Yang Jun, Zhao Shui-Ping, Li Jing, Dong Shao-Zhuang
Department of Cardiology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, PR China.
Cardiovasc Pathol. 2008 Jul-Aug;17(4):219-25. doi: 10.1016/j.carpath.2007.09.005. Epub 2008 Apr 1.
Leptin may play an important role in the development of atherosclerosis. Several transcription genes [including peroxisome proliferator-activated receptor gamma (PPARgamma) and CD36] involved in lipid and glucose metabolism and inflammatory processes may correlate to leptin expression. The aim of this study was to investigate the effect of niacin on serum leptin levels in hypercholesterolemic rabbits and the expression of leptin, PPARgamma, and CD36 in adipocytes from hypercholesterolemic rabbits.
Eighteen rabbits fed with high-cholesterol diet for 8 weeks were randomly divided into two groups: (a) high-cholesterol group (n=6), which is maintained on high-cholesterol diet for 6 weeks, and (b) niacin group (n=6), which receives the same cholesterol diet plus niacin (200 mg/kg/day) for 6 weeks. The control group (n=6) was fed with normal diet for 14 weeks. Subcutaneous adipose was collected for RNA analysis. The direct effect of niacin on leptin release was assayed in hypercholesterolemic rabbit adipocytes. Leptin levels in serum and adipocyte culture supernatant were measured via enzyme-linked immunosorbent assay. RT-PCR was used to evaluate leptin, PPARgamma, and CD36 mRNA expression in adipose and adipocytes.
Compared with the control group, rabbits fed with high-cholesterol diets showed higher levels of serum total cholesterol, low-density lipoprotein cholesterol, and leptin, all of which were significantly reduced by niacin treatment. After 6 weeks of treatment with niacin, the leptin level was significantly decreased by 21.8% (6.87+/-1.58 vs. 8.79+/-1.45, P<.05) and leptin mRNA expression of adipose was significantly lower in rabbits treated with niacin than in those fed with high-cholesterol diet continuously (0.58+/-0.11 vs. 0.73+/-0.15, P<.05). Niacin dose-dependently inhibited leptin secretion and increased CD36 and PPARgamma expression in cultured adipocytes. The reduction of leptin mRNA expression of hypercholesterolemic rabbits by niacin was negatively correlated with the up-regulation of PPARgamma and CD36 mRNA expression by niacin (r=-.69 and r=-.63, respectively, P<.01).
Niacin can reduce serum level and adipose mRNA expression of leptin and up-regulate PPARgamma and CD36 mRNA expression in hypercholesterolemic rabbits.
瘦素可能在动脉粥样硬化的发展中起重要作用。一些参与脂质和葡萄糖代谢以及炎症过程的转录基因[包括过氧化物酶体增殖物激活受体γ(PPARγ)和CD36]可能与瘦素表达相关。本研究的目的是探讨烟酸对高胆固醇血症兔血清瘦素水平以及高胆固醇血症兔脂肪细胞中瘦素、PPARγ和CD36表达的影响。
将18只喂高胆固醇饮食8周的兔子随机分为两组:(a)高胆固醇组(n = 6),继续喂高胆固醇饮食6周;(b)烟酸组(n = 6),在相同胆固醇饮食基础上加用烟酸(200 mg/kg/天)6周。对照组(n = 6)喂正常饮食14周。收集皮下脂肪进行RNA分析。在高胆固醇血症兔脂肪细胞中检测烟酸对瘦素释放的直接作用。通过酶联免疫吸附测定法测量血清和脂肪细胞培养上清液中的瘦素水平。用逆转录-聚合酶链反应(RT-PCR)评估脂肪组织和脂肪细胞中瘦素、PPARγ和CD36 mRNA的表达。
与对照组相比,喂高胆固醇饮食的兔子血清总胆固醇、低密度脂蛋白胆固醇和瘦素水平更高,而烟酸治疗可使所有这些指标显著降低。烟酸治疗6周后,瘦素水平显著降低21.8%(6.87±1.58对8.79±1.45,P<0.05),且烟酸治疗的兔子脂肪组织中瘦素mRNA表达明显低于持续喂高胆固醇饮食的兔子(0.58±0.11对0.73±0.15,P<0.05)。烟酸在培养的脂肪细胞中剂量依赖性地抑制瘦素分泌并增加CD36和PPARγ表达。烟酸使高胆固醇血症兔瘦素mRNA表达降低与烟酸使PPARγ和CD36 mRNA表达上调呈负相关(分别为r = -0.69和r = -0.63,P<0.01)。
烟酸可降低高胆固醇血症兔血清瘦素水平和脂肪组织mRNA表达,并上调PPARγ和CD36 mRNA表达。