Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2008-9-23
pubmed:abstractText
The ABCB1-type multidrug resistance efflux transporter P-glycoprotein (P-gp) has been hypothesized to regulate hypothalamic-pituitary-adrenal axis activity by limiting the access of glucocorticoids to the brain. In vivo systemic administration studies using P-gp-deficient mice have shown increased glucocorticoid entry to the brain compared with wild-type controls. However, these studies did not control for the presence of radiolabeled drug in the capillaries, verify an intact blood-brain barrier, or confirm stability of the glucocorticoids used. In the present study, an in situ brain perfusion method, coupled with capillary depletion and HPLC analyses, was used to quantify brain uptake of [3H]dexa-methasone, [3H]cortisol, and [3H]corticosterone in P-gp-deficient and control mice. A vascular marker was included in these experiments. The results show that brain uptake of [3H]dexamethasone was increased in the frontal cortex, hippocampus, hypothalamus, and cerebellum of P-gp-deficient mice compared with wild-type controls. Brain uptake of [3H]cortisol was increased in the hypothalamus of P-gp-deficient mice compared with wild-type controls, but no differences were detected in other regions. Brain uptake of [3H]corticosterone was not increased in P-gp-deficient mice compared with wild-type controls in any brain areas. After our systemic administration of the same radiolabeled glucocorticoids, HPLC analysis of plasma samples identified additional radiolabeled components, likely to be metabolites. This could explain previous findings from systemic administration studies, showing an effect of P-gp not only for dexamethasone and cortisol, but also for corticosterone. This in situ study highlights the different affinities of dexamethasone, cortisol, and corticosterone for P-gp, and suggests that the entry of the endogenous glucocorticoids into the mouse brain is not tightly regulated by P-gp. Therefore, our current understanding of the role of P-gp in hypothalamic-pituitary-adrenal regulation in mice requires revision.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-10698076, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-10700657, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-10837354, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-11356720, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-11704655, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-11905988, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12213137, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12464451, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12535575, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12784111, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12871829, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-12888779, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-1334712, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-1360010, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-14749091, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-15359572, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-16150912, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-16892207, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-17094122, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-17356567, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-17369055, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-17576845, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-175888, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-2338547, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-2563168, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-447850, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-6482428, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-7589529, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-7903303, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-8763339, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-9108099, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-9449553, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-9528963, http://linkedlifedata.com/resource/pubmed/commentcorrection/18556350-9681461
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ATP-Binding Cassette Transporters, http://linkedlifedata.com/resource/pubmed/chemical/Abcb1b protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents, http://linkedlifedata.com/resource/pubmed/chemical/Carbon Radioisotopes, http://linkedlifedata.com/resource/pubmed/chemical/Corticosterone, http://linkedlifedata.com/resource/pubmed/chemical/Dexamethasone, http://linkedlifedata.com/resource/pubmed/chemical/Glucocorticoids, http://linkedlifedata.com/resource/pubmed/chemical/Hydrocortisone, http://linkedlifedata.com/resource/pubmed/chemical/Octanols, http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoprotein, http://linkedlifedata.com/resource/pubmed/chemical/Sodium Chloride, http://linkedlifedata.com/resource/pubmed/chemical/Sucrose, http://linkedlifedata.com/resource/pubmed/chemical/Tritium
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0013-7227
pubmed:author
pubmed:issnType
Print
pubmed:volume
149
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5244-53
pubmed:dateRevised
2011-6-21
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
A revised role for P-glycoprotein in the brain distribution of dexamethasone, cortisol, and corticosterone in wild-type and ABCB1A/B-deficient mice.
pubmed:affiliation
Pharmaceutical Science Research Division, King's College London, London, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't