Anti-Parkinsonian Activity of Ganoderma Lucidum in Experimentally Induced Parkinson’s Disease

Sana Aslam

Department of Health Sciences, Iqra University North Karachi, Pakistan.

Muhammad Aslam *

Department of Pharmacology, Faculty of Pharmacy, University of Sindh, Jamshoro, Pakistan.

Hania Kauser

Department of Health Sciences, Iqra University North Karachi, Pakistan.

Sara Naqvi

Department of Health Sciences, Iqra University North Karachi, Pakistan.

*Author to whom correspondence should be addressed.


Abstract

Background: Parkinson's illness has been proclaimed as the second most neurodegenerative problem on the planet. Ganoderma lucidum is considered as a genuine restorative mushroom.

Aim: Our study was directed to assess the antiparkinsonian action of Ganoderma lucidum in rotenone-incited Parkinson’s disease in male Wistar rodents.

Methods: The impacts of Ganoderma lucidum were concentrated on catalepsy, muscle rigidity.

Results: Ganoderma lucidum fundamentally decreased the expanded length of catalepsy. Rotenone essentially initiated the disturbance of motor neurons as demonstrated by muscle rigidity of muscles and decreased locomotion. Ganoderma lucidum alleviated the disturbance of motor neurons by rotarod execution and locomotor action of the creatures. The exercises of cell reinforcement proteins catalase and superoxide dismutase, and the level of tripeptide glutathione were essentially diminished by rotenone. Besides, rotenone extended the level of lipid peroxidation thing malondialdehyde. Notwithstanding, Ganoderma lucidum supplementation to rotenone-infused rats essentially extended the degrees of superoxide dismutase, catalase, and glutathione, and diminished the level of malondialdehyde

Conclusion: Our study firmly supports the notion that Ganoderma lucidum has neuroprotective and antiparkinsonian action.

Keywords: Medicinal mushroom, neurodegenerative diseases, reishi


How to Cite

Aslam, S., Aslam, M., Kauser, H. and Naqvi, S. (2021) “Anti-Parkinsonian Activity of Ganoderma Lucidum in Experimentally Induced Parkinson’s Disease”, Journal of Pharmaceutical Research International, 33(52B), pp. 266–275. doi: 10.9734/jpri/2021/v33i52B33626.