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Free Iron, Estrogen and Postmenopausal Osteoporosis

Free Iron, Estrogen and Postmenopausal Osteoporosis
游离铁、雌激素和绝经后骨质疏松症
批准号:
6547330
负责人:
GANG LIU
金额:
$7.5万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-01 至 2004-08-31

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中文摘要
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英文摘要
The goal of this study is to test the hypothesis that loss of estrogen results in loss of control of the levels of free iron in bone which are powerful catalysts for free radical formation, and thus cause oxidative damage. This results in the development of osteoporosis in man postmenopausal women as well as the development of osteopenia in ovariectomized (ovx) adult female rats. To do this, an ovx rat model will be used. Six month old rats will be ovariectomized, followed by a two month period for osteopenia to develop. They will then be treated for three months with (1) estrogen, (2) iron chelator or (3) a combination of estrogen and iron chelator. The animals will be sacrificed at the end of the treatment period and their free iron and mineral levels will be determined by electron paramagnetic (EPR) and x-ray absorptiometry (pDEXA and pOct) respectively. The iron chelator used will be one which has been developed in our laboratory and has been shown to have the ability to efficiently remove heavy metals from bone. The EPR techniques which we will use were also developed in our laboratory. We believe that this small but important project will provide novel insights into the mechanism by which loss of estrogens results in the development of osteoporosis. Moreover, this new approach will permit the reevaluation of the role of estrogen and will expedite the development of novel pharmaceutical agents for the prevention or treatment of osteoporosis.
期刊论文(3)
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科研奖励(0)
会议论文
Variation of long-lived free radicals responsible for the EPR native signal in bone of aged or diseased human females and ovariectomized adult rats.
负责老年或患病人类女性和卵巢切除成年大鼠骨骼中 EPR 天然信号的长寿命自由基的变化。
DOI: 10.1016/j.radmeas.2004.01.040
发表时间: 2005
期刊: Radiation measurements.
影响因子: --
作者: [Kenner,GH, Brik,AB, Liu,G, Haskell,EH, Hayes,RB, Knight,JA, Vajda,EG, Miller,SC, Jee,WSS, Barrus,JK]
通讯作者: Barrus,JK
Acyclonucleoside iron chelators of 1-(2-hydroxyethoxy)methyl-2-alkyl-3-hydroxy-4-pyridinones: potential oral iron chelation therapeutics.
1-(2-羟基乙氧基)甲基-2-烷基-3-羟基-4-吡啶酮的无环核苷铁螯合剂:潜在的口服铁螯合疗法。
DOI: 10.1081/ncn-120030718
发表时间: 2004
期刊: Nucleosides, nucleotides & nucleic acids.
影响因子: --
作者: [Liu,Gang, Men,Ping, Kenner,GerryH, Miller,ScottC, Bruenger,FredW]
通讯作者: Bruenger,FredW
Developing novel therapeutic approaches for osteopenia and osteoporosis in patients with sickle cell disease
  • 批准号:
    9976289
  • 项目类别:
  • 资助金额:
    $24.85万
  • 财政年份:
    2020
  • 负责人:
    GANG LIU
  • 依托单位:
A therapeutic approach for potential prevention of aromatase inhibitor-induced bone loss
  • 批准号:
    9621018
  • 项目类别:
  • 资助金额:
    $22.3万
  • 财政年份:
    2018
  • 负责人:
    GANG LIU
  • 依托单位:
NOVEL THERAPEUTICS FOR POSTMENOPAUSAL OSTEOPOROSIS
  • 批准号:
    8251439
  • 项目类别:
  • 资助金额:
    $18.77万
  • 财政年份:
    2012
  • 负责人:
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  • 依托单位:
Nanoparticle Brain Delivery of Iron Chelators for AD
  • 批准号:
    7588011
  • 项目类别:
  • 资助金额:
    $32.92万
  • 财政年份:
    2007
  • 负责人:
    GANG LIU
  • 依托单位:
海外基金