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大鼠肛门尾骨肌及其对神经刺激和某些药物的反应。

The rat anococcygeus muscle and its response to nerve stimulation and to some drugs.

作者信息

Gillespie J S

出版信息

Br J Pharmacol. 1972 Jul;45(3):404-16. doi: 10.1111/j.1476-5381.1972.tb08097.x.

Abstract
  1. A new smooth muscle preparation, the rat anococcygeus muscle, is described. The muscle is paired, thin, consists of smooth muscle only and the muscle cells are organized in parallel bundles. It has a dense adrenergic innervation distributed throughout the muscle but apparently no cholinergic innervation. The muscles are easily isolated.2. The muscle contracts to noradrenaline, acetylcholine, furmethide, 5-hydroxytryptamine, but not to histamine. Isoprenaline produces contraction at high concentrations. The effects of noradrenaline and acetylcholine are blocked by phentolamine and atropine respectively. The response to isoprenaline is little affected by propranolol.3. The muscle contracts in response to field stimulation or stimulation of extrinsic nerves. This response is completely blocked by phentolamine but unaffected by hexamethonium or atropine.4. Guanethidine 10(-6)-5 x 10(-6)M blocks the motor response to nerve stimulation and potentiates that to noradrenaline. Higher concentrations of guanethidine raise tone. In the presence of raised tone, field stimulation produces an inhibitory response insensitive to hexamethonium but abolished by tetrodotoxin 2 x 10(-7) g/ml. This inhibitory response to stimulation can also be shown after other drugs which raise tone.5. The inhibitory response to nerve stimulation is not mimicked by acetylcholine, isoprenaline or ATP, nor blocked by atropine, phentolamine, phenoxybenzamine, propranolol, hexamethonium or lysergic acid diethylamide.
摘要
  1. 本文描述了一种新的平滑肌标本——大鼠肛门尾骨肌。该肌肉为成对的薄肌,仅由平滑肌组成,肌细胞呈平行束状排列。它有密集的肾上腺素能神经支配,分布于整个肌肉,但显然没有胆碱能神经支配。这些肌肉很容易分离。

  2. 该肌肉对去甲肾上腺素、乙酰胆碱、呋塞米、5-羟色胺有收缩反应,但对组胺无反应。异丙肾上腺素在高浓度时会引起收缩。去甲肾上腺素和乙酰胆碱的作用分别被酚妥拉明和阿托品阻断。普萘洛尔对异丙肾上腺素的反应影响很小。

  3. 该肌肉对场刺激或外在神经刺激有收缩反应。这种反应被酚妥拉明完全阻断,但不受六甲铵或阿托品影响。

  4. 10(-6)-5×10(-6)M的胍乙啶可阻断神经刺激的运动反应,并增强对去甲肾上腺素的反应。更高浓度的胍乙啶可提高肌张力。在肌张力升高的情况下,场刺激会产生一种对六甲铵不敏感但被2×10(-7)g/ml的河豚毒素消除的抑制反应。在其他能提高肌张力的药物作用后,也可出现这种对刺激的抑制反应。

  5. 对神经刺激的抑制反应不能被乙酰胆碱、异丙肾上腺素或ATP模拟,也不能被阿托品、酚妥拉明、苯氧苄胺、普萘洛尔、六甲铵或麦角酸二乙胺阻断。

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Poster communications.壁报交流
Br J Pharmacol. 1993 Oct;110(Suppl):81P-184P. doi: 10.1111/j.1476-5381.1993.tb16292.x.
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