Nursing Pharmacology: Antiviral Drugs
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Antiviral Drugs
Antiviral drugs may target specific steps of viral replication.3
These steps include
Viral binding to host cell surface receptors
Viral entry into the cell
Viral nucleic acid uncoating;
"Early" regulatory protein synthesis, an example being nucleic acid polymerases
New viral RNA or DNA synthesis
Synthesis of "late", structural proteins which may be used in capsid assembly
Viral particle assembly, the maturation step; release of active virions from the cell.3
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Herpes simplex virus type 1 (HSV-1) and herpes simplex virus type 2 (HSV-2) are responsible for a number of infections.1
These infections result in diseases of the mouth, skin, esophagus, brain, or face in the case of HSV-1. 1
HSV-2 infections are more commonly associated with diseases of the genitals, skin, rectum, hands or meninges.
HSV-1 and HSV-2 are implicated in neonatal herpes simplex virus (HSV) infections.
The first effective treatment for relatively less severe HSV and another herpesvirus, varicella-zoster virus (VZV) was developed over 40 years ago and approved in 1982.
Acyclovir is the prototype drug in a group of antiviral agents which must be phosphorylated intracellularly, catalyzed by both viral kinase and host cell enzymes to become the active drug which inhibits viral DNA synthesis.1
Mechanism of Action:
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Acyclovir exhibits selectivity of action mainly affecting viral DNA synthesis NOT mammalian cell DNA synthesis.2
This selectivity depends on acyclovir being a "prodrug" and requiring an initial phosphorylation step to acyclovir monophosphate.
The important point is this phosphorylation step rarely occurs in herpes-infected cells because it is catalyzed by a virus-coded thymidine kinase.
By contrast, very limited acyclovir phosphorylation occurs in unaffected mammalian cells acyclovir affinity for the mammalian thymidine kinase is about 200 times less than that for the viral kinase.1,2
Acyclovir triphosphate exhibits a 40-100 fold higher concentration in HSV viral infected cells compared to uninfected cells.1
Host cell kinases, as described in the figure above, catalyzed multiple additional transphosphorylation steps, ultimately resulting in active drug, acyclovir triphosphate.2
Acyclovir triphosphate is incorporated into viral DNA and as an analogue of 2'-3' dideoxynucleotides, causes early chain termination.2
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Chemistry of Acyclovir and Related Drugs
Acyclovir is classified as an acyclic guanine nucleoside analog which is missing a 3'-hydroxyl on the side chain.1
A closely related drug, valacyclovir is a L-valyl ester prodrug for acyclovir.1
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