蛋白激酶B
PI3K/AKT/mTOR通路
内科学
胰岛素
IRS1
胰岛素受体
内分泌学
胰岛素受体底物
磷酸肌醇3激酶
糖原合酶
IRS2
糖原发生
SOCS3
化学
生物
信号转导
胰岛素抵抗
细胞生物学
医学
车站3
作者
Sayori Wakayama,Abedul Haque,Naoki Koide,Yoshiro Kato,Erdenezaya Odkhuu,Bilegtsaikhan Tsolmongyn,Yoshikazu Naiki,Takayuki Komatsu,Tomoaki Yoshida,Takashi Yokochi
标识
DOI:10.3109/08923973.2014.887096
摘要
The effect of lipopolysaccharide (LPS) on insulin sensitivity in adipocytes were examined by using differentiated 3T3-L1 adipocytes. Insulin-mediated activation of insulin receptor substrate (IRS) 1/2 was inhibited in LPS-pretreated adipocytes and IRS1/2-mediated Akt activation was also attenuated in those cells. LPS inhibited activation of glycogen synthase kinase 3 as a negative regulator of glycogenesis and impaired the glycogen synthesis in response to insulin. LPS-induced activation of phosphoinositide 3-kinase (PI3K) in adipocytes. Involvement of suppressor of cytokine signaling 3 (SOCS3) in LPS-induced IRS1/2 inhibition was excluded. Considering that both insulin and LPS were able to activate the PI3K/Akt signaling pathway, LPS was suggested to impair insulin sensitivity of adipocytes through down-regulating insulin-mediated PI3K/Akt activation.
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