Equal inhibition of HIV replication by stereoisomers of phosphatidyl-azidothymidine. Lack of stereospecificity of lysosomal phospholipase A1. NLM AIDSLINE Important note: Information in this article was accurate in 1993. The state of the art may have changed since the publication date.

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Equal inhibition of HIV replication by stereoisomers of phosphatidyl-azidothymidine. Lack of stereospecificity of lysosomal phospholipase A1.

J Biol Chem. 1992 Oct 5;267(28):20288-92. Unique Identifier : AIDSLINE MED/93015904
Kumar R; Gardner MF; Richman DD; Hostetler KY; Vical Incorporated, San Diego, California 92121.


Abstract: Glycerol-1-P and glycerol-3-P stereoisomers of dipalmitoylphosphatidylazidothymidine were synthesized and found to have equal antiretroviral activity in HIV-infected HT4-6C cells. It was anticipated that the glycerol-1-P isomer would be less active because of slow metabolic conversion by cellular phospholipases A and C, but the antiretroviral results suggested that the human cell line (HT4-6C) may have phospholipases capable of hydrolyzing 2,3-dipalmitoyl-sn-glycerol-1-phospho-5'-azidothymidine (AZT). To evaluate this possibility, we purified lysosomal phospholipase A1, an enzyme known to play a major role in cellular phospholipid catabolism. This enzyme rapidly hydrolyzed both the sn-1 and sn-3 isomers of dipalmitoylphosphatidyl-AZT. We synthesized sn-2,3-dipalmitoyl-glycero-1-phosphocholine and found that it is also hydrolyzed readily by lysosomal phospholipase A1 although the Vmax, 59 mumol mg-1 h-1, is slightly lower than that of the sn-1,2-dipalmitoyl-glycero-3-phosphocholine, 89 mumol mg-1 h-1. In conclusion, our studies show that sn-2,3-dipalmitoyl-glycerol-1-phospho-AZT is equal in antiviral activity to sn-1,2-dipalmitoyl-glycero-3-phospho-AZT in HIV-infected HT4-6C cells. This surprising result is due in part to the lack of stereospecificity of lysosomal phospholipase A1.
Keywords: Animal Antiviral Agents/CHEMISTRY/METABOLISM/*PHARMACOLOGY Cell Line Chromatography, Thin Layer Hela Cells Human HIV-1/*DRUG EFFECTS/PHYSIOLOGY Liver/ENZYMOLOGY Lysosomes/*ENZYMOLOGY Phospholipases A/ISOLATION & PURIF/*METABOLISM Rats Stereoisomers Support, Non-U.S. Gov't Support, U.S. Gov't, Non-P.H.S. Support, U.S. Gov't, P.H.S. Virus Replication/DRUG EFFECTS Zidovudine/*ANALOGS & DERIVATIVES/CHEMISTRY/METABOLISM/ PHARMACOLOGY JOURNAL ARTICLEKWDanimalantiviralagents/chemistry/metabolism/KWDpharmacologycelllinechromatography,thinlayerhelacellshumanhiv-1/KWDdrugeffects/physiologyliver/enzymologylysosomes/KWDenzymologyphospholipasesa/isolation&purif/KWDmetabolismratsstereoisomerssupport,non-uKWDsKWDgov'tsupport,uKWDsKWDgov't,non-pKWDhKWDsKWDsupport,uKWDsKWDgov't,pKWDhKWDsKWDvirusreplication/drugeffectszidovudine/KWDanalogs&derivatives/chemistry/metabolism/pharmacologyjournalarticle
930130
M9310738

Copyright © 1993 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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