Kim E, Na K J
Korea Ginseng and Tobacco Research Institute, Taejon.
Toxicol Appl Pharmacol. 1991 Sep 1;110(2):251-8. doi: 10.1016/s0041-008x(05)80007-9.
Subcutaneous injection of sodium dichromate into male Sprague-Dawley rats immediately produced a variety of metabolic changes in a dose-dependent manner. Serum lactate and glucose were significantly increased after dichromate treatment, reaching maximum levels at 15 and 30 min, respectively. Then, the toxicity progressively diminished. In contrast, a steady increase in blood urea nitrogen (BUN) concentration was caused by dichromate, reaching maximum levels at 60 min after the administration; elevated BUN levels were sustained for several hours thereafter. Unlike KCN (5 mg/kg, ip) and As2O3 (5 mg/kg, ip), dichromate rapidly decreased serum insulin within 15 min after intoxication in doses of 20 and 40 mg/kg; hypoinsulinemia lasted 60 min. However, insulin levels returned to the normal range at 120 min after treatment. Dichromate-induced metabolic disturbance was also observed in the 24 hr-fasted rats, the response of which was similar to normal rats except for later hyperglycemia. In both cases, the duration time was short (30 to 60 min). Adrenalectomy and insulin pretreatment had no effect on dichromate-induced hyperglycemia. These results suggest that dichromate-induced metabolic disturbance results from the concomitant effects of a sudden decrease in serum insulin level and its direct inhibitory effect on carbohydrate metabolism. In addition, the characteristic biphasic pattern of metabolic disturbance might be related to metabolic fate of dichromate in vivo.
向雄性Sprague-Dawley大鼠皮下注射重铬酸钠后,立即以剂量依赖的方式产生了多种代谢变化。重铬酸盐处理后,血清乳酸和葡萄糖显著增加,分别在15分钟和30分钟时达到最高水平。然后,毒性逐渐减弱。相比之下,重铬酸盐导致血尿素氮(BUN)浓度持续升高,给药后60分钟达到最高水平;此后BUN水平升高持续数小时。与氰化钾(5mg/kg,腹腔注射)和三氧化二砷(5mg/kg,腹腔注射)不同,重铬酸盐在中毒后15分钟内,以20mg/kg和40mg/kg的剂量迅速降低血清胰岛素水平;低血糖症持续60分钟。然而,治疗后120分钟胰岛素水平恢复到正常范围。在禁食24小时的大鼠中也观察到重铬酸盐诱导的代谢紊乱,除了后期高血糖外,其反应与正常大鼠相似。在这两种情况下,持续时间都很短(30至60分钟)。肾上腺切除术和胰岛素预处理对重铬酸盐诱导的高血糖没有影响。这些结果表明,重铬酸盐诱导的代谢紊乱是血清胰岛素水平突然下降及其对碳水化合物代谢的直接抑制作用共同作用的结果。此外,代谢紊乱的特征性双相模式可能与重铬酸盐在体内的代谢命运有关。