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Morphine sulfate inhibits bronchoconstriction in subjects with mild asthma whose responses are inhibited by atropine
Abstract:
To determine whether morphine sulfate alters the bronchoconstrictive response to inhalation of distilled water, we gave 13 subjects with mild asthma 0.15 mg/kg morphine sulfate or normal saline intravenously, after which they inhaled increasing volumes of nebulized distilled water from an ultrasonic nebulizer. We constructed stimulus-response curves, and by interpolation determined the provocative output of the nebulizer that resulted in a 50% increase in SRaw from baseline (PO50). On a separate day the subjects inhaled 2.0 mg of atropine sulfate 30 min before they inhaled distilled water. We compared the bronchoconstrictive response after morphine and after atropine with the bronchoconstrictive response after saline by determining the ratio of the PO50 values. Atropine was considered effective in inhibiting bronchoconstriction in 7 of the 13 subjects in whom the ratio of PO50 after atropine to the PO50 after saline was greater than 2.0. By similar criteria, morphine was also considered effective in 5 of these 7 subjects. Neither atropine nor morphine was effective in the remaining 6 subjects. By chi-square analysis, we found a positive correlation between the inhibitory effects of morphine and those of atropine (p less than 0.05). In the 5 subjects in whom morphine was effective, naloxone reversed the inhibitory effect of morphine. Atropine caused significant baseline bronchodilation when compared with placebo (normal saline), whereas morphine did not. We conclude that opiate receptor stimulation by morphine causes inhibition of the vagally mediated component of water-induced bronchoconstriction.
Insights
Morphine sulfate inhibits vagally mediated bronchoconstriction in asthma patients. This effect, linked to opiate receptor stimulation, was reversed by naloxone and correlated with atropine
Area of Science:
- Pulmonary Medicine
- Pharmacology
Background:
- Asthma is characterized by airway hyperresponsiveness.
- Water-induced bronchoconstriction is a model for studying airway reactivity.
- The role of vagal tone in water-induced bronchoconstriction is not fully understood.
Purpose of the Study:
- To investigate the effect of morphine sulfate on water-induced bronchoconstriction in mild asthma.
- To compare the inhibitory effects of morphine sulfate and atropine sulfate on airway reactivity.
Main Methods:
- 13 mild asthma subjects inhaled nebulized distilled water after intravenous administration of morphine sulfate or saline.
- Stimulus-response curves were generated to determine the provocative concentration (PO50) causing a 50% increase in SRaw.
- The effects of morphine and atropine were compared to saline, and naloxone was used to assess opiate receptor involvement.
Main Results:
- Morphine sulfate inhibited water-induced bronchoconstriction in 5 of 13 subjects, an effect correlated with atropine's inhibitory action.
- Naloxone reversed the inhibitory effect of morphine in subjects where it was effective.
- Atropine caused significant baseline bronchodilation, unlike morphine.
Conclusions:
- Opiate receptor stimulation by morphine inhibits the vagally mediated component of water-induced bronchoconstriction.
- Morphine's effect suggests a role for opioid pathways in modulating airway reflexes.
- These findings highlight potential therapeutic targets for managing asthma exacerbations.