Renal Potassium Handling in Aging Rats
Aging is often related to electrolyte disorders. This study was designed to evaluate the renal capacity for K + handling of aging rats submitted to both extreme situations of K + depletion and K + loading. Aging rats were submitted to metabolic assessment, measurement of plasma aldosterone and deter...
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Veröffentlicht in: | Kidney & blood pressure research 1998-01, Vol.21 (6), p.425-431 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aging is often related to electrolyte disorders. This study was designed to evaluate the renal capacity for K + handling of aging rats submitted to both extreme situations of K + depletion and K + loading. Aging rats were submitted to metabolic assessment, measurement of plasma aldosterone and determination of Na + ,K + –ATPase and H + ,K + –ATPase activity in the inner medullary collecting duct (IMCD). During K + depletion, aging rats showed low values of urine K + excretion. After 2 weeks of dietary K + restriction, the plasma K + levels of these animals reached 2.9±0.1 mEq/l without acid–base disorders. During K + loading, aging rats showed a significant increase in urinary K + excretion, with plasma K + remaining at normal levels (4.7±0.1 mEq/l). Plasma aldosterone levels were low in control aging rats but K + intake modulated the levels of this hormone, with K + depletion reducing it and K + loading significantly increasing it. Na + ,K + –ATPase activity increased only in the initial portion of the IMCD of aging rats after 2 weeks of K + depletion. In the distal portion of the IMCD, Na + ,K + –ATPase activity did not change. H + ,K + –ATPase remained unchanged in both the proximal and distal portions of the IMCD of aging rats. During K + loading, there was no change in Na + ,K + –ATPase or H + ,K + –ATPase activity in the proximal or distal portions of the IMCD of aging rats. This study suggests that the senescent kidney responded to K + conservation and excretion under the two extremes of low and high K + intake. |
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ISSN: | 1420-4096 1423-0143 |
DOI: | 10.1159/000025895 |