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Published on: August 6, 2018
Thermal sweat lactate in cystic fibrosis and in normal children
Insights
Cystic fibrosis (CF) patients show altered sweat electrolyte levels. This study found that CF sweat glands maintain normal anaerobic metabolism, suggesting efficient energy use despite ion transport changes.
Area of Science:
- Physiology
- Biochemistry
- Sweat Gland Function
Background:
- Cystic fibrosis (CF) is characterized by abnormal ion transport, affecting sweat composition.
- Previous research indicates altered sodium (Na+) and potassium (K+) handling in CF sweat.
- The metabolic state of CF sweat glands remains incompletely understood.
Purpose of the Study:
- To investigate the association between altered sweat electrolyte excretion and anaerobic metabolism in CF.
- To evaluate sweat lactate excretion rate as an indicator of glandular energy metabolism in CF patients.
Main Methods:
- Forehead sweat was collected from 6 children with CF and 11 healthy children under thermal load (45°C).
- Sweat electrolyte concentrations (Na+, K+, Cl-) and lactate excretion rates were measured.
- Excretion rates were analyzed in relation to sweat flow rate (Qsw).
Main Results:
- In CF patients, Na+, K+, and Cl- concentrations remained constant across varying sweat flow rates.
- Sweat electrolyte excretion rates increased linearly with sweat flow rate in both CF and control groups.
- The slopes for electrolyte excretion were significantly steeper in CF patients compared to controls (p < 0.001).
- Sweat lactate excretion rate increased with sweat flow rate similarly in both CF and control groups.
Conclusions:
- CF sweat glands exhibit normal anaerobic metabolism, as indicated by consistent sweat lactate excretion rates.
- Increased energy expenditure for Na+-K+ exchange and active K+ secretion may explain the observed metabolic profile in CF.
- These findings suggest that CF sweat glands can maintain energy homeostasis despite ion transport abnormalities.
Abstract:
We attempt to determine whether the decrease in Na+ reabsorption and the increase in K+ secretion in sweat of cystic fibrosis patients (CF) were associated with changes in glandular anaerobic metabolism evaluated by forehead sweat lactate excretion rate. 6 CF and 11 normal (C) children, 5 months to 14 years old, were exposed to external thermal load (45 degrees C). The data showed that: 1) Na+, K+ and Cl- concentrations in CF are constant at any flow rate (Qsw); 2) In both groups the excretion rates of Na+, K+ and Cl- increased linearly with Qsw but the slopes in CF were significantly higher than in C (p less than 0.001); 3) Lactate excretion rate increased with Qsw as in CF and C with the same slope. We suggest that an increase in energy expenditure of Na+ - K+ exchange and an active secretion of K+ by the duct could explain the normal energy metabolism that we observed in CF sweat glands.
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