PetBiomics Ltd., Helsinki, Finland.
Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
Metabolomics. 2021 Jun 2;17(6):54. doi: 10.1007/s11306-021-01803-5.
Phenobarbital is a commonly used anticonvulsant for the treatment of canine epileptic seizures. In addition to its central nervous system (CNS) depressing effects, long-term phenobarbital administration affects liver function. However, broader metabolic consequences of phenobarbital treatment are poorly characterized.
To identify metabolic changes in the sera of phenobarbital-treated dogs and to investigate the relationship between serum phenobarbital concentration and metabolite levels.
Leftovers of clinical samples were used: 58 cases with phenobarbital concentrations ranging from 7.8 µg/mL to 50.8 µg/mL, and 25 controls. The study design was cross-sectional. The samples were analyzed by a canine-specific H NMR metabolomics platform. Differences between the case and control groups were evaluated by logistic regression. The linear relationship between metabolite and phenobarbital concentrations was evaluated using linear regression.
Increasing concentrations of glycoprotein acetyls, LDL particle size, palmitic acid, and saturated fatty acids, and decreasing concentrations of albumin, glutamine, histidine, LDL particle concentration, multiple HDL measures, and polyunsaturated fatty acids increased the odds of the sample belonging to the phenobarbital-treated group, having a p-value < .0033, and area under the curve (AUC) > .7. Albumin and glycoprotein acetyls had the best discriminative ability between the groups (AUC: .94). No linear associations between phenobarbital and metabolite concentrations were observed.
The identified metabolites are known to associate with, for example, liver and CNS function, inflammatory processes and drug binding. The lack of a linear association to phenobarbital concentration suggests that other factors than the blood phenobarbital concentration contribute to the magnitude of metabolic changes.
苯巴比妥是一种常用于治疗犬癫痫发作的抗惊厥药物。除了对中枢神经系统(CNS)的抑制作用外,长期使用苯巴比妥还会影响肝功能。然而,苯巴比妥治疗的更广泛的代谢后果尚未得到充分描述。
确定接受苯巴比妥治疗的犬血清中的代谢变化,并研究血清中苯巴比妥浓度与代谢物水平之间的关系。
使用临床样本的剩余物:58 例苯巴比妥浓度范围为 7.8μg/mL 至 50.8μg/mL 的病例和 25 例对照。研究设计为横断面。使用犬特异性 H NMR 代谢组学平台对样本进行分析。通过逻辑回归评估病例组和对照组之间的差异。使用线性回归评估代谢物与苯巴比妥浓度之间的线性关系。
糖蛋白乙酰基、LDL 颗粒大小、棕榈酸和饱和脂肪酸浓度的增加,以及白蛋白、谷氨酰胺、组氨酸、LDL 颗粒浓度、多种 HDL 指标和多不饱和脂肪酸浓度的降低,增加了样本属于苯巴比妥治疗组的可能性,p 值 < .0033,曲线下面积(AUC)> .7。白蛋白和糖蛋白乙酰基在两组之间具有最佳的区分能力(AUC:.94)。未观察到苯巴比妥与代谢物浓度之间的线性关联。
所鉴定的代谢物与例如肝和 CNS 功能、炎症过程和药物结合有关。与苯巴比妥浓度之间缺乏线性关联表明,除了血液中苯巴比妥浓度之外,还有其他因素会导致代谢变化的程度。