Carvacrol Mitigates Bleomycin-Induced Experimental Pulmonary Fibrosis


Turgut N., Gungor H., EKİCİ M., Karayigit M., KARA H.

JOURNAL OF EVOLUTIONARY BIOCHEMISTRY AND PHYSIOLOGY, vol.59, no.5, pp.1577-1593, 2023 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 59 Issue: 5
  • Publication Date: 2023
  • Doi Number: 10.1134/s0022093023050101
  • Journal Name: JOURNAL OF EVOLUTIONARY BIOCHEMISTRY AND PHYSIOLOGY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Academic Search Premier, Animal Behavior Abstracts, BIOSIS
  • Page Numbers: pp.1577-1593
  • Keywords: carvacrol, pulmonary fibrosis, Inducible nitric oxide synthase (iNOS), transforming growth factor-beta 1 (TGF- beta 1), caspase 3
  • Dokuz Eylül University Affiliated: Yes

Abstract

Idiopathic pulmonary fibrosis (IPF) is a serious progressive pulmonary disease of unknown etiology and high mortality. Carvacrol is a natural phenolic monoterpene with various pharmacological effects, especially antioxidant and anti-inflammatory effects. Hence, the present study aimed to investigate the effect of carvacrol on bleomycin (BLM) induced pulmonary fibrosis (PF) in Wistar-albino rats. Rats were administered a single dose of BLM (5mg/kg, intratracheal) or vehicle and treated with carvacrol (100 mg/kg, p.o. for 14 days following BLM administration). For calculating the lung index, the body and lungs were weighed. The Elisa method was used to assess hydroxyproline content, anti-inflammatory, and antioxidant effects. Fibrosis score, collagen deposition and inflammation were evaluated with Hematoxylin-Eosin (HxE) and Masson’s trichrome staining. Inducible nitric oxide synthase (iNOS), transforming growth factor-beta 1 (TGF-β1), and caspase 3 expressions were assessed immunohistochemically. BLM administration significantly diminished glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities and increased malondialdehyde (MDA) levels. BLM also increased tumor necrosis factor alpha (TNF-α) and collagen bundle accumulation. Carvacrol at 100 mg/kg significantly decreased collagen accumulation, MDA, TNF-α levels, iNOS, TGF-1, and caspase 3 expression, while increasing SOD and GPx activity. Histopathological examination supported the findings that carvacrol attenuated the degree of collagen deposition and inflammation. This study revealed that treatment with carvacrol (100 mg/kg) exhibits a potential healing effect on BLM-induced PF by reducing inflammatory and oxidative damages and histopathological alterations, with possible molecular targets being iNOS, TGF-β1 and caspase 3 signaling pathways.