基于属性的预测揭示了肠道分泌作为小分子药物的消除途径
Chen Chen1, Weiping Zhao1, Lin Cao2
1Drug Metabolism and Pharmacokinetics, Drug Discovery, Genentech Inc., South San Francisco, California 94080, United States.
Journal of medicinal chemistry
|August 8, 2025
概括
肠道分泌是药物清除的重要途径,经常被忽视. 这项研究揭示了它的机制,并为药物设计和药理动力学评估提供了新的考虑.
科学领域:
- 药理学 药理学是指药理学的学科.
- 药物新陈代谢 药物新陈代谢
- 药物发现 药物发现 药物发现
背景情况:
- 肝脏和脏通路传统上被视为主要的药物清除途径.
- 新出现的证据表明,直接肠道分泌起着重要作用.
- 肠道分泌往往被低估,因为未吸收的药物和胆道分泌的复杂性.
研究的目的:
- 研究肠道药物分泌的程度和机制.
- 开发基于分子描述器的肠道分泌的预测模型.
- 了解肠道和胆道分泌通路之间的相互作用.
主要方法:
- 使用胆道管入的老鼠进行体内研究.
- 研究了一系列用于肠道分泌的药物库.
- 使用分子描述符开发了一个预测性决策树.
主要成果:
- 被动透性和排泄输送物是大鼠肠道分泌的关键驱动因素.
- 修改单个功能组可以在肠道和胆道路径之间转移药物清除.
- 确定肠道分泌是代谢稳定的小分子药物的主要途径.
结论:
- 肠道分泌是一种至关重要的,但尚未被充分探索的药物清除途径.
- 这些发现为药物清除机制提供了更全面的理解.
- 为药物设计和药理动力学评估策略提供了新的考虑.
相关概念视频
Drug Excretion: Miscellaneous Routes
128
Drug excretion involves various organs, including the liver, intestines, skin, and eyes. In the case of drugs or toxins, they can be actively secreted into bile by transporters in the hepatocyte's canalicular membrane. These substances enter the GI tract during digestion and may be reabsorbed into the body from the intestine. This process, known as enterohepatic recycling, can significantly prolong the presence and effects of a substance in the body. To interrupt this cycle, specific...
128
Drug Elimination: Non-Renal Routes
2.5K
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...
2.5K
Drug Elimination: Overview
1.9K
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...
1.9K
Drug Elimination by Renal Route: Tubular Reabsorption
3.9K
During the process of renal excretion, as the glomerular filtrate progresses to the distal convoluted tubule (DCT), drugs that are highly permeable, lipophilic, and nonionized undergo passive reabsorption from the tubular fluid into the surrounding peritubular capillaries. This reabsorption process restricts their elimination through the kidneys. However, the majority of drugs are either weak acids or weak bases, and their ionization level is dependent on pH. By altering the pH of urine, the...
3.9K
Hepatic Drug Excretion: Influencing Factors
218
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...
218
Hepatic Drug Excretion: Enterohepatic Cycling
1.8K
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...
1.8K


