Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/346069
Title: Evaluation of Antiparkinsons activity of Uncaria rhynchophylla Mentha aquatica and Banisteriopsis caapi plants with Monoamine Oxidase B inhibition potential
Researcher: Biswajit Pal
Guide(s): Suresh Kumar S
Keywords: Antiparkinson s activity
Banisteriopsis caapi plants
Inhibition potential
Mentha aquatica
Monoamine Oxidase B
Uncaria rhynchophylla
University: The Tamil Nadu Dr. M.G.R. Medical University
Completed Date: 2015
Abstract: The study revealed the anti-Parkinson s activity of three herbal extracts (that Uncaria rhynchophylla, Mentha aquatica and Banisteriopsis caapi and its combination) in 6-OHDA induced Parkinson s models. In the standard experimental conditions, all the three extracts showed significant anti-parkinson s activity. The postural and neuro-humoral defects were normalised by the all test drugs. The systematic pharmacological analysis revealed that Uncaria rhynchophylla, Mentha aquatica and Banisteriopsis caapi- plants could be an anti-Parkinson s remedy, and earlier these three plants were ethanopharmacologically proven for its anti oxidant, anti ulcer, antiseptic, antispasmodic, anti diabetic, immunostimulent, anti cancer and CNS activities. The evaluation of anti Parkinson s activities of these plants might be leading to a new drug molecule or herbal moiety which can ameliorate the anti- Parkinson s drug toxicities or can be an anti Parkinson s drug in future. The extracts showed significant anti-Parkinson s activity in 6-OHDA lesioned rat models, but the lead identification was not carried out in this study. The estimated parameters were closely relevant to clinical Parkinsonism and the drug treatment protected the diseased brain of rat. The time constrains to complete this research and nature of experiment made us to restrict experiments specific to pharmacology. Our invention on these herbal drugs shall be an information to further carryout the lead identification for preclinical pharmacology, and we propose suitable lead optimization from these extracts. And we appreciate further detailed molecular studies with these leads in anti-Parkinson s pharmacology and toxicology. From these findings we suggest that, these newlinedrug molecules could be a future drug of choice for the treatment of clinical Parkinsonism. newline newline
Pagination: 146
URI: http://hdl.handle.net/10603/346069
Appears in Departments:Department of Pharmacy

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03_preliminary pages.pdf428.66 kBAdobe PDFView/Open
04_chapter 1.pdf1.21 MBAdobe PDFView/Open
05_chapter 2.pdf325.91 kBAdobe PDFView/Open
06_chapter 3.pdf400.96 kBAdobe PDFView/Open
07_chapter 4.pdf356.24 kBAdobe PDFView/Open
08_chapter 5.pdf737.37 kBAdobe PDFView/Open
09_chapter 6.pdf1.64 MBAdobe PDFView/Open
10_chapter 7.pdf330 kBAdobe PDFView/Open
11_appendix.pdf404.22 kBAdobe PDFView/Open
12_bibliography.pdf412 kBAdobe PDFView/Open
80_recommendation.pdf223.76 kBAdobe PDFView/Open
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