Hunt C D, Herbel J L
USDA, Grand Forks Human Nutrition Research Center, N. Dak.
Magnes Trace Elem. 1991;10(5-6):387-408.
Dietary boron, in concentrations similar to that found in human diets comprised mainly of fruits and vegetables, affects both mineral and energy metabolism. Therefore, the effects of boron on a model system with a perturbed metabolic insulin-vitamin D3 axis was examined. Weanling male rats were fed a ground corn-high protein casein-corn oil-based diet (0.06 mg B/kg; no supplemental vitamin D3) supplemented with B (as orthoboric acid) at 0 or 2.4 mg/kg. After 55 days, all rats were equilibrated in individual metabolic cages for 6 days. After another 6 days, one half of the rats in both dietary groups were injected intraperitoneally with streptozotocin (STZ). All rats were killed 3 days after STZ treatment. STZ affected many aspects of mineral metabolism as expected. Plasma ionized calcium concentrations fell by approximately 10% in STZ-treated rats. Brain and heart mineral metabolism was spared from the toxic effects of STZ whereas spleen mineral metabolism was especially vulnerable to STZ. Supplemental dietary boron increased urinary excretion of calcium in the non-STZ rats but did not affect the plasma concentrations of alkaline phosphatase, ionized calcium or the concentration of calcium in the brains, lungs, kidneys and spleens of those animals. Supplemental dietary boron temporarily reduced the abnormally elevated renal excretion of albumin, potassium and sodium during the acute phase of diabetes mellitus. On the other hand, physiological amounts of dietary boron exacerbated the abnormally elevated rate of collagen breakdown in the STZ animal. Finally, boron may have indirectly affected heart mineral metabolism because dietary boron did not affect cardiac boron concentrations but did affect cardiac copper, calcium, manganese, molybdenum and phosphorus concentrations, primarily in non-STZ rats. The findings suggest that dietary boron has both protective and regulatory roles in mineral metabolism.
饮食中的硼,其浓度与主要由水果和蔬菜构成的人类饮食中发现的浓度相似,会影响矿物质和能量代谢。因此,研究了硼对代谢胰岛素 - 维生素D3轴受到干扰的模型系统的影响。给断乳雄性大鼠喂食以磨碎的玉米 - 高蛋白酪蛋白 - 玉米油为基础的饮食(0.06毫克硼/千克;无补充维生素D3),并添加0或2.4毫克/千克的硼(以硼酸形式)。55天后,所有大鼠在单独的代谢笼中平衡6天。再过6天后,两个饮食组中的一半大鼠腹腔注射链脲佐菌素(STZ)。STZ处理3天后处死所有大鼠。正如预期的那样,STZ影响了矿物质代谢的许多方面。经STZ处理的大鼠血浆离子钙浓度下降了约10%。脑和心脏的矿物质代谢未受STZ毒性影响,而脾脏的矿物质代谢尤其易受STZ影响。补充饮食中的硼增加了非STZ大鼠的尿钙排泄,但不影响这些动物血浆碱性磷酸酶、离子钙的浓度,也不影响其脑、肺、肾和脾脏中的钙浓度。补充饮食中的硼在糖尿病急性期暂时降低了白蛋白、钾和钠异常升高的肾排泄。另一方面,生理量的饮食硼加剧了STZ动物中胶原蛋白分解异常升高的速率。最后,硼可能间接影响了心脏的矿物质代谢,因为饮食中的硼不影响心脏硼浓度,但确实影响了心脏铜、钙、锰、钼和磷的浓度,主要是在非STZ大鼠中。这些发现表明饮食中的硼在矿物质代谢中具有保护和调节作用。