Neuroprotective effects of pink lotus oil in kainic acid-induced epilepsy.

Antioxidants Hippocampus Kainic acid Neurodegeneration Pink lotus essential oil p-Akt activation

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 29 03 2024
revised: 31 08 2024
accepted: 17 09 2024
medline: 9 10 2024
pubmed: 9 10 2024
entrez: 9 10 2024
Statut: epublish

Résumé

Excitotoxicity-induced oxidative stress results in neuronal cell death. Pink lotus essential oil (PLO) is a concentrated volatile oil from lotus blossoms widely used in traditional medicine. This study aimed to explore the possible therapeutic effects of PLO and its underlying mechanisms on kainic acid (KA)-induced oxidative stress and hippocampal cell death in a mouse model of epilepsy. Mice were treated with 100 mg/kg or 200 mg/kg PLO to ameliorate neurodegeneration and seizure-induced behavior induced by KA injection. Pre- and post-treatment of PLO increased antioxidant activities, reduced the seizure score, prevented oxidative stress by increasing GSH and CAT levels, and reduced MDA (malondialdehyde) levels after KA-induced status epilepticus. KA injection created neuronal cell death in the pyramidal layers of CA1 and CA3 subfields of the hippocampus, and affected interneurons in the hilus of the dentate gyrus. PLO treatment notably diminished KA-induced neuronal cell death in these areas through activation of the Akt signaling pathway, increasing reactive astrogliosis, and up-regulation of GDNF expression. Moreover, caspase-3 expression, and microglia activation were significantly decreased in PLO treatments. Taken together, these results suggest that PLO possesses antiepileptic, anti-apoptosic, and neuroprotective effects on KA-induced epileptogenesis indicating that PLO may serve as a dietary supplement option in the treatment of epilepsy or of other neurodegenerative disorders.

Identifiants

pubmed: 39381248
doi: 10.1016/j.heliyon.2024.e38070
pii: S2405-8440(24)14101-1
pmc: PMC11458948
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e38070

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ratchaniporn Kongsui (R)

Division of Physiology, School of Medical Sciences, University of Phayao, 56000, Thailand.

Teera Chanmanee (T)

Division of Anatomy, School of Medical Sciences, University of Phayao, 56000, Thailand.

Tichanon Promsrisuk (T)

Division of Physiology, School of Medical Sciences, University of Phayao, 56000, Thailand.

Lars Klimaschewski (L)

Division of Neuroanatomy, Department of Anatomy Histology and Embryology, Innsbruck Medical University, Innsbruck, 6020, Austria.

Napatr Sriraksa (N)

Division of Physiology, School of Medical Sciences, University of Phayao, 56000, Thailand.

Jinatta Jittiwat (J)

Faculty of Medicine, Mahasarakham University, Maha Sarakham, Maha Sarakham, 44000, Thailand.

Sitthisak Thongrong (S)

Division of Anatomy, School of Medical Sciences, University of Phayao, 56000, Thailand.

Classifications MeSH