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首页> 外文期刊>Life sciences >ANTINOCICEPTIVE EFFECT OF NIFEDIPINE AND VERAPAMIL TESTED ON RATS CHRONICALLY EXPOSED TO NICOTINE AND AFTER ITS WITHDRAWAL
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ANTINOCICEPTIVE EFFECT OF NIFEDIPINE AND VERAPAMIL TESTED ON RATS CHRONICALLY EXPOSED TO NICOTINE AND AFTER ITS WITHDRAWAL

机译:替尼定和维拉帕米对长期暴露于尼古丁和戒断后大鼠的止痛作用

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Antinociceptive effect of nifedipine (15 mg/kg i.p.) and verapamil (10 mg/kg s.c.) was examined in rats chronically exposed to nicotine (6 mg/kg/day via Alzet osmotic pump for 28 days) and after nicotine withdrawal. Sham operated rats served as control for testing DMSO (dimethylsulfoxide, a solvent for nifedipine), nifedipine and verapamil alone. Nociception was measured by the tail-flick technique. Nifedipine, but not verapamil, injected to control rats produced a ceiling tail-flick latency (20 sec) 30 min after the injection, lasting for 10 min. In rats exposed to chronic nicotine for 3 days, nifedipine treatment exhibited ceiling tail-flick latency within 10 min lasting for 80 min. Tested in rats exposed to nicotine for 3 weeks, nifedipine treatment produced this effect 25 min after the injection lasting for 60 min. Nicotine withdrawal abolished this effect. Verapamil did not exhibit any significant changes in tail-flick latencies. These data support our hypothesis that smoking patients treated with nifedipine could be at a potential risk in developing a high pain threshold and missing the first sign of heart attack - a chest pain. [References: 15]
机译:在长期暴露于尼古丁(6 mg / kg /天,通过Alzet渗透泵治疗28天)和尼古丁戒断后的大鼠中,观察了硝苯地平(15 mg / kg i.p.)和维拉帕米(10 mg / kg s.c.)的抗伤害作用。假手术的大鼠作为对照,分别测试DMSO(二甲亚砜,硝苯地平的溶剂),硝苯地平和维拉帕米。通过甩尾技术测量伤害感受。注射硝苯地平(而非维拉帕米)以控制大鼠后,在注射后30分钟产生上限甩尾潜伏期(20秒),持续10分钟。在暴露于慢性尼古丁3天的大鼠中,硝苯地平治疗在10分钟内表现出天花板甩尾潜伏期,持续80分钟。在暴露于尼古丁3周的大鼠中进行了测试,硝苯地平治疗在注射60分钟后25分钟产生了这种效果。尼古丁戒断消除了这种作用。维拉帕米的甩尾潜伏期未显示任何显着变化。这些数据支持了我们的假设,即用硝苯地平治疗的吸烟患者可能会出现高疼痛阈值并错过心脏病发作的第一个迹象-胸痛的潜在风险。 [参考:15]

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