Determination of Therapeutic and Safety Effects of Zygophyllum coccineum Extract in Induced Inflammation in Rats

Author:

Yosri Mohammed1ORCID,Elaasser Mahmoud M.1ORCID,Abdel-Aziz Marwa M.1ORCID,Hassan Marwa M.2,Alqhtani Abdulmohsen Hussen3ORCID,Al-Gabri Naif45ORCID,Ali Ahmed B. A.6ORCID,Pokoo-Aikins A.7ORCID,Amin Basma H.1ORCID

Affiliation:

1. The Regional Center for Mycology and Biotechnology, Al Azhar University, Nasr City, Cairo, Egypt

2. Anatomy and Embryology Department, Faculty of Medicine, Helwan University, Egypt

3. Animal Production Department, Food and Agriculture Sciences College, King Saud University, Riyadh, Saudi Arabia

4. Department of Pathology, Faculty of Veterinary Medicine, Thamar University, Yemen

5. Laboratory of Pathology, Salam Veterinary Group, Buraydah, Al Qassim 51911, Saudi Arabia

6. Department of Animal and Veterinary Science, Clemson University, SC, USA

7. US National Poultry Research Center, Toxicology & Mycotoxin Research Unit, USDA, ARS, Athens, GA 30605, USA

Abstract

Background. Z. coccineum is a facultative plant with many medicinal applications. This study examined the anti-inflammatory activity of Zygophyllum coccineum (Z. coccineum) in an arthritis animal model. Materials and Methods. Seventy-Six Wistar Albino rats of either sex randomly divided into six groups (12/each). The inflammation model was done using Complete Freund’s Adjuvant in albino rats. The anti-inflammatory activities of the extract were estimated at different dose levels (15.6, 31, and 60 mg/kg) as well as upon using methotrexate (MTX) as a standard drug (0.3 mg/kg). Paw volume and arthritis index scores have been tested in all examined animals’ treatments. Histological examination of joints was also performed. Flow cytometric studies were done to isolated osteoclasts. Cytokines assay as well as biochemical testing was done in the examined samples. Results. In vitro studies reported an IC50 of 15.6 μg/ml for Z. coccineum extract in lipoxygenase inhibition assay (L.O.X.). Moreover, it could be noticed that isorhamnetin-3-O-glucoside, tribuloside, and 7-acetoxy-4-methyl coumarin were the most common compounds in Z. coccineum extract separated using L.C.–ESI-TOF–M.S. (liquid chromatography-electrospray ionization ion-trap time-of-flight mass spectrometry). Microscopic examinations of synovial tissue and hind limb muscles revealed the effect of different doses of Z. coccineum extract on restoring chondrocytes and muscles structures. Osteoclast size and apoptotic rate examinations revealed the protective effect of Z. coccineum extract on osteoclast. The results upon induction of animals and upon treatment using of MTX significantly increased apoptotic rate of osteoclast compared to control, while using of 15.6 μg/ml. for Z. coccineum extract lead to recover regular apoptotic rate demonstrating the protective effect of the extract. Z. coccineum extract regulated the secretion of proinflammatory and anti-inflammatory cytokines. Biochemical tests indicated the safety of Z. coccineum extract on kidney and liver functions. Conclusion. Z. coccineum extract has efficient and safe anti-inflammatory potential in an induced rat model.

Funder

King Saud University

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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