Khoja S M, Abuelgassim A O, al-Bar O A
Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia.
Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1996 Nov;115(3):217-21. doi: 10.1016/s0742-8413(96)00080-1.
The effect of sodium orthovanadate on the activity of 6-phosphofructo-1-kinase (PFK) in the epithelial cells of rat small intestine was investigated. Injection of vanadate (2.5 mg/rat) into rats at 2-day intervals per week for two consecutive weeks resulted in a significant decrease in the maximal activities and activity ratios (activity at 0.5 mM fructose-6-phosphate at pH 7.0/activity at pH 8.0 [v0.5/V]) of the partially purified PFK in rat jejunum. Also, the sensitivity of jejunal PFK to inhibition by ATP increased in rats treated with vanadate. The addition of 1 microM fructose-2,6-biphosphate and 50 microM AMP in the assays released the enzyme inhibition by ATP, and no significant difference was seen between vanadate-injected and control rats. Moreover, the extent of activation with 1 microM fructose-2,6-bisphosphate was significantly higher (79%) in vanadate-injected rats than in control rats (26%). The present results indicate that rat jejunal PFK is highly inhibited with vanadate in vivo. Therefore, although vanadate has been considered to be an insulin-like agent, because of its insulin-like effects on adipocytes and skeletal muscle, the present results may indicate that this behavior could not be applicable to normal rat tissues, because the effect of vanadate on jejunal PFK is clearly opposite that of insulin.
研究了原钒酸钠对大鼠小肠上皮细胞中6-磷酸果糖-1-激酶(PFK)活性的影响。每周间隔2天给大鼠注射钒酸盐(2.5毫克/只大鼠),连续两周,导致大鼠空肠中部分纯化的PFK的最大活性和活性比(pH 7.0时0.5毫摩尔/升6-磷酸果糖的活性/pH 8.0时的活性[v0.5/V])显著降低。此外,用钒酸盐处理的大鼠空肠PFK对ATP抑制的敏感性增加。在测定中加入1微摩尔/升果糖-2,6-二磷酸和50微摩尔/升AMP可解除ATP对酶的抑制,注射钒酸盐的大鼠和对照大鼠之间未见显著差异。此外,注射钒酸盐的大鼠中1微摩尔/升果糖-2,6-二磷酸的激活程度(79%)显著高于对照大鼠(26%)。目前的结果表明,大鼠空肠PFK在体内被钒酸盐高度抑制。因此,尽管钒酸盐由于其对脂肪细胞和骨骼肌的胰岛素样作用而被认为是一种胰岛素样剂,但目前的结果可能表明这种行为不适用于正常大鼠组织,因为钒酸盐对空肠PFK的作用与胰岛素明显相反。