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Insulin attenuates TNFα-induced hemopexin mRNA: An anti-inflammatory action of insulin in rat H4IIE hepatoma cells

机译:胰岛素减弱TNFα诱导的血红素mRNA的表达:胰岛素在大鼠H4IIE肝癌细胞中的抗炎作用

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Proinflammatory cytokines, including TNF-α and IL-6, can contribute to insulin resistance. Conversely, insulin has some actions that can be considered anti-inflammatory. Hemopexin is a Class 2 acute phase reactant and control of its transcription is predominantly regulated by IL-6, with TNF-α and IL-1β also inducing hemopexin gene expression. Thus, we asked whether insulin could inhibit the ability of TNF-α to stimulate hemopexin mRNA expression. In cultured rat hepatoma (H4IIE) cells, TNF-α significantly increased hemopexin mRNA accumulation. The TNF-α-induced increase of hemopexin mRNA was dramatically attenuated by insulin, even though TNF-α reduced peak insulin activation of ERK. Thus, even though TNF-α can contribute to insulin resistance, the residual insulin response was still able to counteract TNF-α actions. Highlights ? The TNF-α-induced increase of hemopexin mRNA was dramatically attenuated by insulin. ? This occurred even though TNF-α significantly decreased insulin activation of ERK. ? This suggests an additional mechanism for the anti-inflammatory action of insulin. ? Cytokine-induced insulin resistance does not abolish insulin’s anti-inflammatory effect.
机译:包括TNF-α和IL-6在内的促炎细胞因子可导致胰岛素抵抗。相反,胰岛素具有一些可被视为抗炎的作用。血红蛋白是2类急性期反应物,其转录控制主要受IL-6调节,TNF-α和IL-1β也会诱导血红蛋白基因表达。因此,我们询问胰岛素是否可以抑制TNF-α刺激血红素mRNA表达的能力。在培养的大鼠肝癌(H4IIE)细胞中,TNF-α显着增加了血红蛋白mRNA的积累。尽管TNF-α降低了ERK的峰值胰岛素激活,但胰岛素显着减弱了TNF-α诱导的血红蛋白mRNA的增加。因此,即使TNF-α有助于胰岛素抵抗,残留的胰岛素反应仍然能够抵消TNF-α的作用。强调 ?胰岛素可显着减弱TNF-α诱导的血红蛋白mRNA的增加。 ?即使TNF-α显着降低了ERK的胰岛素激活,这种情况仍然发生。 ?这提示了胰岛素抗炎作用的另一种机制。 ?细胞因子诱导的胰岛素抵抗不会消除胰岛素的抗炎作用。

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