首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >SYNTHESIS AND EVALUATION OF ANTIDIABETIC PROPERTIES OF A ZINC MIXED LIGAND COMPLEX IN HIGH-FAT DIET - LOW-DOSE STREPTOZOTOCIN-INDUCED DIABETIC RATS
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SYNTHESIS AND EVALUATION OF ANTIDIABETIC PROPERTIES OF A ZINC MIXED LIGAND COMPLEX IN HIGH-FAT DIET - LOW-DOSE STREPTOZOTOCIN-INDUCED DIABETIC RATS

机译:高脂肪饮食-低剂量链脲佐菌素诱导的糖尿病大鼠锌混合配体的抗糖尿病性能的合成与评价。

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Objective: Due to the multifactorial and multisystemic nature of diabetes mellitus (DM), it is often treated with a combination of therapeutic agents. Earlier, we have synthesized and characterized several organozinc complexes and evaluated their safety and antidiabetic properties in experimental DM. In the present study, a new zinc mixed ligand (metformin-3-hydroxyflavone) was synthesized and characterized by various spectral studies and its antidiabetic properties were evaluated in high-fat diet (HFD) fed – low-dose streptozotocin (STZ)-induced Type 2 D (T2D) in rats. Methods: The zinc mixed ligand complex was characterized by spectral studies. The toxicity and dosage fixation studies were carried out as per OECD guidelines 423. HFD fed low-dose STZ-induced T2DM in rats was used as the experimental model. The hypoglycemic efficacy of the complex was evaluated through oral glucose tolerance test, homeostasis model assessment of insulin resistance (IR), QUICK I and by determining the status of important biochemical parameters. The activities of marker enzymes such as aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase were assayed. Metformin was used as a standard drug. Results: The spectral data evidenced the synthesis of a new zinc mixed ligand complex. The biochemical studies evidenced that the oral administration of the complex at a concentration of 10 mg/kg b.w/rat/day for 30 days to diabetic rats significantly improved the glucose homeostasis which was comparable to metformin treatment (50 mg/kg b.w). Conclusion: The zinc mixed complex possesses significant antidiabetic properties in ameliorating IR and stimulatory properties.
机译:目的:由于糖尿病(DM)的多因素和多系统性质,通常需要结合多种治疗药物进行治疗。先前,我们已经合成和表征了几种有机锌配合物,并在实验DM中评估了它们的安全性和抗糖尿病性。在本研究中,合成了一种新的锌混合配体(metformin-3-hydroxyflavone),并通过各种光谱研究对其进行了表征,并在高脂饮食(HFD)喂养–低剂量链脲佐菌素(STZ)诱导下评估了其抗糖尿病特性大鼠2型D(T2D)。方法:通过光谱研究表征了锌混合配体配合物。根据OECD指南423进行毒性和剂量固定研究。以HFD喂食低剂量STZ诱导的大鼠T2DM为实验模型。通过口服葡萄糖耐量试验,胰岛素抵抗(IR),QUICK I稳态模型评估以及确定重要生化参数的状态来评估复合物的降血糖功效。测定了诸如天冬氨酸转氨酶,丙氨酸转氨酶和碱性磷酸酶等标记酶的活性。二甲双胍用作标准药物。结果:光谱数据证明了新的锌混合配体配合物的合成。生化研究表明,以10 mg / kg b.w /大鼠/天的浓度向糖尿病大鼠口服该复合物30天可显着改善葡萄糖稳态,这与二甲双胍治疗(50 mg / kg b.w)相当。结论:锌复合配合物在改善IR和刺激性方面具有显着的抗糖尿病作用。

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