Adrenoreceptors in the rat costo‐uterine muscle were compared with those in the uterine horn. The responses of electrically‐stimulated preparations of both tissues to isoprenaline and phenylephrine were investigated in the absence and presence of phentolamine and propranolol to block α‐ and β‐adrenoreceptors respectively. Preparations were taken from rats at known stages of the four‐day oestrous cycle.
Both adrenoreceptor agonists consistently inhibited contractions in both tissues; threshold sensitivity to isoprenaline was similar for both tissues and at all cycle stages. The same held true for phenylephrine, which was only approximately 1/400 as potent as isoprenaline. A generally similar pattern was observed when concentrations producing maximum inhibition were compared; however during proestrus, phenylephrine was more potent in producing maximal responses in uterine horns than in costo‐uterine muscles.
Phentolamine had no effect on inhibitory responses to isoprenaline in either tissue, nor to phenylephrine in costo‐uterine muscles, but slightly enhanced the inhibitory action of phenylephrine in uterine horns from proestrous rats. Propranolol blocked the inhibitory effects of both drugs, revealing an excitatory effect of phenylephrine in the uterine horns at proestrus.
These observations, and estimates of pA2 values for propranolol against both agonists, indicate that β‐adrenoreceptors insensitive to cyclical fluctuations in ovarian hormone levels, are predominant in the uterine horn and may be the exclusive adrenoreceptor present in the costo‐uterine muscle. In the uterine horn a small sub‐population of excitatory α‐adrenoreceptors, the presence of which is masked by β‐adrenoreceptors, can be demonstrated during proestrus. These receptors may be dependent upon the presence of the endometrium and/or the circular smooth muscle layer. The costo‐uterine muscle, which lacks excitatory α‐adrenoreceptors, could serve as a useful model of the longitudinal layer of the myometrium in investigations of drug actions at β‐adrenoreceptors.