Shukla Ruchi, Padhye Subhash, Modak Manisha, Ghaskadbi Saroj S, Bhonde Ramesh R
Tissue Engineering and Banking Laboratory, National Centre for Cell Science, Pune University Campus, Ganeshkind, Pune 411007, India.
Rev Diabet Stud. 2007 Spring;4(1):33-43. doi: 10.1900/RDS.2007.4.33. Epub 2007 May 10.
Organic vanadium compounds offer several advantages in the treatment of diabetes, yet they are impractical to use because of known side effects. In order to ameliorate the side effects of vanadium, we conjugated it with quercetin to form bis(quercetinato)oxovanadium IV (BQOV). This study evaluates the effect of BQOV treatment on carbohydrate metabolism and overall oxidative stress in streptozotocin-induced (STZ) diabetic mice. Administration of BQOV orally to diabetic mice for 3 weeks led to a reduction of blood glucose levels and the animals exhibited normal glucose tolerance at the end of the study period. The increase in glucose uptake by skeletal muscle and liver as well as the normalization of mRNA levels of G-6-Pase and glucokinase in the liver after BQOV treatment pointed to improvements in carbohydrate metabolism. The analysis of the antioxidant status of serum, liver and pancreas revealed reduced oxidative stress in BQOV-treated animals compared to untreated diabetic controls. Serum analyses for kidney and liver function showed that BQOV treatment provoked total protection of the kidney and partial protection of the liver from diabetogenic insults. The number of insulin-positive cells and the amount of pancreatic insulin in treated mice (1.2038 +/- 0.34 ng/mg tissue) did not account for pancreatic regeneration but suggested an insulin-mimetic action on the part of BQOV. Moreover, administration of BQOV for 3 weeks did not show any visible side-effects. This data indicate that BQOV is a safe and potent agent for diabetes treatment, because it is able to improve carbohydrate metabolism and to reduce overall oxidative stress.
有机钒化合物在糖尿病治疗方面具有诸多优势,但由于已知的副作用,它们在实际应用中并不实用。为了改善钒的副作用,我们将其与槲皮素结合,形成双(槲皮素)氧钒(IV)(BQOV)。本研究评估了BQOV治疗对链脲佐菌素诱导(STZ)的糖尿病小鼠碳水化合物代谢和整体氧化应激的影响。给糖尿病小鼠口服BQOV 3周可导致血糖水平降低,并且在研究期结束时动物表现出正常的葡萄糖耐量。BQOV治疗后骨骼肌和肝脏对葡萄糖摄取的增加以及肝脏中G-6-Pase和葡萄糖激酶mRNA水平的正常化表明碳水化合物代谢得到改善。血清、肝脏和胰腺抗氧化状态的分析显示,与未治疗的糖尿病对照组相比,BQOV治疗的动物氧化应激降低。肾脏和肝脏功能的血清分析表明,BQOV治疗可使肾脏得到完全保护,肝脏得到部分保护免受糖尿病损伤。治疗小鼠中胰岛素阳性细胞的数量和胰腺胰岛素的量(1.2038 +/- 0.34 ng/mg组织)并不说明胰腺再生,但表明BQOV具有胰岛素模拟作用。此外,给予BQOV 3周未显示任何明显的副作用。这些数据表明BQOV是一种安全有效的糖尿病治疗药物,因为它能够改善碳水化合物代谢并降低整体氧化应激。