FK506 is neuroprotective in a model of antiretroviral toxic neuropathy

Sanjay C. Keswani, Bani Chander, Chiler Hasan, John W. Griffin, Justin C. McArthur, Ahmet Hoke

Research output: Contribution to journalArticlepeer-review

72 Scopus citations


Antiretroviral toxic neuropathy is the most common neurological complication of human immunodeficiency virus infection. This painful neuropathy not only affects the quality of life of human immunodeficiency virus-infected patients but also severely limits viral suppression strategies. We have developed an in vitro model of this toxic neuropathy to better understand the mechanism of neurotoxicity and to test potential neuroprotective compounds. We show that among the dideoxynucleosides, ddC appears to be the most neurotoxic, followed by ddI and then d4T. This reflects their potency in causing neuropathy. AZT, which does not cause a peripheral neuropathy in patients, does not cause significant neurotoxicity in our model. Furthermore, in this model, we show that the immunophilin ligand FK506 but not cyclosporin A prevents the development of neurotoxicity by ddC, as judged by amelioration of ddC-induced "neuritic pruning, " neuronal mitochondrial depolarization, and neuronal necrotic death. This finding suggests a calcineurin-independent mechanism of neuroprotection. As calcineurin inhibition underlies the immunosuppressive properties of these clinically used immunophilin ligands, this holds promise for the neuroprotective efficacy of nonimmunosuppressive analogs of FK506 in the prevention or treatment of antiretroviral toxic neuropathy.

Original languageEnglish (US)
Pages (from-to)57-64
Number of pages8
JournalAnnals of neurology
Issue number1
StatePublished - Jan 1 2003

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology


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