TY - JOUR
T1 - Antitumoral Activity of Cecropia Pachystachya Leaves Extract in Vitro and in Vivo Model of Rat Glioma
T2 - Brain and Blood Effects
AU - Bona, Natália Pontes
AU - Pedra, Nathalia Stark
AU - Spohr, Luiza
AU - da Silva dos Santos, Francieli
AU - Saraiva, Juliane Torchelsen
AU - Carvalho, Fabiano Barbosa
AU - da Cruz Fernandes, Marilda
AU - Fernandes, Ana Sofia
AU - Saraiva, Nuno
AU - Martins, Marta Filipa
AU - Tavares, Rejane Giacomelli
AU - Spanevello, Roselia Maria
AU - Aguiar, Mayara Sandrielly Soares de
AU - Stefanello, Francieli Moro
N1 - © 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2024/10
Y1 - 2024/10
N2 - 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.
AB - 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.
KW - 5'-Nucleotidase/metabolism
KW - Adenosine Deaminase/metabolism
KW - Animals
KW - Antineoplastic Agents, Phytogenic/pharmacology
KW - Antioxidants/pharmacology
KW - Brain Neoplasms/drug therapy
KW - Brain/drug effects
KW - Cecropia Plant/chemistry
KW - Cell Line, Tumor
KW - Cell Survival/drug effects
KW - Disease Models, Animal
KW - Glioma/drug therapy
KW - Male
KW - Plant Extracts/pharmacology
KW - Plant Leaves/chemistry
KW - Rats
KW - Rats, Wistar
KW - Reactive Oxygen Species/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85187879393&partnerID=8YFLogxK
U2 - 10.1007/s12035-024-04086-8
DO - 10.1007/s12035-024-04086-8
M3 - Article
C2 - 38483655
AN - SCOPUS:85187879393
SN - 0893-7648
VL - 61
SP - 8234
EP - 8252
JO - Molecular Neurobiology
JF - Molecular Neurobiology
IS - 10
ER -