Oral supplementation of gossypin during lead exposure protects alteration in heme synthesis pathway and brain oxidative stress in rats

被引:48
作者
Gautam, Pratibha [1 ]
Flora, S. J. S. [1 ]
机构
[1] Def Res & Dev Estab, Div Pharmacol & Toxicol, Gwalior 474002, India
关键词
Gossypin supplementation; Lead toxicity; Heme synthesis pathways; Blood and tissue lead concentrations; Rats; ACID; ANTIOXIDANTS;
D O I
10.1016/j.nut.2009.06.008
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Objective: The objective was to study the efficacy of oral supplementation of gossypin, a flavonoid, during lead exposure in preventive alterations in the heme synthesis pathway, brain oxidation, and tissue lead uptake in rats Methods: Male rats were used for the experiment and were exposed to lead (0 5% in drinking water) or lead plus oral supplementation of gossypin (25 or 100 mg/kg) for 3 wk to determine the preventive effect of gossypin against lead toxicity. Animals were sacrificed after 3 wk for various biochemical variables suggestive of oxidative stress and heme synthesis pathway in addition to the concentration of lead in the blood and brain Results: Exposure to lead produced significant inhibition in the activity of blood delta-aminolevulinic acid dehydratase accompanied by an increase in urinary delta-aminolevulinic acid and the levels of reactive oxygen species. There were significant alterations in the levels of glutathione, thiobarbituric acid-reactive substances, reactive oxygen species, and superoxide dismutase activity on lead exposure Most of these alterations were significantly prevented by oral coadministration of gossypin. particularly at the dose of 100 mg/kg Conclusion: The antioxidant and moderate chelating properties of oral gossypin suggest a promising role in use either as a nutritional supplement during lead exposure or as a complementary chelating agent during chelation therapy (C) 2010 Elsevier Inc All netts reserved
引用
收藏
页码:563 / 570
页数:8
相关论文
共 36 条
  • [1] Pb2+ promotes lipid oxidation and alterations in membrane physical properties
    Adonaylo, VN
    Oteiza, PI
    [J]. TOXICOLOGY, 1999, 132 (01) : 19 - 32
  • [2] Aebi H., 1984, METHOD ENZYMOL, P125
  • [3] Bechara EJ., 1993, Quim Nova, V16, P385
  • [4] BERLIN A, 1974, Z KLIN CHEM KLIN BIO, V12, P389
  • [5] Exposure to lead (Pb) and the developmental origin of oxidative DNA damage in the aging brain
    Bolin, Celeste M.
    Basha, Riyaz
    Cox, David
    Zawia, Nasser H.
    Maloney, Bryan
    Lahiri, Debomoy K.
    Cardozo-Pelaez, Fernando
    [J]. FASEB JOURNAL, 2006, 20 (02) : 788 - +
  • [6] URINARY DELTA-AMINOLEVULINIC ACID (ALA) LEVELS IN LEAD POISONING .2. CORRELATION OF ALA VALUES WITH CLINICAL FINDINGS IN 250 CHILDREN WITH SUSPECTED LEAD INGESTION
    DAVIS, JR
    ABRAHAMS, RH
    FISHBEIN, WI
    FABREGA, EA
    [J]. ARCHIVES OF ENVIRONMENTAL HEALTH, 1968, 17 (02): : 164 - +
  • [7] TISSUE SULFHYDRYL GROUPS
    ELLMAN, GL
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) : 70 - 77
  • [8] Ercal Nuran, 2001, Current Topics in Medicinal Chemistry, V1, P529, DOI 10.2174/1568026013394831
  • [9] FERNANDEZ SP, 2009, NEUROCHEM R IN PRESS
  • [10] Response of lead-induced oxidative stress and alterations in biogenic amines in different rat brain regions to combined administration of DMSA and MiADMSA
    Flora, S. J. S.
    Saxena, Geetu
    Gautam, Pratibha
    Kaur, Pushpinder
    Gill, Kiran Dip
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 2007, 170 (03) : 209 - 220