Abstract
The effect of CDS, an endogenous brain substance that specifically displaces bound [3H]clonidine and [3H]rauwolscine in rat brain membranes and human platelets, has been tested in isolated, field-stimulated rat vas deferens. CDS, obtained after an extensive purification procedure as a single peak from an HPLC sizing column, inhibited the electrically stimulated rat vas deferens similarly to the inhibitory action of clonidine, an α2-agonist. The effective dose of CDS as an inhibitor of the vas deferens is equivalent to its effective dose in displacing specifically bound [3H]clonidine in rat brain membranes. Furthermore, the CDS inhibition of the twitch response is reversed by two α2-adrenergic antagonists, yohimbine and phentolamine. From these results, it is suggested that CDS extracted from brain, with affinity for clonidine sites, may be involved in the non-adrenergic fast response of the sympathetic transmission of the vas deferens.
| Original language | English |
|---|---|
| Pages (from-to) | 184-190 |
| Number of pages | 7 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 134 |
| Issue number | 1 |
| DOIs | |
| State | Published - 14 Jan 1986 |
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