Chang H Y, Chen C W, Hsiue T R, Chen C R
Department of Internal Medicine, College of Medicine, National Cheng Kung University Hospital, Tainan, Taiwan R.O.C.
J Formos Med Assoc. 1994 Sep;93(9):788-96.
To assess the effect of endothelium-derived relaxing factor (EDRF) on the diaphragmatic microcirculation under basal conditions and after vasodilator stimulation, prepared diaphragms from anesthetized rats were studied. With bicarbonate-buffered Ringer's solution suffusing the diaphragm, the microcirculatory blood flow was recorded by laser-Doppler flowmetry (QLDF). Drugs were applied to the surface of the diaphragm. Five series of experiments were performed. In Series 1, the effects of acetylcholine (ACh, 10(-4) M) and sodium nitroprusside (SNP, 3 x 10(-6) M) were measured before and after 15 minutes suffusion of N omega-nitro-L-arginine methyl ester (L-NAME, 10(-4) M). Trend analyses revealed that the vasodilator effect of SNP was not affected, while that of ACh was abolished by L-NAME. In Series 2, both ACh and SNP elicited a concentration-dependent increase in QLDF. In Series 3, following 15 minutes suffusion with L-NAME (10(-4) M), there was no change in baseline QLDF and the ACh-induced QLDF change was abolished, while the effect of SNP was maintained. In Series 4, five minutes of pretreatment with L-arginine (L-arg, 10(-2) M), followed by co-administration of L-arg (10(-2) M) and L-NAME (10(-4) M) for another 15 minutes, did not prevent the inhibitory effect on ACh-induced QLDF change by L-NAME. In Series 5, 20 minutes application of L-arg (10(-2) M) alone did not affect baseline QLDF. Also, L-arg did not influence the ACh-induced vasodilating response, whereas it slightly increased the SNP-induced vasodilating response.(ABSTRACT TRUNCATED AT 250 WORDS)
为评估内皮源性舒张因子(EDRF)在基础条件下以及血管舒张剂刺激后对膈微循环的影响,对来自麻醉大鼠制备好的膈进行了研究。用碳酸氢盐缓冲的林格氏液灌注膈,通过激光多普勒血流仪(QLDF)记录微循环血流量。将药物应用于膈表面。进行了五组实验。在第1组实验中,在灌注Nω-硝基-L-精氨酸甲酯(L-NAME,10⁻⁴ M)15分钟前后,测量乙酰胆碱(ACh,10⁻⁴ M)和硝普钠(SNP,3×10⁻⁶ M)的作用。趋势分析显示,SNP的血管舒张作用未受影响,而ACh的血管舒张作用被L-NAME消除。在第2组实验中,ACh和SNP均引起QLDF浓度依赖性增加。在第3组实验中,灌注L-NAME(10⁻⁴ M)15分钟后,基线QLDF无变化,ACh诱导的QLDF变化被消除,而SNP的作用得以维持。在第4组实验中,用L-精氨酸(L-arg,10⁻² M)预处理5分钟,然后将L-arg(10⁻² M)和L-NAME(10⁻⁴ M)共同给药15分钟,未能阻止L-NAME对ACh诱导的QLDF变化的抑制作用。在第5组实验中,单独应用L-arg(10⁻² M)20分钟未影响基线QLDF。此外,L-arg不影响ACh诱导的血管舒张反应,而它略微增加了SNP诱导的血管舒张反应。(摘要截断于250字)