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Hypothalamic digoxin, hemispheric chemical dominance, and chronic bronchitis emphysema
Ravi Kumar Kurup1, Parameswara Achutha Kurup
1Department of Neurology, Medical College Hospital, Trivandrum, Kerala, India. kvgnair@satyam.net.in
The International Journal of Neuroscience
|September 10, 2003
Summary
Chronic bronchitis emphysema is linked to altered isoprenoid pathway metabolites and left-hemispheric dominance. These biochemical changes may reflect brain function alterations impacting lung health.
Area of Science:
- Biochemistry
- Pulmonology
- Neuroscience
Background:
- The isoprenoid pathway yields critical metabolites: endogenous digoxin, dolichol, and ubiquinone.
- Chronic bronchitis emphysema (CBE) involves complex biochemical and potentially neurological factors.
- Hemispheric dominance is increasingly recognized for its influence on physiological processes.
Purpose of the Study:
- To investigate the isoprenoid pathway's role in chronic bronchitis emphysema pathogenesis.
- To explore the association between hemispheric dominance and CBE.
- To identify biochemical markers and their correlation with brain function in CBE patients.
Main Methods:
- Assessed isoprenoid pathway metabolites in CBE patients.
- Utilized the dichotic listening test to determine hemispheric dominance.
- Analyzed biochemical markers including digoxin, dolichol, ubiquinone, free radicals, and glycoconjugates.
- Correlated biochemical findings with hemispheric dominance patterns.
Main Results:
- CBE patients exhibited elevated endogenous digoxin and dolichol, decreased ubiquinone, and increased free radicals.
- All CBE patients displayed left-hemispheric dominance.
- Biochemical profiles in CBE mirrored those in individuals with right hemispheric dominance.
- Increased free radicals and altered glycoconjugate metabolism contribute to immune activation and disease pathology.
Conclusions:
- Altered isoprenoid pathway and left-hemispheric dominance are implicated in chronic bronchitis emphysema.
- Endogenous digoxin and free radical generation may drive immune activation in CBE.
- Biochemical changes in CBE suggest a link to altered brain function and hemispheric dominance.