Barrios Vicente, Guerra-Cantera Santiago, Martín-Rivada Álvaro, Canelles Sandra, Campillo-Calatayud Ana, Arilla-Ferreiro Eduardo, Frago Laura M, Chowen Julie A, Argente Jesús
Department of Endocrinology, Hospital Infantil Universitario Niño Jesús, Instituto de Investigación La Princesa, E-28009 Madrid, Spain.
Network Center for Biomedical Research on Obesity and Nutrition, Instituto de Salud Carlos III (CIBEROBN, ISCIII), E-28009 Madrid, Spain.
Biomedicines. 2022 Jun 21;10(7):1465. doi: 10.3390/biomedicines10071465.
Leptin is involved in the modulation of insulin signaling in peripheral tissues, being closely associated with changes in lipid metabolism. This adipokine modifies inflammatory pathways that can interact with insulin targets in peripheral organs; however, the mechanisms remain unclear. Inflammatory and insulin signaling targets, cytokines, adiponectin, irisin and non-esterified fatty acid (NEFA) levels and enzymes of fatty acid anabolism were studied in the gastrocnemius of chronic centrally infused leptin (L), pair-fed and control rats. The phosphorylation of signal transducer and activator of transcription 3 (STAT3) and c-Jun -terminal kinase (JNK) was reduced in L rats (59% and 58%, respectively). The phosphorylation of the insulin receptor and Akt and adiponectin and irisin content was increased in L rats (154%, 157%, 308% and 329%, respectively). The levels of glucose-6-phosphate dehydrogenase, the mRNA content of acetyl Co-A carboxylase and NEFA concentrations were diminished in the muscles of L rats (59%, 50% and 61%, respectively). The activation of JNK correlated positively with STAT3 phosphorylation, tumoral necrosis factor-α and NEFA and negatively with irisin and Akt phosphorylation. These data suggest that the activation of insulin signaling targets and a decrease in NEFA content are associated with a reduction in muscle inflammation parameters, suggesting that leptin may integrate these pathways.
瘦素参与外周组织中胰岛素信号的调节,与脂质代谢变化密切相关。这种脂肪因子可改变炎症信号通路,而这些通路可与外周器官中的胰岛素靶点相互作用;然而,其机制仍不清楚。我们研究了慢性经中枢注射瘦素的大鼠(L组)、配对喂养大鼠和对照大鼠腓肠肌中炎症和胰岛素信号靶点、细胞因子、脂联素、鸢尾素以及非酯化脂肪酸(NEFA)水平和脂肪酸合成代谢酶。L组大鼠中信号转导和转录激活因子3(STAT3)和c-Jun末端激酶(JNK)的磷酸化水平降低(分别降低59%和58%)。L组大鼠中胰岛素受体、Akt以及脂联素和鸢尾素含量的磷酸化水平升高(分别升高154%、157%、308%和329%)。L组大鼠肌肉中葡萄糖-6-磷酸脱氢酶水平、乙酰辅酶A羧化酶的mRNA含量以及NEFA浓度均降低(分别降低59%、50%和61%)。JNK的激活与STAT3磷酸化、肿瘤坏死因子-α和NEFA呈正相关,与鸢尾素和Akt磷酸化呈负相关。这些数据表明,胰岛素信号靶点的激活以及NEFA含量的降低与肌肉炎症参数的减少有关,提示瘦素可能整合这些信号通路。