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J Clin Exp Tox 2017 | Volume 1 | Issue 2

Toxicology and Pharmacology

November 01-02, 2017 | Toronto, Canada

International Conference on

A

number of processes are thought to contribute to the

development of epilepsy including increased excitatory

synaptic transmission, neuronal cell death and development

of aberrant innervations pattern in part arising from axonal

growth. Recent findings indicate that adhesion molecules

and their receptors play an important role in these processes

and contribute significantly in epileptogenesis. Among the

adhesion molecules, cell surface glycoproteins CD44 and

CD90 are reported to be up-regulated after neuronal injury

or epilepsy. Focus of this study was to evaluate the effect

of classical anticonvulsants i.e., diazepam and phenytoin and

an essential oil of

Allium cepa

AC-31B on the expression of

these markers in the PTZ-induced model of epilepsy. Here

we tested the hypothesis that anticonvulsant therapy that

can reduce the level of CD44/CD90 expression

in vivo

model

of epileptogenesis can be used to control the underlying

process of epileptogenesis. Targeting CD44/CD90 might be

a novel therapeutic target in neurological disorders. Mice

weighing 20-25 gm were subjected to PTZ-induced kindling

and their seizure-related behaviors were monitored. Once

stage 4 seizures were prominent, animals were sacrificed and

the brain samples were collected for the determination of

CD44/CD90 expression. The results revealed that AC-31B not

only halts the development of epileptogenesis in PTZ-kindled

mice but also significantly reduced the expression of CD44/

CD90. Based on these observations, we suggest that AC-31B

can be effectively used to control the underlying pathology

of epileptogenesis. This finding uncovers a potential effect

of AC-31B in epileptogenesis and may provide a new

therapeutic target that can be harnessed for the prevention

of epilepsy development or progression.

e

:shabana.simjee@iccs.edu

Nature’s own remedies:

Allium cepa

- does it offer new options for the treatment of epilepsy?

Shabana Usman Simjee

1, 2

and Humera Perveen

1

, Uzair Nisar

1

, Maha Shahid

1

and

Marium Askani

1

1

H E J Research Institute of Chemistry, Pakistan

2

University of Karachi, Pakistan