Investigation of Neuroprotective Effect of n-Hexane Extract of Cissampelos pareira in Ischemic Stroke-Induced Nerve Damage and Underlying Mechanisms

Author:

Khalid Muhammad Sohaib1ORCID,Sarwar Sadia1,Shah Fawad Ali2,Alamro Abir3,Algamdi Amani Ahmed3,Alghamdi Suad4,Malik Imran5

Affiliation:

1. Cell Culture Lab, Department of Pharmacognosy, Riphah Institute of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan

2. Swat College of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Swat, Khyber Pukthankhwa, Pakistan

3. Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia

4. Department of Medical Laboratory, College of Applied Medical Sciences, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia

5. Department of Pharmacology, Riphah Institute of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan

Abstract

Objective: Cissampelos pareira Linn. (Menispermaceae) has been reported for improving memory and cognitive behavior, and also as a folk remedy, for various neurodegenerative disorders. We investigated Cissampelos pareira for evaluating its neuroprotective effect on rodent model of focal cerebral ischemia. Methods: Male Sprague–Dawley rats (270-300 g) were subjected to permanent middle cerebral artery occlusion (MCAO). The animals were divided into five groups as control, MCAO, and MCAO +  Cissampelos pareira ( n-hexane, ethyl acetate (EtOAc), and methanol (MeOH) extracts; 50 mg/kg; n = 14). The expression of various inflammatory factors and enzymes including cyclooxygenase (COX-2), c-Jun N-terminal Kinase (p-JNK), and nuclear factor kappa-light-chain-enhancer of activated B cells (p-NF-κB) was detected in response to disease and extracts by immunohistochemistry and enzyme-linked immunosorbent assay. Results: The n-hexane extract (LD50 > 5.0 g/kg) reduced the infarction area significantly from in n-hexane extract + MCAO group, reversed neuronal death ( P < .01), and relieved the neurobehavioral deficits. The reduced levels of antioxidant enzymes (GST, GSH, CAT, SOD, and GPx), in case of MCAO were significantly elevated in response to n-hexane extract. 1,2-benzenedicarboxylic acid was detected (through gas chromatography/mass spectrometry) as the major component in n-hexane extract. Conclusion: n-hexane extract has the potential to be of therapeutic value in stroke patients, and thus further studies are warranted to elucidate the neuroprotective effects of this extract.

Publisher

SAGE Publications

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