Zeisel S H, DaCosta K A, Edrise B M, Fox J G
Carcinogenesis. 1986 May;7(5):775-8. doi: 10.1093/carcin/7.5.775.
Dimethylamine is important because it is a precursor of nitrosodimethylamine, a suspected carcinogen in man. Significant quantities of dimethylamine and nitrite are found in gastric fluid, and conditions in the stomach are favorable for nitrosodimethylamine formation. Little is known about the origins of dimethylamine in gastric fluid. Studies were performed to determine whether dimethylamine can be transported from blood to gastric fluid. There was no diurnal variation of the dimethylamine content in gastric fluid or blood from untreated dogs. We administered 50 mg/kg dimethylamine i.v. to dogs and ferrets and collected blood and gastric fluid samples at timed intervals. In both species we observed similar kinetics of dimethylamine distribution into biologic fluids. Dimethylamine concentrations in blood and gastric fluid rose rapidly during the first minutes after treatment. Blood dimethylamine concentrations peaked within 30 min after the dose (rising from 10 to 430 nmol/ml in the dogs, and from 30 to 430 nmol/ml in the ferrets). Dimethylamine concentrations in blood slowly decreased thereafter. Gastric fluid dimethylamine concentrations continued to rise for 3 h after the dose (from 40 to 540 nmol/ml in the dogs, and from 40 to 1056 nmol/ml in the ferrets). Gastric fluid dimethylamine remained elevated for more than 5 h. Between 1 h and 5 h after treatment, gastric fluid dimethylamine concentrations were significantly higher than blood dimethylamine concentrations (by greater than 2.5 X). In gastric fluid from control animals, dimethylamine concentration exceeded monomethylamine concentration, which in turn was higher than trimethylamine concentration. Administration of dimethylamine transiently increased gastric fluid monomethylamine content, but had little effect upon trimethylamine concentration. These data demonstrate that dimethylamine is efficiently transported from blood into gastric fluid.
二甲胺很重要,因为它是亚硝基二甲胺的前体,而亚硝基二甲胺是一种被怀疑对人体有致癌性的物质。胃液中存在大量的二甲胺和亚硝酸盐,而且胃部环境有利于亚硝基二甲胺的形成。关于胃液中二甲胺的来源知之甚少。开展了多项研究以确定二甲胺是否能够从血液转运至胃液中。未接受治疗的犬的胃液和血液中,二甲胺含量没有昼夜变化。我们给犬和雪貂静脉注射50 mg/kg二甲胺,并在不同时间间隔采集血液和胃液样本。在这两个物种中,我们观察到二甲胺在生物体液中的分布动力学相似。治疗后的最初几分钟内,血液和胃液中的二甲胺浓度迅速上升。给药后30分钟内血液中的二甲胺浓度达到峰值(犬从10 nmol/ml升至430 nmol/ml,雪貂从30 nmol/ml升至430 nmol/ml)。此后血液中的二甲胺浓度缓慢下降。给药后3小时内,胃液中的二甲胺浓度持续上升(犬从40 nmol/ml升至540 nmol/ml,雪貂从40 nmol/ml升至1056 nmol/ml)。胃液中的二甲胺在5小时以上一直保持在较高水平。治疗后1小时至5小时之间,胃液中的二甲胺浓度显著高于血液中的二甲胺浓度(高出2.5倍以上)。在对照动物的胃液中,二甲胺浓度超过了单甲胺浓度,而单甲胺浓度又高于三甲胺浓度。给予二甲胺会使胃液中单甲胺含量短暂增加,但对三甲胺浓度影响不大。这些数据表明,二甲胺能有效地从血液转运至胃液中。