Dose-Dependent Behavioral and Antioxidant Effects of Quercetin and Methanolic and Acetonic Extracts fromHeterotheca inuloideson Several Rat Tissues following Kainic Acid-InducedStatus Epilepticus

Author:

Carmona-Aparicio Liliana1ORCID,Cárdenas-Rodríguez Noemí1ORCID,Delgado-Lamas Guillermo2,Pedraza-Chaverri José3ORCID,Montesinos-Correa Hortencia4,Rivera-Espinosa Liliana5,Torres-Espíndola Luz María5,Hernández Maria Eugenia6ORCID,López-Aceves Teresita17,Pérez-Lozano Diana Leticia1,Hernández-Velasco Natalia1,Narváez-Delgado Omar1,Gutiérrez-Alejandre Ana Paulina1,Fuentes-Mejía Monserrat1,Bello-Robles Edith1,Martínez-Ponce Karina1,Sánchez-Valle Vicente1,Sampieri Aristides8,Granados-Rojas Leticia1,Coballase-Urrutia Elvia1ORCID

Affiliation:

1. Laboratory of Neuroscience, National Institute of Pediatrics, Mexico City 04530, Mexico

2. Chemistry Institute, UNAM, Mexico City 04150, Mexico

3. Department of Biology, Faculty of Chemistry, UNAM, Mexico City 04150, Mexico

4. Service of Endocrinology, National Institute of Pediatrics, Mexico City 04530, Mexico

5. Laboratory of Pharmacology, National Institute of Pediatrics, Mexico City 04530, Mexico

6. Subdirection of Clinical Research, National Institute of Psychiatry, Mexico City 14370, Mexico

7. Faculty of Chemistry, Autonomous University of Sinaloa, Sinaloa 80000, Mexico

8. Department of Comparative Biology, Faculty of Sciences, UNAM, Mexico City 04150, Mexico

Abstract

Kainic acid (KA) has been used to study the neurotoxicity induced afterstatus epilepticus(SE) due to activation of excitatory amino acids with neuronal damage. Medicinal plants can protect against damage caused by KA-induced SE; in particular, organic extracts ofHeterotheca inuloidesand its metabolite quercetin display antioxidant activity and act as hepatoprotective agents. However, it is unknown whether these properties can protect against the hyperexcitability underlying the damage caused by KA-induced SE. Our aim was to study the protective effects (with regard to behavior and antioxidant activity) of administration of natural products methanolic (ME) and acetonic (AE) extracts and quercetin (Q) fromH. inuloidesat doses of 30 mg/kg (ME30, AE30, and Q30 groups), 100 mg/kg (ME100, AE100, and Q100 groups), and 300 mg/kg (ME300, AE300, and Q300 groups) against damage in brain regions of male Wistar rats treated with KA. We found dose-dependent effects on behavioral and biochemical studies in the all-natural product groupsvs.the control group, with decreases in seizure severity (Racine’s scale) and increases in seizure latency (p<0.05in the ME100, AE100, Q100, and Q300 groups andp<0.01in the AE300 and ME300 groups); on lipid peroxidation and carbonylated proteins in all brain tissues (p<0.0001); and on GPx, GR, CAT, and SOD activities with all the treatments vs. KA (p0.001). In addition, there were strong negative correlations between carbonyl levels and latency in the group treated with KA and in the group treated with methanolic extract in the presence of KA (r=0.9919,p=0.0084). This evidence suggests that organic extracts and quercetin fromH. inuloidesexert anticonvulsant effects via direct scavenging of reactive oxygen species (ROS) and modulation of antioxidant enzyme activity.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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