• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Effects of β-citryl-L-glutamic acid and its metal ion-complex on the iron-dependent formation of free radicals

Research Project

Project/Area Number 16591776
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Ophthalmology
Research InstitutionKobe Gakuin University

Principal Investigator

MIYAKE Masaharu  Kobe Gakuin University, The Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (50093943)

Co-Investigator(Kenkyū-buntansha) HAMADA Michiko  Kobe Gakuin University, The Faculty of Pharmaceutical Sciences, Assistant Professor, 薬学部, 実験助手 (10248106)
Project Period (FY) 2004 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2006: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 2005: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2004: ¥1,400,000 (Direct Cost: ¥1,400,000)
Keywordsβ-citryl-L-glutamate, / iron / copper / competitive inhibitor, / xanthine oxidase / chelation / Feイオン依存性フリーラジカル / SOD様活性 / XOD抑制活性 / 鉄イオン依存性フリーラジカル
Research Abstract

We previously isolated a novel compound containing glutamate and citrate residue from a newborn rat brain and identified it as β-citryl-L-glutamate (β-CG). This compound appears at high concentrations (300〜600μM) during the period characterized by the growth and differentiation of neurons in developing rats, and then disappears with maturation,
Thin-layer chromatography results have shown that β-CG form a complex with ferrous ion and is also associated with calcium, magnesium, manganese, zinc, nickel, cobalt, and copper, where it has no affinity for ferric, potassium, or sodium ion. β-CG is able to solubilize iron more effectively from Fe(OH)_2 than Fe(OH)_3, and its Fe-solubilizing activities are inhibited by the presence of divalent metals in the following order, Co>Ca=Zn>Mp>Cu.
Both β-CG and deferoxamine inhibited the iron-dependent degradation of deoxyribose in a dose-dependent manner. In contrast, EDTA activated that degradation at a low concentration, and had scant effects at a hig … More her concentration. EDTA strongly inhibited bleomycin-iron-dependent damage to DNA, while both β-CG and deferoxamine showed slight stimulatory effects at low concentrations, whereas they inhibited the damage in a dose-dependent fashion at high concentrations.
Among various metal ion-complexes, only Cu-β-CG complex showed SOD activity in an assay system with xanthine-xanthine oxidase. Cu-EDTA complex also demonstrated SOD activity as did β-CG, while both Cu-and Mn-deferoxamine had strong SOD activities.
The Cu-complexes of β-CG and deferoxamine showed a concentration-dependent inhibition of xanthine oxidase, while those of glutamate and citrate also demonstrated inhibitory effects, in contrast to the Cu-complex of GHK, which showed only a weak inhibitory effect, and the complexes of EDTA and bathocuproine, which had no effect. Further, free Cu^<2+> alone was also found to inhibit xanthine oxidase. Using Lineweaver-Burk plots, the type of inhibition for Cu-β-CG and free Cu^<2+> were examined, and both compounds demonstrated competitive inhibition Less

Report

(4 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report
  • 2004 Annual Research Report

URL: 

Published: 2004-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi