Curcumin Protects against Arsenic and Cadmium-Induced Lung Toxicity in Rats by Modulating Bax/Bcl-2/caspase-3 Pathway: In Vivo and In Silico Approaches


Kulcanay Şahin İ., Gür B., Cengiz M., Ertekin R., Vejselova Sezer C., Bayrakdar A., ...Daha Fazla

Journal of biochemical and molecular toxicology, cilt.40, sa.2, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 40 Sayı: 2
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1002/jbt.70707
  • Dergi Adı: Journal of biochemical and molecular toxicology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Chemical Abstracts Core, EMBASE, Environment Index, MEDLINE
  • Anahtar Kelimeler: arsenic, cadmium, curcumin, in silico, lung toxicity
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

The present study aims to investigate the putative protective role of curcumin (CUR) against oxidative stress and lung damage caused by a heavy metal mixture (Cd+As) with cadmium (Cd) + arsenic (As). Wistar albino rats were randomly divided into five experimental groups: Control, 0.44 + 5.55 mg/kg Cd+As, 100 mg/kg CUR, 100 CUR + Cd+As, and 200 CUR + Cd+As groups. The Cd+As increased malondialdehyde levels and oxidative stress. However, it also led to a decrease in levels of glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) in lung tissue homogenates. Different doses of CUR effectively prevented Cd+As-induced lipid peroxidation and suppression of antioxidant capacity in lung tissue. Also, lung tissue administered Cd+As showed elevated levels of congestion, inflammation, alveolar damage, and apoptosis, as evidenced by decreased Bcl-2 and increased expression levels of Bax and caspase-3. The high dose remarkably improved lung injury in Cd+As-injected rats, better than the low dose. The results show that CUR treatment is effective in protecting against Cd+As-induced lipid peroxidation and reducing the negative effects of metal mixture on antioxidant status. This study suggests that CUR may be a potential new approach for the prevention/treatment of Cd+As-induced pulmonary toxicity and possibly other lung diseases associated with oxidative stress and inflammation. Furthermore, in silico studies on how CUR and Cd+As treatments affect the activities of the enzymes CAT and GPx1 showed that ROS induced by Cd+As treatment caused changes in the enzymes CAT and GPx1, while CAT was modulated by CUR treatment, whereas GPx1 was not modulated.