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Inhibition of sickling in vitro by three purine-based antiviral agents: an approach to the treatment of sickle cell disease.
- Source :
-
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2003 Sep-Oct; Vol. 31 (2), pp. 286-90. - Publication Year :
- 2003
-
Abstract
- As a result of an in vitro screening effort the antiviral agent acyclovir was found to inhibit aggregation of hemoglobin S and the sickling of erythrocytes from individuals with sickle cell disease. Sickling of the erythrocytes was significantly inhibited at 200 microg/ml under essentially anaerobic conditions, considerably more hypoxic than the conditions in which sickling occurs in sickle cell patients. The structurally related guanine-based antiviral agents ganciclovir, valacyclovir, and penciclovir were also tested. Valacyclovir and ganciclovir showed comparable anti-sickling activity at concentrations similar to that of acyclovir. An examination of the shared structural characteristics of the four guanine derivatives linked anti-sickling activity to the presence of an oxygen atom alpha to the N9 of the guanine moiety. These findings suggest a new approach in the search for new agents for the treatment of patients with sickle cell disease.
- Subjects :
- Acyclovir chemistry
Acyclovir pharmacology
Anemia, Sickle Cell pathology
Antiviral Agents chemistry
Antiviral Agents therapeutic use
Cell Aggregation
Cell Separation
Erythrocytes metabolism
Erythrocytes pathology
Ganciclovir chemistry
Ganciclovir pharmacology
Hemoglobin, Sickle metabolism
Humans
Oxygen metabolism
Valacyclovir
Valine chemistry
Valine pharmacology
Acyclovir analogs & derivatives
Anemia, Sickle Cell drug therapy
Antiviral Agents pharmacology
Erythrocytes drug effects
Hemoglobin, Sickle drug effects
Valine analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1079-9796
- Volume :
- 31
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Blood cells, molecules & diseases
- Publication Type :
- Academic Journal
- Accession number :
- 12972037
- Full Text :
- https://doi.org/10.1016/s1079-9796(03)00156-6