Abstract
Many studies have reported greater drug uptake into brain than that predicted based upon existing models using the free fraction (fu) of drug in arterial serum. To explain this difference, circulating plasma proteins have been suggested to interact with capillary membrane in vivo to produce a conformational change that favors net drug dissociation and elevation of fu. Albumin, the principal binding protein in plasma, has two main drug binding sites, Sudlow I and II. We tested this hypothesis using drugs that bind selectively to either site I (warfarin) or site II (ibuprofen), as well as mixed ligands that have affinity for both sites (tolbutamide and valproate). Brain uptake was determined in the presence and absence of albumin using the in situ rat brain perfusion technique. Unidirectional brain uptake transfer constants (Kin) were measured and compared with those predicted using the modified Kety-Crone-Renkin model: Kin = F(1 – e–fu × PSu/F), where F is perfusion flow and PSu is the permeability-surface area product to free drug of brain capillaries. The results demonstrated good agreement between measured and predicted Kin over a 100-fold range in perfusion fluid albumin concentration using albumin from three different species (i.e., human, bovine, and rat), as well as whole-rat serum. Kin decreased in the presence of albumin in direct proportion to perfusion fluid fu with constant PSu. The results show that brain uptake of selected Sudlow site I and II ligands matches that predicted by the modified Kety-Crone-Renkin model with no evidence for enhanced dissociation.
Footnotes
-
This work was supported in part by Grant NS052484 from the National Institutes of Health (to Q.R.S.).
-
doi:10.1124/jpet.105.097402.
-
ABBREVIATIONS: PSu, permeability-surface area product; LSC, liquid scintillation counting.
- Received October 18, 2005.
- Accepted January 9, 2006.
- The American Society for Pharmacology and Experimental Therapeutics
JPET articles become freely available 12 months after publication, and remain freely available for 5 years.Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page.
|