Maternal separation influences hepatic drug-metabolizing CYP450 gene expression without pathological changes in adult mice.

Q3 Pharmacology, Toxicology and Pharmaceutics
Yazun Bashir Jarrar, Walaa' Ashour, Abdalla Madani, Qais Jarrar, Dina Abulebdah, Yahya F Jamous, Samah Y Labban, Mariam Tazkarji
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引用次数: 0

Abstract

Objectives: The principal motive of this study is to explore the influence maternal separation (MS) exhibits on the mRNA expression of major drug metabolizing-cyp450s in parallel with the assessment of pathological changes that can be induced by MS in the livers of experimental mice.

Methods: Eighteen Balb/c mouse pups, comprising of both males and females, were separated from their mothers after birth. Following a six-week period during when the pups became adults, the mice were sacrificed and their livers were isolated for analysis of weight, pathohistological alterations, and the mRNA expression of drug metabolizing cyp450 genes: cyp1a1, cyp3a11, cyp2d9, and cyp2c29.

Results: The study demonstrated that MS markedly downregulated (p<0.05) the mRNA expression of all tested drug-metabolizing cyp450s in livers of female and male mice. Furthermore, the mRNA levels of major drug-metabolizing cyp450s were notably lower (p<0.05) in livers of female MS mice as compared with male MS mice. It was found that values of the total body weight and liver weight of MS mice did not vary significantly (p>0.05) from those of the control groups. Additionally, histological examination revealed that the hepatic tissue of MS mice was normal, similar to that of the control mice.

Conclusions: In summary, MS downregulates the gene expression of major hepatic drug-metabolizing cyp450s without inducing pathological alterations in the livers of mice. These findings provide an explanation for the heterogeneity in pharmacokinetics and drug response of patients with early life stress.

母体分离会影响成年小鼠肝脏药物代谢 CYP450 基因的表达,但不会导致病理变化。
研究目的本研究的主要目的是探讨母体分离(MS)对主要药物代谢-cyp450s mRNA表达的影响,同时评估MS可在实验小鼠肝脏中诱发的病理变化:方法:18 只雌雄 Balb/c 小鼠幼崽出生后即与母鼠分离。方法:18 只雌雄 Balb/c 小鼠在出生后即与母鼠分离,在幼鼠长大成人的六周后,将小鼠处死并分离其肝脏,分析重量、病理组织学改变以及药物代谢 cyp450 基因(cyp1a1、cyp3a11、cyp2d9 和 cyp2c29)的 mRNA 表达:研究表明,与对照组相比,多发性硬化症的基因表达明显降低(P0.05)。此外,组织学检查显示 MS 小鼠的肝组织正常,与对照组相似:综上所述,MS能下调肝脏主要药物代谢cyp450s的基因表达,但不会引起小鼠肝脏的病理改变。这些发现为早期生活压力患者的药代动力学和药物反应的异质性提供了解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Basic and Clinical Physiology and Pharmacology
Journal of Basic and Clinical Physiology and Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
3.90
自引率
0.00%
发文量
53
期刊介绍: The Journal of Basic and Clinical Physiology and Pharmacology (JBCPP) is a peer-reviewed bi-monthly published journal in experimental medicine. JBCPP publishes novel research in the physiological and pharmacological sciences, including brain research; cardiovascular-pulmonary interactions; exercise; thermal control; haematology; immune response; inflammation; metabolism; oxidative stress; and phytotherapy. As the borders between physiology, pharmacology and biochemistry become increasingly blurred, we also welcome papers using cutting-edge techniques in cellular and/or molecular biology to link descriptive or behavioral studies with cellular and molecular mechanisms underlying the integrative processes. Topics: Behavior and Neuroprotection, Reproduction, Genotoxicity and Cytotoxicity, Vascular Conditions, Cardiovascular Function, Cardiovascular-Pulmonary Interactions, Oxidative Stress, Metabolism, Immune Response, Hematological Profile, Inflammation, Infection, Phytotherapy.
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