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豚鼠膀胱的肾上腺素能受体

Adrenoreceptors of the guinea-pig urinary bladder.

作者信息

Dave K C, Dhattiwala A S

出版信息

Br J Pharmacol. 1976 Sep;58(1):37-41. doi: 10.1111/j.1476-5381.1976.tb07690.x.

Abstract

1 Adrenaline, noradrenaline and isoprenaline (5 mug/ml) did not affect the resting tone of the isolated urinary bladder of the guinea-pig. 2 The catecholamines (1-2 mug/ml) inhibited neuronally evoked contractions at various stimulation frequencies; the inhibition was maximum at 2 Hz and minimum at 50 Hz. Isoprenaline produced maximum inhibition. 3 Propranolol (0.5 mug/ml) completely blocked the catecholamine-induced inhibition at all the frequencies employed. The concentration-response curves of isoprenaline at 2, 10 and 50 Hz were characteristically shifted by propranolol (50 ng/ml). Phenoxybenzamine (0.2 mug/ml) was totally ineffective. 4 In some experiments adrenaline significantly raised the tone of the bladder exposed to propranolol; this effect could be blocked by phenoxybenzamine. 5 Acetylcholine-induced bladder contractions were inhibited by adrenaline (2 mug/ml); the inhibition was completely blocked by propranolol (0.5 mug/ml). 6 The results indicate the presence of an inhibitory beta-adrenoceptor and suggest the possibility of an excitatory alpha-adrenoceptor in guinea-pig urinary bladder.

摘要
  1. 肾上腺素、去甲肾上腺素和异丙肾上腺素(5微克/毫升)对豚鼠离体膀胱的静息张力无影响。

  2. 儿茶酚胺(1 - 2微克/毫升)在不同刺激频率下抑制神经诱发的收缩;在2赫兹时抑制作用最大,在50赫兹时最小。异丙肾上腺素产生的抑制作用最大。

  3. 普萘洛尔(0.5微克/毫升)在所有使用的频率下完全阻断了儿茶酚胺诱导的抑制作用。普萘洛尔(50纳克/毫升)使异丙肾上腺素在2、10和50赫兹时的浓度 - 反应曲线发生特征性移位。酚苄明(0.2微克/毫升)完全无效。

  4. 在一些实验中,肾上腺素显著提高了暴露于普萘洛尔的膀胱的张力;这种作用可被酚苄明阻断。

  5. 乙酰胆碱诱导的膀胱收缩被肾上腺素(2微克/毫升)抑制;这种抑制作用被普萘洛尔(0.5微克/毫升)完全阻断。

  6. 结果表明豚鼠膀胱中存在抑制性β - 肾上腺素能受体,并提示可能存在兴奋性α - 肾上腺素能受体。

相似文献

1
Adrenoreceptors of the guinea-pig urinary bladder.豚鼠膀胱的肾上腺素能受体
Br J Pharmacol. 1976 Sep;58(1):37-41. doi: 10.1111/j.1476-5381.1976.tb07690.x.
5
Betadrenoceptors in urinary bladder.
Arch Int Pharmacodyn Ther. 1976 Aug;222(2):193-9.
7
Beta-adrenoceptors in the detrusor of guinea pig bladder.
J Smooth Muscle Res. 1998 Oct-Dec;34(5-6):233-42. doi: 10.1540/jsmr.34.233.

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