Vidarabine: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 1: Line 1:
'''Vidarabine''' is an [[antiviral drug]] that is primarily used in the treatment of [[Herpes simplex virus]] infections, as well as in the treatment of varicella zoster (chickenpox and shingles) and Epstein-Barr virus. It is a type of [[nucleoside analogue]], a class of drugs that are known to inhibit the synthesis of viral DNA.
{{Short description|Antiviral medication}}
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002295
| IUPAC_name = 9-β-D-Arabinofuranosyladenine
| image = Vidarabine.svg
| image2 = Mechanism_of_action_of_vidarabine.gif
}}


== History ==
'''Vidarabine''', also known as '''adenine arabinoside''' or '''ara-A''', is an [[antiviral drug]] that was one of the first antiviral agents to be developed and used in clinical practice. It is primarily used for the treatment of [[herpes simplex virus]] (HSV) infections, particularly in cases of [[herpes simplex encephalitis]] and [[herpes zoster]] in immunocompromised patients.


Vidarabine was first synthesized in the 1960s by the [[National Cancer Institute]] as part of a program to develop antiviral drugs. It was initially used as a topical ointment to treat herpes simplex virus infections of the skin and mucous membranes. In the 1970s, it was approved by the [[Food and Drug Administration]] (FDA) for use in the treatment of systemic herpes simplex virus infections and varicella zoster virus infections.
==History==
Vidarabine was first synthesized in the 1960s and was initially investigated for its potential as an [[anticancer]] agent. However, its antiviral properties were soon recognized, leading to its development as an antiviral medication. It was approved for medical use in the United States in 1976.


== Mechanism of Action ==
==Mechanism of Action==
[[File:Mechanism_of_action_of_vidarabine.gif|Mechanism of action of vidarabine|thumb|right]]
Vidarabine works by inhibiting viral [[DNA polymerase]], an enzyme critical for viral DNA replication. It is a nucleoside analog, meaning it mimics the natural nucleosides that are the building blocks of DNA. Once incorporated into viral DNA, vidarabine causes premature chain termination, effectively halting viral replication.


Vidarabine works by inhibiting the replication of viral DNA. It is converted into its active form, vidarabine triphosphate, by cellular enzymes. This active form then inhibits the activity of DNA polymerase, an enzyme that is necessary for the replication of the virus. By inhibiting this enzyme, vidarabine prevents the virus from replicating and spreading.
==Pharmacokinetics==
Vidarabine is administered intravenously due to its poor oral bioavailability. It is rapidly deaminated to arabinosyl hypoxanthine, which is less active. The drug is primarily excreted by the kidneys.


== Side Effects ==
==Clinical Uses==
Vidarabine is used in the treatment of severe HSV infections, including:
* [[Herpes simplex encephalitis]]
* [[Neonatal herpes simplex]]
* [[Herpes zoster]] in immunocompromised patients


The most common side effects of vidarabine are nausea, vomiting, and diarrhea. Other side effects can include fever, rash, and changes in blood counts. In rare cases, vidarabine can cause serious side effects such as neurotoxicity and bone marrow suppression.
==Side Effects==
 
Common side effects of vidarabine include nausea, vomiting, diarrhea, and headache. More serious side effects can include [[neurotoxicity]] and [[bone marrow suppression]].
== Resistance ==
 
Resistance to vidarabine can occur in patients who have been treated with the drug for a long period of time. This resistance is usually due to mutations in the viral DNA polymerase that make it less susceptible to the inhibitory effects of vidarabine.
 
== See Also ==


==Related Pages==
* [[Antiviral drug]]
* [[Antiviral drug]]
* [[Herpes simplex virus]]
* [[Herpes simplex virus]]
* [[Varicella zoster virus]]
* [[Nucleoside analog]]
* [[Epstein-Barr virus]]
* [[Nucleoside analogue]]


[[Category:Antiviral drugs]]
[[Category:Antiviral drugs]]
[[Category:Herpes]]
[[Category:Purines]]
[[Category:Medicine]]
[[Category:World Health Organization essential medicines]]
 
{{Medicine-stub}}
<gallery>
File:Vidarabine.svg|Vidarabine
File:Mechanism_of_action_of_vidarabine.gif|Mechanism of action of vidarabine
</gallery>
<gallery>
File:Vidarabine.svg|Chemical structure of Vidarabine
File:Mechanism_of_action_of_vidarabine.gif|Mechanism of action of Vidarabine
</gallery>

Latest revision as of 10:53, 23 March 2025

Antiviral medication


Vidarabine
File:Vidarabine.svg
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number
PubChem
DrugBank
ChemSpider
KEGG


Vidarabine, also known as adenine arabinoside or ara-A, is an antiviral drug that was one of the first antiviral agents to be developed and used in clinical practice. It is primarily used for the treatment of herpes simplex virus (HSV) infections, particularly in cases of herpes simplex encephalitis and herpes zoster in immunocompromised patients.

History[edit]

Vidarabine was first synthesized in the 1960s and was initially investigated for its potential as an anticancer agent. However, its antiviral properties were soon recognized, leading to its development as an antiviral medication. It was approved for medical use in the United States in 1976.

Mechanism of Action[edit]

File:Mechanism of action of vidarabine.gif
Mechanism of action of vidarabine

Vidarabine works by inhibiting viral DNA polymerase, an enzyme critical for viral DNA replication. It is a nucleoside analog, meaning it mimics the natural nucleosides that are the building blocks of DNA. Once incorporated into viral DNA, vidarabine causes premature chain termination, effectively halting viral replication.

Pharmacokinetics[edit]

Vidarabine is administered intravenously due to its poor oral bioavailability. It is rapidly deaminated to arabinosyl hypoxanthine, which is less active. The drug is primarily excreted by the kidneys.

Clinical Uses[edit]

Vidarabine is used in the treatment of severe HSV infections, including:

Side Effects[edit]

Common side effects of vidarabine include nausea, vomiting, diarrhea, and headache. More serious side effects can include neurotoxicity and bone marrow suppression.

Related Pages[edit]