Role of CAPE in reducing oxidative stress in animal models with traumatic brain injury

Abstract Introduction The central nervous system (CNS) is the most metabolically active organ characterized by high oxygen demand and relatively low anti-oxidative activity, which makes neurons and glia highly susceptible to damage by reactive oxygen and nitrogen byproducts as well as neurodegener...

Full description

Saved in:
Bibliographic Details
Main Authors: Rizha Anshori Nasution, -, Andi Asadul Islam, Andi, Mochammad Hatta, Mochammad, Prihantono, -, Agus Turchan, Agus, Nasrullah, -, Muhammad Faruk, Muhammad
Format: Article PeerReviewed
Language:English
Indonesian
English
Published: Elsevier
Subjects:
Online Access:https://repository.unair.ac.id/126190/1/19%20artikel.pdf
https://repository.unair.ac.id/126190/2/19A_Karil.pdf
https://repository.unair.ac.id/126190/3/19%20Turnitin.pdf
https://repository.unair.ac.id/126190/
https://www.sciencedirect.com/science/article/pii/S2049080120302181
https://doi.org/10.1016/j.amsu.2020.07.036
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universitas Airlangga
Language: English
Indonesian
English
Description
Summary:Abstract Introduction The central nervous system (CNS) is the most metabolically active organ characterized by high oxygen demand and relatively low anti-oxidative activity, which makes neurons and glia highly susceptible to damage by reactive oxygen and nitrogen byproducts as well as neurodegeneration. Free radicals are associated with secondary injuries that occur after a primary brain injury. Some of these free radical products include F2-Isoprostane (F2-IsoPs), malondialdehyde (MDA), 4-hydroxy-2-nonenal (4-HNE) and acrolein. Methods In this study we measured serum F2-IsoPs levels as markers of free radical activity in 10–12 week-old male Sprague-Dawley rats weighing 200–300 g, all rats (n = 10) subjected with a head injury according to the modified marmourou model, then divided into 2 groups, one group treated with CAPE (Caffeic Acid Phenethyl Ester) (n = 5) and the other not treated with CAPE (n = 5), serum levels in the two groups were compared starting from day-0 (before brain injury), day-4 and day-7. Results We found lower F2-IsoPs levels in the group that received the CAPE treatment compared to the group that did not receive the CAPE treatment. Conclusion CAPE is capable of significantly reducing oxidative stress in brain injury.