| Literature DB >> 34356608 |
Rima El-Dirany1,2, Hawraa Shahrour2,3, Zeinab Dirany4, Fadi Abdel-Sater2, Gustavo Gonzalez-Gaitano4, Klaus Brandenburg5, Guillermo Martinez de Tejada3, Paul A Nguewa1.
Abstract
Anti-microbial peptides (AMPs), small biologically active molecules, produced by different organisms through their innate immune system, have become a considerable subject of interest in the request of novel therapeutics. Most of these peptides are cationic-amphipathic, exhibiting two main mechanisms of action, direct lysis and by modulating the immunity. The most commonly reported activity of AMPs is their anti-bacterial effects, although other effects, such as anti-fungal, anti-viral, and anti-parasitic, as well as anti-tumor mechanisms of action have also been described. Their anti-parasitic effect against leishmaniasis has been studied. Leishmaniasis is a neglected tropical disease. Currently among parasitic diseases, it is the second most threating illness after malaria. Clinical treatments, mainly antimonial derivatives, are related to drug resistance and some undesirable effects. Therefore, the development of new therapeutic agents has become a priority, and AMPs constitute a promising alternative. In this work, we describe the principal families of AMPs (melittin, cecropin, cathelicidin, defensin, magainin, temporin, dermaseptin, eumenitin, and histatin) exhibiting a potential anti-leishmanial activity, as well as their effectiveness against other microorganisms.Entities:
Keywords: Cathelicidin; Cecropin; Defensin; Dermaseptin; Eumentin; Histatin; Leishmania; Magainin; Melittin; Temporin; anti-bacterial; anti-fungal; anti-microbial peptides (AMPs); anti-parasitic; anti-tumor; anti-viral; bacteria; parasite
Year: 2021 PMID: 34356608 DOI: 10.3390/biom11070984
Source DB: PubMed Journal: Biomolecules ISSN: 2218-273X