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Abstract

Ruta graveolens is a plant commonly found in north Africa and south Europe. It is reported  that Ruta graveolens is used traditionally for epilepsy and some other illnesses. The acute and sub-acute effects of alcoholic extract residue were tested  for possible antiepileptic  and skeletal muscle relaxation activity. The effect of extract on rat spontaneous motor activity (SMA) was also investigated using open filed. We previously proved the anticonvulsant activity of the plant against pentylenetetrazol and electrically induced  convulsions. Therefore in this study strychnine  was used to induce convulsions in order to explore the mechanism of anticonvulsant activity of the plant. The skeletal muscle relaxation activity of Ruta graveolens was studied using pull-up and rod hanging tests in rats. At concentration of 5%w/v  the extract protected mice against strychnine induced myoclonic jerks and death. The pull-up and rod hanging tests pointed to a skeletal muscle relaxant activity at higher concentrations. Ruta graveolens extract also significantly decreased the  number of squares visited by rats in open field apparatus at all tested concentrations (7.5-20%w/v). However, the significant decrease in number of rearings was noticed at concentrations of above 10%w/v.  The results indicate that Ruta graveolens contains compound(s) capable to inhibit convulsions, decrease SMA  and/or diminish skeletal muscle tone in animal models. This data and the previously generated data together point to a general depression trend of CNS produced by  Ruta graveolens.

Keywords

Ruta graveolens Strychnine Spontaneous motor activity Skeletal muscle relaxation

Article Details

How to Cite
Shaban E. A. Saad, Suher M. Aburawi, Isabel Fong, Salem O. Abdalla, Abdurrahim A. Elouzi, Hend M. Shubar, & Madiha T. Al-gadamsy. (2021). Studying the effects of Ruta graveolens on spontaneous motor activity, skeletal muscle tone and strychnine induced convulsions in albino mice and rats. International Journal of Research in Pharmacology & Pharmacotherapeutics, 4(1), 53-58. https://doi.org/10.61096/ijrpp.v4.iss1.2015.53-58

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