EXPRESSION OF PLASMA-MEMBRANE CALCIUM-PUMP MESSENGER-RNA IN RAT INTESTINE - EFFECT OF AGE AND 1,25-DIHYDROXYVITAMIN-D

被引:31
作者
ARMBRECHT, HJ
BOLTZ, MA
WONGSURAWAT, N
机构
[1] ST LOUIS UNIV,SCH MED,DEPT MED,ST LOUIS,MO 63125
[2] ST LOUIS UNIV,SCH MED,DEPT BIOCHEM,ST LOUIS,MO 63125
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1994年 / 1195卷 / 01期
关键词
CALCIUM PUMP; INTESTINE; AGE; 1,25-DIHYDROXYVITAMIN D; (RAT);
D O I
10.1016/0005-2736(94)90016-7
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
The capacity of the small intestine to actively transport Ca declines markedly with increasing age in the rat. The basal-lateral plasma membrane Ca pump is thought to be an important component of the active transport mechanism. Therefore, the purpose of this study was to determine if there are changes in the expression of the intestinal Ca pump with age, mRNA levels were quantitated by Northern and dot blot analysis using a cDNA probe based on the sequence of the plasma membrane Ca pump expressed in the rat intestine (PMCA1). In the duodenum, Ca pump mRNA levels were 3-4-times higher in young (2 months) rats compared to adult (12 months) and old (27 months) rats. In the ileum, Ca pump mRNA Levels were one third those of the duodenum, and ileal levels were higher in young rats compared to adult rats. These changes in mRNA levels with age and segment were significantly correlated with Ca pump activity as measured in basal-lateral membrane vesicles in vitro. To determine intestinal responsiveness to 1,25(OH)(2)D, rats were fed a strontium diet to induce vitamin D deficiency. In young animals, 1,25(OH)(2)D significantly increased Ca pump mRNA levels 4-fold in the duodenum. 1,25(OH)(2)D had a similar effect in the adult duodenum. These studies demonstrate that there are changes in Ca pump mRNA levels with age and intestinal segment. Since there was no change in the capacity of 1,25(OH)(2)D to increase Ca pump mRNA levels, the decline in Ca pump expression may be due to the age-related decrease in serum 1,25(OH)(2)D rather than to decreased responsiveness to 1,25(OH)(2)D.
引用
收藏
页码:110 / 114
页数:5
相关论文
共 21 条
[1]  
ALEVIZAKI CC, 1973, J NUCL MED, V14, P760
[2]   MODIFICATION OF ATP-DEPENDENT CA-2+ TRANSPORT IN RAT PAROTID BASOLATERAL MEMBRANES DURING AGING [J].
AMBUDKAR, IS ;
KUYATT, BL ;
ROTH, GS ;
BAUM, BJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1988, 43 (01) :45-60
[3]   EFFECT OF AGE ON INTESTINAL CALCIUM-ABSORPTION AND ADAPTATION TO DIETARY CALCIUM [J].
ARMBRECHT, HJ ;
ZENSER, TV ;
BRUNS, MEH ;
DAVIS, BB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1979, 236 (06) :E769-E774
[4]   EXPRESSION OF CALBINDIN-D DECREASES WITH AGE IN INTESTINE AND KIDNEY [J].
ARMBRECHT, HJ ;
BOLTZ, M ;
STRONG, R ;
RICHARDSON, A ;
BRUNS, MEH ;
CHRISTAKOS, S .
ENDOCRINOLOGY, 1989, 125 (06) :2950-2956
[5]   CALCIUM-TRANSPORT BY BASAL LATERAL MEMBRANE-VESICLES FROM RAT SMALL-INTESTINE DECREASES WITH AGE [J].
ARMBRECHT, HJ ;
DOUBEK, WG ;
PORTER, SB .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 944 (03) :367-373
[6]   EFFECT OF 1,25-DIHYDROXYVITAMIN D3 ON INTESTINAL CALCIUM-ABSORPTION IN STRONTIUM-FED RATS [J].
ARMBRECHT, HJ ;
WASSERMAN, RH ;
BRUNS, MEH .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1979, 192 (02) :466-473
[7]   AGE-RELATED-CHANGES IN CALCIUM AND PHOSPHORUS UPTAKE BY RAT SMALL-INTESTINE [J].
ARMBRECHT, HJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 882 (03) :281-286
[8]   ADAPTATION TO DIETARY CALCIUM AND PHOSPHORUS RESTRICTION CHANGES WITH AGE IN THE RAT [J].
ARMBRECHT, HJ ;
ZENSER, TV ;
GROSS, CJ ;
DAVIS, BB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1980, 239 (05) :E322-E327
[9]   EFFECT OF VITAMIN-D METABOLITES ON INTESTINAL CALCIUM-ABSORPTION AND CALCIUM-BINDING PROTEIN IN YOUNG AND ADULT-RATS [J].
ARMBRECHT, HJ ;
ZENSER, TV ;
DAVIS, BB .
ENDOCRINOLOGY, 1980, 106 (02) :469-475
[10]   VITAMIN-D AND ADAPTATION TO DIETARY CALCIUM AND PHOSPHATE DEFICIENCIES INCREASE INTESTINAL PLASMA-MEMBRANE CALCIUM-PUMP GENE-EXPRESSION [J].
CAI, Q ;
CHANDLER, JS ;
WASSERMAN, RH ;
KUMAR, R ;
PENNISTON, JT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (04) :1345-1349