A bitter flavonoid gum from Dorema aucheri accelerate wound healing in rats: Involvement of Bax/HSP 70 and hydroxyprolin mechanisms

Author:

Ahmed Khaled Abdul‐Aziz1,Jabbar Ahmed A.j.2ORCID,Raouf Mohammed M. Hussein M.3,Al‐Qaaneh Ayman M.4,Mothana Ramzi A.5,Alanzi Abdullah R.5,Abdullah Fuad Othman6,hassan Rawaz Rizgar7,Abdulla Mahmood Ameen8,Saleh Musher Ismael9,Hasson Sidgi10

Affiliation:

1. Associate Professor at Department of Medical Laboratory Sciences Faculty of Allied Medical Sciences Al‐Ahliyya Amman University Amman Jordan

2. Department of Medical Laboratory Technology Erbil Technical Health and Medical College Erbil Polytechnic University Erbil Iraq

3. Department of Biomedical Sciences College of Applied Science Cihan University‐Erbil Erbil Kurdistan Region Iraq

4. Department of Allied Health Sciences Al‐Balqa Applied University (BAU) Al‐Salt Jordan

5. Department of Pharmacognosy College of Pharmacy King Saud University Riyadh Saudi Arabia

6. Department of Chemistry College of Science Salahaddin University‐Erbil Kurdistan Region Erbil Kurdistan Region Iraq

7. Department of Medical Laboratory Science College of Science Knowledge University Erbil Iraq

8. Department of Medical Analysis Faculty of Applied Science Tishk International University Erbil Iraq

9. Department of Chemistry Faculty of Science and Health Koya University Koya KOY45 Erbil Kurdistan Region Iraq

10. School of Pharmacy and Biomolecular Sciences Liverpool John Moores University Liverpool UK

Abstract

AbstractBackgroundDorema aucheri gum (DAG) is a bitter flavonoid gum widely used for numerous medicinal purposes including wound recovery. The present work investigates the acute toxicity and wound‐healing effects of DAG in excisional skin injury in rats.Materials and methodsSprague Dawley rats (24) were clustered into four groups, each rat had a full‐thickness excisional dorsal neck injury (2.00 cm) and addressed with 0.2 mL of the following treatments for 15 days: Group A (vehicle), rats addressed with normal saline; Group B, rats received intrasite gel; C and D, rats addressed with 250 and 500 mg/kg of DAG, respectively.ResultsThe results revealed the absence of any toxic signs in rats who received oral dosages of 2 and 5 g/kg of DAG. Wound healing was significantly accelerated following DAG treatments indicated by smaller open areas and higher wound contraction percentages compared to vehicle rats. Histological evaluation revealed higher fibroblast formation, collagen deposition, and noticeably lower inflammatory cell infiltration in granulated skin tissues of DAG‐addressed rats compared to vehicle rats. DAG treatment caused significant modulation of immunohistochemical proteins (decreased Bax and increased HSP 70) and inflammatory mediators (reduced TNF‐α, IL‐6, and magnified IL‐10), which were significantly varied compared to vehicle rats. Moreover, topical DAG treatment led to significant upregulation of the hydroxyproline (HDX) (collagen) and antioxidant content. At the same time, decreased the lipid peroxidation (MDA) levels in healed tissues obtained from DAG‐treated rats.ConclusionThe present wound contraction by DAG might be linked with the modulatory effect of its phytochemicals (polysaccharides, flavonoids, and phenolic) on the cellular mechanisms, which justify their folkloric use and provokes further investigation as therapeutic drug additives for wound contraction.

Funder

King Saud University

Publisher

Wiley

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