Endogenous digoxin-like immunoactivity and diabetes mellitus: facts and hypotheses

Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na +-K +-ATPase which increase the total amount of intracellular stored calcium (Ca 2+ i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to...

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Bibliographic Details
Published in:Medical hypotheses 1997-09, Vol.49 (3), p.271-275
Main Authors: Martinka, E., Galajada, P., Ochodnicky, M., Lichardus, B., Straka, S., Mokan, M.
Format: Article
Language:English
Subjects:
Biological and medical sciences
Cardiotonic agents
Cardiovascular system
Diabetes Mellitus - physiopathology
Diabetes Mellitus, Type 2 - physiopathology
Diabetic Angiopathies - physiopathology
Diabetic Nephropathies - physiopathology
Digoxin - analysis
Glucose - metabolism
Humans
Hyperinsulinism
Hypertension - physiopathology
Immunoassay
Insulin - metabolism
Insulin Secretion
Medical sciences
Models, Biological
Ouabain - analysis
Pharmacology. Drug treatments
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Summary:Substances with digoxin- and ouabain-like immunoactivity (DLIA) are specific inhibitors of Na +-K +-ATPase which increase the total amount of intracellular stored calcium (Ca 2+ i). In diabetic patients, DLIA levels have been reported to be increased. Although this increase is probably secondary to sodium retention and volume expansion (induced in diabetic subjects by hyperinsulinemia and/or diabetic nephropathy), the question arises of whether it has pathophysiological consequences: namely, whether substances with DLIA, via their effect on Na +-K +-ATPase activity and Ca 2+ i stores, could in diabetic subjects facilitate development of hypertension and/or modulate insulin sensitivity or insulin secretion. Clinical findings of correlations of DLIA to blood pressure, insulin levels and to degree of insulin resistance, together with experimental findings of decreased Na +-K +-ATPase activity, increased Ca 2+ i and decreased Mg 2+ i n both diabetic and hypertensioe subjects, support these hypotheses. However, the issue of whether or not these relations are causative and whether or not defects in intracellular milieu are primary or secondary to non-insulin-dependent diabetes mellitus has not been resolved yet. Moreover, pathogenesis of both diabetes mellitus and hypertension is multifactorial and includes many other factors. Therefore, further efforts should be made to elucidate the exact role of substances with DLIA in diabetes mellitus.
ISSN:0306-9877
1532-2777
DOI:10.1016/S0306-9877(97)90212-7