Taurine attenuated methotrexate-induced intestinal injury by regulating NF-κB/iNOS and Keap1/Nrf2/HO-1 signals

• Published in: Life sciences (1973) 2022-12, Vol.311 (Pt A), p.121180, Article 121180
• Main Authors: Hassanein, Emad H.M., Althagafy, Hanan S., Atwa, Ahmed M., Kozman, Magy R., Kotb El-Sayed, Mohamed.I., Soubh, Ayman A.
• Format: Article
• Language: English
• Subjects: adverse effects; Animals; antioxidants; Antioxidants - pharmacology; apoptosis; Caco-2 Cells; Caspase-3; cytoglobin; cytokines; cytotoxicity; drug therapy; Humans; Intestinal injury; intestinal mucosa; Keap1/Nrf2/HO-1; Kelch-Like ECH-Associated Protein 1 - metabolism; Methotrexate; Methotrexate - pharmacology; NF-E2-Related Factor 2 - metabolism; NF-kappa B - metabolism; NF-κB/iNOS; protective effect; Rats; Signal Transduction; Taurine; Taurine - pharmacology
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2022.121180

Methotrexate (MTX) is a well-known and widely used cytotoxic chemotherapeutic agent. However, intestinal mucosa damage is a serious adverse effect of MTX. Taurine (TUR) is a sulfur-containing free β-amino acid with antioxidant and therapeutic value against several diseases. The current study aimed to determine the protective effect of TUR against MTX-induced intestinal injury. Rats were allocated into four groups. The first group received vehicles only. The second group received TUR at a dose of 250 mg/kg i.p. For induction of intestinal injury, the rats in the third group were given MTX once at a dose of 20 mg/kg, i.p. The fourth group received TUR 7 days before and 7 days after MTX, as previously described. TUR significantly attenuated the cytokine release by suppressing NF-κB and iNOS expressions. Moreover, cotreatment with TUR attenuated the increased MDA level while it enhanced the antioxidant GSH and SOD levels mediated by effective downregulation of Keap1 expression, while the expression of Nrf2, HO-1, and cytoglobin were up-regulated. Additionally, TUR mitigated the apoptosis and proliferation indices by decreasing the elevated levels of intestinal PCNA and caspase-3. Finally, TUR potently increased the cytotoxic activity of MTX toward Caco-2, MCF-7, and A549 cancer cells. In conclusion, TUR was a promising agent for relieving MTX-mediated intestinal injury via various antioxidant, anti-inflammatory, and antiapoptotic mechanisms.