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相似文献

1
The accumulation of adenosine in rabbit intestinal muscle.腺苷在兔肠肌中的蓄积。
Br J Pharmacol. 1974 Apr;50(4):569-74. doi: 10.1111/j.1476-5381.1974.tb08590.x.
2
Some effects of dipyridamole, hexobendine and lidoflazine on inhibitory processes in rabbit duodenum.潘生丁、己酮可可碱和利多氟嗪对兔十二指肠抑制过程的某些作用。
Br J Pharmacol. 1974 Apr;50(4):609-11. doi: 10.1111/j.1476-5381.1974.tb08598.x.
3
Influence of hexobendine, dipyridamole, dilazep, lidoflazine, inosine and purine riboside on adenosine uptake by the isolated epithelium of guinea pig jejunum.己酮可可碱、双嘧达莫、地拉齐普、利多氟嗪、肌苷和嘌呤核苷对豚鼠空肠离体上皮细胞摄取腺苷的影响。
Pharmacology. 1978;16(1):54-60. doi: 10.1159/000136747.
4
Measurement of adenosine metabolism and uptake in smooth muscle and effects of adenosine transport inhibitors.平滑肌中腺苷代谢与摄取的测量以及腺苷转运抑制剂的作用
J Pharmacol Exp Ther. 1984 May;229(2):564-70.
5
Potentiation of the effects of exogenously applied ATP and purinergic nerve stimulation on the guinea-pig taenia coli by dipyridamole and hexobendine.双嘧达莫和己酮可可碱对豚鼠结肠带中外源性应用ATP和嘌呤能神经刺激作用的增强
Eur J Pharmacol. 1972 Sep;19(3):343-50. doi: 10.1016/0014-2999(72)90100-8.
6
Adenosine uptake by erythrocytes of man, rat and guinea-pig and its inhibition by hexobendine and dipyridamole.人、大鼠和豚鼠红细胞对腺苷的摄取及其被己酮可可碱和双嘧达莫的抑制作用。
Biochem Pharmacol. 1975 Jan 1;24(1):154-6. doi: 10.1016/0006-2952(75)90331-7.
7
Effects of some purine derivatives on the guinea-pig trachea and their interaction with drugs that block adenosine uptake.某些嘌呤衍生物对豚鼠气管的作用及其与阻断腺苷摄取药物的相互作用。
Br J Pharmacol. 1976 May;57(1):51-7. doi: 10.1111/j.1476-5381.1976.tb07655.x.
8
Calcium entry blocking activity of dilazep in dog coronary artery.双嘧达莫在犬冠状动脉中的钙内流阻滞活性。
Pharmacology. 1986;33(3):148-56. doi: 10.1159/000138212.
9
Adenosine and dipyridamole: actions and interactions on the contractile response of guinea-pig ileum to high frequency electrical field stimulation.腺苷与双嘧达莫:对豚鼠回肠对高频电场刺激的收缩反应的作用及相互作用
Br J Pharmacol. 1985 Mar;84(3):765-71. doi: 10.1111/j.1476-5381.1985.tb16159.x.
10
[Comparative investigation on the vitro inhibition of adenosine decomposition by dilazep].[双嘧达莫对腺苷分解的体外抑制作用的比较研究]
Arzneimittelforschung. 1974 Nov;24(11A Suppl):1901-5.

引用本文的文献

1
Potentiation by dilazep on the negative inotropic effect of adenosine on guinea-pig atria.地拉卓对腺苷对豚鼠心房负性肌力作用的增强作用。
Br J Pharmacol. 1980 Feb;68(2):343-9. doi: 10.1111/j.1476-5381.1980.tb10423.x.
2
Some effects of dipyridamole, hexobendine and lidoflazine on inhibitory processes in rabbit duodenum.潘生丁、己酮可可碱和利多氟嗪对兔十二指肠抑制过程的某些作用。
Br J Pharmacol. 1974 Apr;50(4):609-11. doi: 10.1111/j.1476-5381.1974.tb08598.x.
3
Identification of separate receptors for adenosine and adenosine 5'-triphosphate in causing relaxations of the isolated taenia of the guinea-pig caecum.腺苷和5'-三磷酸腺苷在引起豚鼠盲肠离体带状肌松弛中各自受体的鉴定。
Br J Pharmacol. 1976 Jun;57(2):305-10. doi: 10.1111/j.1476-5381.1976.tb07480.x.

