All Blood Brain Barrier Cell Types Demonstrate Capability to Influence Differential Tenofovir and Emtricitabine Metabolism and Transport in the Brain
The blood brain barrier (BBB) represents a significant obstacle in brain drug penetration that challenges efforts in the treatment of neurological disorders. Therapeutically targeting the brain requires interactions with each BBB cell type, including endothelial cells, pericytes, and astrocytes. Yet, the relative contribution of these BBB cell types to the mechanisms that facilitate brain drug disposition is not well characterized. Here, we use first-line antiretroviral therapies, tenofovir (TFV) and emtricitabine (FTC), as models to investigate the mechanisms of drug transport and metabolism at the BBB that may influence access of the drug to the brain. We evaluated regional and cell-type-specific drug metabolism and transport mechanisms using rhesus macaques and in vitro treatment of primary human cells. We report heterogeneous distribution of TFV, FTC, and their active metabolites, which cerebrospinal fluid measures could not reflect. We found that all BBB cell types possessed functional drug-metabolizing enzymes and transporters that promoted TFV and FTC uptake and pharmacologic activation. Pericytes and astrocytes emerged as pharmacologically dynamic cells that rival hepatocytes and were uniquely susceptible to modulation by disease and treatment. Together, our findings demonstrate the importance of considering the BBB as a unique pharmacologic entity rather than viewing it as an extension of the liver, as each cell type possesses distinct drug metabolism and transport capacities that contribute to differential brain drug disposition. Further, our work highlights pharmacologically active pathways at the BBB that may regulate brain drug disposition and impact therapeutic efforts to alleviate neurologic disease.
Authors
- Dionna W. Williams (ORCID: https://orcid.org/0000-0001-5029-2628)
- Benjamin C. Orsburn (ORCID: https://orcid.org/0000-0002-0774-3750)
- Hannah Wilkins
- Ahmed Warshanna
- Stephen Knerler
- Rodnie Colón Ortiz (ORCID: https://orcid.org/0000-0002-3977-1019)
- Kate Haas
Institutions
- Johns Hopkins University (US)
- Emory University (US)
- Johns Hopkins Medicine (US)
Publication Details
- Journal
- ACS Pharmacology & Translational Science
- Published
- 2024-10-18
- DOI
- https://doi.org/10.1021/acsptsci.4c00510
- Citations
- 2
- Primary Topic
- Adenosine and Purinergic Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.80
Funders
- Emory University
- Johns Hopkins University
- University of Dundee
- National Institutes of Health
- Center for AIDS Research, University of Washington
- National Institute on Aging
- National Institute on Drug Abuse
- National Institute of General Medical Sciences
- National Institute of Allergy and Infectious Diseases