Changes in sodium or glucose filtration rate modulate expression of glucose transporters in renal proximal tubular cells of rat

被引:164
作者
Vestri, S
Okamoto, MM
de Freitas, HS
dos Santos, RA
Nunes, MT
Morimatsu, M
Heimann, JC
Machado, UF [1 ]
机构
[1] Univ Sao Paulo, Dept Phys & Biophys, Inst Biomed Sci, Sao Paulo, Brazil
[2] Hokkaido Univ, Sch Vet Med, Dept Biomed Sci, Sapporo, Hokkaido, Japan
[3] Univ Sao Paulo, Sch Med, Dept Nephrol, Sao Paulo, Brazil
关键词
SGLT2; SGLT1; GLUT2; GLUT1; rat kidney;
D O I
10.1007/s00232-001-0036-y
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
Renal glucose reabsorption is mediated by luminal sodium-glucose cotransporters (SGLTs) and basolateral facilitative glucose transporters (GLUTs). The modulators of these transporters are not known, and their substrates glucose and Na+ are potential candidates. In this study we examined the role of glucose and Na+ filtration rate on gene expression of glucose transporters in renal proximal tubule. SGLT1, SGLT2, GLUT1 and GLUT2 mRNAs were assessed by Northern blotting; and GLUT1 and GLUT2 proteins were assessed by Western blotting. Renal cortex and medulla samples from control rats (C), diabetic rats (D) with glycosuria, and insulin-resistant 15-month old rats (I) without glycosuria; and from normal (NS), low (LS), and high (HS) Na+-diet fed rats were studied. Compared to C and I rats, D rats increased (P < 0.05) gene expression of SGLT2 by similar to 36%, SGLT1 by similar to 20%, and GLUT2 by similar to 100%, and reduced (P < 0.05) gene expression of GLUT1 by more than 50%. Compared to NS rats, HS rats increased (P < 0.05) SCLT2, GLUT2, and GLUT1 expression by <similar to>100%. with no change in SGLT1 mRNA expression, and LS rats increased (P < 0.05) GLUT1 gene expression by <similar to>150% with no changes in other transporters. In summary, the results showed that changes in glucose or Na+ filtrated rate modulate the glucose transporters gene expression in epithelial cells of the renal proximal tubule.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 23 条
[11]  
Hoffman B B, 1995, Curr Opin Nephrol Hypertens, V4, P406, DOI 10.1097/00041552-199509000-00006
[12]   OBESITY IS THE MAJOR CAUSE OF ALTERATIONS IN INSULIN-SECRETION AND CALCIUM FLUXES BY ISOLATED ISLETS FROM AGED RATS [J].
MACHADO, UF ;
NOGUEIRA, CR ;
CARPINELLI, AR .
PHYSIOLOGY & BEHAVIOR, 1992, 52 (04) :717-721
[13]   REDUCED CONTENT AND PRESERVED TRANSLOCATION OF GLUCOSE-TRANSPORTER (GLUT-4) IN WHITE ADIPOSE-TISSUE OF OBESE MICE [J].
MACHADO, UF ;
SHIMIZU, I ;
SAITO, M .
PHYSIOLOGY & BEHAVIOR, 1994, 55 (04) :621-625
[14]  
NATH KA, 1992, AM J KIDNEY DIS, V20, P1
[15]   STRUCTURE AND FUNCTION CHANGES IN THE ENDOCRINE PANCREAS OF AGING RATS WITH REFERENCE TO THE MODULATING EFFECTS OF EXERCISE AND CALORIC RESTRICTION [J].
REAVEN, EP ;
REAVEN, GM .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (01) :75-84
[16]   The kidney: An unwilling accomplice in syndrome X [J].
Reaven, GM .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1997, 30 (06) :928-931
[17]   EFFECT OF DIETARY-SODIUM CHLORIDE ON INSULIN-RECEPTOR NUMBER AND MESSENGER-RNA LEVELS IN RAT-KIDNEY [J].
SECHI, LA ;
GRIFFIN, CA ;
SCHAMBELAN, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (01) :F31-F38
[18]   Regulation of glomerular and proximal tubule renin mRNA by chronic changes in dietary NaCl [J].
Tank, JE ;
Henrich, WL ;
Moe, OW .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 273 (06) :F892-F898
[19]  
Vestri S, 1998, BRAZ ARCH BIOL TECHN, V41, P194
[20]  
Wright EM, 1997, J EXP BIOL, V200, P287