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FRUCTOSE REABSORPTION BY RAT PROXIMAL TUBULES: ROLE OF SODIUM-LINKED COTRANSPORTERS AND THE EFFECT OF DIETARY FRUCTOSE.

07:00 EST 19th December 2018 | BioPortfolio

Summary of "FRUCTOSE REABSORPTION BY RAT PROXIMAL TUBULES: ROLE OF SODIUM-LINKED COTRANSPORTERS AND THE EFFECT OF DIETARY FRUCTOSE."

Fructose consumption has increased due to widespread use of high-fructose corn syrup by the food industry. Renal proximal tubules are thought to reabsorb fructose. However, fructose reabsorption (J) by proximal tubules has not yet been directly demonstrated, nor the effects of dietary fructose on J. This segment express sodium-glucose linked transporters (SGLTs) 1, 2, 4 and 5, and glucose transporters (GLUTs) 2 and 5. SGLT4 and 5 transport fructose but SGLT1 and 2 don't. Knocking out SGLT5 increases urinary fructose excretion. We hypothesize that J in the S2 portion of the proximal tubule is mediated by luminal entry via SGLT4/5 and basolateral exit by GLUT2, and that it is enhanced by a fructose-enriched diet. We measured J by proximal straight tubules from rats consuming either tap water (Controls) or 20% fructose (FRU). Basal J in Controls was 14.1±1.5 pmol/mm/min. SGLT inhibition with phlorizin reduced J to 4.9±1.4 pmol/mm/min ( p<0.008), while removal of Na diminished J by 86±5% (p<0.0001). A fructose-enriched diet increased J from 12.8 ± 2.5 to 19.3±0.5 pmol/mm/min, 51% increase ( p<0.03). Using immunofluorescence, we detected luminal SGLT4 and SGLT5 and basolateral GLUT2; GLUT5 was undetectable. The expression of apical transporters SGLT4 and SGLT5 was higher in FRU than in Controls; 137±10% ( p<0.01) and 38±14% ( p<0.04) respectively. GLUT2 was also elevated by 88±27% ( p<0.02) in FRU. We conclude that J by proximal tubules occurs primarily via sodium-linked cotransport processes and a fructose-enriched diet enhances reabsorption. Transport across luminal and basolateral membranes is likely mediated by SGLT4/5 and GLUT2, respectively.

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Name: American journal of physiology. Renal physiology
ISSN: 1522-1466
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Medical and Biotech [MESH] Definitions

An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.

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A sodium-hydrogen antiporter expressed primarily by EPITHELIAL CELLS in the kidneys, it localizes to the apical membrane of the PROXIMAL KIDNEY TUBULE, where it functions in sodium and water reabsorption and possibly calcium homeostasis. It also is expressed in heart, brain, and lung tissues and is resistant to AMILORIDE inhibition.

A non-electrogenic sodium-dependent phosphate transporter. It is found primarily in apical membranes of PROXIMAL RENAL TUBULES.

An electrogenic sodium-dependent phosphate transporter. It is present primarily in BRUSH BORDER membranes of PROXIMAL RENAL TUBULES.

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