipine控释剂对自发性高血压大鼠(SHR)一氧化氮(NO)及诱导性一氧化氮合酶(iNOS)的影响。方法本实验为随机对照的实验研究,在山东大学医学院实验室完成。实验动物为近交SHR大鼠21只。实验动物被随机分3组:生理盐水对照组7只,Nifedipine正常剂量组7只,Nifedipine低剂量组7只。每天灌胃一次,连续15 d,末次给药后摘眼球取血并取大鼠心、肺分别测定血清NO和iNOS的含量。结果:灌胃15 d后,正常剂量组的NO含量为(135±7.7)ptnol/L,与生理盐水组(102.3±4.6)ptnol/L相比,差异有显著性意义(P<0.01);正常剂量组心、肺组织块中iNOS活性降低,为(1.15±0.18),差异有显著性意义(P<0.01);与低剂量组(1.77±0.23)相比,差异亦有显著性意义(P<0.05)。结论Nifedipine能在有效降低血压的同时,提高血清NO的含量,并且对抗血压增高所造成的iNOS的活性增强(或二者互为因果)。Objective: To study the effect of Nifedipine on nitric oxide(NO) and inducible nitric oxide synthase(iNOS) in spontaneous hypertension rats. Methods: A randomly controlled trial study was made. The research was accomplished in Shandong University Medical College. Twenty-one spontaneous hypertension rats were divided into the control group, normal and low doses Nifedipine groups. The drugs were administered once a day by gastrogavage for 15 successive days. Blood was collected from the eye-balls and the viscera pulmo to determine the NO and iNOS in the serum after the last time. Results: The NO in the serum in the normal dose group was 135±7.7μmol/L, and 121±6.4μmol/L in the low dose group, which were both significantly higher than those in the control group (P 〈 0.01 and P 〈 0.01). It was also observed that the iNOS activity was significantly depressed in the normal dose (1.15±0.18) and the low dose (1.77±0.23) Nifedipine groups than that in the controls (2.43±0.76) (P 〈 0.05). Conclusion: Nifedipine can low the pressure and at the came time can raise NO in the serum and depress the activity of iNOS caused by the hypertension.
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