Protective activity of Ruta chalepensis methanolic extract against nephrotoxicity and testicular damage induced by Carbon tetrachloride on albino male mice

Author:

Yahya Haider N.1,Okhti Zahraa A.2,Al-Ezzy Ruqaya M.3,Mhawesh Ahmed A.4,Alsaed Afnan A.4

Affiliation:

1. Plant Biotechnology department, College of Biotechnology, Al-Nahrain University, Iraq.

2. Clinical Laboratory Sciences department, College of Pharmacy, Mustansiriyah University, Iraq.

3. Molecular and Medical Biotechnology Department, College of Biotechnology, Al-Nahrain University, Iraq.

4. Department of Molecular and Medical Biotechnology, College of Biotechnology, Al-Nahrain University, Iraq.

Abstract

Herbal medicinal products can contain whole or partially prepared plant components from plant leaves, bark, stems, flowers and seeds.They are administered orally, inhaled or directly applied in the skin. Ruta chalepensis is a wild herb of the Mediterranean region used by many countries in herbal medicine. The existence of bioactive molecules responsible for their pharmacological properties has been shown by phytochemical screening. Results of kidney protective activity of plant. Showed that: for total cholesterol, the effect was dose dependant (50 and 100 mg\kg) in which the plant decreased it in compared to positive and negative groups (162.1±1.83 and 154.6±1.11 mg\dl) compared to (202.1±1.13 and 167.5±2.96 mg\dl) respectively. For total protein, creatinin and albumin the plant also had the ability to keep it near control groups compared to CCL4group.While the results of interaction groups indicated the ability of plant to provide protection against CCL4 damage. the plant possessed the ability to keep testosterone, progesterone and estrogen hormones level near normal in compared to CCL4 treated group (2.96±0.03, 1.93±0.01 and 3.63±0.04 ng\dl); (11.51±4.12, 9.85±2.18 and 11.78±3.42 ng\ml); (29.07±7.21, 30.11±9.11 and 30.67±8.98 ng\ml) for 50,100 mg\kg and negative control respectively. While for interaction group the results showed the ability of plant to counteract the damaged caused by CCL4 (1.67±0.01, 2.54±0.02); (10.42±2.21, 13.65±4.37); (39.74±10.13, 35.45±9.91) for testosterone, progesterone and estrogen hormones in Ruta chalepensis +CCL4 at dose (50 +0.02%) and (100+0.02%) respectively. All results of histo-architecture for kidney and testis showed the ability of plant to counteract any necrosis and abnormality caused by CCL4.

Publisher

A and V Publications

Subject

Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

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