Summary
In vivo prostatic secretion was collected from retired breeder Sprague Dawley rats using a method for isolated perfusion of the rat prostatic urethra. Enzymatic acid phosphatase determination was performed on the collected effluent. Control acid phosphatase secretion was 24.2±2.7 nm over 30 minutes. Intravenous phenylephrine 5 mg/kg stimulated a 10 fold increase in acid phosphatase secretion. The secretion seen with phenylephrine was dose dependent and could be blocked with prazosin, but not yohimbine, atropine, or propranolol. Intravenous β-adrenergic agonist isoproterenol caused no increase in the secretion of rat prostatic acid phosphatese. Intravenous administration of the cholinergic agonist pilocarpine also resulted in a dose dependent rise in acid phosphatase secretion. The stimulation seen could be blocked by atropine but not phentolamine or propranolol. The stimulation of acid phosphatase secretion seen with α1 adrenergic or cholinergic agonists was not additive. Intravenous vasoactive intestinal peptide did not stimulate acid phosphatase secretion nor did it augment the secretion induced by α1 adrenergic or cholinergic agonists. Release of acid phosphatase into rat prostatic exocrine secretion is under both α1 adrenergic and cholinergic control.
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Jacobs, S.C., Story, M.T. Autonomic control of acid phosphatase exocrine secretion by the rat prostate. Urol. Res. 17, 311–315 (1989). https://doi.org/10.1007/BF00262989
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DOI: https://doi.org/10.1007/BF00262989