![]() |
|
|
SP Markey, RW Colburn, IJ Kopin and RL Aamodt
Radiolabeled bromocriptine was administered to rats and monkeys and its tissue distribution, rate of excretion and metabolism were determined. In both species, [82Br]bromocriptine is predominantly concentrated in the liver, metabolized and then excreted through bile. Extractable free drug is undetectable in blood after 30 min. After 2 hr, the estimated concentration of free drug in rat brain is 2 x 10(-8) M. Terminal phase half-lives of radiolabel excretion were 2.9 days for the rat and 27.3 days for the monkey. The retained organically bound 82Br is present in a form more polar than bromocriptine.
This article has been cited by other articles:
![]() |
C. Li, P. Chen, and M. S. Smith Neuropeptide Y and Tuberoinfundibular Dopamine Activities Are Altered during Lactation: Role of Prolactin Endocrinology, January 1, 1999; 140(1): 118 - 123. [Abstract] [Full Text] |
||||
![]() |
D. Valente, M. Delaforge, S. Urien, D. Guivarc'H, R. Vienet, J.-M. Grognet, and E. Ezan Metabolite Involvement in Bromocriptine-Induced Prolactin Inhibition in Rats J. Pharmacol. Exp. Ther., September 1, 1997; 282(3): 1418 - 1424. [Abstract] [Full Text] |
||||