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腺苷与甲基黄嘌呤对中枢嘌呤能系统的行为相互作用。

Behavioral interaction of adenosine and methylxanthines on central purinergic systems.

作者信息

Coffin V L, Taylor J A, Phillis J W, Altman H J, Barraco R A

出版信息

Neurosci Lett. 1984 Jun 15;47(2):91-8. doi: 10.1016/0304-3940(84)90412-9.

Abstract

Mice implanted with chronic indwelling cannulae were injected in the lateral cerebral ventricle with adenosine (ADO); an adenosine analogue, 5'-N-ethylcarboxamidoadenosine (NECA); a potent adenosine uptake inhibitor, papaverine (PAP); and a methylxanthine, 3-isobutyl-1-methylxanthine (IBMX). All drugs produced dose-related decreases in spontaneous locomotor activity and the order of potency for locomotor depression was: NECA much greater than IBMX greater than ADO, PAP. Further, the behavioral interaction of i.p. injections of caffeine with drug-induced locomotor depression was examined at a dose of caffeine which had no effect on locomotor activity when given alone. Caffeine antagonized the depressant effects of NECA at all doses. However, doses of IBMX producing only behavioral depression, in combination with caffeine, elicited pronounced behavioral stimulation. At higher doses of ADO and PAP, caffeine antagonized their depressant effects whereas at the lower doses of ADO and PAP in combination with caffeine there was behavioral stimulation. These results suggest there is a complex behavioral interaction between methylxanthines and central purinergic systems.

摘要

给植入慢性留置套管的小鼠侧脑室注射腺苷(ADO);一种腺苷类似物,5'-N-乙基羧酰胺腺苷(NECA);一种强效腺苷摄取抑制剂,罂粟碱(PAP);以及一种甲基黄嘌呤,3-异丁基-1-甲基黄嘌呤(IBMX)。所有药物均使自发运动活动呈剂量依赖性降低,运动抑制的效力顺序为:NECA远大于IBMX大于ADO、PAP。此外,在单独给药时对运动活动无影响的咖啡因剂量下,研究了腹腔注射咖啡因与药物诱导的运动抑制之间的行为相互作用。咖啡因在所有剂量下均拮抗NECA的抑制作用。然而,仅产生行为抑制的IBMX剂量与咖啡因联合使用时,会引起明显的行为兴奋。在较高剂量的ADO和PAP时,咖啡因拮抗它们的抑制作用,而在较低剂量的ADO和PAP与咖啡因联合使用时,则出现行为兴奋。这些结果表明甲基黄嘌呤与中枢嘌呤能系统之间存在复杂的行为相互作用。

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