Oenanthe Javanica Extract Protects Against Experimentally Induced Ischemic Neuronal Damage via its Antioxidant Effects.
- Author:
Joon Ha PARK
;
Jeong Hwi CHO
;
In Hye KIM
;
Ji Hyeon AHN
;
Jae-Chul LEE
;
Bai Hui CHEN
;
Bich-Na SHIN
;
Hyun-Jin TAE
;
Ki-Yeon YOO
;
SeongKweon HONG
;
Il Jun KANG
;
Moo-Ho WON
1
;
Jong-Dai KIM
2
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Antioxidants; metabolism; therapeutic use; Gerbillinae; Glutathione Peroxidase; metabolism; Hippocampus; drug effects; metabolism; Ischemic Attack, Transient; prevention & control; Male; Oenanthe; chemistry; Plant Extracts; therapeutic use
- From: Chinese Medical Journal 2015;128(21):2932-2937
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDWater dropwort (Oenanthe javanica) as a popular traditional medicine in Asia shows various biological properties including antioxidant activity. In this study, we firstly examined the neuroprotective effect of Oenanthe javanica extract (OJE) in the hippocampal cornus ammonis 1 region (CA1 region) of the gerbil subjected to transient cerebral ischemia.
METHODSGerbils were established by the occlusion of common carotid arteries for 5 min. The neuroprotective effect of OJE was estimated by cresyl violet staining. In addition, 4 antioxidants (copper, zinc superoxide dismutase [SOD], manganese SOD, catalase, and glutathione peroxidase) immunoreactivities were investigated by immunohistochemistry.
RESULTSPyramidal neurons in the CA1 region showed neuronal death at 5 days postischemia; at this point in time, all antioxidants immunoreactivities disappeared in CA1 pyramidal neurons and showed in many nonpyramidal cells. Treatment with 200 mg/kg, not 100 mg/kg, OJE protected CA1 pyramidal neurons from ischemic damage. In addition, 200 mg/kg OJE treatment increased or maintained antioxidants immunoreactivities. Especially, among the antioxidants, glutathione peroxidase immunoreactivity was effectively increased in the CA1 pyramidal neurons of the OJE-treated sham-operated and ischemia-operated groups.
CONCLUSIONOur present results indicate that treatment with OJE can protect neurons from transient ischemic damage and that the neuroprotective effect may be closely associated with increased or maintained intracellular antioxidant enzymes by OJE.