Key result
Intravenously administered exogenous dopamine acted as a transient but potent depressant of respiration in anesthetized dogs.
Why the study?
Does intravenously administered dopamine depress respiration in anesthetized dogs?
Does intravenously administered dopamine depress respiration in anesthetized dogs?
Intravenous dopamine acts as a transient but potent respiratory depressant in anesthetized dogs, highlighting a potential adverse effect to consider during shock treatment.
May prompt respiratory monitoring in anesthetized canine models; leaves open translation to human shock therapy.
Dopamine has increasingly become the drug of choice for treating patients with cardiogenic shock (1, 2). Numerous studies on the cardiovascular actions of dopamine revealed that dopamine itself has a specific action, which is distinct from its stimulating actions on α- and β-adrenergic receptors (3). This action is associated with specific dopamine receptors, except for those in the central nervous system, which exist mainly in the renal and mesenteric vascular beds. The specific action of dopamine is partly antagonized by haloperidol or chlorpromazine (3). In contrast, there are relatively few reports concerning the respiratory actions of dopamine. In our studies we found that exogenous dopamine was a transient but potent depressant of respiration in anesthetized dogs. Dopamine therapy in the treatment of shock is a comparatively new maneuver, and the therapeutic value and adverse effects are still open to assessment. Using anesthetized dogs, the respiratory and cardiovascular effects of dopamine, especially as a depressant of respiration, were examined. The current concepts of dopamine as an inhibitory modulator in respiratory control were then studied.
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Yasuhara et al. (1980) studied Anesthetized dogs. Intravenously administered dopamine was evaluated on Respiratory and cardiovascular effects. Intravenously administered exogenous dopamine acted as a transient but potent depressant of respiration in anesthetized dogs.
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