Assessing the Protective Role of Epigallocatechin Gallate (EGCG) against Water-Pipe Smoke-Induced Toxicity: A Comparative Study on Gene Expression and Histopathology

• Published in: Molecules (Basel, Switzerland) Vol. 28; no. 22; p. 7502
• Main Authors: Al-Awaida, Wajdy, Goh, Khang Wen, Al-Ameer, Hamzeh J, Gushchina, Yulia Sh, Torshin, Vladimir I, Severin, Alexandr E, Al Bawareed, Omar, Srour, Besan, Al Farraj, Jude, Hamad, Islam
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.11.2023
• Subjects: Analysis; antioxidant genes; Antioxidants; Catechin; Cytokines; Drinking water, Bottled; Enzymes; epigallocatechin gallate (EGCG); Free radicals; Gene expression; Genes; Genetic research; Green tea; Histochemistry; Inflammation; inflammatory markers; Kidneys; Liver; Oxidative stress; Smoking; Tea; Tumor necrosis factor; Water pipes; water-pipe smoke
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules28227502

Exposure to water-pipe smoking, whether flavored or unflavored, has been shown to instigate inflammation and oxidative stress in BALB/c mice. This consequently results in alterations in the expression of inflammatory markers and antioxidant genes. This study aimed to scrutinize the impact of Epigallocatechin gallate (EGCG)—a key active component of green tea—on inflammation and oxidative stress in BALB/c mice exposed to water-pipe smoke. The experimental setup included a control group, a flavored water-pipe smoke (FWP) group, an unflavored water-pipe smoke (UFWP) group, and EGCG-treated flavored and unflavored groups (FWP + EGCG and UFWP + EGCG). Expression levels of IL-6, IL1B, TNF-α, CAT, GPXI, MT−I, MT−II, SOD−I, SOD−II, and SOD-III were evaluated in lung, liver, and kidney tissues. Histopathological changes were also assessed. The findings revealed that the EGCG-treated groups manifested a significant decline in the expression of inflammatory markers and antioxidant genes compared to the FWP and UFWP groups. This insinuates that EGCG holds the capacity to alleviate the damaging effects of water-pipe smoke-induced inflammation and oxidative stress. Moreover, enhancements in histopathological features were observed in the EGCG-treated groups, signifying a protective effect against tissue damage induced by water-pipe smoking. These results underscore the potential of EGCG as a protective agent against the adverse effects of water-pipe smoking. By curbing inflammation and oxidative stress, EGCG may aid in the prevention or mitigation of smoking-associated diseases.