Larsucosterol (DUR-928) trimethylamine 是一种胆固醇代谢物,是一种有效的肝 X 受体 (LXR) 拮抗剂。Larsucosterol trimethylamine 是一种有效的内源性脂肪生成调节剂。Larsucosterol trimethylamine 通过降低 mRNA 水平和抑制 SREBP-1 的激活抑制胆固醇的生物合成。
生物活性 | Larsucosterol (DUR-928) trimethylamine, acholesterolmetabolite, is a potentliver X receptor (LXR)antagonist. Larsucosterol trimethylamine as a potent endogenous regulator decreases lipogenesis. Larsucosterol trimethylamine inhibits thecholesterolbiosynthesis via decreasing mRNA levels and inhibiting the activation of SREBP-1[1][2][3]. |
体外研究 (In Vitro) | Larsucosterol (DUR-928; 0-25 μM; 8 h; HepG2 cells) trimethylamine inhibits cholesterol biosynthesis by decreasing HMG-CoA reductase mRNA levels and decreases free [14C] cholesterol in a dose-dependent manner[1]. Larsucosterol (0-25 μM; 6 h; HepG2 cells) trimethylamine inhibits HMG-CoA reductase expression by inhibition of both SREBP1 activation and expression in hepatocytes[1]. Larsucosterol (0-50 μM; 48 h) trimethylamine increases cell proliferation and decreases apoptosis in macrophages[2]. Larsucosterol (0-25 μM; 48 h; macrophages) trimethylamine inhibits activation of liver oxysterol receptor LXRα[2].
Cell Proliferation Assay[2] Cell Line: | Macrophages | Concentration: | 0, 5, 10, 15, 20, and 25 μM | Incubation Time: | 48 hours | Result: | Induces cell proliferation and relative cell number after treatment for 48 h were 120% at 25 μM. |
Apoptosis Analysis[2] Cell Line: | Macrophages | Concentration: | 0, 10, 20, 30, 40 and 50 μM | Incubation Time: | 48 hours | Result: | Did not significantly affect the numbers of apoptotic or live cells. |
Western Blot Analysis[1] Cell Line: | HepG2 cells | Concentration: | 0, 3, 6, 12, and 25 μM | Incubation Time: | 6 hours | Result: | Inhibited the activation of SREBP-1 and SREBP-2, and subsequently inhibit the expression HMG-CoA reductase. |
Western Blot Analysis[2] Cell Line: | Macrophages | Concentration: | 0, 3, 6, 12, and 25 μM | Incubation Time: | 48 hours | Result: | Decreased LXRα levels in the nuclei in a does-dependent manner. |
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体内研究 (In Vivo) | Larsucosterol (DUR-928; 25 mg/kg; i.p.; twice in 14 hours; C57BL/6J mice with nonalcoholic fatty liver diseases (NAFLD) model) trimethylamine reduces serum lipid levels in mice fed a high-fat diet[3]. Larsucosterol (25 mg/kg; i.p.; twice in 14 hours; C57BL/6J mice with nonalcoholic fatty liver diseases (NAFLD) model) trimethylamine suppressed the expression of the genes and inhibits ABCA1 expressionde. Larsucosterolcreases nuclear SREBP-1 Protein levels and cytoplasmic FAS and ACC1 protein levels in liver tissue[3]. Larsucosterol (25 mg/kg; i.p.; once every 3 days for 6 weeks; C57BL/6J mice with nonalcoholic fatty liver diseases (NAFLD) model) trimethylamine protects the liver from injury by suppressing hepatic inflammation[3].
Animal Model: | Female C57BL/6J mice with nonalcoholic fatty liver diseases (NAFLD) model[3] | Dosage: | 25 mg/kg | Administration: | Intraperitoneal injection; twice in 14 hours | Result: | Decreased plasma TG, CHOL, and HDL-C by 40, 15, and 20%, respectively. Reduced the mRNA levels of SREBP-1c, ACC1, and FAS by 46, 57, and 49%, respectively. Suppressed ABCA1 expression. Suppressed nuclear SREBP-1, cytoplasmic ACC1, and FAS protein levels by 74, 58, and 47%, respectively.
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Animal Model: | Female C57BL/6J mice with nonalcoholic fatty liver diseases (NAFLD) model[3] | Dosage: | 25 mg/kg | Administration: | Intraperitoneal injection; once every 3 days for 6 weeks | Result: | Decreased plasma cholesterol levels. Reduced serum alkaline phosphatase, ALT, and AST levels.
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运输条件 | Room temperature in continental US; may vary elsewhere. |
储存方式 | Powder | -20°C | 3 years | | 4°C | 2 years | In solvent | -80°C | 6 months | | -20°C | 1 month |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(65.44 mM;Need ultrasonic) 配制储备液 1 mM | 1.9634 mL | 9.8170 mL | 19.6340 mL | 5 mM | 0.3927 mL | 1.9634 mL | 3.9268 mL | 10 mM | 0.1963 mL | 0.9817 mL | 1.9634 mL |
*请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。 |