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典型的腺苷A(2A)受体激动剂CGS 21680与腺苷A(1)和A(2A)受体基因敲除小鼠大脑皮层的结合。

Binding of the prototypical adenosine A(2A) receptor agonist CGS 21680 to the cerebral cortex of adenosine A(1) and A(2A) receptor knockout mice.

作者信息

Lopes Luísa V, Halldner Linda, Rebola Nelson, Johansson Björn, Ledent Catherine, Chen Jian Fan, Fredholm Bertil B, Cunha Rodrigo A

机构信息

Laboratory of Neurosciences, Faculty of Medicine, University of Lisbon, Portugal.

出版信息

Br J Pharmacol. 2004 Mar;141(6):1006-14. doi: 10.1038/sj.bjp.0705692. Epub 2004 Mar 1.

Abstract
  1. 2-p-(2-carboxyethylphenethylamino-5'-ethylcarboxamidoadenosine) (CGS 21680) is considered the reference compound to study adenosine A(2A) receptors. However, CGS 21680 binding in the cerebral cortex, where adenosine A(1) receptors are predominant, displays a mixed A(2A)/A(1) receptor pharmacology. We now use adenosine A(1) and A(2A) receptor knockout mice to investigate the characteristics of cortical [(3)H]CGS 21680 binding. 2. [(3)H]CGS 21680 binding to the cerebral cortex was strongly reduced in adenosine A(1) receptor knockout mice, but only slightly reduced in A(2A) receptor knockout mice compared with the corresponding wild-type littermates. 3. Another selective A(2A) receptor ligand, [(3)H]-5-amino-7-(2-phenylethyl)-2-(2-furyl)-pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine ([(3)H]SCH 58261), displayed a saturable binding to mouse cortical membranes, albeit with a binding density 20 times lower than that of striatal membranes, and this [(3)H]SCH58261 binding was abolished in both striatal and cortical membranes of A(2A) receptor knockout mice and unchanged in A(1) receptor knockout mice. 4. The presence of A(2A) receptors in cortical neurons was further confirmed by Western blot in mouse cortical nerve terminal membranes. 5. It is concluded that, although A(2A) receptors are present in the cerebral cortex, the purportedly selective A(2A) receptor agonist [(3)H]CGS 21680 binds in the cerebral cortex to an entity that requires the presence of adenosine A(1) receptors. Thus, CGS 21680 should be used with care in all preparations where adenosine A(1) receptors out-number A(2A) receptors.
摘要
  1. 2 - 对 -(2 - 羧乙基苯乙氨基 - 5'- 乙基甲酰胺基腺苷)(CGS 21680)被视为研究腺苷A(2A)受体的参考化合物。然而,在腺苷A(1)受体占主导的大脑皮层中,CGS 21680的结合表现出A(2A)/A(1)受体的混合药理学特性。我们现在使用腺苷A(1)和A(2A)受体基因敲除小鼠来研究皮层中[(3)H]CGS 21680结合的特性。2. 与相应的野生型同窝小鼠相比,[(3)H]CGS 21680与大脑皮层的结合在腺苷A(1)受体基因敲除小鼠中显著降低,但在A(2A)受体基因敲除小鼠中仅略有降低。3. 另一种选择性A(2A)受体配体,[(3)H]-5 - 氨基 - 7 -(2 - 苯乙基)- 2 -(2 - 呋喃基)- 吡唑并[4,3 - e]-1,2,4 - 三唑并[1,5 - c]嘧啶([(3)H]SCH 58261),与小鼠皮层膜呈现出可饱和的结合,尽管其结合密度比纹状体膜低20倍,并且这种[(3)H]SCH58261结合在A(2A)受体基因敲除小鼠的纹状体和皮层膜中均被消除,而在A(1)受体基因敲除小鼠中保持不变。4. 通过蛋白质印迹法在小鼠皮层神经末梢膜中进一步证实了皮层神经元中存在A(2A)受体。5. 得出的结论是,尽管大脑皮层中存在A(2A)受体,但所谓的选择性A(2A)受体激动剂[(3)H]CGS 21680在大脑皮层中与一种需要腺苷A(1)受体存在的实体结合。因此,在腺苷A(1)受体数量超过A(2A)受体的所有制剂中,应谨慎使用CGS 21680。

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