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大鼠大脑皮层切片中的腺苷和环磷酸腺苷:腺苷摄取抑制剂和腺苷脱氨酶抑制剂的作用

Adenosine and cyclic AMP in rat cerebral cortical slices: effects of adenosine uptake inhibitors and adenosine deaminase inhibitors.

作者信息

Nimit Y, Skolnick P, Daly J W

出版信息

J Neurochem. 1981 Mar;36(3):908-12. doi: 10.1111/j.1471-4159.1981.tb01680.x.

DOI:10.1111/j.1471-4159.1981.tb01680.x
PMID:6259294
Abstract

The endogenous levels of adenosine functionally linked to cyclic AMP systems in rat cerebral cortical slices are regulated by both adenosine deaminase and adenosine uptake systems. 2'-Deoxycoformycin (2'-DCF), an adenosine deaminase inhibitor, slightly increased basal, adenosine, and norepinephrine-elicited accumulations of cyclic AMP, whereas dipyridamole, an uptake inhibitor, had an even greater effect on cyclic AMP accumulations under the same conditions. Combinations of 2'-DCF and dipyridamole elicited a greater effect than either compound alone. Neither 2'-DCF nor dipyridamole significantly augmented accumulations of cyclic AP elicited by a depolarizing agent, veratridine, suggesting that the adenosine "released" during neuronal depolarization of brain slices is not as subject to inactivation by uptake or deamination as endogenous adenosine in control brain slices. The accumulation of cyclic AMP elicited by a combination of norepinephrine and veratridine was greater than additive. The response to a pure beta-adrenergic agonist, isoproterenol, was not potentiated by 2'-DCF, dipyridamole, or veratridine, consonant with minimal interaction of endogenous adenosine with beta-adrenergic systems.

摘要

与大鼠大脑皮层切片中环磷酸腺苷(cAMP)系统功能相关的内源性腺苷水平受腺苷脱氨酶和腺苷摄取系统的调节。腺苷脱氨酶抑制剂2'-脱氧助间型霉素(2'-DCF)略微增加了基础状态下、腺苷以及去甲肾上腺素引发的cAMP积累,而摄取抑制剂双嘧达莫在相同条件下对cAMP积累的影响更大。2'-DCF和双嘧达莫联合使用产生的效果比单独使用任一化合物都要大。2'-DCF和双嘧达莫均未显著增强由去极化剂藜芦定引发的环磷腺苷(cyclic AP)积累,这表明在脑片神经元去极化过程中“释放”的腺苷不像对照脑片中的内源性腺苷那样容易受到摄取或脱氨作用的失活影响。去甲肾上腺素和藜芦定联合引发的cAMP积累大于两者相加的效果。对纯β-肾上腺素能激动剂异丙肾上腺素的反应未被2'-DCF、双嘧达莫或藜芦定增强,这与内源性腺苷与β-肾上腺素能系统的相互作用最小一致。

相似文献

1
Adenosine and cyclic AMP in rat cerebral cortical slices: effects of adenosine uptake inhibitors and adenosine deaminase inhibitors.大鼠大脑皮层切片中的腺苷和环磷酸腺苷:腺苷摄取抑制剂和腺苷脱氨酶抑制剂的作用
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Biochem Pharmacol. 1980 Feb;29(2):187-93. doi: 10.1016/0006-2952(80)90327-5.

引用本文的文献

1
The anticonvulsant BW534U87 depresses epileptiform activity in rat hippocampal slices by an adenosine-dependent mechanism and through inhibition of voltage-gated Na+ channels.抗惊厥药物BW534U87通过腺苷依赖性机制并通过抑制电压门控性钠通道来抑制大鼠海马切片中的癫痫样活动。
Br J Pharmacol. 1999 Nov;128(5):1011-20. doi: 10.1038/sj.bjp.0702881.
2
The ionic basis of adenosine receptor actions on post-ganglionic neurones in the rat.腺苷受体对大鼠节后神经元作用的离子基础。
J Physiol. 1983 Mar;336:607-20. doi: 10.1113/jphysiol.1983.sp014600.
3
Effects of deoxyadenosine on the activation of ADA inhibited T & B cells.
脱氧腺苷对腺苷脱氨酶抑制的T细胞和B细胞激活的影响。
Clin Exp Immunol. 1982 Dec;50(3):587-95.
4
Endogenous adenosine as a modulator of hippocampal acetylcholine release.内源性腺苷作为海马乙酰胆碱释放的调节剂。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Oct;327(4):319-25. doi: 10.1007/BF00506243.
5
Similarities of adenosine uptake systems in astrocytes and neurons in primary cultures.原代培养的星形胶质细胞和神经元中腺苷摄取系统的相似性。
Neurochem Res. 1986 Nov;11(11):1507-24. doi: 10.1007/BF00965770.
6
Presynaptic P1-purinoceptors in jejunal branches of the rabbit mesenteric artery and their possible function.兔肠系膜动脉空肠支中的突触前P1嘌呤受体及其可能的功能。
J Physiol. 1988 Mar;397:13-29. doi: 10.1113/jphysiol.1988.sp016985.
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On the role, inactivation and origin of endogenous adenosine at the frog neuromuscular junction.关于内源性腺苷在青蛙神经肌肉接头处的作用、失活及来源
J Physiol. 1987 Mar;384:571-85. doi: 10.1113/jphysiol.1987.sp016470.
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On the adenosine receptor and adenosine inactivation at the rat diaphragm neuromuscular junction.关于大鼠膈肌神经肌肉接头处的腺苷受体及腺苷失活
Br J Pharmacol. 1988 May;94(1):109-20. doi: 10.1111/j.1476-5381.1988.tb11505.x.