Antitumoral Activity of Cecropia Pachystachya Leaves Extract in Vitro and in Vivo Model of Rat Glioma: Brain and Blood Effects

Natália Pontes Bona, Nathalia Stark Pedra, Luiza Spohr, Francieli da Silva dos Santos, Juliane Torchelsen Saraiva, Fabiano Barbosa Carvalho, Marilda da Cruz Fernandes, Ana Sofia Fernandes, Nuno Saraiva, Marta Filipa Martins, Rejane Giacomelli Tavares, Roselia Maria Spanevello, Mayara Sandrielly Soares de Aguiar, Francieli Moro Stefanello

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

The aim of this study was to investigate the antiglioma effect of Cecropia pachystachya Trécul (CEC) leaves extract against C6 and U87 glioblastoma (GB) cells and in a rat preclinical GB model. The CEC extract reduced in vitro cell viability and biomass. In vivo, the extract decreased the tumor volume approximately 62%, without inducing systemic toxicity. The deficit in locomotion and memory and an anxiolytic-like behaviors induced in the GB model were minimized by CEC. The extract decreased the levels of reactive oxygen species, nitrites and thiobarbituric acid reactive substances and increased the activity of antioxidant enzymes in platelets, sera and brains of GB animals. The activity of NTPDases, 5'-nucleotidase and adenosine deaminase (ADA) was evaluated in lymphocytes, platelets and serum. In platelets, ATP and AMP hydrolysis was reduced and hydrolysis of ADP and the activity of ADA were increased in the control, while in CEC-treated animals no alteration in the hydrolysis of ADP was detected. In serum, the reduction in ATP hydrolysis was reversed by CEC. In lymphocytes, the increase in the hydrolysis of ATP, ADP and in the activity of ADA observed in GB model was altered by CEC administration. The observed increase in IL-6 and decrease in IL-10 levels in the serum of GB animals was reversed by CEC. These results demonstrate that CEC extract is a potential complementary treatment to GB, decreasing the tumor size, while modulating aspects of redox and purinergic systems.

Original languageEnglish
Pages (from-to)8234-8252
Number of pages19
JournalMolecular Neurobiology
Volume61
Issue number10
DOIs
Publication statusPublished - Oct 2024

Bibliographical note

© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Funding

This research was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico and Fundação de Amparo à Pesquisa do Rio Grande do Sul (FAPERGS). This study was financed in part by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior- Brasil (CAPES) – Finance code 001. Authors also acknowledge Fundação para a Ciência e a Tecnologia (FCT) through projects UIDB/04567/2020 and UIDP/04567/2020 to CBIOS.

FundersFunder number
Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul
Conselho Nacional de Desenvolvimento Científico e Tecnológico
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Fundação para a Ciência e a TecnologiaUIDP/04567/2020, UIDB/04567/2020

    Keywords

    • 5'-Nucleotidase/metabolism
    • Adenosine Deaminase/metabolism
    • Animals
    • Antineoplastic Agents, Phytogenic/pharmacology
    • Antioxidants/pharmacology
    • Brain Neoplasms/drug therapy
    • Brain/drug effects
    • Cecropia Plant/chemistry
    • Cell Line, Tumor
    • Cell Survival/drug effects
    • Disease Models, Animal
    • Glioma/drug therapy
    • Male
    • Plant Extracts/pharmacology
    • Plant Leaves/chemistry
    • Rats
    • Rats, Wistar
    • Reactive Oxygen Species/metabolism

    Fingerprint

    Dive into the research topics of 'Antitumoral Activity of Cecropia Pachystachya Leaves Extract in Vitro and in Vivo Model of Rat Glioma: Brain and Blood Effects'. Together they form a unique fingerprint.

    Cite this