Limitations of Current Therapeutic Options, Possible Drug Targets and Scope of Natural Products in Control of Leishmaniasis
- PMID: 28443518
- DOI: 10.2174/1389557517666170425105129
Limitations of Current Therapeutic Options, Possible Drug Targets and Scope of Natural Products in Control of Leishmaniasis
Abstract
Soon after the identification of Leishmania parasite as a causative agent, the pentavalent antimony compounds have been the mainstay to treat all forms of leishmaniasis. Due to growing incidences of antimony resistant parasites and unavailability of true antileishmanial compounds, few drugs like pentamidine (antimicrobial), amphotericin B (antifungal) or miltefosine (antitumor) are currently being used but these are associated with serious side effects. Unfortunately, the emergence of amphotericin B and miltefosine resistant parasites in clinical settings has further questioned their sustained use in leishmanial control. Moreover, the parameters of protective immunity are not well understood in leishmanial pathogenesis therefore, a vaccine candidate, either prophylactic or preventive, is still an unrealized goal. In addition, the emergence of insecticide resistance sand flies in disease endemic regions also stance a big threat for the current elimination strategies. Therefore, in lieu of the limited drug regimen and unavailability of a vaccine, the necessity of a true antileishmanial agent is always there. Although, leishmanial infections have been neglected for many decades but recent studies have identified potential drug targets that could be targeted to control the growth of parasites. In recent past many compounds derived from natural sources have also been shown to possess excellent antiparasitic potential; however, most of these studies are limited to primary evaluation and only a few have reached to clinical levels. In this review, we discuss the limitations of current drug regimen, explore possible drug targets of Leishmania species and summarize wide range of compounds isolated from various natural sources that are worth screening as antileishmanial drug candidates.
Keywords: Antileishmanial compounds; dermal; drug resistance; leishmaniasis; natural products; parasites.
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.
Similar articles
-
Natural product based leads to fight against leishmaniasis.Bioorg Med Chem. 2014 Jan 1;22(1):18-45. doi: 10.1016/j.bmc.2013.11.048. Epub 2013 Dec 4. Bioorg Med Chem. 2014. PMID: 24355247 Review.
-
Leishmaniasis: current status of available drugs and new potential drug targets.Asian Pac J Trop Med. 2012 Jun;5(6):485-97. doi: 10.1016/S1995-7645(12)60084-4. Asian Pac J Trop Med. 2012. PMID: 22575984 Review.
-
Leishmania treatment and prevention: Natural and synthesized drugs.Eur J Med Chem. 2018 Dec 5;160:229-244. doi: 10.1016/j.ejmech.2018.10.022. Epub 2018 Oct 11. Eur J Med Chem. 2018. PMID: 30342363 Review.
-
Screening natural products database for identification of potential antileishmanial chemotherapeutic agents.Interdiscip Sci. 2011 Sep;3(3):217-31. doi: 10.1007/s12539-011-0101-x. Epub 2011 Sep 29. Interdiscip Sci. 2011. PMID: 21956744
-
Marine Algae as Source of Novel Antileishmanial Drugs: A Review.Mar Drugs. 2017 Oct 29;15(11):323. doi: 10.3390/md15110323. Mar Drugs. 2017. PMID: 29109372 Free PMC article. Review.
Cited by
-
In Vitro Antileishmanial and Antitrypanosomal Activities of Plicataloside Isolated from the Leaf Latex of Aloe rugosifolia Gilbert & Sebsebe (Asphodelaceae).Molecules. 2022 Feb 18;27(4):1400. doi: 10.3390/molecules27041400. Molecules. 2022. PMID: 35209185 Free PMC article.
-
(-)-T-Cadinol-a Sesquiterpene Isolated From Casearia sylvestris (Salicaceae)-Displayed In Vitro Activity and Causes Hyperpolarization of the Membrane Potential of Trypanosoma cruzi.Front Pharmacol. 2021 Nov 3;12:734127. doi: 10.3389/fphar.2021.734127. eCollection 2021. Front Pharmacol. 2021. PMID: 34803682 Free PMC article.
-
Applications of Nanomaterials in Leishmaniasis: A Focus on Recent Advances and Challenges.Nanomaterials (Basel). 2019 Dec 9;9(12):1749. doi: 10.3390/nano9121749. Nanomaterials (Basel). 2019. PMID: 31818029 Free PMC article. Review.
-
A Betulinic Acid Derivative, BA5, Induces G0/G1 Cell Arrest, Apoptosis Like-Death, and Morphological Alterations in Leishmania sp.Front Pharmacol. 2022 Mar 22;13:846123. doi: 10.3389/fphar.2022.846123. eCollection 2022. Front Pharmacol. 2022. PMID: 35392556 Free PMC article.
-
High resolution melting analysis and detection of Leishmania resistance: the role of multi drug resistance 1 gene.Genes Environ. 2021 Aug 11;43(1):36. doi: 10.1186/s41021-021-00210-5. Genes Environ. 2021. PMID: 34380574 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous