Iron supplementation prevents the development of iron deficiency in rats with omeprazole-induced hypochlorhydria

被引:5
作者
da Conceiçao, EC
Shuhama, T
Izumi, C
de Freitas, O [1 ]
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Dept Ciencias Farmaceut, BR-14049 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Dept Quim & Fis, BR-14049 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Fac Med Ribeirao Preto, Ctr Quim Prot, Ribeirao Preto, SP, Brazil
关键词
omeprazole; hypochlorhydria; iron supplementation; iron deficiency;
D O I
10.1016/S0271-5317(01)00313-X
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
Gastric acidity is an important luminal factor for non-heme iron absorption. The effect of iron supplementation (1 mg Fe/kg body weight) was studied in rats submitted to hypochlorhydria by daily oral administration of omeprazole (40 mu mol/kg). Forty (40) rats received omeprazole (experimental group) and 20 rats received vehicle (control group) for 4 weeks. At the end of this period, 10 animals from each group were sacrificed. The remaining rats in the control group continued receiving vehicle alone for 2 additional weeks. The experimental group was divided into three subgroups of 10 rats each. One subgroup received omeprazole alone, and the other subgroups received omeprazole plus iron supplementation with iron sulphate (Fe+2) or iron-peptide complex (Fe+3) for 2 additional weeks. After 4 weeks of treatment, the group that received omeprazole presented an increase of serum transferrin and a decrease of hepatic iron levels. However, only after 6 weeks did a decrease of haemoglobin occur in this subgroup. Supplementation started during the 5th week prevented the decrease of haemoglobin, improved the transferrin levels but did not cause hepatic iron to return to control levels. These results suggest that iron deficiency due to hypochlorhydria could be prevented by iron supplementation and that the two iron sources were equally efficient in this respect. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1201 / 1208
页数:8
相关论文
共 26 条
[1]  
[Anonymous], PREVENTING CONTROLLI
[2]  
ARNOLD R, 1994, ALIMENT PHARM THER, V8, P65
[3]  
CHAMPAGNE ET, 1988, J AM COLL NUTR, V7, P499
[4]  
Conrad ME, 2000, AM J HEMATOL, V64, P287, DOI 10.1002/1096-8652(200008)64:4<287::AID-AJH9>3.0.CO
[5]  
2-L
[6]   BIOCHEMICAL BASIS FOR THE MANIFESTATIONS OF IRON-DEFICIENCY [J].
DALLMAN, PR .
ANNUAL REVIEW OF NUTRITION, 1986, 6 :13-40
[7]   IRON-DEFICIENCY [J].
FINCH, CA ;
COOK, JD .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1984, 39 (03) :471-477
[8]   INHIBITION OF IRON-ABSORPTION BY OMEPRAZOLE IN RAT MODEL [J].
GOLUBOV, J ;
FLANAGAN, P ;
ADAMS, P .
DIGESTIVE DISEASES AND SCIENCES, 1991, 36 (04) :405-408
[9]   IRON, COPPER AND ZINC-METABOLISM OF RATS FED VARIOUS LEVELS AND TYPES OF TEA [J].
GREGER, JL ;
LYLE, BJ .
JOURNAL OF NUTRITION, 1988, 118 (01) :52-60
[10]  
HENRY RJ, 1974, CLIN CHEM PRINCIPLES, P1131