School of Food and Drug, Luoyang Normal University, Luoyang 471934, China.
Beijing Academy of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China.
Molecules. 2022 Sep 7;27(18):5786. doi: 10.3390/molecules27185786.
The novel biochanin A-chromium(III) complex was synthesized by chelating chromium with biochanin A (BCA). The structure of the complex was determined and the complex ([CrBCA]) was composed of chromium(III) and three ligands, and the chromium content was 55 μg/mg. The hypoglycemic activity of the complex was studied in db/db mice and C57 mice. The sub-acute toxicity test of the complex was carried out by the maximum limit method in KM mice. The hypoglycemic activity showed that the complex could reduce the weight of db/db mice and lower the fasting blood glucose and random blood glucose levels. The complex also improved the organ index, oral glucose tolerance test (OGTT) and insulin tolerance test (ITT) results of db/db mice, and some of the indicators were similar to those of the positive control group after treatment with the complex. The histopathology study showed significant improvements in the liver, kidney, pancreas and skeletal muscle compared with the diabetes model group. The complex also showed a significant improvement in serum biochemical indices and antioxidant enzyme activities, as well as glycogen levels. The sub-acute toxicity study showed that the complex did not cause death or any dangerous symptoms during the study. In addition, the sub-acute toxicity study showed that the complex had no significant effect on the serum biochemical indices, antioxidant capacity and organs of normal mice. This study showed that [CrBCA] had good hypoglycemic activity in vivo and had no sub-acute toxicity. This work provides an important reference for the development of functional hypoglycemic foods or drugs.
新型生物查尔酮 A-铬(III)配合物通过与生物查尔酮 A(BCA)螯合铬合成。确定了配合物的结构,该配合物([CrBCA])由铬(III)和三个配体组成,铬含量为 55μg/mg。研究了配合物在 db/db 小鼠和 C57 小鼠中的降血糖活性。采用 KM 小鼠最大耐受量法进行了配合物的亚急性毒性试验。降血糖活性表明,配合物可降低 db/db 小鼠的体重,降低空腹血糖和随机血糖水平。该配合物还改善了 db/db 小鼠的器官指数、口服葡萄糖耐量试验(OGTT)和胰岛素耐量试验(ITT)结果,经配合物治疗后,部分指标与阳性对照组相似。组织病理学研究表明,与糖尿病模型组相比,肝脏、肾脏、胰腺和骨骼肌均有明显改善。配合物还显著改善了血清生化指标和抗氧化酶活性以及糖原水平。亚急性毒性研究表明,在研究过程中,配合物未引起死亡或任何危险症状。此外,亚急性毒性研究表明,配合物对正常小鼠的血清生化指标、抗氧化能力和器官无明显影响。本研究表明[CrBCA]在体内具有良好的降血糖活性,无亚急性毒性。这项工作为功能性降血糖食品或药物的开发提供了重要参考。