在斑马鱼的药理动力学和残留物消除Diazepam
Hong-Liang Xiao1, Si-Ting Li1, Ting-Ting Li1
1Guangdong Provincial Key Laboratory of Veterinary Pharmaceutics, Development and Safety Evaluation, South China Agricultural University, Guangzhou, P.R. China.
Journal of veterinary pharmacology and therapeutics
|January 10, 2026
概括
斑马鱼中的泽残留物被快速吸收和分发,但缓慢排出,造成食品安全风险. 这项研究详细介绍了迪亚泽帕姆.
科学领域:
- 水生物质毒理学研究
- 药理动力学 药理动力学
- 食品安全分析 食品安全分析
背景情况:
- 在水产养殖中被泽 (DZP) 污染造成了严重的食品安全问题.
- 了解DZP的药理动力学和水生生物中的残留物消除对于风险评估至关重要.
研究的目的:
- 调查斑马鱼中代谢 (DZP) 的药理动力学和残留物消除模式.
- 为评估与水产养殖中DZP相关的食品安全风险提供数据.
主要方法:
- 斑马鱼通过浴暴露在1mg/L的DZP中24小时.
- 用非分组分析确定了药理动力学参数.
- 在150天内监测残留物消除,分析代谢物诺迪亚泽帕姆 (NDZP),氧泽帕姆 (OZP) 和特马泽帕姆 (TZP).
主要成果:
- DZP及其代谢物 (NDZP,OZP,TZP) 迅速被斑马鱼吸收并广泛分布.
- 药物动力学参数表明缓慢的消除 (T1/2 = 4.25-11.78小时).
- 150天后,DZP残留物持续显著 (0.54±0.2μg/kg),而代谢物更早清除.
结论:
- 斑马鱼表现出DZP及其代谢物的缓慢消除,突出显示了生物积累的潜力.
- 这些发现强调了需要严格监测水产养殖中的DZP,以确保食品安全.
- 这项研究为评估其他小型食用鱼类的DZP风险提供了一个框架.
相关概念视频
Drug Elimination: The Concept of Clearance
Drug elimination refers to removing drugs from the body, either through urine by the kidneys or through bile by the liver. Drug clearance is a pharmacokinetic parameter that measures the efficiency of drug removal from the bloodstream within a specific time frame. It is calculated as the rate at which a drug is eliminated from plasma divided by the plasma concentration of the drug.
Drug clearance is not limited to renal excretion but encompasses all organs involved in drug elimination,...
Drug clearance is not limited to renal excretion but encompasses all organs involved in drug elimination,...
Drug Elimination: Non-Renal Routes
The liver plays a pivotal role in eliminating drugs and their metabolites, primarily through a process known as biliary excretion. This process involves the hepatocytes, the primary cells in the liver that generate bile. A range of transporters actively expels polar drugs or hydrophilic drug metabolites into the bile, which transports the drugs and metabolites into the small intestine. From here, they are eventually expelled from the body through feces. In some instances, the original drug or a...
Drug Elimination: Overview
Drug elimination involves many complex processes and does not necessarily differentiate between distribution and elimination. It is divided into two primary components: excretion and biotransformation.
Excretion refers to removing a drug from the body, either in its unchanged form or as its metabolites. Nonvolatile and polar drugs are primarily excreted through the kidneys, with other pathways including bile, sweat, saliva, and milk. Volatile drugs such as anesthetic gases are excreted via the...
Excretion refers to removing a drug from the body, either in its unchanged form or as its metabolites. Nonvolatile and polar drugs are primarily excreted through the kidneys, with other pathways including bile, sweat, saliva, and milk. Volatile drugs such as anesthetic gases are excreted via the...
Hepatic Drug Excretion: Enterohepatic Cycling
Enterohepatic cycling involves the active secretion of drugs and their metabolites into the bile via transporters in the canalicular membrane of hepatocytes. This secretion is an integral part of the digestive process, releasing these substances into the gastrointestinal (GI) tract.
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
Hepatic Drug Excretion: Influencing Factors
The biliary system of the liver, crucial for bile secretion and drug excretion, comprises intrahepatic bile ducts that merge to form the common hepatic duct. This duct, carrying hepatic bile, combines with the cystic duct, draining the gallbladder and forming the common bile duct, which empties into the duodenum. Bile, produced by hepatic cells lining the bile canaliculi, is composed primarily of water, bile salts, pigments, electrolytes, and lesser amounts of cholesterol and fatty acids. Bile...
Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance
The elimination half-life and drug clearance of drugs following nonlinear kinetics can vary with dosage. The Michaelis-Menten parameters and drug concentration influence these factors. As the dose increases, the elimination half-life tends to lengthen, resulting in a reduction in clearance and a disproportionately larger area under the curve. The total clearance can be derived from the Michaelis-Menten equation for drugs following a one-compartment model.
A study on guinea pigs examined the...
A study on guinea pigs examined the...


