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关于嘌呤能抑制性神经支配存在于兔门静脉而非豚鼠门静脉的比较药理学和组织化学证据。

Comparative pharmacological and histochemical evidence for purinergic inhibitory innervation of the portal vein of the rabbit, but not guinea-pig.

作者信息

Burnstock G, Crowe R, Wong H K

出版信息

Br J Pharmacol. 1979 Mar;65(3):377-88. doi: 10.1111/j.1476-5381.1979.tb07841.x.

Abstract

1 Intramural nerve stimulation elicited a powerful relaxation of the longitudinal muscle of the rabbit portal vein in the presence of atropine and guanethidine, but not of the guinea-pig portal vein.2 Intramural nerve stimulation of the rabbit portal vein produced a 13 fold increase in release of (3)H-adenyl compounds after preloading with [(3)H]-adenosine. About 50% of this release was abolished by guanethidine. All release was abolished by tetrodotoxin. No significant release of radioactive compounds was observed during intramural nerve stimulation of the guinea-pig portal vein in the presence of guanethidine, although there was a 6 fold increase in release of radioactivity in the absence of drugs.3 Histochemical studies using quinacrine, which binds ATP showed a fine fluorescent nerve plexus, nerve bundles, and ganglion cells in the rabbit portal vein, but not in the guinea-pig portal vein. This plexus was still present after chemical sympathectomy with 6-hydroxydopamine.4 Adenosine 5'-triphosphate (ATP) relaxed the rabbit portal vein, but usually produced a biphasic response, consisting of a contraction followed by a relaxation, of the guinea-pig portal vein.5 Prostaglandins E(1) and E(2) caused contraction of the rabbit portal vein. Indomethacin, a prostaglandin synthesis inhibitor, potentiated the relaxations of the rabbit portal vein produced by both non-adrenergic, non-cholinergic nerve stimulation and ATP.6 High concentrations of antazoline and phentolamine, which antagonize purinergic responses in the guinea-pig taenia coli, caused a loss of basal tone so that it was not possible to assess their effects on the responses of the portal vein to either non-adrenergic, non-cholinergic nerve stimulation, or ATP.7 Comparison of the results on the portal vein of the rabbit and guinea-pig provides support for the view that: (i) quinacrine fluorescence can be used to localize purinergic nerves and that the rabbit portal vein is supplied by these nerves; (ii) ATP is released from adrenergic nerve fibres, although, based on histochemical analysis, about 3 to 7 times less than is released from purinergic nerve fibres.

摘要
  1. 在阿托品和胍乙啶存在的情况下,壁内神经刺激可引起兔门静脉纵行肌强力舒张,但对豚鼠门静脉无效。

  2. 用[³H] - 腺苷预加载后,兔门静脉的壁内神经刺激使(³H) - 腺苷化合物的释放增加了13倍。胍乙啶可消除约50%的这种释放。河豚毒素可消除所有释放。在胍乙啶存在的情况下,豚鼠门静脉壁内神经刺激期间未观察到放射性化合物的显著释放,尽管在无药物时放射性释放增加了6倍。

  3. 使用结合ATP的喹吖因进行的组织化学研究显示,兔门静脉中有精细的荧光神经丛、神经束和神经节细胞,而豚鼠门静脉中没有。用6 - 羟基多巴胺进行化学交感神经切除后,该神经丛仍然存在。

  4. 三磷酸腺苷(ATP)可使兔门静脉舒张,但通常对豚鼠门静脉产生双相反应,包括先收缩后舒张。

  5. 前列腺素E₁和E₂可引起兔门静脉收缩。前列腺素合成抑制剂吲哚美辛可增强非肾上腺素能、非胆碱能神经刺激和ATP引起的兔门静脉舒张。

  6. 高浓度的安他唑啉和酚妥拉明可拮抗豚鼠结肠带中的嘌呤能反应,导致基础张力丧失,因此无法评估它们对门静脉对非肾上腺素能、非胆碱能神经刺激或ATP反应的影响。

  7. 对兔和豚鼠门静脉结果的比较支持以下观点:(i)喹吖因荧光可用于定位嘌呤能神经,兔门静脉由这些神经供应;(ii)ATP从肾上腺素能神经纤维释放,尽管根据组织化学分析,其释放量比嘌呤能神经纤维少约3至7倍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b619/1668636/99a1db2ff466/brjpharm00426-0033-a.jpg

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