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Possible Neuroprotective Mechanisms Of Ginseng And Rutin In Experimental Model Of Head Injury Induced Cognitive Dysfunction | 64306
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Introduction: Head injury is a major cause of disability and death. Possible role of neuroinflammation, nitric oxide, microglia
and oxidative stress have been suggested in the pathophysiology of traumatic brain injury related complications such as
cognitive dysfunction.
Objective: Therefore, the present study was designed to explore the possible role of ginseng and rutin and its interaction with
nitric oxide modulator and microglial inhibitor against experimental of head injury induced behavioral, biochemical and
molecular alterations.
Materials & Methods: Wistar rats were exposed to head injury by using weight-drop method. Following injury and a postinjury
rehabilitation period of two weeks, animals were administered vehicle/drugs for another two weeks.
Results: Traumatic brain injury caused significant memory impairment in Morris water maze task as evident from increase
in escape latency and total distance travelled to reach the hidden platform. Time spent in target quadrant and frequency of
appearance in target quadrant was also significantly decreased in head trauma rats. Further, there was a significant increase
in oxidative stress (elevated malondialdehyde, nitrite concentration and decreased reduced glutathione, superoxide dismutase
and catalase levels), neuroinflammation (TNF-α and IL-6) and acetylcholinesterase levels in both cortex and hippocampal
regions of traumatized rat brain. Ginseng (100-200 mg/kg), Rutin (20-80) treatment for two weeks significantly attenuated
all these behavioral, biochemical and molecular alterations, suggesting their neuroprotective effect. Further, combination of
sub effective doses of ginseng (50 and 100 mg/kg) or rutin (40, 80) with microglia inhibitor as well as nitric oxide modulators
significantly modulates their protective effect respectively. The present study suggests that these flavanoids produce their
neuroprotective effect by involving microglial as well as nitric oxide pathways.
Conclusion: The study further provides a hope that these flavanoids could be used effectively for the management of brain
traumatic injury and related complication.