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Specific binding of serotonin in rat lung
The American Journal of Physiology
|January 1, 1985
Summary
Mammalian lungs actively inactivate serotonin (5-HT) and possess distinct 5-HT receptors in mitochondria and microsomes. These lung serotonin receptors may explain known and unknown 5-HT actions.
Area of Science:
- Pulmonary Pharmacology
- Neurotransmitter Receptor Research
- Cellular Biology
Background:
- Mammalian lungs are known to store and inactivate serotonin (5-HT) through an active uptake and metabolism process.
- Serotonin exhibits direct effects on lung tissues, including smooth muscle constriction, indicating the presence of 5-HT receptors.
Purpose of the Study:
- To identify and characterize specific serotonin (5-HT) binding sites within different lung tissue fractions.
- To investigate the affinity and capacity of these 5-HT binding sites in mitochondrial and microsomal fractions.
Main Methods:
- Utilized saturation analysis of 5-[3H]HT binding to purified outer and inner mitochondrial membranes.
- Performed binding assays on purified lung microsomal fractions.
- Determined dissociation constants (Kd) and maximum binding capacities for identified sites.
Main Results:
- Identified high-affinity, high-capacity 5-HT binding in outer mitochondrial membranes (Kd = 8.3 nM).
- Detected a low-capacity 5-HT binding site in inner mitochondrial membranes (Kd = 25.2 nM).
- Characterized a high-capacity 5-HT binding site in lung microsomal fractions (Kd = 14.8 nM).
Conclusions:
- The lung serves as a primary site for serotonin inactivation.
- The presence of multiple specific 5-HT receptors in lung mitochondria and microsomes suggests roles in known and potentially novel 5-HT-mediated lung functions.