Biomedical subjects
Publications and source records attributed to W L Collier.
Using mature (12 months), old (70 months) rabbits and 3H-labeled spiroperidol, the characteristics of renal artery dopamine receptors were studied. In old age the dissociation constant of [3H]spiroperidol was unchanged, while maximum specific binding was reduced more than 45%. The present data seem to indicate an impairment of peripheral dopaminergic function in ageing.
The effect of dopamine on 3'-5'-cyclic adenosine monophosphate (cAMP) generation in the rabbit superior mesenteric artery was studied in order to identify dopamine receptors. Dopamine added to homogenates of superior mesenteric artery increased the concentration of cAMP. The stimulation of cAMP levels elicited by dopamine was unaffected by alpha or beta-adrenergic receptor blocking agents but was remarkably reduced by the dopamine receptor blocking agents fluphenazine and haloperidol. The findings appear to indicate that the effects of dopamine on rabbit superior mesenteric artery are mediated through activation of the adenylate-cyclase cAMP system.
The effect of dopamine on 3',5'-cyclic adenosine monophosphate (cAMP) generation in the rabbit renal artery was studied. Dopamine added to homogenates of rabbit renal artery increased the concentration of cAMP. The stimulation of cAMP levels elicited by dopamine was remarkably reduced by the dopamine receptor antagonists fluphenazine and haloperidol, but it was unaffected by the ergot-like dopaminergic agonist bromocriptine. These findings appear to indicate that the effects of dopamine on rabbit renal artery are mediated through a D1 receptor.
Age-related changes in the density of the noradrenergic perivascular plexus supplying the uterine artery and its intrauterine branches were studied in rats 4, 12 and 24 months old using the glyoxylic acid fluorescence technique. Moreover, uterine noradrenaline levels were determined by means of high pressure liquid chromatography with electrochemical detection. No changes in the density of noradrenergic innervation or in uterine noradrenaline levels were noticeable in 12 month in comparison with 4 month rats. In contrast, a significant decrease in the density of the noradrenergic perivascular plexus of uterine artery and of its intrauterine branches as well as decrease in noradrenaline concentrations of uterine horns and cervix were observed in 24 month rats. The above findings indicate an age-related impairment of uterine noradrenergic innervation.
By using combined radioreceptor binding and autoradiographic techniques, we were able to localize the GABA 'A' receptor agonist 3H-muscimol in the rat choroid plexus. Within sections of rat choroid plexus, 3H-muscimol was bound specifically with a KD of 37 nM and a Bmax of 253 pmol/mg tissue. These values are consistent with the labelling of GABA 'A' receptor sites. The autoradiographic studies demonstrated that 3H-muscimol was attached to the epithelium of the choroid plexus. The blood vessels of the plexus did not exhibit specific labelling. Examination of these data suggests the existence of GABAergic mechanisms which control cerebrospinal fluid production or flow.
The effect of in vitro addition of dopamine on the 3'-5'-cyclic adenosine monophosphate (cAMP) generating system of rabbit internal carotid and middle cerebral artery was studied. Dopamine increased cAMP levels in a dose-dependent manner in both arteries. The DA1-receptor antagonist SCH 23390 decreased the dopamine-elicited cAMP increase. On the contrary, the DA2-receptor antagonist L-sulpiride caused an increase in dopamine-dependent cAMP levels. The simultaneous addition of SCH 23390 and of L-sulpiride abolished any effect of dopamine on cAMP content. The DA2-receptor agonists bromocriptine and co-dergocrine decreased cAMP levels. The above findings indicate the existence in the rabbit internal carotid and middle cerebral artery of 2 types of dopamine receptors mediating respectively, the increase (DA1-effect) and the decrease (DA2-effect) of cAMP levels.