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Published on: January 19, 2019
Enhanced antiscrapie effect using combination drug treatment.
David A Kocisko1, Byron Caughey, John D Morrey
1Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA. DKocisko@niaid.nih.gov
Combination treatment with pentosan polysulfate and Fe(III)meso-tetra(4-sulfonatophenyl)porphine extended survival times in mice with scrapie disease. This synergistic approach shows promise for treating transmissible spongiform encephalopathies and other protein-misfolding diseases.
Area of Science:
- Neuroscience
- Pharmacology
- Biochemistry
Background:
- Transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases.
- Protein-misfolding diseases share common pathogenic mechanisms.
- Effective treatments for TSEs are currently lacking.
Purpose of the Study:
- To evaluate the efficacy of a combination therapy for scrapie, a model TSE.
- To determine if pentosan polysulfate and Fe(III)meso-tetra(4-sulfonatophenyl)porphine act synergistically.
Main Methods:
- Mice were inoculated with scrapie.
- Combination treatment with pentosan polysulfate and Fe(III)meso-tetra(4-sulfonatophenyl)porphine was initiated at 14 or 28 days post-inoculation.
- Survival times were monitored.
Main Results:
- Combination therapy significantly increased survival times in scrapie-infected mice.
- The observed increase in survival suggests a synergistic effect between the two compounds.
- Treatment initiated later post-inoculation still demonstrated efficacy.
Conclusions:
- Combination therapy with pentosan polysulfate and Fe(III)meso-tetra(4-sulfonatophenyl)porphine is a promising therapeutic strategy for TSEs.
- The synergistic action of these compounds in vivo warrants further investigation.
- This approach may be applicable to other protein-misfolding diseases.
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