Regner A, Ramirez G, Belló-Klein A, Souza D
Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Neurochem Res. 1998 Apr;23(4):519-24. doi: 10.1023/a:1022430501454.
Glutamate significantly increased levels of spontaneous chemiluminescence (CL) in rat hippocampal slices incubated under hypoxic conditions. Although it has been previously shown that guanine nucleotides (GN) displace glutamate from several of its receptors, in our study only GMP, as well as the glutamate antagonist MK-801, was able to reverse the increase in CL provoked by glutamate. On the other hand, not only GTP or Gpp(NH)p failed to reverse the action of glutamate, but they increased CL production like glutamate. This effect of GTP/Gpp(NH)p was also reversed by GMP. We concluded that, under neurotoxic conditions, GMP acted as an antagonist and GTP or Gpp(NH)p acted as agonists of glutamate. These results reinforced the evidence of the existence of extracellular site(s) for GN and indicated a possible role for GN in excitotoxicity.
谷氨酸显著增加了在缺氧条件下孵育的大鼠海马切片中的自发化学发光(CL)水平。尽管先前已经表明鸟嘌呤核苷酸(GN)可从其几种受体上取代谷氨酸,但在我们的研究中,只有鸟苷酸(GMP)以及谷氨酸拮抗剂MK-801能够逆转谷氨酸引起的CL增加。另一方面,不仅三磷酸鸟苷(GTP)或鸟苷5′-三磷酸(Gpp(NH)p)未能逆转谷氨酸的作用,而且它们像谷氨酸一样增加了CL的产生。GTP/Gpp(NH)p的这种作用也被GMP逆转。我们得出结论,在神经毒性条件下,GMP作为拮抗剂起作用,而GTP或Gpp(NH)p作为谷氨酸的激动剂起作用。这些结果进一步证明了GN存在细胞外位点,并表明GN在兴奋性毒性中可能发挥作用。