Kuo Kung-Kai, Wu Bin-Nan, Liu Chung-Pin, Yang Tzu-Yang, Kao Li-Pin, Wu Jiunn-Ren, Lai Wen-Ter, Chen Ing-Jun
Division of Hepatobiliopancreatic Surgery, Kaohsiung Medical University Hospital.
Department of Pharmacology, School of Medicine, College of Medicine.
J Lipid Res. 2015 Nov;56(11):2070-84. doi: 10.1194/jlr.M057547. Epub 2015 Sep 8.
The phosphodiesterase inhibitor (PDEI)/eNOS enhancer KMUP-1, targeting G-protein coupled receptors (GPCRs), improves dyslipidemia. We compared its lipid-lowering effects with simvastatin and explored hormone-sensitive lipase (HSL) translocation in hepatic fat loss. KMUP-1 HCl (1, 2.5, and 5 mg/kg/day) and simvastatin (5 mg/kg/day) were administered in C57BL/6J male mice fed a high-fat diet (HFD) by gavage for 8 weeks. KMUP-1 inhibited HFD-induced plasma/liver TG, total cholesterol, and LDL; increased HDL/3-hydroxy-3-methylglutaryl-CoA reductase (HMGR)/Rho kinase II (ROCK II)/PPARγ/ABCA1; and decreased liver and body weight. KMUP-1 HCl in drinking water (2.5 mg/200 ml tap water) for 1-14 or 8-14 weeks decreased HFD-induced liver and body weight and scavenger receptor class B type I expression and increased protein kinase A (PKA)/PKG/LDLRs/HSL expression and immunoreactivity. In HepG2 cells incubated with serum or exogenous mevalonate, KMUP-1 (10(-7)∼10(-5) M) reversed HMGR expression by feedback regulation, colocalized expression of ABCA1/apolipoprotein A-I/LXRα/PPARγ, and reduced exogenous geranylgeranyl pyrophosphate/farnesyl pyrophosphate (FPP)-induced RhoA/ROCK II expression. A guanosine 3',5'-cyclic monophosphate (cGMP) antagonist reversed KMUP-1-induced ROCK II reduction, indicating cGMP/eNOS involvement. KMUP-1 inceased PKG and LDLRs surrounded by LDL and restored oxidized LDL-induced PKA expresion. Unlike simvastatin, KMUP-1 could not inhibit (14)C mevalonate formation. KMUP-1 could, but simvastatin could not, decrease ROCK II expression by exogenous FPP/CGPP. KMUP-1 improves HDL via PPARγ/LXRα/ABCA1/Apo-I expression and increases LDLRs/PKA/PKG/HSL expression and immunoreactivity, leading to TG hydrolysis to lower hepatic fat and body weight.
靶向G蛋白偶联受体(GPCRs)的磷酸二酯酶抑制剂(PDEI)/内皮型一氧化氮合酶(eNOS)增强剂KMUP-1可改善血脂异常。我们将其降脂效果与辛伐他汀进行了比较,并探讨了激素敏感性脂肪酶(HSL)在肝脏脂肪减少中的转位情况。通过灌胃给高脂饮食(HFD)喂养的C57BL/6J雄性小鼠给予盐酸KMUP-1(1、2.5和5mg/kg/天)和辛伐他汀(5mg/kg/天),持续8周。KMUP-1抑制了HFD诱导的血浆/肝脏甘油三酯、总胆固醇和低密度脂蛋白;增加了高密度脂蛋白/3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)/Rho激酶II(ROCK II)/过氧化物酶体增殖物激活受体γ(PPARγ)/ATP结合盒转运体A1(ABCA1);并降低了肝脏和体重。饮用水中添加盐酸KMUP-1(2.5mg/200ml自来水)1 - 14周或8 - 14周可降低HFD诱导的肝脏和体重以及B类I型清道夫受体的表达,并增加蛋白激酶A(PKA)/蛋白激酶G(PKG)/低密度脂蛋白受体(LDLRs)/HSL的表达和免疫反应性。在与血清或外源性甲羟戊酸孵育的HepG2细胞中,KMUP-1(10⁻⁷ ∼ 10⁻⁵ M)通过反馈调节逆转HMGR的表达,使ABCA1/载脂蛋白A-I/肝X受体α(LXRα)/PPARγ共定位表达,并降低外源性香叶基香叶基焦磷酸/法尼基焦磷酸(FPP)诱导的RhoA/ROCK II表达。一种环磷酸鸟苷(cGMP)拮抗剂逆转了KMUP-1诱导的ROCK II减少,表明cGMP/eNOS参与其中。KMUP-1增加了被低密度脂蛋白包围的PKG和LDLRs,并恢复了氧化低密度脂蛋白诱导的PKA表达。与辛伐他汀不同,KMUP-1不能抑制(14)C甲羟戊酸的形成。KMUP-1可以,但辛伐他汀不能,通过外源性FPP/CGPP降低ROCK II的表达。KMUP-1通过PPARγ/LXRα/ABCA1/载脂蛋白I(Apo-I)表达改善高密度脂蛋白,并增加LDLRs/PKA/PKG/HSL的表达和免疫反应性,导致甘油三酯水解以降低肝脏脂肪和体重。