Molecular effects of photodynamic therapy with curcumin on Leishmania major promastigotes.

Leishmania Curcumin Gene expression PDT Photodynamic therapy

Journal

Parasitology research
ISSN: 1432-1955
Titre abrégé: Parasitol Res
Pays: Germany
ID NLM: 8703571

Informations de publication

Date de publication:
29 Feb 2024
Historique:
received: 12 09 2023
accepted: 05 02 2024
medline: 29 2 2024
pubmed: 29 2 2024
entrez: 28 2 2024
Statut: epublish

Résumé

Leishmaniasis is a neglected disease mainly affecting low-income populations. Conventional treatment involves several side effects, is expensive, and, in addition, protozoa can develop resistance. Photodynamic therapy (PDT) is a promising alternative in treating the disease. PDT involves applying light at a specific wavelength to activate a photosensitive compound (photosensitizer, PS), to produce reactive oxygen species (ROS). Curcumin and its photochemical characteristics make it a good candidate for photodynamic therapy. Studies evaluating gene expression can help to understand the molecular events involved in the cell death caused by PDT. In the present study, RNA was extracted from promastigotes from the control and treated groups after applying PDT. RT-qPCR was performed to verify the expression of the putative ATPase beta subunit (ATPS), ATP synthase subunit A (F0F1), argininosuccinate synthase 1 (ASS), ATP-binding cassette subfamily G member 2 (ABCG2), glycoprotein 63 (GP63), superoxide dismutase (FeSODA), and glucose-6-phosphate dehydrogenase (G6PDH) genes (QR). The results suggest that PDT altered the expression of genes that participate in oxidative stress and cell death pathways, such as ATPS, FeSODA, and G6PD. The ATP-F0F1, ASS, and GP63 genes did not have their expression altered. However, it is essential to highlight that other genes may be involved in the molecular mechanisms of oxidative stress and, consequently, in the death of parasites.

Identifiants

pubmed: 38418645
doi: 10.1007/s00436-024-08155-8
pii: 10.1007/s00436-024-08155-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

146

Subventions

Organisme : Coordination for the Improvement of Higher Education Personnel - Brazil (CAPES)
ID : 001
Organisme : São Paulo State Research Support Foundation (FAPESP)
ID : 2016/12211-4
Organisme : São Paulo State Research Support Foundation (FAPESP)
ID : 2016/12211-4
Organisme : São Paulo State Research Support Foundation (FAPESP)
ID : 2016/12211-4
Organisme : São Paulo State Research Support Foundation (FAPESP)/CEPOF
ID : 2013/07276-1
Organisme : São Paulo State Research Support Foundation (FAPESP)/CEPOF
ID : 2013/07276-1
Organisme : Financiadora de Estudos e Projetos
ID : 01.13.0275.00

