Análogos e derivados da piperina com potencial atividade antiparasitária: revisão sistemática com avaliação do risco de viésadaptada para estudos in vitro
Piperine analogs and derivatives with potentialantiparasitic activity: systematic review with riskof-bias assessment adapted for in vitro studies
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Objetivo: Analizar el perfil de análogos y derivados de piperina que tienen actividad antiparasitaria contra los géneros Leishmania y Trypanosoma. Métodos: El estudio fue una revisión sistemática, que utilizó los descriptores: Piperina (Piperine), análogos y derivados (análogos y derivados), Leishmaniasis (Leishmaniasis), Trypanosoma (Trypanosoma), antiparasitarios (agentes antiparasitarios) en las siguientes bases de datos: Virtual Biblioteca de Salud (BVS), Biblioteca Nacional de Medicina (PubMed), (Scientific Electronic Library Online) SciELO, (Elsevier Database) ScienceDirect, Scopus y Embase. En el proceso de catalogación de los estudios se utilizó la lista de verificación de elementos de informes preferidos para revisiones sistemáticas y metanálisis (PRISMA). Además, se realizó una adaptación para evaluar el riesgo de sesgo de los estudios in vitro utilizando la herramienta de la Oficina de Evaluación y Traducción de la Salud (OHAT). Resultados: Inicialmente se encontraron 659 estudios en las bases de datos y luego de aplicar procedimientos específicos de selección de inclusión y exclusión se seleccionaron 10 artículos científicos. Conclusión: La investigación demostró que los análogos y derivados de la piperina mostraron actividad potencial contra las formas evolutivas de parásitos del género Leishmania y Trypanosoma.
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- Moreira RRD, Santos AGD, Carvalho FA, Perego CH, Crevelin EJ, Crotti AEM, Nakamura C.V. Antileishmanial activity of Melampodium divaricatum and Casearia sylvestris essential oils on Leishmania amazonensis. Revista do Instituto de Medicina Tropical de São Paulo, 2019; 61. https://doi.org/10.1590/S1678-9946201961033.
- World Health Organization. Leishmaniasis factsheet. Geneva: World Health Organization, 2020; Disponível em: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis.
- Ikeogu NM, Akaluka GN, Edechi CA, Salako ES, Onyilagha C, Barazandeh AF, Uzonna JE. Leishmania immunity: advancing immunotherapy and vaccine development. Microorganisms, 2020;8(8):1201. https://doi.org/10.3390/microorganisms8081201.
- Franco JR, Simarro PP, Diarra A, Jannin JG. Epidemiology of human African trypanosomiasis. Clinical epidemiology, 2014; 257-275. https://doi.org/10.2147/CLEP.S39728.
- Costa PRR. Produtos naturais como ponto de partida para a descoberta de novas substâncias bioativas: Candidatos a fármacos com ação antiofídica, anticâncer e antiparasitária. Revista Virtual de Química, 2009;1(1):58-66. https://doi.org/10.5935/1984-6835.20090008.
- Barreiro EJ, Fraga CAM. Química Medicinal-: As bases moleculares da ação dos fármacos. Artmed Editora, 2014. https://docs.bvsalud.org/biblioref/2023/06/1436553/tese-de-doutorado-fabio-navarro-baltazar-fabio-navarro.pdf
- Pal Singh, I., & Choudhary, A. Piperine and derivatives: trends in structure-activity relationships. Current topics in medicinal chemistry, 2015;15(17): 1722-1734. https://doi.org/10.2174/1568026615666150427123213.
- Da Silva YC, Silva EMS, Fernandes NDS, Lopes NL, Orlandi P.P, Nakamura CV, Costa EV, Da Veiga Júnior VF. Antimicrobial substances from Amazonian Aniba (Lauraceae) species. Natural Product Research, 2021;35(5):849-852. https://doi.org/10.1080/14786419.2019.1603225.
- Wang J, Wang W, Xiong H, Song, D, Cao X. Natural phenolic derivatives based on piperine scaffold as potential antifungal agents. BMC chemistry, 2020; 14:1-12. https://doi.org/10.1186/s13065-020-00676-4.
- Yasir A, Ishtiaq S, Jahangir M, Ajaib M, Salar U, Khan KM. Biology-oriented synthesis (BIOS) of piperine derivatives and their comparative analgesic and antiinflammatory activities. Medicinal Chemistry, 2018;14(3):269-280. https://doi.org/10.2174/1573406413666170623083810.
- Da Silva MA, Passarini GM, Martinez LDN, Fialho SN, Sales Jr PA, Fokoue HH, Kuenh CC. Atividade Tripanocida in vitro de amidas naturais e seus respectivos análogos sintéticos. South American Journal of Basic Education, Technical and Technological, 2020;7(1):186-197. https://teste-periodicos.ufac.br/index.php/SAJEBTT/article/view/2714.
- Mancini MC, Sampaio RF. Quando o objeto de estudo é a literatura: estudos de revisão. Brazilian Journal of Physical Therapy, 2007;10. https://doi.org/10.1590/S1413-35552006000400001
- Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, Moher D. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. International journal of surgery, 2021;88: 105906. https://doi.org/10.1016/j.ijsu.2021.105906.
