Affiliations 

  • 1 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 Food Technology, College of Agricultural Engineering Sciences, Salaheddin University-Erbil, Erbil, Kurdistan Region, Iraq
  • 4 Department of Allied Health Sciences, Al-Balqa Applied University (BAU), Al-Salt, Jordan
  • 5 Department of Pathology, Faculty of Veterinary Medicine, Aksaray University, Aksaray, Turkey
  • 6 Department of Biomedical Sciences, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
  • 7 Department of Medical Laboratory Science, College of Science, Knowledge University, Erbil, Iraq
  • 8 Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia
  • 9 Department of Medical Analysis, Faculty of Applied Science, Tishk International University-Erbil, Erbil, Iraq
  • 10 School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK
Skin Res Technol, 2024 May;30(5):e13727.
PMID: 38711343 DOI: 10.1111/srt.13727

Abstract

Wound healing is a complex, intricate, and dynamic process that requires effective therapeutic management. The current study evaluates the wound healing potentials of methanolic extract of Cuminum cyminum L. seeds (CCS) in rats. Sprague Dawley (24) rats were distributed into four cages, wounds produced on the back of the neck, and received two daily topical treatments for 14 days: A, rats received normal saline; B, wounded rats treated with intrasite gel; C and D, rats received 0.2 mL of 250 and 500 mg/kg of CCS, respectively. After that, wound area and closure percentage were evaluated, and wound tissues were dissected for histopathological, immunohistochemical, and biochemical examinations. Acute toxicity trials of methanolic extract of CCS showed the absence of any physiological changes or mortality in rats. CCS application caused a significant reduction in wound size and a statistically elevated percentage of wound contraction than those of vehicle rats. CCS treatment caused significant up-regulation of collagen fiber, fibroblasts, and fewer inflammatory cells (inflammation) in granulation tissues. TGF-β1 (angiogenetic factor) was significantly more expressed in CCS-treated rats in comparison to normal saline-treated rats; therefore, more fibroblasts transformed into myofibroblasts (angiogenesis). CCS-treated rats showed remarkable antioxidant potentials (higher SOD and CAT enzymes) and decreased MDA (lipid peroxidation) levels in their wound tissue homogenates. Hydroxyproline amino acid (collagen) was significantly up-regulated by CCS treatment, which is commonly related to faster wound closure area. The outcomes suggest CCS as a viable new source of pharmaceuticals for wound treatment.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.