Role of TLR4 signaling pathway in the mitigation of damaged lung by low-dose gamma irradiation.
Hanan A FahmyMarwa Abd El Hameed MohmadMai H MekkawyEman F S TahaPublished in: Cell biochemistry and function (2023)
Organisms frequently suffer negative effects from large doses of ionizing radiation. However, radiation is not as hazardous at lower doses as was once believed. The current study aims to evaluate the possible radio-adaptive effect induced by low-dose radiation (LDR) in modulating high-dose radiation (HDR) and N-nitrosodiethylamine (NDEA)-induced lung injury in male albino rats. Sixty-four male rats were randomly divided into four groups: Group 1 (control): normal rats; Group 2 (D): rats given NDEA in drinking water; Group 3 (DR): rats administered with NDEA then exposed to fractionated HDR; and Group 4 (DRL): rats administered with NDEA then exposed to LDR + HDR. In the next stage, malondialdehyde (MDA), glutathione reduced (GSH), catalase (CAT), and superoxide dismutase (SOD) levels in the lung tissues were measured. Furthermore, the enzyme-linked immunoassay analysis technique was performed to assess the Toll-like receptor 4 (TLR4), interleukin-1 receptor-associated kinase 4 (IRAK4), and mitogen-activated protein kinases (MAPK) expression levels. Histopathological and DNA fragmentation analyses in lung tissue, in addition to hematological and apoptosis analyses of the blood samples, were also conducted. Results demonstrated a significant increase in antioxidant defense and a reduction in MDA levels were observed in LDR-treated animals compared to the D and DR groups. Additionally, exposure to LDR decreased TLR4, IRAK4, and MAPK levels, decreased apoptosis, and restored all the alterations in the histopathological, hematological parameters, and DNA fragmentation, indicating its protective effects on the lung when compared with untreated rats. Taken together, LDR shows protective action against the negative effects of subsequent HDR and NDEA. This impact may be attributable to the adaptive response induced by LDR, which decreases DNA damage in lung tissue and activates the antioxidative, antiapoptotic, and anti-inflammatory systems in the affected animals, enabling them to withstand the following HDR exposure.
Keyphrases
- toll like receptor
- low dose
- signaling pathway
- oxidative stress
- high dose
- drinking water
- dna damage
- inflammatory response
- anti inflammatory
- immune response
- nuclear factor
- cell cycle arrest
- pi k akt
- cell death
- circulating tumor
- poor prognosis
- gene expression
- endoplasmic reticulum stress
- radiation induced
- diabetic rats
- health risk
- epithelial mesenchymal transition
- multidrug resistant
- nitric oxide
- breast cancer cells
- gram negative
- binding protein
- risk assessment
- newly diagnosed
- long non coding rna