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鸟嘌呤核苷酸抑制代谢型谷氨酸受体激活诱导的环磷酸腺苷(cAMP)积累。

Guanine nucleotides inhibit cAMP accumulation induced by metabotropic glutamate receptor activation.

作者信息

Tasca C I, Cardoso L F, Martini L H, Ramírez G, Souza D O

机构信息

Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Trindade, Florianópolis, SC, Brasil.

出版信息

Neurochem Res. 1998 Feb;23(2):183-8. doi: 10.1023/a:1022480825290.

Abstract

Metabotropic glutamate receptors (mGluRs) have been shown to modulate adenylate cyclase activity via G-proteins. In the present study we report similar results to the previously observed in the literature, showing that glutamate and the metabotropic agonists, 1S,3R-ACPD or quisqualate induced cAMP accumulation in hippocampal slices of young rats. Moreover, guanine nucleotides GTP, GDP or GMP, inhibited the glutamate-induced cAMP accumulation. By measuring LDH activity in the buffer surrounding the slices, we showed that the integrity of the slices was maintained, indicating that the effect of guanine nucleotides was extracellular. GMP, GDPbeta-S or Gpp(NH)p abolished quisqualate-induced cAMP accumulation. GDPbeta-S or Gpp(NH)p but not GMP inhibited 1S,3R-ACPD-induced cAMP accumulation. The response evoked by glutamate was also abolished by the mGluR antagonists: L-AP3 abolished glutamate-induced cAMP accumulation in a dose-dependent manner and MCPG was effective only at the 2 mM dose. DNQX was ineffective. We are reporting here, an inhibition induced by guanine nucleotides, via an extracellular site (s), similar to the observed with classical glutamate antagonists on a cellular response evoked by mGluR agonists.

摘要

代谢型谷氨酸受体(mGluRs)已被证明可通过G蛋白调节腺苷酸环化酶活性。在本研究中,我们报告了与先前文献中观察到的相似结果,表明谷氨酸以及代谢型激动剂1S,3R-ACPD或喹啉酸可诱导幼鼠海马切片中cAMP积累。此外,鸟嘌呤核苷酸GTP、GDP或GMP可抑制谷氨酸诱导的cAMP积累。通过测量切片周围缓冲液中的乳酸脱氢酶(LDH)活性,我们表明切片的完整性得以维持,这表明鸟嘌呤核苷酸的作用是细胞外的。GMP、GDPβ-S或Gpp(NH)p可消除喹啉酸诱导的cAMP积累。GDPβ-S或Gpp(NH)p而非GMP可抑制1S,3R-ACPD诱导的cAMP积累。mGluR拮抗剂也可消除谷氨酸引发的反应:L-AP3以剂量依赖性方式消除谷氨酸诱导的cAMP积累,而MCPG仅在2 mM剂量时有效。DNQX无效。我们在此报告,鸟嘌呤核苷酸通过细胞外位点诱导的抑制作用,类似于经典谷氨酸拮抗剂对mGluR激动剂引发的细胞反应所观察到的抑制作用。

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