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钨酸钠对泊洛沙姆407诱导高血脂昆明小鼠模型血脂的影响
引用本文:王培琴,杨东升,孙静,赵艳威. 钨酸钠对泊洛沙姆407诱导高血脂昆明小鼠模型血脂的影响[J]. 武警医学院学报, 2013, 22(4): 249-251
作者姓名:王培琴  杨东升  孙静  赵艳威
作者单位:1. 武警乌鲁木齐指挥学院门诊部,新疆乌鲁木齐,830049
2. 新疆医科大学附属肿瘤医院麻醉科,新疆乌鲁木齐,830000
3. 武警后勤学院药理学教研室,天津,300162
摘    要:【目的】研究钨酸钠对泊洛沙姆407诱导的高血脂昆明小鼠模型血脂的影响。【方法】昆明小鼠给予钨酸钠(100或200mg/kg)灌胃,连续3 d,末次给药1 h后,腹腔注射泊洛沙姆407 0.3 g/kg,于注射后的4、24及48 h,取血测定甘油三酯和胆固醇含量,注射泊洛沙姆407后24 h血样同时测定高密度脂蛋白-胆固醇的含量。【结果】与正常组的甘油三酯(6.30±0.87)mmol/L相比,泊洛沙姆407腹腔注射4 h后,诱导昆明小鼠出现明显的高甘油三酯血症(233.99±37.94)mmol/L,预先给予钨酸钠处理,能明显降低血清甘油三酯水平[低剂量钨酸钠组:(207.13±29.85)mmol/L;高剂量钨酸钠组:(131.50±46.07)mmol/L,P〈0.05],此作用可持续到造模后的48 h。造模后的24 h,钨酸钠的降血清胆固醇的作用最明显[对照组:(6.07±0.70)mmol/L;低剂量钨酸钠组:(3.04±0.40)mmol/L;高剂量钨酸钠组:(1.81±0.40)mmol/L,P〈0.05]。造模后的24 h,预处理钨酸钠能明显升高血清高密度脂蛋白-胆固醇水平[对照组:(1.97±0.40)mmol/L;低剂量钨酸钠组:(2.70±0.42)mmol/L;高剂量钨酸钠组:(3.73±0.81)mmol/L,P〈0.05]。【结论】钨酸钠对于泊洛沙姆407诱导的高血脂昆明小鼠模型具有降脂作用。

关 键 词:钨酸钠  泊洛沙姆407  昆明小鼠  高血脂

Effects of sodium tungstate on poloxamer 407-induced hyperlipidemic Kunming mouse model
WANG Pei-qin , YANG Dong-sheng , SUN Jing , ZHAO Yan-wei. Effects of sodium tungstate on poloxamer 407-induced hyperlipidemic Kunming mouse model[J]. Acta Academiae Medicinae CPAPF, 2013, 22(4): 249-251
Authors:WANG Pei-qin    YANG Dong-sheng    SUN Jing    ZHAO Yan-wei
Affiliation:(Out-patient Department of Urumqi Command College of Chinese People's Armed Police Forces, Urumqi, 830049, China)
Abstract:[Objective] To investigate the effects of sodium tungstate on serum lipids level in poloxamer 407-induced hyperlipidemic mouse. [ Methods ] Before a bolus of poloxamer 407 (0.3 g/kg) was given intraperitoneally, Kunming mice were pretreated intragastrically with sodium tungstate (100 or 200mg/kg) for 3 days. Blood triacylglycerol (TG) and cholesterol (CHO) were measured at 0, 4, 24 and 48 h after the poloxamer 407 injection, and the blood high density lipoprotein cholesterol (HDL-CHO) level of 24 h were measured. [ Results] Compared to normal group (6.30 ± 0.87) mmol/L, poloxamer 407 induced marked hypertriglyceridemia in Kunming mice (233.99 ± 37.94) mmol/L after intraperitoneal injection for 4 h. Pretreatment with sodium tungstate, could significantly reduce serum triglyceride levels (low dose of sodium tungstate group: (207.13 ± 29.85) mmol/L, high dose sodium tungstate group: (131.50 ± 46.07) mmol/L, the hypolipidemic effect of sodium tungstate is still obvious after 48 h (P 〈 0.05). The most obvious lowering cholesterol of sodium tungstate can be observed after building the model of 24 h [control group: (6.07 ± 0.70) mmol/L; low dose of sodium tungstate group: (3.04 ± 0.40) mmol/L; high doses of sodium tungstate group: (1.81 ± 0.40) mmol/L, P 〈0.05]. After building the model of 24 h, pretreatment with sodium tungstate group can obviously increase the serum HDL-CHO [control group:(1.97 ± 0.40) mmol/L; low dose of sodium tungstate group: (2.70 ± 0.42) mmol/L, high doses of sodium tungstate group: (3.73 ± 0.81) mmol/L, P 〈 0.05]. [Conclusion] Sodium tungstate may have a hypolipidemic effects on poloxamer 407-induced hyperlipidemic Kunming mice and represent a potentially useful approach for the treatment of lipid metabolic disturbances.
Keywords:Sodium tungstate  Poloxamer 407  Kunming mice  Hyperlipidemic
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