摘要
To investigate whether lactic acid could inhibit the LPS-activation of NF-κB p65 in rat intestinal mucosa microvascular endothelial cells （RIMMVECs）, RIMMVECs, cultured in vitro, were pretreated with different concentrations of lactic acid and then exposed to lipopolysaccharide （LPS）. Cells and cell culture media were then collected at different time intervals. Production of tumor necrosis factor-a （TNF-a） and interleukin-6 （IL-6） was examined at the protein level by enzyme-linked immunosorbent assay. The influence of lactic acid on the LPS-activation of NF-κB was examined at mRNA and protein levels by real-time quantitative PCR and Western blot analysis, respectively. TNF-a and IL-6 protein levels were significantly decreased after pretreatment with lactic acid compared with cells exposed to LPS only. After pretreatment with 7.5, 5.0, and 2.5 μL mL-1 lactic acid, NF-κB mRNA levels were increased by 1.51-, 2.62- and 3.00-fold, respectively, compared with levels in control cells without LPS treatment. Western blot analysis indicated that the level of NF-κB p65 in the lactic acid-pretreated group was significantly lower than that in the group treated with LPS only （positive control） and was unchanged compared with the group without LPS treatment （blank control）. These results suggest that lactic acid may inhibit LPS-activation of NF-κB, leading to the down-regulation of TNF-a and IL-6.
To investigate whether lactic acid could inhibit the LPS-activation of NF-κB p65 in rat intestinal mucosa microvascular endothelial cells （RIMMVECs）, RIMMVECs, cultured in vitro, were pretreated with different concentrations of lactic acid and then exposed to lipopolysaccharide （LPS）. Cells and cell culture media were then collected at different time intervals. Production of tumor necrosis factor-a （TNF-a） and interleukin-6 （IL-6） was examined at the protein level by enzyme-linked immunosorbent assay. The influence of lactic acid on the LPS-activation of NF-κB was examined at mRNA and protein levels by real-time quantitative PCR and Western blot analysis, respectively. TNF-a and IL-6 protein levels were significantly decreased after pretreatment with lactic acid compared with cells exposed to LPS only. After pretreatment with 7.5, 5.0, and 2.5 μL mL-1 lactic acid, NF-κB mRNA levels were increased by 1.51-, 2.62- and 3.00-fold, respectively, compared with levels in control cells without LPS treatment. Western blot analysis indicated that the level of NF-κB p65 in the lactic acid-pretreated group was significantly lower than that in the group treated with LPS only （positive control） and was unchanged compared with the group without LPS treatment （blank control）. These results suggest that lactic acid may inhibit LPS-activation of NF-κB, leading to the down-regulation of TNF-a and IL-6.
基金
supported by the Natural Science Foundation of Beijing, China (6072007)
the Project for the Establishment and Development of Swine Disease Clinical Diagnosis, China (KM200910020002)
