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豚鼠输精管中肾上腺素能运动传递的反证。

Evidence against adrenergic motor transmission in the guinea-pig vas deferens.

作者信息

Ambache N, Zar M A

出版信息

J Physiol. 1971 Jul;216(2):359-89. doi: 10.1113/jphysiol.1971.sp009530.

Abstract
  1. Field stimulation of desheathed preparations of guinea-pig vas deferens, treated with a ganglion-blocking agent, has revealed the presence of two tetrodotoxin-susceptible components in the motor response, suggesting the existence of two sets of post-ganglionic motor nerve fibres of different excitability: one set responding maximally to pulses of 0.1-0.4 msec; the other, to pulses of 2 msec. No distinction could be made pharmacologically between the two components.2. Cooling potentiated that component in the twitch-responses which was due to stimulation of the more excitable fibres.3. The sensitivity of the longitudinal muscle to the motor action of noradrenaline was low and was subject to considerable animal variation. But normal responses to post-ganglionic field stimulation were elicited in noradrenaline-insensitive preparations, in which the twitches elicited by 5 pulses could not be matched with noradrenaline, even 100-125 mug/ml.4. In some forty experiments, small doses of noradrenaline inhibited the twitch-responses evoked by either set of motor fibres. This inhibition differed from that produced by isoprenaline in two respects. Firstly, propranolol did not antagonize the noradrenaline inhibition, thus excluding an action on beta-adrenoceptors; and secondly, noradrenaline did not depress contractions elicited by muscarine or by 5-methylfurmethide.5. Phenoxybenzamine, 10(-6) g/ml., produced a thousandfold reduction in the sensitivity of the muscle to the motor action of noradrenaline, without any decrease in the height of the twitches elicited by 0.1 or 1 msec pulses.6. The twitch-responses were not affected by combined alpha + beta adrenoceptor blockade with phentolamine and propranolol.7. Tyramine, amphetamine, tranylcypromine and prostaglandin E(2) inhibited the twitches but potentiated the contractile effect of noradrenaline.8. The twitch-responses and their inhibition by noradrenaline were present in preparations taken from reserpinized animals.9. Although the twitch-responses could be paralysed by bretylium or guanethidine, the foregoing results excluded adrenergic transmission at the motor endings. Cholinergic transmission was also excluded by negative findings with anticholinesterases, atropine, nicotine and (+)-tubocurarine.10. Motor transmission by histamine, 5-hydroxytryptamine, gamma-aminobutyric acid or ATP was also excluded.
摘要
  1. 用神经节阻断剂处理的豚鼠输精管去鞘制剂的场刺激显示,运动反应中存在两种对河豚毒素敏感的成分,这表明存在两组兴奋性不同的节后运动神经纤维:一组对0.1 - 0.4毫秒的脉冲反应最大;另一组对2毫秒的脉冲反应最大。从药理学上无法区分这两种成分。

  2. 冷却增强了因刺激较易兴奋的纤维而产生的抽搐反应中的该成分。

  3. 纵肌对去甲肾上腺素运动作用的敏感性较低,且存在相当大的动物个体差异。但在对去甲肾上腺素不敏感的制剂中,对节后场刺激仍能引发正常反应,在这些制剂中,5个脉冲引发的抽搐即使在100 - 125微克/毫升的去甲肾上腺素作用下也无法与之匹配。

  4. 在约四十个实验中,小剂量的去甲肾上腺素抑制了由任何一组运动纤维引发的抽搐反应。这种抑制在两个方面与异丙肾上腺素产生的抑制不同。首先,普萘洛尔不能拮抗去甲肾上腺素的抑制作用,因此排除了对β - 肾上腺素能受体的作用;其次,去甲肾上腺素不会抑制毒蕈碱或5 - 甲基糠甲铵引发的收缩。

  5. 10⁻⁶克/毫升的酚苄明使肌肉对去甲肾上腺素运动作用的敏感性降低了一千倍,而0.1或1毫秒脉冲引发的抽搐高度没有任何降低。

  6. 酚妥拉明和普萘洛尔联合进行α + β肾上腺素能受体阻断对抽搐反应没有影响。

  7. 酪胺、苯丙胺、反苯环丙胺和前列腺素E₂抑制抽搐,但增强了去甲肾上腺素的收缩作用。

  8. 从利血平化动物身上获取的制剂中存在抽搐反应及其被去甲肾上腺素抑制的现象。

  9. 虽然布雷迪宁或胍乙啶可使抽搐反应麻痹,但上述结果排除了运动终末的肾上腺素能传递。抗胆碱酯酶、阿托品、尼古丁和(+) - 筒箭毒碱的阴性结果也排除了胆碱能传递。

  10. 组胺、5 - 羟色胺、γ - 氨基丁酸或ATP的运动传递也被排除。

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Action of bretylium and guanethidine at the neuromuscular junction.溴苄铵和胍乙啶在神经肌肉接头处的作用。
Br J Pharmacol Chemother. 1961 Dec;17(3):372-9. doi: 10.1111/j.1476-5381.1961.tb01123.x.
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The innervation of the vas deferens of the guinea-pig.豚鼠输精管的神经支配。
J Physiol. 1967 Sep;192(2):463-78. doi: 10.1113/jphysiol.1967.sp008309.

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