本文引用的文献

1
[Effect of hexabendin on oxygen consumption, energetics and substrate metabolism of the heart. II. Studies with intravenously administered single doses].己环苯对心脏耗氧量、能量代谢及底物代谢的影响。II. 静脉注射单剂量的研究
Arzneimittelforschung. 1966 Jun;16(6):692-7.
2
Potentiation of adenosine and the adenine nucleotides by dipyridamole.双嘧达莫对腺苷和腺嘌呤核苷酸的增强作用。
Br J Pharmacol Chemother. 1966 Nov;28(2):218-27. doi: 10.1111/j.1476-5381.1966.tb01888.x.
3
Enhancement of coronary vasodilating action of ATP and adenosine by lidoflazine.利多氟嗪增强ATP和腺苷的冠状血管舒张作用。
Circ Res. 1968 Jan;22(1):43-8. doi: 10.1161/01.res.22.1.43.
4
Neuronal uptake processes for amines and amino acids.
Adv Biochem Psychopharmacol. 1970;2:109-32.
5
Specificity of adenosine uptake into the heart and inhibition by dipyridamole.腺苷摄取入心脏的特异性及双嘧达莫对其的抑制作用。
Eur J Pharmacol. 1970 Mar;9(3):265-8. doi: 10.1016/0014-2999(70)90221-9.
6
Effects of isoprenaline and phenylephrine on energy-rich phosphate compounds and glucose-6-phosphate in smooth and cardiac muscle.异丙肾上腺素和去氧肾上腺素对平滑肌和心肌中高能磷酸化合物及6-磷酸葡萄糖的影响。
Br J Pharmacol. 1971 Nov;43(3):593-603. doi: 10.1111/j.1476-5381.1971.tb07189.x.
7
A species difference in the uptake of adenosine by heart.心脏对腺苷摄取的种属差异。
Biochem Pharmacol. 1971 Dec;20(12):3359-65. doi: 10.1016/0006-2952(71)90440-0.
8
The potentiation of the action of adenosine on the guinea-pig heart.腺苷对豚鼠心脏作用的增强效应。
Biochem Pharmacol. 1973 Feb 1;22(3):341-8. doi: 10.1016/0006-2952(73)90415-2.
9
Some effects of dipyridamole, hexobendine and lidoflazine on inhibitory processes in rabbit duodenum.潘生丁、己酮可可碱和利多氟嗪对兔十二指肠抑制过程的某些作用。
Br J Pharmacol. 1974 Apr;50(4):609-11. doi: 10.1111/j.1476-5381.1974.tb08598.x.
10
Purinergic nerves.嘌呤能神经
Pharmacol Rev. 1972 Sep;24(3):509-81.

腺苷在兔肠肌中的蓄积。

The accumulation of adenosine in rabbit intestinal muscle.

作者信息

Hulme M E, Weston A H

出版信息

Br J Pharmacol. 1974 Apr;50(4):569-74. doi: 10.1111/j.1476-5381.1974.tb08590.x.

DOI:10.1111/j.1476-5381.1974.tb08590.x
PMID:4447859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1776717/
Abstract

1 Strips of longitudinal muscle from rabbit intestine accumulated radioactivity when exposed to [(3)H]-adenosine.2 Accumulation of radioactivity was not sodium-dependent or ouabain-sensitive, but was reduced by cooling, zero glucose plus bubbling with N(2), 2,4,dinitrophenol, dipyridamole, hexobendine and lidoflazine.3 After 7 min exposure to [(3)H]-adenosine, the tissue was found to contain radioactive adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP) and adenosine itself in the approximate ratio 13: 6: 4: 1.4 In the presence of dipyridamole, hexobendine or lidoflazine (each 1 muM), the amounts of radioactive ATP, ADP, AMP and adenosine were reduced with the concentration of adenosine not significantly different from controls.5 It is concluded that energy-dependent uptake of adenosine does not occur in the longitudinal muscle of rabbit intestine. Adenosine enters the tissue by a passive process and rapidly becomes phosphorylated giving rise to apparently high tissue: medium ratios.6 The drugs dipyridamole, hexobendine and lidoflazine appear to reduce the accumulation of radioactivity by preventing the formation of adenosine phosphate derivatives.

摘要
  1. 兔肠纵行肌条在暴露于[³H] - 腺苷时会积累放射性。

  2. 放射性的积累不依赖于钠,对哇巴因不敏感,但会因冷却、零葡萄糖加氮气鼓泡、2,4 - 二硝基苯酚、双嘧达莫、己酮可可碱和利多氟嗪而减少。

  3. 在暴露于[³H] - 腺苷7分钟后,发现组织中含有放射性的三磷酸腺苷(ATP)、二磷酸腺苷(ADP)、一磷酸腺苷(AMP)和腺苷本身,其近似比例为13:6:4:1。

  4. 在双嘧达莫、己酮可可碱或利多氟嗪(各1μM)存在的情况下,放射性ATP、ADP、AMP和腺苷的量减少,腺苷浓度与对照组无显著差异。

  5. 得出结论,兔肠纵行肌中不存在腺苷的能量依赖性摄取。腺苷通过被动过程进入组织并迅速磷酸化,导致组织与介质的比例明显升高。

  6. 双嘧达莫、己酮可可碱和利多氟嗪似乎通过阻止磷酸腺苷衍生物的形成来减少放射性的积累。