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Azim M, Khan SA, Ullah S, Ullah S, Anjum SI (2021) Therapeutic advances in the topical treatment of cutaneous leishmaniasis: a review. PLoS Negl Trop Dis 15:1–15. https://doi.org/10.1371/journal.pntd.0009099
doi: 10.1371/journal.pntd.0009099
Ceccarelli M, Galluzzi L, Migliazzo A, Magnani M (2014) Detection and characterization of Leishmania (Leishmania) and Leishmania (Viannia) by SYBR green-based real-time PCR and high resolution melt analysis targeting kinetoplast minicircle DNA. PLoS One 9:. https://doi.org/10.1371/journal.pone.0088845
de Melo Mendes MV, Tempone AG, TreigerBorborema SE (2019) Antileishmanial activity of H1-antihistamine drugs and cellular alterations in Leishmania (L.) infantum. Acta Trop 195:6–14. https://doi.org/10.1016/j.actatropica.2019.04.017
doi: 10.1016/j.actatropica.2019.04.017 pubmed: 31002807
Giorgio V, Burchell V, Schiavone M et al (2017) Ca2+ binding to F-ATP synthase β subunit triggers the mitochondrial permeability transition. EMBO Rep 18:1065–1076. https://doi.org/10.15252/embr.201643354
doi: 10.15252/embr.201643354 pubmed: 28507163 pmcid: 5494526
Goswami S, Dhar G, Mukherjee S, Adhya S (2006) A bifunctional tRNA import receptor from Leishmania mitochondria. Proc Natl Acad Sci U S A 103:8354–8359. https://doi.org/10.1073/pnas.0510869103
doi: 10.1073/pnas.0510869103 pubmed: 16714384 pmcid: 1482498
Hellemond JJ Van, Tielens AGM (1997) Inhibition of the respiratory chain results in a reversible metabolic arrest in leishmania promastigotes. Mol Biochem Parasitol  85(1):135–138. https://doi.org/10.1016/S0166-6851(97)02828-4
Kharkwal GB, Sharma SK, Huang YY, Dai T, Hamblin MR (2011) Photodynamic therapy for infections: clinical applications. Lasers Surg Med 43:755–767. https://doi.org/10.1002/lsm.21080
doi: 10.1002/lsm.21080 pubmed: 22057503 pmcid: 3449167
Manzano JI, Perea A, León-Guerrero D, Campos-Salina J, Piacenza L, Castanys S, Gamarro F (2017) Leishmania LABCG1 and LABCG2 transporters are involved in virulence and oxidative stress: functional linkage with autophagy. Parasit Vectors 10:1–12. https://doi.org/10.1186/s13071-017-2198-1
doi: 10.1186/s13071-017-2198-1
Marcolino LMC, Pereira AHC, Pinto JG, Mamone LA, Ferreira-Strixino J (2021) Cellular and metabolic changes after photodynamic therapy in Leishmania promastigotes. Photodiagnosis Photodyn Ther 35:102403. https://doi.org/10.1016/j.pdpdt.2021.102403
doi: 10.1016/j.pdpdt.2021.102403 pubmed: 34161856
Mittra B, Laranjeira-Silva MF, Miguel DC, de Menezes JPB, Andrews NW (2017) The iron-dependent mitochondrial superoxide dismutase SODA promotes Leishmania virulence. J Biol Chem 292:12324–12338. https://doi.org/10.1074/jbc.M116.772624
doi: 10.1074/jbc.M116.772624 pubmed: 28550086 pmcid: 5519379
Mondal S, Roy JJ, Bera T (2014) Characterization of mitochondrial bioenergetic functions between two forms of Leishmania donovani – a comparative analysis. J Bioenerg Biomembr 46:395–402. https://doi.org/10.1007/s10863-014-9569-5
doi: 10.1007/s10863-014-9569-5 pubmed: 25107348
Nafisi S, Adelzadeh M, Norouzi Z, Sarbolouki MN (2009) Curcumin binding to DNA and RNA. DNA Cell Biol 28:201–208. https://doi.org/10.1089/dna.2008.0840
doi: 10.1089/dna.2008.0840 pubmed: 19364279
Olivier M, Atayde VD, Isnard A, Hassani K, Shio MT (2012) Leishmania virulence factors: focus on the metalloprotease GP63. Microbes Infect 14:1377–1389. https://doi.org/10.1016/j.micinf.2012.05.014
doi: 10.1016/j.micinf.2012.05.014 pubmed: 22683718
Ouakad M, Bahi-Jaber N, Chenik M, Louzir H (2007) Selection of endogenous reference genes for gene expression analysis in Leishmania major developmental stages. Parasitol Res 101:473–477. https://doi.org/10.1007/s00436-007-0491-1
doi: 10.1007/s00436-007-0491-1 pubmed: 17318579
Pereira AHC, Marcolino LMC, Pinto JG, Ferreira-Strixino J (2021) Evaluation of the photodynamic therapy with curcumin on L. braziliensis and L. major amastigotes. Antibiotics 10:. https://doi.org/10.3390/antibiotics10060634
Pfaffl WM (2001) A new mathematical model for relative quantification in real-time RT–PCR. Oxford Univ Press 29:2003–2007. https://doi.org/10.1093/nar/29.9.e45
doi: 10.1093/nar/29.9.e45
Pinto JG, Fontana LC, de Oliveira MA, Kurachi C, Rainiero LJ, Ferreira-Strixino J (2016) In vitro evaluation of photodynamic therapy using curcumin on Leishmania major and Leishmania braziliensis. Lasers Med Sci 31:883–890. https://doi.org/10.1007/s10103-016-1928-5
doi: 10.1007/s10103-016-1928-5 pubmed: 27056699
Sardar AH, Jardim A, Ghosh AK et al (2016) Genetic manipulation of Leishmania donovani to explore the involvement of argininosuccinate synthase in oxidative stress management. PLoS Negl Trop Dis 10:1–25. https://doi.org/10.1371/journal.pntd.0004308
doi: 10.1371/journal.pntd.0004308
Szlasa W, Supplitt S, Drąg-Zalesińska M, Przystypski D, Kotowski K, Szewczyk, Kasperkiewicz P, Saczko J, Kulbacka J (2020) Effects of curcumin based PDT on the viability and the organization of actin in melanotic (A375) and amelanotic melanoma (C32) – in vitro studies. Biomed Pharmacother 132:. https://doi.org/10.1016/j.biopha.2020.110883
Veronica J, Chandrasekaran S, Dayakar A, Devender M, Prajapati VK, Sundar S, Maurya R (2019) Iron superoxide dismutase contributes to miltefosine resistance in Leishmania donovani. FEBS J 286:3488–3503. https://doi.org/10.1111/febs.14923
doi: 10.1111/febs.14923 pubmed: 31087522
Wikene KO, Bruzell E, Tønnesen HH (2015) Characterization and antimicrobial phototoxicity of curcumin dissolved in natural deep eutectic solvents. Eur J Pharm Sci 80:26–32. https://doi.org/10.1016/j.ejps.2015.09.013
doi: 10.1016/j.ejps.2015.09.013 pubmed: 26410725

Auteurs

Luciana Maria Cortez Marcolino (LMC)

Photobiology Applied to Health (PhotoBioS Lab), Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil.

Juliana Guerra Pinto (JG)

Photobiology Applied to Health (PhotoBioS Lab), Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil.

Isabelle Ferreira (I)

Photobiology Applied to Health (PhotoBioS Lab), Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil.

Bruno Henrique Godoi (BH)

Photobiology Applied to Health (PhotoBioS Lab), Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil.

Renata de Azevedo Canevari (R)

Cancer Molecular Biology Laboratory, Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil.

Juliana Ferreira-Strixino (J)

Photobiology Applied to Health (PhotoBioS Lab), Universidade Do Vale Do Paraíba, Av. Shishima Hifumi, 2911, Urbanova, São José Dos Campos, SP, Brazil. jufestrixino@gmail.com.

Classifications MeSH