Boyce B F, Yates A J, Mundy G R
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7877.
Endocrinology. 1989 Nov;125(5):2780-3. doi: 10.1210/endo-125-5-2780.
Single daily injections of recombinant human interleukin-1 alpha (IL-1 alpha) or interleukin-1 beta (IL-1 beta) were given for 1-3 days to normal mice, and blood ionized calcium concentrations were measured before and at various times after each injection. Mean blood calcium levels fell significantly in both groups of animals 3 h after the first IL-1 injections and returned to pretreatment values at 5 h. However, at 24 and 48 h mean values were significantly higher than those in saline-heated controls. Despite this progressive underlying increase in mean blood ionized calcium concentrations, blood calcium concentrations also fell significantly 3 h after the second and third IL-1 injections. The transient decrease in blood calcium was prevented by treatment with indomethacin and, thus, appears to be prostaglandin mediated. Hypocalcemia was not observed after single bolus injections of tumor necrosis factor-alpha or -beta (lymphotoxin). These findings suggest that IL-1 is a potential mediator of the hypocalcemia that occurs in up to 40% of patients with bacteremic sepsis and severe tissue injury and is associated with an increased mortality rate.
对正常小鼠每日单次注射重组人白细胞介素-1α(IL-1α)或白细胞介素-1β(IL-1β),持续1 - 3天,在每次注射前及注射后的不同时间测量血液离子钙浓度。在首次注射IL-1后3小时,两组动物的平均血钙水平均显著下降,并在5小时恢复到注射前水平。然而,在24小时和48小时时,平均值显著高于生理盐水加热对照组。尽管血液离子钙平均浓度有这种逐渐升高的趋势,但在第二次和第三次注射IL-1后3小时,血钙浓度仍显著下降。吲哚美辛治疗可防止血钙的短暂下降,因此,血钙下降似乎是由前列腺素介导的。单次推注肿瘤坏死因子-α或-β(淋巴毒素)后未观察到低钙血症。这些发现表明,IL-1是低钙血症的潜在介质,在高达40%的菌血症性败血症和严重组织损伤患者中会发生低钙血症,且与死亡率增加有关。