Balogh Zoltán, Fóris Gabriella, Kosztáczky Béla, Paragh György, Seres Ildikó, Zsíros Emese, Kónya Gabriella, Paragh György
First Department of Medicine, Medical and Health Science Center, University of Debrecen, Nagyerdei krt. 98, Debrecen H-4012, Hungary.
Peptides. 2007 Oct;28(10):2081-3. doi: 10.1016/j.peptides.2007.07.004. Epub 2007 Jul 12.
In human monocytes 100 ng/mL leptin increased both statin-inhibitable free radical and cholesterol production in vitro. In our recent study, we aimed to elucidate the concentration dependence of observed leptin-effect. Following leptin stimulation cholesterol synthesis was measured in the presence of inhibitors to determine affected signal pathways. Leptin at low (10-100 ng/mL) concentrations increased [(14)C]acetate incorporation, whereas at 250 ng/mL and higher concentrations it suppressed cholesterol synthesis. HMG CoA reductase, phosphatidyl-3-kinase (PI3K) and mitogen activated protein kinase (MAPK) were involved in mediating leptin effects at low concentrations, whereas the cholesterol synthesis suppression was abolished by inhibitors of protein kinase C (PKC) and PI3K.
在人单核细胞中,100 ng/mL的瘦素在体外可增加他汀类药物可抑制的自由基和胆固醇生成。在我们最近的研究中,我们旨在阐明所观察到的瘦素效应的浓度依赖性。在瘦素刺激后,在存在抑制剂的情况下测量胆固醇合成,以确定受影响的信号通路。低浓度(10 - 100 ng/mL)的瘦素增加了[(14)C]乙酸盐的掺入,而在250 ng/mL及更高浓度时,它抑制了胆固醇合成。3-羟基-3-甲基戊二酰辅酶A还原酶、磷脂酰-3-激酶(PI3K)和丝裂原活化蛋白激酶(MAPK)参与介导低浓度时的瘦素效应,而蛋白激酶C(PKC)和PI3K的抑制剂可消除胆固醇合成的抑制作用。