The ATP-binding cassette proteins ABCB1 and ABCC1 as modulators of glucocorticoid action

被引:14
作者
Devine, Kerri [1 ,2 ]
Villalobos, Elisa [1 ]
Kyle, Catriona J. [1 ]
Andrew, Ruth [1 ]
Reynolds, Rebecca M. [1 ]
Stimson, Roland H. [1 ]
Nixon, Mark [1 ]
Walker, Brian R. [1 ,2 ]
机构
[1] Univ Edinburgh, BHF Ctr Cardiovasc Sci, Queens Med Res Inst, Edinburgh, Midlothian, Scotland
[2] Newcastle Univ, Translat & Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国惠康基金;
关键词
BLOOD-BRAIN-BARRIER; MULTIDRUG-RESISTANCE PROTEIN-1; MDR1A P-GLYCOPROTEIN; PITUITARY-ADRENAL AXIS; DRUG TRANSPORTER; 11-BETA-HYDROXYSTEROID DEHYDROGENASE; PLASMA-CORTICOSTERONE; REPLACEMENT THERAPY; TISSUE DISTRIBUTION; ADDISONS-DISEASE;
D O I
10.1038/s41574-022-00745-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Responses to hormones that act through nuclear receptors are controlled by modulating hormone concentrations not only in the circulation but also within target tissues. The role of enzymes that amplify or reduce local hormone concentrations is well established for glucocorticoid and other lipophilic hormones; moreover, transmembrane transporters have proven critical in determining tissue responses to thyroid hormones. However, there has been less consideration of the role of transmembrane transport for steroid hormones. ATP-binding cassette (ABC) proteins were first shown to influence the accumulation of glucocorticoids in cells almost three decades ago, but observations over the past 10 years suggest that differential transport propensities of both exogenous and endogenous glucocorticoids by ABCB1 and ABCC1 transporters provide a mechanism whereby different tissues are preferentially sensitive to different steroids. This Review summarizes this evidence and the new insights provided for the physiology and pharmacology of glucocorticoid action, including new approaches to glucocorticoid replacement.
引用
收藏
页码:112 / 124
页数:13
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