首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Stimulation of rat cerebellar guanosine 35-cyclic monophosphate (cyclic GMP) levels: effects of amino acid antagonists.
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Stimulation of rat cerebellar guanosine 35-cyclic monophosphate (cyclic GMP) levels: effects of amino acid antagonists.

机译:刺激大鼠小脑鸟苷35-环一磷酸(环GMP)水平:氨基酸拮抗剂的作用。

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摘要

1 The ability of glutamate, aspartate and related neuroexcitants to produce large calcium-dependent increases in the levels of guanosine 3',5'-cyclic monophosphate (cyclic GMP) in immature rat cerebellar slices has been demonstrated. 2 These effects were inhibited by selective antagonist compounds, indicating the presence of at least two types of excitatory amino acid receptor mediating the cyclic GMP response. 3 Protoveratrine also produced large increases in cyclic GMP, and this action was antagonized by L-glutamate diethylester suggesting that released endogenous glutamate, subsequently interacting with its postsynaptic receptors, is the predominant mechanism. 4 The kinetic characteristics of several of the inhibitor compounds were investigated.
机译:1证明了谷氨酸,天冬氨酸和相关神经兴奋剂在未成熟大鼠小脑切片中产生大量的钙依赖性鸟嘌呤3',5'-环一磷酸(环GMP)水平的能力。 2这些作用被选择性拮抗剂化合物抑制,表明存在至少两种类型的介导循环GMP反应的兴奋性氨基酸受体。 3 Protoveratrine也会使环状GMP大量增加,并且该作用被L-谷氨酸二乙酯拮抗,表明释放的内源性谷氨酸随后是其与突触后受体相互作用的主要机制。 4研究了几种抑制剂化合物的动力学特性。

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