Mongold J J, Cros G H, Vian L, Tep A, Ramanadham S, Siou G, Diaz J, McNeill J H, Serrano J J
Laboratory of Pharmacodynamics, Faculty of Pharmacy, Montpellier, France.
Pharmacol Toxicol. 1990 Sep;67(3):192-8. doi: 10.1111/j.1600-0773.1990.tb00812.x.
This study explored some toxicological aspects of vanadyl sulphate (VOSO4) treatment of rats made diabetic with a single intravenous injection of streptozotocin (60 mg/kg). Administered in drinking water (0.25, 0.5, 0.75 or 1 mg of VOSO4, 5H2O ml) VOSO4 treatment partially or totally corrected some of the alterations associated with the diabetic state (hyperglycaemia, polydipsia, polyphagia, high cholesterol and triglycerides levels) and did not produce any changes in various plasma or blood cell parameters which were not previously altered by diabetes. Measurement of vanadium levels indicated that tissues accumulated vanadium in the following order of concentrations: bone greater than kidney greater than spleen greater than liver greater than lung greater than or equal to muscle greater than blood. Histopathological studies did not reveal any difference in liver, stomach, ileum, spleen, heart and lung from control, non-treated diabetic or VOSO4-treated diabetic animals. Kidney of all non-treated diabetic animals showed an epithelial cellular swelling of distal tubules while only 2 of 6 VOSO4-treated diabetic animals showed this alteration. Cellular degeneration of pancreas B-cells was less marked in VOSO4-treated that in non-treated diabetic animals. The study indicates that VOSO4 may be a potential antidiabetic agent.
本研究探讨了用硫酸氧钒(VOSO4)治疗单次静脉注射链脲佐菌素(60 mg/kg)致糖尿病大鼠的一些毒理学方面。将VOSO4(0.25、0.5、0.75或1 mg的VOSO4·5H2O/ml)加入饮用水中给予,VOSO4治疗部分或完全纠正了一些与糖尿病状态相关的改变(高血糖、多饮、多食、高胆固醇和甘油三酯水平),并且未对糖尿病之前未改变的各种血浆或血细胞参数产生任何变化。钒水平的测量表明,组织中钒的积累浓度顺序为:骨>肾>脾>肝>肺≥肌肉>血液。组织病理学研究未发现对照动物、未治疗的糖尿病动物或VOSO4治疗的糖尿病动物在肝、胃、回肠、脾、心脏和肺方面有任何差异。所有未治疗的糖尿病动物的肾远端小管上皮细胞肿胀,而在VOSO4治疗的糖尿病动物中,6只只有2只出现这种改变。与未治疗的糖尿病动物相比,VOSO4治疗的糖尿病动物胰腺B细胞的细胞变性不那么明显。该研究表明,VOSO4可能是一种潜在的抗糖尿病药物。