Lubis Adisaputra Ramadhinara, Widia Fina, Soegondo Sidartawan, Setiawati Arini
Faculty of Medicine, University of Indonesia, Jl. Salemba 6, Jakarta Pusat.
Acta Med Indones. 2008 Apr;40(2):89-95.
Obesity is one of the risk factors in various chronic diseases and malignancy. It may result from excess accumulation of body fat. This condition may be caused by dysfunction of appetite-regulating pathways and energy balance due to leptin resistance. Leptin, a 16 kDa hormone, is the most important regulator of appetite and energy balance in the body. Most individuals with obesity have leptin resistance characterized by increased leptin blood levels. Some possibilities of mechanism involved in leptin resistance have been proposed by researchers despite the fact that it is still being studied hitherto. One of the mechanisms considered to have a role in leptin resistance is disruption in signal transduction process through Janus-activating kinase2-signal transducer and activator of transcription 3 (JAK2-STAT3) pathway on leptin receptors by suppressor of cytokine signaling-3 (SOCS-3). SOCS-3 is a protein that inhibits the signal transduction process of various cytokines in the body, including leptin. SOCS-3 expression is induced by leptin and SOCS-3 activation will inhibit STAT3 phosphorylation which is important in signal transmission on leptin receptors. Such inhibition will consequently cause leptin resistance characterized by dysfunction of leptin biological function.
肥胖是多种慢性疾病和恶性肿瘤的危险因素之一。它可能是由于体内脂肪过度堆积所致。这种情况可能是由于瘦素抵抗导致食欲调节途径和能量平衡功能障碍引起的。瘦素是一种16 kDa的激素,是体内食欲和能量平衡的最重要调节因子。大多数肥胖个体存在瘦素抵抗,其特征是血液中瘦素水平升高。尽管瘦素抵抗至今仍在研究中,但研究人员已经提出了一些与瘦素抵抗相关的机制可能性。细胞因子信号抑制因子3(SOCS-3)被认为在瘦素抵抗中起作用的机制之一是通过抑制Janus激活激酶2-信号转导和转录激活因子3(JAK2-STAT3)途径破坏瘦素受体上的信号转导过程。SOCS-3是一种抑制体内各种细胞因子信号转导过程的蛋白质,包括瘦素。SOCS-3的表达由瘦素诱导,SOCS-3的激活将抑制STAT3磷酸化,而STAT3磷酸化在瘦素受体的信号传递中很重要。这种抑制将因此导致以瘦素生物学功能障碍为特征的瘦素抵抗。