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Research Article Free access | 10.1172/JCI114700

Progressive increases in luminal glucose stimulate proximal sodium absorption in normal and diabetic rats.

N Bank and H S Aynedjian

Department of Medicine, Montefiore Medical Center, Bronx, New York 10467.

Find articles by Bank, N. in: PubMed | Google Scholar

Department of Medicine, Montefiore Medical Center, Bronx, New York 10467.

Find articles by Aynedjian, H. in: PubMed | Google Scholar

Published July 1, 1990 - More info

Published in Volume 86, Issue 1 on July 1, 1990
J Clin Invest. 1990;86(1):309–316. https://doi.org/10.1172/JCI114700.
© 1990 The American Society for Clinical Investigation
Published July 1, 1990 - Version history
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Abstract

The effect of progressive increases in intraluminal glucose concentration on proximal tubule sodium absorption was studied in normal and streptozotocin diabetic rats by microperfusion. Each tubule was perfused twice, with and without glucose added to the perfusion fluid. Net sodium and water absorption were markedly enhanced by 300-500 mg% intraluminal glucose in both normal and diabetic rats. Substituting the transported but nonmetabolized glucose analogue, alpha-methyl D-glucoside for glucose also resulted in marked stimulation of sodium absorption, whereas substituting bicarbonate and acetate for chloride in the perfusion solution inhibited the effect of glucose. These observations suggest that the stimulation of sodium absorption by glucose was mediated by the brush border Na/glucose cotransporter. Sodium concentration and osmolality were found to fall markedly to hypotonic levels when high glucose concentrations were in the perfusion fluid. This luminal hypotonicity may be an important driving force for proximal fluid absorption. In poorly controlled diabetes, high filtered glucose concentrations may lead to enhanced proximal sodium and water absorption, which could in turn contribute to volume expansion, hypertension, and renal hypertrophy.

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