Activation of NF-κB and its regulation on IL-6 expression during LPSinduced liver injury
Wang Yong-tang
Abstract
Wang Yong-tang
Abstract
Objective: To explore the kinetics of the activation of nuclear factor-kappa B (NF-κB) and its regulation of interleukin-6 (IL-6) expression during LPS induced liver injury. Methods: Kunming mice were randomly divided into 4 groups in order to observe the does-effect relationship at 3 h: normal saline solution (control) group, low (1 mg/kg), middle (5 mg/kg), and high (10 mg/kg) LPS-induced groups; 6 groups in order to observe the time-effect relationship of 5 mg/kg LPS injection: normal saline solution (control) group, 0.5, 1, 3, 5 and 8 h groups; pyrrolidine dithiocarbamate (PDTC) intervened groups (3 h): normal saline solution (control) group, 5 mg/kg LPS, 200 mg/kg PDTC, and 200 mg/kg PDTC+5 mg/kg LPS groups. NF-κB activities of Kupffer cells were determined with electrophoretic mobility shift assay (EMSA) and expression levels of IL-6 were measured with enzyme-linked immunosorbent assay (ELISA). Results: Does-effect of NF-κB activities in Kupffer cells after LPS injection 3 h: NF-κB activation could be detected in 1 mg/kg LPS group, reached the highest level in 5 mg/kg LPS group, and persisted in 10 mg/kg LPS group; time-course after 5 mg/kg LPS injection: the DNA-binding activity was observable at 0.5 h after LPS injection, increased significantly at 3 h, and persisted for at least 8 h; in addition, antioxidant PDTC could inhibit the activation of NF-κB significantly. The kinetics of IL-6 level in liver tissues during LPS-induced liver injury were that IL-6 level after 3 h of injection increased first and then reduced; the same trend was observed in the time-course on IL-6 level after LPS injection; PDTC could significantly inhibit the release of IL-6. Correlation analyses revealed that IL-6 level was significantly and positively correlated with the activation of NF-κB.Conclusion: NF-κB in Kupffer cells can be activitied during LPS-induced liver injury to some extent, and NF-κB may have some regulation on the expression of IL-6.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To explore the kinetics of the activation of nuclear factor-kappa B (NF-κB) and its regulation of interleukin-6 (IL-6) expression during LPS induced liver injury. Methods: Kunming mice were randomly divided into 4 groups in order to observe the does-effect relationship at 3 h: normal saline solution (control) group, low (1 mg/kg), middle (5 mg/kg), and high (10 mg/kg) LPS-induced groups; 6 groups in order to observe the time-effect relationship of 5 mg/kg LPS injection: normal saline solution (control) group, 0.5, 1, 3, 5 and 8 h groups; pyrrolidine dithiocarbamate (PDTC) intervened groups (3 h): normal saline solution (control) group, 5 mg/kg LPS, 200 mg/kg PDTC, and 200 mg/kg PDTC+5 mg/kg LPS groups. NF-κB activities of Kupffer cells were determined with electrophoretic mobility shift assay (EMSA) and expression levels of IL-6 were measured with enzyme-linked immunosorbent assay (ELISA). Results: Does-effect of NF-κB activities in Kupffer cells after LPS injection 3 h: NF-κB activation could be detected in 1 mg/kg LPS group, reached the highest level in 5 mg/kg LPS group, and persisted in 10 mg/kg LPS group; time-course after 5 mg/kg LPS injection: the DNA-binding activity was observable at 0.5 h after LPS injection, increased significantly at 3 h, and persisted for at least 8 h; in addition, antioxidant PDTC could inhibit the activation of NF-κB significantly. The kinetics of IL-6 level in liver tissues during LPS-induced liver injury were that IL-6 level after 3 h of injection increased first and then reduced; the same trend was observed in the time-course on IL-6 level after LPS injection; PDTC could significantly inhibit the release of IL-6. Correlation analyses revealed that IL-6 level was significantly and positively correlated with the activation of NF-κB.Conclusion: NF-κB in Kupffer cells can be activitied during LPS-induced liver injury to some extent, and NF-κB may have some regulation on the expression of IL-6.
Key concepts: Pyrrolidine dithiocarbamate, Chemistry, Saline, Liver injury, Electrophoretic mobility shift assay, NF-κB, Endocrinology, Kupffer cell