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Mol Neurobiol ; 61(10): 8234-8252, 2024 Oct.
Article in English | MEDLINE | ID: mdl-38483655

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.


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