Bacterial Lipase Neutralized Toxicity of Lipopolysaccharide on Chicken Embryo Cardiac Tissue
Afsaneh Bagherzadeh1, Hamidreza Vaziri1, Fatemeh Sokouti Nasimi2
1Department of Biology, Faculty of Science, Guilan University, Rasht, Iran.
Abstract:
It has been shown that near all organs, especially the cardiovascular system, are affected by bacterial lipopolysaccharide via the activation of Toll-like receptor signaling pathways. Here, we tried to find the blunting effect of bacterial lipase on lipopolysaccharide (LPS)-induced cardiac tissue toxicity in chicken embryos. 7-day fertilized chicken eggs were divided randomly into different groups as follows; Control, Normal Saline, LPS (0.1, 0.5 and 1 mg/kbw), and LPS (0.1, 0.5 and 1 mg/kbw) plus 5 mg/ml Lipase. On day 17, the hearts were sampled. The expression of genes such as GATA4, NKX2.5, EGFR, TRIF, and NF-ƙB was monitored using real-time PCR analysis. Using western blotting, we measured NF-ƙB protein level. Total antioxidant capacity, glutathione peroxidase, and Catalase activity were also studied. Microvascular density and anterior wall thickness were monitored in histological samples using H&E staining. High dose of LPS (1 mg/kbw) increased the expression of TRIF but not NF-ƙB compared to the control group (p < 0.05). We found a statistically significant reduction in groups that received LPS + Lipase compared to the control and LPS groups (p < 0.05). Western blotting revealed that the injection of Lipase could reduce LPS-induced NF-ƙB compared to the control group (p < 0.05). The expression of GATA4, NKx2.5, and EGFR was not altered in the LPS group, while the simultaneous application of LPS and Lipase significantly reduced GATA4, NKx2.5, and EGFR levels below the control (p < 0.05). We found non-significant differences in glutathione peroxidase, and Catalase activity in all groups (p > 0.05), while total antioxidant capacity was increased in groups that received LPS + Lipase. Anterior wall thickness was diminished in LPS groups and the use of both lipase and LPS returned near-to-control values (p < 0.05). Despite a slight increase in microvascular density, we found statistically non-significant differences in all groups (p > 0.05). Bacterial lipase reduces detrimental effects of LPS on chicken embryo heart induced via Toll-like receptor signaling pathway.
Insights
Bacterial lipase effectively mitigates lipopolysaccharide (LPS)-induced cardiac toxicity in chicken embryos by modulating Toll-like receptor signaling pathways, offering a protective effect against cardiovascular damage.
Area of Science:
- Cardiovascular research
- Immunology
- Toxicology
Background:
- Bacterial lipopolysaccharide (LPS) triggers Toll-like receptor (TLR) signaling, adversely affecting organs, particularly the cardiovascular system.
- Understanding LPS-induced cardiac toxicity is crucial for developing therapeutic interventions.
Purpose of the Study:
- To investigate the protective effects of bacterial lipase against LPS-induced cardiac tissue toxicity in chicken embryos.
- To elucidate the molecular mechanisms underlying lipase's protective action.
Main Methods:
- Chicken embryos were exposed to varying doses of LPS and bacterial lipase.
- Gene expression (GATA4, NKX2.5, EGFR, TRIF, NF-κB) was analyzed using real-time PCR.
- NF-κB protein levels were assessed via Western blotting.
- Antioxidant capacity and enzyme activities were measured.
- Histological analysis evaluated microvascular density and anterior wall thickness.
Main Results:
- LPS (1 mg/kbw) increased TRIF expression, while lipase co-administration significantly reduced LPS-induced NF-κB levels.
- LPS exposure altered cardiac gene expression (GATA4, NKX2.5, EGFR), with lipase partially restoring normal levels.
- Total antioxidant capacity increased with lipase treatment, while anterior wall thickness was preserved.
- No significant changes were observed in glutathione peroxidase or catalase activity.
Conclusions:
- Bacterial lipase demonstrates a blunting effect on LPS-induced cardiac toxicity in chicken embryos.
- Lipase may exert protective effects by modulating TLR signaling pathways and enhancing antioxidant capacity.
- These findings suggest potential therapeutic applications for bacterial lipase in managing LPS-related cardiovascular complications.
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