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http://hdl.handle.net/10603/331207
Title: | Evaluation of phosphoinositide 3 kinase mammalian target of rapamycin and their dual inhibition in experimental epilepsy |
Researcher: | Vyas, Preeti |
Guide(s): | Vohora, Divya |
Keywords: | Clinical Pre Clinical and Health Pharmacology and Pharmacy Pharmacology and Toxicology |
University: | Jamia Hamdard University |
Completed Date: | 2021 |
Abstract: | The evidences from various studies show the association of peripheral and neuronal newlineinflammation with complex pathophysiology of status epilepticus (SE). In this view, the newlinepresent work attempted to develop a model of neuronal inflammation mediated SE by newlinecombining both epileptic and inflammatory components of the disease and also to mimic SE newlineco-morbid with systemic inflammation by peripheral administration of the lipopolysaccharide newline(LPS) 2 hours prior to the pilocarpine induction in C57BL/6 mice. We evaluated the anti newlineconvulsant and neuroprotective effects of 7-day prophylactic treatment with three newlineconventional anti-epileptic drugs (Sodium valproate, SVP 300 mg/kg p.o.; Carbamazepine newlineCBZ 100 mg/kg p.o.; Levetiracetam; LEV 200 mg/kg p.o.) of widespread clinical use. Morris newlinewater maze and Rota rod tests were carried out 24-hours post-exposure to evaluate the newlineneurobehavioral co-morbidities associated with neuroinflammation-mediated status newlineepilepticus. Upon priming with LPS, the loss of protection against pilocarpine-induced newlineseizures was observed by SVP and CBZ, however, LEV showed protection by delaying the newlineseizures. Dramatic elevation in the seizure severity and neuronal loss demonstrated the newlinepossible pro-convulsant effect of LPS in the pilocarpine model. Also, the decreased cytokine newlinelevels by the AEDs showed their association with NF-and#954;B, IL-1and#946;, IL-6, TNF-and#945; and TGF-b newlinepathways in PILO model. However, loss of protective activities of SVP and CBZ and only a newlinepartial efficacy of LEV in LPS+PILO model is suggestive of the possibility of involvement newlineof some other neuroinflammatory-pathway involved in the same. Over-activation of newlinephosphoinositide-3-kinases is associated with both neuroinflammation and seizures. Herein, newlinewe speculate PI3K/Akt/mTOR pathway as promising therapeutic target for neuroinflammation-mediated seizures and associated neurodegeneration. Firstly, we cultured HT22 cells for detection of the downstream cell signaling events activated in newline......... |
Pagination: | xxii, 247 |
URI: | http://hdl.handle.net/10603/331207 |
Appears in Departments: | Department of Pharmacology |
Files in This Item:
File | Description | Size | Format | |
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01_title page.pdf | Attached File | 288.04 kB | Adobe PDF | View/Open |
02_certificate.pdf | 465.47 kB | Adobe PDF | View/Open | |
03_preliminary pages.pdf | 721.05 kB | Adobe PDF | View/Open | |
04_chapter 1.pdf | 796.79 kB | Adobe PDF | View/Open | |
05_chapter 2.pdf | 922.14 kB | Adobe PDF | View/Open | |
06_chapter 3.pdf | 1.52 MB | Adobe PDF | View/Open | |
07_chapter 4.pdf | 2.99 MB | Adobe PDF | View/Open | |
08_chapter 5.pdf | 3.5 MB | Adobe PDF | View/Open | |
09_chapter 6.pdf | 753.59 kB | Adobe PDF | View/Open | |
10_chapter 7.pdf | 2.75 MB | Adobe PDF | View/Open | |
11_bibliography.pdf | 939.46 kB | Adobe PDF | View/Open | |
12_appendix i.pdf | 1.31 MB | Adobe PDF | View/Open | |
80_recommendation.pdf | 404.21 kB | Adobe PDF | View/Open | |
abstract.pdf | 78.44 kB | Adobe PDF | View/Open |
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