- Sterne JAC, Hernán MA, Reeves BC, Savović J, Berkman ND, Viswanathan M, Henry D, Altman DG et al. ROBINS-I: a tool for assessing risk of bias in non-randomized studies of interventions. BMJ, 2016;355: [i4919]. https://doi.org/10.1136/bmj.i4919.
- Hooijmans CR, Rovers MM, De Vries R.B, Leenaars M, Ritskes-Hoitinga M, Langendam MW. SYRCLE’s risk of bias tool for animal studies. BMC medical research methodology, 2014;14: 1-9. https://doi.org/10.1186/1471-2288-14-43.
- Office of Health Assessment and Translation (OHAT). National Institute of Environmental Health Sciences. OHAT risk of bias rating tool for human and animal studies. US Department of Health and Human Services, 2015. https://ntp.niehs.nih.gov/sites/default/files/ntp/ohat/pubs/riskofbiastool_508.pdf.
- Rooney AA, Boyles AL, Wolfe MS, Bucher JR, Thayer KA. Systematic review and evidence integration for literature-based environmental health science assessments. Environmental health perspectives, 2014;122(7):711-718. https://doi.org/10.1289/ehp.13079.
- Hilal-Dandan R, Brunton L. Manual de farmacologia e terapêutica de Goodman & Gilman. AMGH Editora, 2015. https://books.google.com.br/books?hl=pt-BR&lr=&id=ofidBgAAQBAJ&oi=fnd&pg=PT2&dq=Manual+de+farmacologia+e+terap%C3%AAutica+de+Goodman+%26+Gilman.&ots=TfM9vji7gs&sig=Oc7iBO9uHAcJ3-wyXcg3XOQOSQQ#v=onepage&q=Manual%20de%20farmacologia%20e%20terap%C3%AAutica%20de%20Goodman%20%26%20Gilman.&f=false.
- Da Silva MA, Fokoue HH, Fialho SN, Dos Santos APDA, Rossi NR, Gouveia ADJ, ... Kuehn CC. Antileishmanial activity evaluation of a natural amide and its synthetic analogs against Leishmania (V.) braziliensis: an integrated approach in vitro and in silico. Parasitology Research, 2021;120(6): 2199-2218. https://link.springer.com/article/10.1007/s00436-021-07169-w.
- Da Silva TF. Abordagens da química medicinal para o planejamento de protótipos de fármacos. Revista Virtual de Química, 2013: 5(5), 921-933. https://doi.org/10.5935/1984-6835.20130066.
- Nepomuceno LL, Carvalho LD, Soares NP, Cruz VDS, Arnhold E, Ferreira JL, ... Samylla MCS. Padronização metodológica in vitro do ensaio colorimétrico MTT para avaliação da atividade de formazan e dosagem do fármaco: padronização do teste colorimétrico MTT. Farmacologia Aplicada à Enfermagem: Aspectos Teóricos e Práticos, 2021; 149-161. https://downloads.editoracientifica.org/articles/201202541.pdf.
- Folgueras-Flatschart AV, Gomes BC, Leve F, da Cunha Boldrini L. A importância do controle de qualidade de culturas utilizadas em ensaios biológicos e no desenvolvimento de pesquisas na área de saúde. Vigilância Sanitária em Debate: Sociedade, Ciência & Tecnologia, 2018; 6(1), 96-108. https://doi.org/10.22239/2317-269X.01083.
- Ribeiro TS, Freire-de-Lima L, Previato JO, Mendonça-Previato L, Heise N, de Lima MEF. Toxic effects of natural piperine and its derivatives on epimastigotes and amastigotes of Trypanosoma cruzi. Bioorganic & medicinal chemistry letters, 2004; 14(13), 3555-3558. https://doi.org/10.1016/j.bmcl.2004.04.019.
- Da Silva Ferreira W, Freire-de-Lima L, Saraiva VB, Alisson-Silva F, Mendonça-Previato L, Previato JO, ... de Lima MEF. Novel 1, 3, 4-thiadiazolium-2-phenylamine chlorides derived from natural piperine as trypanocidal agents: chemical and biological studies. Bioorganic & medicinal chemistry, 2008; 16(6), 2984-2991. https://doi.org/10.1016/j.bmc.2007.12.049.
- Regasini LO, Cotinguiba F, Passerini GD, Bolzani VDS, Cicarelli RMB, Kato M J, Furlan M. Trypanocidal activity of Piper arboreum and Piper tuberculatum (Piperaceae). Revista Brasileira de Farmacognosia, 2009; 19, 199-203. https://doi.org/10.1590/S0102-695X2009000200003.
- Singh IP, Jain SK, Kaur A, Singh S, Kumar R, Garg P, Arora SK. Synthesis and antileishmanial activity of piperoyl-amino acid conjugates. European journal of medicinal chemistry, 2010; 45(8), 3439-3445. https://doi.org/10.1016/j.ejmech.2010.04.033.
