The pharmacokinetic properties of yohimbine in the conscious rat

• Published in: Naunyn-Schmiedeberg's archives of pharmacology 1988-05, Vol.337 (5), p.583-587
• Main Authors: HUBBARD, J. W, PFISTER, S. L, BIEDIGER, A. M, HERZIG, T. C, KEETON, T. K
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Brain - metabolism; Cardiovascular system; Chromatography, High Pressure Liquid; Injections, Intravenous; Male; Medical sciences; Pharmacology. Drug treatments; Rats; Rats, Inbred Strains; Spectrometry, Fluorescence; Vasodilator agents. Cerebral vasodilators; Yohimbine - blood; Yohimbine - pharmacokinetics
• ISSN: 0028-1298; 1432-1912
• DOI: 10.1007/BF00182736

We used high performance liquid chromatography with fluorescence detection to measure the concentration of yohimbine in serum and brain of conscious Sprague-Dawley rats at various times after the i.v. injection of 1 mg/kg of yohimbine. The serum concentration-time profile of yohimbine was biphasic with a rapid distribution phase (t1/2 alpha = 0.048 h) followed by a very slow elimination phase t1/2 beta = 16.3 h). The clearance of yohimbine was 11 ml/h.kg-1, and the volume of distribution was 259 ml/kg. Increasing doses (0.3, 1 and 3 mg/kg, i.v.) of yohimbine produced non-linear increases in serum yohimbine concentration. Yohimbine entered the brain rapidly (5,000 ng/g at 5 min after 1 mg/kg, i.v.) and disappeared from brain with a t1/2 beta of 7.7 h. In contrast to serum yohimbine concentration, increasing doses of yohimbine (0.3, 1 and 3 mg/kg) produced linear increases in brain yohimbine concentration, a phenomenon which is consistent with concentration-dependent binding of yohimbine to plasma proteins. The rapid entry of yohimbine into the brain, the slow rate of elimination of yohimbine from serum and brain and the linear relationship of brain yohimbine concentration as a function of dose should be taken into consideration whenever yohimbine is to be used as a probe of alpha 2-adrenoceptor function in vivo.