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对大鼠梨状前皮质中内源性腺苷的调控可调节癫痫易感性。

Manipulation of endogenous adenosine in the rat prepiriform cortex modulates seizure susceptibility.

作者信息

Zhang G, Franklin P H, Murray T F

机构信息

College of Pharmacy, Oregon State University, Corvallis.

出版信息

J Pharmacol Exp Ther. 1993 Mar;264(3):1415-24.

PMID:8450475
Abstract

A1 adenosine receptors in the rat prepiriform cortex play an important role in the inhibition of bicuculline methiodide-induced convulsions. In the present study we evaluated manipulation of endogenous adenosine in this brain area as a strategy to effect seizure suppression. All compounds evaluated were unilaterally microinjected into the rat prepiriform cortex. Administration of exogenous adenosine afforded a dose-dependent protection (ED50 = 48.1 +/- 8.4 nmol) against bicuculline methiodide-induced seizures, and these anticonvulsant effects were significantly potentiated by treatment with an adenosine kinase inhibitor, 5'-amino-5'-deoxyadenosine; by the adenosine transport blockers, dilazep or nitrobenzylthioinosine 5'-monophosphate; and by an adenosine deaminase inhibitor, 2'-deoxycoformycin. When administered alone, 5'-amino-5'-deoxyadenosine, 5'-iodotubercidin and dilazep were found to be highly efficacious as anticonvulsants with respective ED50 values of 2.6 +/- 0.8, 4.0 +/- 2.7 and 5.6 +/- 1.5 nmol. In contrast, 2'-deoxycoformycin was both less potent and less efficacious. These results suggest that accumulation of endogenous adenosine may contribute to seizure suppression, and that adenosine kinase and adenosine transport may play a pivotal role in the regulation of extracellular levels of adenosine in the central nervous system. The adenosine antagonist, 8-(p-sulfophenyl)theophylline, increased markedly the severity of bicuculline methiodide-induced seizures. Moreover, reduction of extracellular adenosine formation by a focal injection of an ecto-5'-nucleotidase inhibitor, alpha, beta-methyleneadenosine diphosphate, produced generalized seizures (ED50 = 37.3 +/- 22.7 nmol). Together the proconvulsant effect of an adenosine receptor antagonist and the convulsant action of an ecto-5'-nucleotidase inhibitor further support the role of endogenous adenosine as a tonically active antiepileptogenic substance in the rat prepiriform cortex.

摘要

大鼠梨状前皮质中的A1腺苷受体在抑制荷包牡丹碱甲碘化物诱导的惊厥中起重要作用。在本研究中,我们评估了对该脑区中内源性腺苷的调控作为一种抑制癫痫发作的策略。所有评估的化合物均单侧微量注射到大鼠梨状前皮质中。给予外源性腺苷可提供剂量依赖性保护(ED50 = 48.1 +/- 8.4 nmol)以对抗荷包牡丹碱甲碘化物诱导的癫痫发作,并且这些抗惊厥作用通过用腺苷激酶抑制剂5'-氨基-5'-脱氧腺苷、腺苷转运阻滞剂双嘧达莫或硝基苄基硫代肌苷5'-单磷酸以及腺苷脱氨酶抑制剂2'-脱氧助间型霉素处理而显著增强。单独给药时,发现5'-氨基-5'-脱氧腺苷、5'-碘杀结核菌素和双嘧达莫作为抗惊厥药具有高效性,各自的ED50值分别为2.6 +/- 0.8、4.0 +/- 2.7和5.6 +/- 1.5 nmol。相比之下,2'-脱氧助间型霉素的效力和效果均较差。这些结果表明内源性腺苷的积累可能有助于癫痫发作的抑制,并且腺苷激酶和腺苷转运可能在调节中枢神经系统中腺苷的细胞外水平方面起关键作用。腺苷拮抗剂8-(对磺基苯基)茶碱显著增加了荷包牡丹碱甲碘化物诱导的癫痫发作的严重程度。此外,通过局部注射胞外5'-核苷酸酶抑制剂α,β-亚甲基腺苷二磷酸减少细胞外腺苷的形成会产生全身性癫痫发作(ED50 = 37.3 +/- 22.7 nmol)。腺苷受体拮抗剂的促惊厥作用和胞外5'-核苷酸酶抑制剂的惊厥作用共同进一步支持了内源性腺苷在大鼠梨状前皮质中作为一种持续起作用的抗癫痫发生物质的作用。

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