- Ferreira C, Soares DC, Barreto-Junior CB, Nascimento MT, Freire-de-Lima L, Delorenzi JC, Lima MEF, Atella GC, Folly E, Carvalho TMU, Saraiva EM, Pinto-da-Silva LH. Leishmanicidal effects of piperine, its derivatives, and analogues on Leishmania amazonensis. Phytochemistry, 2011; 72(17), 2155-2164. https://doi.org/10.1016/j.phytochem.2011.08.006.
- Naz T, Mosaddik A, Rahman MM, Muhammad I, Haque ME, Cho SK. Antimicrobial, antileishmanial and cytotoxic compounds from Piper chaba. Natural product research, 2012; 26(11), 979-986. https://doi.org/10.1080/14786419.2010.535166.
- Franklim TN, Freire-de-Lima L, De Nazareth Sá Diniz J, Previato JO, Castro RN, Mendonça-Previato L, De Lima MEF. Design, synthesis and trypanocidal evaluation of novel 1, 2, 4-triazoles-3-thiones derived from natural piperine. Molecules, 2013; 18(6), 6366-6382. https://doi.org/10.3390/molecules18066366.
- Da Silva Carrara V, Cunha-Júnior EF, Torres-Santos EC, Corrêa AG, Monteiro JL, Demarchi IG, Cortez DAG. Antileishmanial activity of amides from Piper amalago and synthetic analogs. Revista Brasileira de Farmacognosia, 2013; 23(3), 447-454. https://doi.org/10.1590/S0102-695X2013005000022.
- Fernandes ÍA, de Almeida L, Ferreira PE, Marques MJ, Rocha RP, Coelho LF, Carvalho DT, Viegas JrC. Synthesis and biological evaluation of novel piperidine-benzodioxole derivatives designed as potential leishmanicidal drug candidates. Bioorganic & Medicinal Chemistry Letters, 2015; 25(16), 3346-3349. https://doi.org/10.1016/j.bmcl.2015.05.068.
- Wansri R, Lin ACK, Pengon J, Kamchonwongpaisan S, Srimongkolpithak N, Rattanajak R, Chamni S. Semi-synthesis of N-aryl amide analogs of piperine from Piper nigrum and evaluation of their antitrypanosomal, antimalarial, and anti-SARS-CoV-2 main protease activities. 2022; Molecules, 27(9), 2841. https://doi.org/10.3390/molecules27092841.
- Serban G. 2-Amino-1, 3, 4-thiadiazoles as prospective agents in trypanosomiasis and other parasitoses. Acta Pharmaceutica, 2020; 70(3), 259-290. https://doi.org/10.2478/acph-2020-0031.
- Oliveira JPGD. Síntese de novos híbridos moleculares entre a estrutura privilegiada 7-cloroquinolina e adutos de morita-baylis-hillman candidatos a fármacos antitumorais e antiparasitários, 2019. https://repositorio.ufpb.br/jspui/handle/123456789/20227.
- Ramos PK, Diniz JA, Silva EO, Quaresma JA, Saraiva EM, Seabra SH, ... Souza W. Characterization in vivo and in vitro of a strain of Leishmania (Viannia) shawi from the Amazon Region. Parasitology International, 2009; 58(2), 154-160. https://doi.org/10.1016/j.parint.2009.01.009.
- Naz T, Mosaddik A, Rahman MM, Muhammad I, Haque ME, Cho SK. Antimicrobial, antileishmanial and cytotoxic compounds from Piper chaba. Natural product research, 2012; 26(11), 979-986. https://doi.org/10.1080/14786419.2010.535166.
- Ferreira WS, Franklim TN, Lopes ND, de Lima MEF. Piperina, seus análogos e derivados: potencial como antiparasitários. Revista Virtual de Química, 2012; 4(3), 208-224. https://doi.org/10.5935/1984-6835.20120018.
- Da Silva MA, Da Silva FB, Passarini GM, Fialho SN, Dos Santos APDA, Martinez LDN, ... Kuehn CC. PIPLARTINE AND PIPERINE: a review of their biological activities. South American Journal of Basic Education, Technical and Technological, 2019; 6(2), 818-858. https://teste-periodicos.ufac.br/index.php/SAJEBTT/article/view/2774.
- Baltazar FN. Otimização de novos candidatos a fármacos para Leishmaniose Visceral Canina. Tese (Doutorado em Ciências) - Secretaria de Estado da Saúde de São Paulo, 119 p, 2022. https://docs.bvsalud.org/biblioref/2023/06/1436553/tese-de-doutorado-fabio-navarro-baltazar-fabio-navarro.pdf.
- Castro LHE. Desenvolvimento de triazóis derivados da piperina inibidores da CYP51 de Trypanosoma cruzi: otimização de um modelo de previsão de atividade teórica, síntese e atividade in vitro. Tese (Doutorado em Química, Química Orgânica) - Instituto de Química, Universidade Federal Rural do Rio de Janeiro, 175 p, 2021. https://tede.ufrrj.br/jspui/handle/jspui/6553.