Suppr超能文献

氨茶碱对纹状体神经元吗啡反应的阻断作用:腺苷介导阿片类药物作用的证据。

Blockade of striatal neurone responses to morphine by aminophylline: evidence for adenosine mediation of opiate action.

作者信息

Perkins M N, Stone T W

出版信息

Br J Pharmacol. 1980 May;69(1):131-7. doi: 10.1111/j.1476-5381.1980.tb10892.x.

Abstract

1 The responses of cortical and striatal neurones to morphine and adenosine applied iontophoretically have been studied in the male rat. 2 The majority of cells (57%) within the corpus striatum were profoundly inhibited, and a smaller proportion (18%) excited by morphine. Adenosine depressed the firing rate of 30/44 cells in the striatum, excitation never being observed. In contrast, the responses of cortical cells to morphine were typically weak and required longer ejection pulses to effect comparable changes in firing rate. 3 Aminophylline applied iontophoretically, as an anion, proved able to antagonize reversibly both morphine and adenosine in parallel. 4 On a number of cells, gamma-aminobutyric acid (GABA) was used as a control depressant but aminophylline did not appear to reduce these responses. 5 The responses to morphine (both inhibitory and excitatory) were not easily antagonized by naloxone. Typically, excitatory reponses were easier to antagonize than the inhibitory ones. 6 It is concluded that a consequence of the interaction of morphine with its receptors may be the release of adenosine which subsequently produces the inhibition observed with morphine.

摘要
  1. 已经在雄性大鼠中研究了皮层和纹状体神经元对离子导入法施加的吗啡和腺苷的反应。2. 纹状体内的大多数细胞(57%)受到深度抑制,较小比例(18%)的细胞被吗啡兴奋。腺苷降低了纹状体中30/44个细胞的放电率,从未观察到兴奋现象。相比之下,皮层细胞对吗啡的反应通常较弱,需要更长的喷射脉冲才能在放电率上产生类似的变化。3. 离子导入法施加的氨茶碱作为阴离子,被证明能够同时可逆地拮抗吗啡和腺苷。4. 在一些细胞上,γ-氨基丁酸(GABA)被用作对照性抑制剂,但氨茶碱似乎并未降低这些反应。5. 对吗啡的反应(包括抑制性和兴奋性)不易被纳洛酮拮抗。通常,兴奋性反应比抑制性反应更容易被拮抗。6. 得出的结论是,吗啡与其受体相互作用的一个结果可能是腺苷的释放,随后腺苷产生了观察到的吗啡引起的抑制作用。

相似文献

2
Is adenosine the mediator of opiate action on neuronal firing rate?
Nature. 1979 Sep 20;281(5728):227-8. doi: 10.1038/281227a0.
3
Morphine and norepinephrine-induced antinociception at the spinal level is mediated by adenosine.
Neuroreport. 1994 Jul 21;5(12):1441-4. doi: 10.1097/00001756-199407000-00009.
4
Adenosine and opiate-like substances mediates antinociception at the spinal cord.
Brain Res. 1995 Feb 27;673(1):170-4. doi: 10.1016/0006-8993(94)01464-s.
7
Lamina-specific effects of morphine and naloxone in dorsal horn of rat spinal cord in vitro.
J Neurophysiol. 1991 Dec;66(6):1941-50. doi: 10.1152/jn.1991.66.6.1941.
10
Neuronal responses to extracellularly applied cyclic AMP:Role of the adenosine receptor.
Experientia. 1978 Apr 15;34(4):481-2. doi: 10.1007/BF01935940.

引用本文的文献

1
Theophylline does not affect morphine inhibition of the isolated vas deferens.
Br J Pharmacol. 1981 Jul;73(3):787-9. doi: 10.1111/j.1476-5381.1981.tb16816.x.
2
Theophylline inhibition of renal and cerebral nucleoside formation.
Br J Pharmacol. 1981 Jun;73(2):467-9. doi: 10.1111/j.1476-5381.1981.tb10444.x.
3
4
Antagonism of enkephalin action on acetylcholine release by methylxanthines: lack of a purine link.
Br J Pharmacol. 1983 Dec;80(4):727-34. doi: 10.1111/j.1476-5381.1983.tb10064.x.

本文引用的文献

2
Depression of corticospinal cells by various purines and pyrimidines.
Can J Physiol Pharmacol. 1974 Dec;52(6):1226-9. doi: 10.1139/y74-162.
4
5
Cyclic adenosine monophosphate antagonism of morphine analgesia.
J Pharmacol Exp Ther. 1973 May;185(2):336-46.
6
Actions of glutamic acid on spinal neurones.
Exp Brain Res. 1973 Mar 29;17(1):35-49. doi: 10.1007/BF00234562.
7
The effect of adenosine on the release of the transmitter from the phrenic nerve of the rat.
J Physiol. 1972 Aug;224(3):629-45. doi: 10.1113/jphysiol.1972.sp009916.
9
The effects of AMP on the potential of rat cerebral cortical neurones.
Can J Physiol Pharmacol. 1976 Oct;54(5):787-90. doi: 10.1139/y76-110.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验