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It is rapidly and completely absorbed from the gut and is mainly excreted in the bile and faeces
Publication types Review Bromocriptine, a D2 receptor agonist, was administered intravenously (1mg/kg) to anesthetized rats
In the present study we have attempted to determine whether bromocriptine therapy causes qualitative changes in plasma human growth hormone (hGH) in acromegaly
Besides, BC represents a novel therapeutic option in type 2 diabetes (T2DM); however, the precise mechanisms are not completely unveiled
At the start of the perfusion, BCT at the concentration of 10 or 100 ng/ml
6 to 4
A total of 16 metabolites of bromocriptine could be isolated from rat bile and incubates of rat liver cell preparations using [6-methyl-14C]bromocriptine as substrate