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吉非贝齐及其与二甲双胍联合应用对胰岛素抵抗型 2 型糖尿病大鼠 IL-10 和脂联素的多效性作用及抗动脉粥样硬化治疗。

Gemfibrozil and its combination with metformin on pleiotropic effect on IL-10 and adiponectin and anti-atherogenic treatment in insulin resistant type 2 diabetes mellitus rats.

机构信息

Department of Pharmacology, Gyan Vihar School of Pharmacy, Suresh Gyan Vihar University, Mahal, Jagatpura, Jaipur 302025, Rajasthan, India.

出版信息

Inflammopharmacology. 2013 Apr;21(2):137-45. doi: 10.1007/s10787-012-0154-4. Epub 2012 Oct 31.

Abstract

AIM

Gemfibrozil is a PPAR-α ligand that inhibits the progression of atherosclerosis in insulin resistance type 2 diabetes mellitus (IR type 2 DM). Gemfibrozil, poor anti-hyperglycemic combined with metformin, evaluated for MMP-9, IL-10 and adiponectin beyond glycemic control.

ESSENTIAL METHODS

IR type 2 DM induced by administering streptozotocin (90 mg/kg, i.p.) in neonatal rat model. IR type 2 DM rats at 6-week age treated for 8 weeks with (1) gemfibrozil (140 mg/kg od) and (2) gemfibrozil (70 mg/kg bid) + metformin (60 mg/kg bid). At the end, risk parameters like MMP-9, IL-10 and adiponectin were evaluated by ELISA kits.

MAIN RESULTS

Gemfibrozil reduced the MMP-9 levels (-25.740 %) (106.772 ± 7.201 ng/ml vs. 80.231 ± 7.023 ng/ml, P < 0.01); increased adiponectin (68.321 %) (8.781 ± 1.111 μg/ml vs. 14.782 ± 1.055 μg/ml) and IL-10 (155.687 %) (334.208 ± 26.307 pg/ml vs. 853.472 ± 23.172 pg/ml, P < 0.001), but poor glycemic control (-6.169 %) (167.5 ± 16.037 vs. 157.167 ± 3.911, P = ns), hence combined with metformin showed synergistic activity, reduced the MMP-9 levels (-16.992 %) (106.772 ± 7.201 ng/ml vs. 89.941 ± 8.636 ng/ml, P < 0.05) and increased adiponectin (39.870 %) (8.781 ± 1.111 μg/ml vs. 12.282 ± 0.782 μg/ml) and, IL-10 (80.136 %) (334.208 ± 26.307 pg/ml vs. 602.029 ± 39.668 pg/ml, P < 0.01) had good glycemic control (-28.856 %) (167.5 ± 16.037 mg/dl vs. 129.167 ± 4.214 mg/dl, P < 0.05).

OVERALL CONCLUSIONS

Gemfibrozil plus metformin decrease MMP-9, increase IL-10 and adiponectin acting as anti-atherogenic, anti-inflammatory and immunomodulatory in IR type 2 DM.

摘要

目的

吉非贝齐是一种过氧化物酶体增殖物激活受体-α配体,可抑制胰岛素抵抗 2 型糖尿病(IR 型 2 型糖尿病)的动脉粥样硬化进展。吉非贝齐与二甲双胍联合使用具有较差的抗高血糖作用,除了血糖控制外,还评估了 MMP-9、IL-10 和脂联素。

方法

采用链脲佐菌素(90mg/kg,腹腔注射)诱导新生大鼠模型诱导 IR 型 2 型糖尿病。6 周龄的 IR 型 2 型糖尿病大鼠用(1)吉非贝齐(140mg/kg,每日一次)和(2)吉非贝齐(70mg/kg,每日两次)+二甲双胍(60mg/kg,每日两次)治疗 8 周。最后,通过 ELISA 试剂盒评估 MMP-9、IL-10 和脂联素等风险参数。

主要结果

吉非贝齐降低 MMP-9 水平(-25.740%)(106.772±7.201ng/ml 比 80.231±7.023ng/ml,P<0.01);增加脂联素(68.321%)(8.781±1.111μg/ml 比 14.782±1.055μg/ml)和 IL-10(155.687%)(334.208±26.307pg/ml 比 853.472±23.172pg/ml,P<0.001),但血糖控制不佳(-6.169%)(167.5±16.037 比 157.167±3.911,P=ns),因此与二甲双胍联合使用具有协同作用,降低 MMP-9 水平(-16.992%)(106.772±7.201ng/ml 比 89.941±8.636ng/ml,P<0.05)并增加脂联素(39.870%)(8.781±1.111μg/ml 比 12.282±0.782μg/ml)和 IL-10(80.136%)(334.208±26.307pg/ml 比 602.029±39.668pg/ml,P<0.01)具有良好的血糖控制(-28.856%)(167.5±16.037mg/dl 比 129.167±4.214mg/dl,P<0.05)。

结论

吉非贝齐联合二甲双胍可降低 MMP-9、增加 IL-10 和脂联素,在 IR 型 2 型糖尿病中具有抗动脉粥样硬化、抗炎和免疫调节作用。

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