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Published on: November 7, 2017
Uremic cardiomyopathy: role of circulating digitalis like substances
Behram Mohmand1, Deepak K Malhotra, Joseph I Shapiro
1Department of Medicine, Medical College of Ohio, 3120 Glendale Avenue, Toledo, Ohio 43614-5089, USA.
Insights
Patients with chronic renal failure develop cardiac problems and oxidative stress due to increased digitalis-like substances. These substances may be the cause of both the cardiomyopathy and the systemic oxidant stress observed in these patients.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Chronic renal failure is associated with cardiac dysfunction, specifically diastolic dysfunction and left ventricular hypertrophy.
- Elevated levels of digitalis-like substances are observed in patients with chronic renal failure.
- An unexplained systemic oxidant stress state is also a characteristic of chronic renal failure.
Purpose of the Study:
- To investigate the potential role of digitalis-like substances in the development of cardiomyopathy and oxidant stress in chronic renal failure.
- To explore the mechanism by which digitalis-like substances might induce cardiac myocyte hypertrophy.
Main Methods:
- The study proposes a mechanism linking digitalis-like substances to cellular processes.
- It references existing data on digitalis-like substances, sodium pump interaction, and reactive oxygen species production.
- It also considers findings on cardiac myocyte hypertrophy in cell culture and oxidant stress in patients.
Main Results:
- Digitalis-like substances bind to the sodium pump, initiating a signal cascade.
- This cascade involves the production of reactive oxygen species.
- This process has been shown to induce hypertrophy in cultured cardiac myocytes.
Conclusions:
- Digitalis-like substances are proposed as the causative agents for cardiomyopathy in renal failure.
- These substances are also implicated as the cause of the systemic oxidant stress state in chronic renal failure patients.
Abstract:
Patients with chronic renal failure develop a cardiomyopathy characterized by marked diastolic dysfunction and left ventricular hypertrophy. Interestingly, they also have substantial increases in the circulating concentrations of digitalis like substances. Digitalis like substances produce reactive oxygen species as part of the signal cascade induced by binding to the sodium pump and patients, and this signal cascade appears to induce hypertrophy of cardiac myocytes grown in culture. Also, patients with chronic renal failure develop an oxidant stress state without a known mechanism. From these data, we propose that it is these digitalis like substances which cause cardiomyopathy of renal failure as well as the systemic oxidant stress state.
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