Literature DB >> 21140187

Peroxisome proliferator activating receptor (PPAR) in cerebral malaria (CM): a novel target for an additional therapy.

S Balachandar1, A Katyal.   

Abstract

Cerebral malaria (CM) is a global life-threatening complication of Plasmodium infection and represents a major cause of morbidity and mortality among severe forms of malaria. Despite developing knowledge in understanding mechanisms of pathogenesis, the current anti-malarial agents are not sufficient due to drug resistance and various adverse effects. Therefore, there is an urgent need for the novel target and additional therapy. Recently, peroxisome proliferator-activated receptor (PPAR) a nuclear receptors (NR) and agonists of its isoforms (PPARγ, PPARα and PPARβ/δ) have been demonstrated to exhibit anti-inflammatory and immunomodulatory properties, which are driven to a new approach of research on inflammatory diseases. Although many studies on PPARs have confirmed their diverse biological role, there is a lack of knowledge of its therapeutic use in CM. The major objective of this review is to explore the possible experimental studies to link these two areas of research. We focus on the data describing the beneficial effects of this receptor in inflammation, which is observed as a basic pathology in CM. In conclusion, PPARs could be a novel target in treating inflammatory diseases, and continued work with the available and additional agonists screened from various sources may result in a potential new treatment for CM.

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Year:  2010        PMID: 21140187     DOI: 10.1007/s10096-010-1122-9

Source DB:  PubMed          Journal:  Eur J Clin Microbiol Infect Dis        ISSN: 0934-9723            Impact factor:   3.267


  165 in total

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3.  An N-ethyl-N-nitrosourea (ENU)-induced dominant negative mutation in the JAK3 kinase protects against cerebral malaria.

Authors:  Silayuv E Bongfen; Ian-Gael Rodrigue-Gervais; Joanne Berghout; Sabrina Torre; Pablo Cingolani; Sean A Wiltshire; Gabriel A Leiva-Torres; Louis Letourneau; Robert Sladek; Mathieu Blanchette; Mark Lathrop; Marcel A Behr; Samantha Gruenheid; Silvia M Vidal; Maya Saleh; Philippe Gros
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6.  Pathway-GPS and SIGORA: identifying relevant pathways based on the over-representation of their gene-pair signatures.

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Review 7.  The molecular mechanisms of action of PPAR-γ agonists in the treatment of corneal alkali burns (Review).

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Journal:  Int J Mol Med       Date:  2016-08-04       Impact factor: 4.101

  7 in total

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