Antiviral therapy for chikungunya (CHIKV) and Zika (ZIKV) viruses: A pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2] increases spermidine/spermine N1-acetyltransferase (SAT) expression, depletes spermidine and Spermine levels, and restricts Chikungunya and Zika viruses replication via up regulation of its target gene, 09/October/2017, 11.29 pm

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Introduction: What they say

A study from the Viral Populations and Pathogenesis Unit, Institut Pasteur, CNRS UMR 3569, 25–28 rue du Dr. Roux, 75724 Paris Cedex 15, France shows that “Interferon-Induced Spermidine-Spermine Acetyltransferase and Polyamine Depletion Restrict Zika and Chikungunya Viruses.”  This research paper was published in the 10 August 2016 issue of the journal “Cell Host and microbe” [One of the best research journals  in Infectious biology with an I.F of 12.552] by Prof. Marco Vignuzzi, Bryan C. Mounce and others.


What we say: 

On the foundation of this interesting finding, Dr L Boominathan PhD, Director-cum-chief Scientist of GBMD, reports, for the first time, that: Antiviral therapy for chikungunya (CHIKV) and Zika (ZIKV) viruses: A pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2] increases spermidine/spermine N1-acetyltransferase (SAT) expression, depletes spermidine and Spermine levels, and restricts Chikungunya and Zika viruses replication via up regulation of its target gene


What is known?

Prof. Marco Vignuzzi’s research team has recently shown that induction of type I interferon results in: a) upregulation of SAT1; b) depletion of spermidine and spermine levels; and c) inhibition of Chikungunya and Zika viruses production. They have further validated this by showing that exogenous administration of Polyamines (spermidine and spermine) restores virus replication.


From Research findings to Therapeutic opportunity:

This study suggests a small molecule-based antiviral therapy against RNA viruses such as Chikungunya virus (CHIKV) and Zika virus (ZIKV).

price-300

A pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2], by increasing the expression of its target gene, it may increase the expression of spermidine/spermine N1-acetyltransferase (SAT1) (Figure 1). Thereby, it may: (1) decrease polyamine spermidine and spermine levels; (2) stall CHIKV and ZIKV replication; (3) promote clearance of Zika and Chikungunya Viruses; and (4) strengthen antiviral immunity against RNA viruses.

Figure 1 Mechanistic insights into how a pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2]   functions as an antiviral agent. APGJ2 functions as an antiviral agent by inhibiting the replication of Chikungunya and Zika viruses through induction of SAT

Figure 2. APGJ2 functions as an antiviral agent through induction of SAT

Thus, pharmacological formulations encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2]  or their analogues, either alone or in combination with other drugs” may be used to treat infections caused by chikungunya (CHIKV) and Zika (ZIKV) viruses.


Details of the research findings:

Idea Proposed/Formulated (with experimental evidence) by: Dr L Boominathan Ph.D.

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Undisclosed information: How does A pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2]  decrease the expression of spermidine/spermine N1-acetyltransferase (SAT1)?

Amount: $300#

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# Research cooperation


References:

Web: http://genomediscovery.org or http://newbioideas.com

Citation: Boominathan, L,  Antiviral therapy for chikungunya (CHIKV) and Zika (ZIKV) viruses: A pharmaceutical mixture encompassing Artesunate and 15-Deoxy-Delta-12,14-prostaglandin J2 (15d-PGJ2) [APGJ2] increases spermidine/spermine N1-acetyltransferase (SAT) expression, depletes spermidine and Spermine levels, and restricts Chikungunya and Zika viruses replication via up regulation of its target gene, 09/October/2017, 11.26 pm, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org

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