Li Yucheng, Zheng Xueli, Yang Gongshe
Laboratory of Animal Fat Deposition and Muscle Development, College of Animal Sciences and Technology, Northwest A & F University, Yangling 712100, China.
Sheng Wu Gong Cheng Xue Bao. 2008 Sep;24(9):1613-9. doi: 10.1016/s1872-2075(08)60068-0.
Leptin, a cytokine predominantly secreted from fat tissue, plays an important role in regulating organism energy balance. Leptin can stimulate lipolysis, but the mechanism is unclear. In order to study the molecular mechanism of leptin stimulating lipolysis, we systemically studied the mRNA expression of key lipolytic enzymes. Morphological observation, Oil Red O staining and RT-PCR were used to identify pig primary adipocytes; commercial kits were used to measure the glycerol and FFA release; Semiquantitative RT-PCR was used to detect the mRNA expression of key lipolytic enzymes. The results showed that 100 nmol/L leptin up-regulated the mRNA expression of ATGL, TGH-2, HSL, MGL and LPL (P<0.01), but down-regulated the Perilipin mRNA expression (P<0.01). At the same time, leptin promoted the glycerol release in a dose dependent manner (P<0.01), but had no effect on the FFA release (P>0.05). These indicate that leptin may mainly stimulate lipolysis in pig primary adipocytes by up-regulating the expression of ATGL, MGL, LPL and down-regulating the expression of Perilipin. The unchanged FFA release may be resulted from Leptin promoting UCPs mRNA expression and increasing FFA expenditure.
瘦素是一种主要由脂肪组织分泌的细胞因子,在调节机体能量平衡中发挥重要作用。瘦素可刺激脂肪分解,但其机制尚不清楚。为研究瘦素刺激脂肪分解的分子机制,我们系统研究了关键脂肪分解酶的mRNA表达。采用形态学观察、油红O染色和RT-PCR鉴定猪原代脂肪细胞;使用商业试剂盒测定甘油和游离脂肪酸(FFA)释放量;采用半定量RT-PCR检测关键脂肪分解酶的mRNA表达。结果显示,100 nmol/L瘦素上调了脂肪甘油三酯脂肪酶(ATGL)、甘油二酯脂肪酶-2(TGH-2)、激素敏感性脂肪酶(HSL)、单酰甘油脂肪酶(MGL)和脂蛋白脂肪酶(LPL)的mRNA表达(P<0.01),但下调了围脂滴蛋白(Perilipin)的mRNA表达(P<0.01)。同时,瘦素以剂量依赖性方式促进甘油释放(P<0.01),但对FFA释放无影响(P>0.05)。这些表明,瘦素可能主要通过上调ATGL、MGL、LPL的表达及下调Perilipin的表达来刺激猪原代脂肪细胞中的脂肪分解。FFA释放未改变可能是由于瘦素促进解偶联蛋白(UCPs)mRNA表达并增加了FFA消耗。