Kosicka-Noworzyń Katarzyna, Romaniuk-Drapała Aleksandra, Sheng Yi-Hua, Yohn Christine, Brunetti Luigi, Kagan Leonid
Department of Physical Pharmacy and Pharmacokinetics, Poznan University of Medical Sciences, Rokietnicka 3, Poznań 60-806, Poland; Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.
Department of Clinical Chemistry and Molecular Diagnostics, Poznan University of Medical Sciences, Rokietnicka 3, Poznań 60-806, Poland; Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.
Biomed Pharmacother. 2025 Jun;187:118155. doi: 10.1016/j.biopha.2025.118155. Epub 2025 May 12.
Implications of obesity extend beyond the association with various health conditions, impacting physiological changes that affect the liver and the activity of metabolizing enzymes. Given the prevalence of obesity and the risk for drug-drug interactions owing to the comorbidity burden, the current drug dosage recommendations may need reevaluation for patients with obesity. This study evaluated the implications of obesity on the gene expression of hepatic drug-metabolizing enzymes. As drug clearance is an essential pharmacokinetic parameter for maintaining drug dosing regimens, investigating alterations in metabolizing enzymes expression is a critical step.
Human liver samples were collected post-mortem from 32 individuals and classified into the control (18.5 ≤ BMI <25 kg/m; range 18.9-24.4 kg/m; median 2.3 kg/m) and the study group (BMI ≥25 kg/m; range 25.1-55.5 kg/m; median 31.2 kg/m). Real-time quantitative PCR was performed for the analysis of 168 drug-metabolizing enzymes.
Our studies revealed several potential physiologically relevant differences, but the statistical significance was reached only for ALDH3B1, PTGS1, and CEL (all being up-regulated in the study group).
The study adds to our understanding of the mechanisms of pharmacokinetic changes in overweight and obesity. The findings require further exploration on the protein level, through proteomic and functional studies.
肥胖的影响不仅限于与各种健康状况的关联,还会影响影响肝脏的生理变化以及代谢酶的活性。鉴于肥胖的普遍性以及由于合并症负担导致药物相互作用的风险,当前针对肥胖患者的药物剂量建议可能需要重新评估。本研究评估了肥胖对肝脏药物代谢酶基因表达的影响。由于药物清除率是维持给药方案的关键药代动力学参数,因此研究代谢酶表达的变化是关键步骤。
从32名个体的尸体中收集人类肝脏样本,并分为对照组(18.5≤体重指数<25kg/m;范围18.9 - 24.4kg/m;中位数2.3kg/m)和研究组(体重指数≥25kg/m;范围25.1 - 55.5kg/m;中位数31.2kg/m)。对168种药物代谢酶进行实时定量PCR分析。
我们的研究揭示了一些潜在的生理相关差异,但仅醛脱氢酶3B1(ALDH3B1)、前列腺素内过氧化物合酶1(PTGS1)和羧酯酶(CEL)达到统计学显著性(在研究组中均上调)。
该研究增进了我们对超重和肥胖患者药代动力学变化机制的理解。这些发现需要通过蛋白质组学和功能研究在蛋白质水平上进一步探索。