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首页> 外文期刊>Neurourology and urodynamics. >Effects of phenazopyridine on rat bladder primary afferent activity, and comparison with lidocaine and acetaminophen.
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Effects of phenazopyridine on rat bladder primary afferent activity, and comparison with lidocaine and acetaminophen.

机译:吩唑并吡啶对大鼠膀胱初级传入活性的影响,并与利多卡因和对乙酰氨基酚进行比较。

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AIMS: The clinical indication of phenazopyridine is unclear, it has been used clinically in conditions with increased bladder sensation as in cystitis and bladder pain syndrome/interstitial cystitis. We explored the effect of phenazopyridine on afferent nerve activity by direct measurement of both Adelta- and C-fibers in the rat, and compared the outcome with the effects of lidocaine (a local anesthetic) and of acetaminophen (an analgesic). METHODS: Female Sprague-Dawley rats were used. Under urethane anesthesia, single nerve fibers primarily originating from the bladder were identified in the L6 dorsal root by electrical stimulation of the left pelvic nerve and by bladder distention. By conduction velocity (2.5 m/sec) the fibers were defined as Adelta-fiber or C-fiber. The afferent activity in response to constant bladder filling was measured before the drug administration. Then, phenazopyridine (0.1-3 mg/kg) or lidocaine (0.3-3 mg/kg) or acetaminophen (1-10 mg/kg) was administrated intravenously. After drug administration, the afferent activity of bladder fillings was measured again. RESULTS: All drugs significantly increased bladder compliance, in a dose-dependent way. Twenty-eight single afferent fibers (Adelta-fibers: n = 13, C-fibers: n = 15) were isolated. Intravenous administration of phenazopyridine significantly decreased dose-dependently only the Adelta-fiber but not the C-fiber activity. Also acetaminophen significantly decreased only Adelta-fiber activity, but it was not dose-dependently completely. Lidocaine inhibited both the Adelta- and C-fiber activities. CONCLUSIONS: This study shows that phenazopyridine can directly inhibit the mechanosensitive Adelta-fibers in the normal rat bladder. This finding might explain its clinical effect in conditions of bladder hypersensitivity.
机译:目的:吩唑并吡啶的临床适应症尚不清楚,已在临床上用于膀胱感觉增加的情况,如膀胱炎和膀胱疼痛综合征/间质性膀胱炎。我们通过直接测量大鼠中的Adelta和C纤维探索了吩唑并吡啶对传入神经活动的影响,并将结果与​​利多卡因(局部麻醉药)和对乙酰氨基酚(镇痛药)的作用进行了比较。方法:使用雌性Sprague-Dawley大鼠。在氨基甲酸乙酯麻醉下,通过左骨盆神经的电刺激和膀胱扩张,在L6背根中发现了主要源自膀胱的单条神经纤维。通过传导速度(2.5m / sec),纤维被定义为Adelta纤维或C纤维。在给药前测量对恒定膀胱充盈的传入活性。然后,静脉内施用苯并吡啶(0.1-3mg / kg)或利多卡因(0.3-3mg / kg)或对乙酰氨基酚(1-10mg / kg)。给药后,再次测量膀胱充盈的传入活动。结果:所有药物均以剂量依赖性方式显着增加膀胱顺应性。分离出二十八根单根传入纤维(Adelta纤维:n = 13,C纤维:n = 15)。静脉给药吩唑并吡啶仅剂量依赖性地显着降低Adelta-纤维活性,而不显着降低C-纤维活性。对乙酰氨基酚也仅显着降低了阿德塔纤维的活性,但并非完全依赖剂量。利多卡因同时抑制Adelta和C纤维的活性。结论:这项研究表明,吩唑并吡啶可直接抑制正常大鼠膀胱中的机械敏感性Adelta纤维。这一发现可能解释了其在膀胱超敏反应条件下的临床效果。

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