Affiliation:
1. Departments of Medicine, and Clinical Biochemistry and Metabolic Medicine, Royal Victoria Infirmary and University of Newcastle upon Tyne, U.K.
Abstract
1. The role of the large intestine in the maintenance of K+ balance in uraemic patients established on long-term dialysis was studied with a rectal dialysis technique in 14 normal subjects, ten normokalaemic patients undergoing chronic ambulatory peritoneal dialysis (CAPD), and seven patients undergoing haemodialysis. Dietary K+ intakes in the normal subjects, CAPD patients and haemodialysis patients were 80–100 mmol/24 h, 70–80 mmol/24 h and 60–70 mmol/24 h, respectively.
2. At an initial intraluminal K+ concentration of 45 mmol/l, rectal K+ secretion in the CAPD patients (2.4 ± 0.4 μmol h−-1cm−-2) was greater than in normal subjects (1.2 ± 0.2 μmol h−-1 cm−-2, P < 0.02). Under similar conditions, rectal K+ secretion was also greater in the haemodialysis patients than in normal subjects, both pre-dialysis (3.7 ± 0.4 μmol h−-1 cm−-2, P < 0.001) and post-dialysis (2.4 ± 0.5 μmol h−-1 cm−-2, P < 0.05), even though haemodialysis decreased plasma K+ concentration from 5.3 ± 0.1 mmol/l to 3.5 ± 0.2 mmol/l (P < 0.001).
3. There were no significant differences in rectal Na+ absorption, rectal potential difference, plasma aldosterone concentration, or total body K+ content (measured by whole-body counting of 40K), between the normal subjects and either the CAPD or the haemodialysis patients.
4. These results indicate that K+ homoeostasis is maintained in uraemic patients undergoing long-term dialysis by a combination of K+ losses during dialysis, and enhanced large intestinal K+ excretion. The role of the large intestine appears to be particularly important at higher dietary K+ intakes, and the K+ secretory process is sensitive to changes in plasma K+ concentration.
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