Antiretroviral effects of glycerophospholipid stereoisomers of AZT on HIV replication in HT4-6C cells. NLM AIDSLINE Important note: Information in this article was accurate in 1990. The state of the art may have changed since the publication date.

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Antiretroviral effects of glycerophospholipid stereoisomers of AZT on HIV replication in HT4-6C cells.

Int Conf AIDS. 1990 Jun 20-23;6(1):186 (abstract no. Th.A.265). Unique Identifier : AIDSLINE ICA6/10026590
Kumar R; Richman DD; Hostetler KY; Vical Inc, San Diego, CA, USA


Abstract: OBJECTIVE: Macrophages are an important target for anti-HIV therapies. We previously reported the synthesis of sn-3 phosphatidylAZT (pAZT), a phospholipid prodrug of azidothymidine (AZT, zidovudine) which was active in HIV-infected cells. pAZT can be targeted to macrophages in vivo. We wished to determine if the sn-1 derivative is also effective in HIV-infected cells since most of the cellular phospholipases are stereospecific for sn-3 phosphoglycerides. METHODS: We synthesized sn-1, sn-3, and racemic dipalmitoylglycerophosphoAZT from the corresponding isopropylidene glycerols by coupling with AZT-monophosphate followed by deblocking and acylation of the hydroxyls of glycerol with palmitic anhydride. Lipid vesicles containing 10 mole % of the pAZTs were incubated with HT4-6C cells after infection with the LAV-1BRU strain of HIV in a plaque reduction assay. RESULTS: sn-3 pAZT reduced plaque formation by 50% (ID50) at 2.1 uM versus 2.2 uM for the sn-1 derivative while racemic pAZT had an IC50 of 2.7 uM. None of these differences were statistically significant (n=3). CONCLUSIONS: Contrary to expectations, the sn-1 and sn-3 derivatives of pAZT were equally effective in reducing HIV replication of HT4-6C cells. This is a surprising result since most cellular phospholipases are thought to be specific for the sn-3 glycerophospholipids. Intact pAZTs have no intrinsic activity against HIV reverse transcriptase (RT). Therefore, the sn-1 pAZT must be degraded in the cell by enzymatic processes which are still uncharacterized before being converted to AZT-triphosphate, the inhibitor of RT.
Keywords: Cell Line Human HIV/*DRUG EFFECTS/PHYSIOLOGY Prodrugs/*PHARMACOLOGY Stereoisomers Virus Replication/*DRUG EFFECTS Zidovudine/*PHARMACOLOGY ABSTRACTKWDcelllinehumanhiv/KWDdrugeffects/physiologyprodrugs/KWDpharmacologystereoisomersvirusreplication/KWDdrugeffectszidovudine/KWDpharmacologyabstract
901230
M90C3532

Copyright © 1990 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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