» Articles » PMID: 35111411

Anti- Activity of 8-hydroxyquinoline and Its Synergistic Effect with Amphotericin B Deoxycholate Against

Overview
Journal PeerJ
Date 2022 Feb 3
PMID 35111411
Authors
Affiliations
Soon will be listed here.
Abstract

() is responsible for visceral leishmaniasis in patients with no known underlying immunodeficiency, and visceral or disseminated cutaneous leishmaniasis in HIV-infected patients. The available anti- drugs for treatment have limitations such as high toxicity and variable efficacy. To improve the therapeutic index of anti- drugs, the search for a new drug or a new natural compound in combination therapy instead of using monotherapy to reduce drug side effect and have high efficacy is required. In this study, anti- activity of 8-hydroxyquinoline (8HQN) and its synergistic effect with amphotericin B (AmB) against were evaluated for the first time. These results showed that 8HQN presented anti- activity against with IC 1.60 ± 0.28 and 1.56 ± 0.02 µg/mL for promastigotes and intracellular amastigotes, respectively. The selectivity index (SI) value of 8HQN was 79.84 for promastigotes and 82.40 for intracellular amastigotes, which highlight promising results for the use of 8HQN in the treatment of -infected host cells. Interestingly, four combinations of 8HQN and AmB provided synergistic effects for intracellular amastigotes and showed no toxic effects to host cells. These results provided information of using a combination therapy in treating this species leads to further development of therapy and can be considered as an alternative treatment for leishmaniasis.

Citing Articles

An update on infections: Transmission, clinical characteristics, and treatment.

Ahmadi S, Hataminejad M, Esboei B, Hosseini S, Fakhar M Parasite Epidemiol Control. 2024; 27:e00386.

PMID: 39507769 PMC: 11538800. DOI: 10.1016/j.parepi.2024.e00386.


Synergistic Effects of Artesunate in Combination with Amphotericin B and Miltefosine against : Potential for Dose Reduction and Enhanced Therapeutic Strategies.

Intakhan N, Saeung A, Rodrigues Oliveira S, Pereira M, Chanmol W Antibiotics (Basel). 2024; 13(9).

PMID: 39334981 PMC: 11428804. DOI: 10.3390/antibiotics13090806.


High Selectivity of 8-Hydroxyquinoline on and Species Correlates with a Potent Therapeutic Activity In Vivo.

de Lima S, Jesus J, Raminelli C, Laurenti M, Passero L Pharmaceuticals (Basel). 2023; 16(5).

PMID: 37242490 PMC: 10221700. DOI: 10.3390/ph16050707.

References
1.
Short B, Vargas M, Thomas J, OHanlon S, Enright M . In vitro activity of a novel compound, the metal ion chelating agent AQ+, against clinical isolates of Staphylococcus aureus. J Antimicrob Chemother. 2005; 57(1):104-9. DOI: 10.1093/jac/dki428. View

2.
Dardari Z, Lemrani M, Bahloul A, Sebban A, Hassar M, Kitane S . Antileishmanial activity of a new 8-hydroxyquinoline derivative designed 7-[5'-(3'-phenylisoxazolino)methyl]-8-hydroxyquinoline: preliminary study. Farmaco. 2004; 59(3):195-9. DOI: 10.1016/j.farmac.2003.11.001. View

3.
Lage L, Barichello J, Pagliara Lage D, Mendonca D, Carvalho A, Rodrigues M . An 8-hydroxyquinoline-containing polymeric micelle system is effective for the treatment of murine tegumentary leishmaniasis. Parasitol Res. 2016; 115(11):4083-4095. DOI: 10.1007/s00436-016-5181-4. View

4.
Allam G, Eweas A, Abuelsaad A . In vivo schistosomicidal activity of three novels 8-hydroxyquinoline derivatives against adult and immature worms of Schistosoma mansoni. Parasitol Res. 2013; 112(9):3137-49. DOI: 10.1007/s00436-013-3490-4. View

5.
Laranjeira-Silva M, Hamza I, Perez-Victoria J . Iron and Heme Metabolism at the Leishmania-Host Interface. Trends Parasitol. 2020; 36(3):279-289. PMC: 7161743. DOI: 10.1016/j.pt.2019.12.010. View