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Occurrence of D-aspartic acid and N-methyl-D-aspartic acid in rat neuroendocrine tissues and their role in the modulation of luteinizing hormone and growth hormone release
被引:212
作者:
D'Aniello, A
Di Fiore, MM
Fisher, GH
Milone, A
Seleni, A
D'Aniello, S
Perna, AF
Ingrosso, D
机构:
[1] Staz Zool Anton Dohrn, Dept Biochem & Mol Biol & Neurobiol, I-80121 Naples, Italy
[2] Univ Naples 2, Dept Sci Vita, I-81100 Caserta, Italy
[3] Barry Univ, Dept Chem, Miami Shores, FL 33161 USA
[4] CNR, Ist Chim Mol Interesse Biol, I-80072 Arco Felice Napoli, Italy
[5] Dept Radioimmunol, Lab Igea, I-80027 Naples, Italy
[6] Univ Naples 2, Inst Nephrol, Sch Med, I-80131 Naples, Italy
[7] Univ Naples 2, Inst Biochem Macromol, Sch Med, I-80138 Naples, Italy
关键词:
D-Asp;
NMDA;
methyltransferase;
S-adenosylmethionine;
NMDA synthase;
testosterone;
progesterone;
endocrine glands;
nervous system;
D O I:
10.1096/fasebj.14.5.699
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Using two specific and sensitive fluorometric/HPLC methods and a GC-MS method, alone and in combination with D-aspartate oxidase, we have demonstrated for the first time that N-methyl-D-aspartate (NMDA), in addition to D-aspartate (D-Asp), is endogenously present as a natural molecule in rat nervous system and endocrine glands. Both of these amino acids are mostly concentrated at nmol/g levels in the adenohypophysis, hypothalamus, brain, and testis. The adenohypophysis maximally showed the ability to accumulate D-Asp when the latter is exogenously administered. In vivo experiments, consisting of the i.p. injection of D-Asp, showed that D-Asp induced both growth hormone and luteinizing hormone (LH) release. However, in vitro experiments showed that D-Asp was able to induce LH release from adenohypophysis only when this gland was co-incubated with the hypothalamus. This is because D-Asp also induces the release of GnRH from the hypothalamus, which in turn is directly responsible for the D-Asp-induced LH secretion from the pituitary gland. Compared to D-Asp, NMDA elicits its hormone release action at concentrations similar to 100-fold lower than D-Asp. D-AP5, a specific NMDA receptor antagonist, inhibited D-Asp and NMDA hormonal activity, demonstrating that these actions are mediated by NMDA receptors. NMDA is biosynthesized from D-Asp by an S-adeno- sylmethionine-dependent enzyme, which we tentatively denominated as NMDA synthase.-D'Aniello, A., Di Fiore, M. M., Fisher, G. H., Milone, A., Seleni, A., D'Aniello, S., Perna, A. F., Ingrosso, D. Occurrence of D-aspartic acid and N-methyl-D-aspartic acid in rat neuroendocrine tissues and their role in the modulation of luteinizing hormone and growth hormone release.
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页码:699 / 714
页数:16
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