TY - JOUR
T1 - The excitatory effect of dopamine on isolated canine tracheal smooth muscle
AU - SHUE, CHUNG‐HUNG ‐H
AU - CHEN, CHING‐JU ‐J
PY - 1990/10
Y1 - 1990/10
N2 - Abstract— The effect of exogenous dopamine on canine tracheal smooth muscle has been studied in‐vitro. Dopamine at concentrations over 10−5 M induced contractions of tracheal muscle strips and repeated exposures resulted in desensitization (tachyphylaxis) of the muscle. The sensitivity of the response varied dramatically among muscle strips. At lower concentrations, dopamine caused neither muscle relaxation nor inhibition of contractions evoked by 10−6 M acetylcholine. Both a dopaminergic antagonist, haloperidol (10−5 and 10−4 M), and an α‐adrenoceptor antagonist, phentolamine (10−7 to 10−5 M), attenuated the contraction to 10−3 M dopamine. The β‐adrenoceptor antagonist, propranolol (10−8 to 10−6 M), enhanced the contraction. However, the contraction could only be abolished by phentolamine at 10−4 M. Thus, in canine tracheal smooth muscle, the contractile response to dopamine is predominantly through the activity of α‐adrenoceptors and the role of dopaminergic receptors is vague. It is suggested that the weakness of the dopamine‐induced contraction results from an antagonism between α‐ and β‐adrenoceptor effects and the dopamine tachyphylaxis may reflect a gradually decreased activation of the α‐adrenoceptor mechanism in comparison with the β‐adrenoceptor mechanism. 1990 Royal Pharmaceutical Society of Great Britain
AB - Abstract— The effect of exogenous dopamine on canine tracheal smooth muscle has been studied in‐vitro. Dopamine at concentrations over 10−5 M induced contractions of tracheal muscle strips and repeated exposures resulted in desensitization (tachyphylaxis) of the muscle. The sensitivity of the response varied dramatically among muscle strips. At lower concentrations, dopamine caused neither muscle relaxation nor inhibition of contractions evoked by 10−6 M acetylcholine. Both a dopaminergic antagonist, haloperidol (10−5 and 10−4 M), and an α‐adrenoceptor antagonist, phentolamine (10−7 to 10−5 M), attenuated the contraction to 10−3 M dopamine. The β‐adrenoceptor antagonist, propranolol (10−8 to 10−6 M), enhanced the contraction. However, the contraction could only be abolished by phentolamine at 10−4 M. Thus, in canine tracheal smooth muscle, the contractile response to dopamine is predominantly through the activity of α‐adrenoceptors and the role of dopaminergic receptors is vague. It is suggested that the weakness of the dopamine‐induced contraction results from an antagonism between α‐ and β‐adrenoceptor effects and the dopamine tachyphylaxis may reflect a gradually decreased activation of the α‐adrenoceptor mechanism in comparison with the β‐adrenoceptor mechanism. 1990 Royal Pharmaceutical Society of Great Britain
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U2 - 10.1111/j.2042-7158.1990.tb06571.x
DO - 10.1111/j.2042-7158.1990.tb06571.x
M3 - Article
C2 - 1982149
AN - SCOPUS:0025064493
SN - 0022-3573
VL - 42
SP - 732
EP - 734
JO - Journal of Pharmacy and Pharmacology
JF - Journal of Pharmacy and Pharmacology
IS - 10
ER -