神经回路相关的生物标志物用于精神病学药物开发:一个行业的观点
Patricio O'Donnell1, Derek L Buhl2, Jason Johannesen3
1Translational Medicine, Alto Neuroscience, Mountain View, CA, USA. podonnell@altoneuroscience.com.
Advances in neurobiology
|November 19, 2024
概括
开发精神药物需要更好的工具来测量神经生物学效应并识别患者子组. 本综述探讨了量化大脑电路调节的方法,这对于推进药物开发至关重要.
科学领域:
- 神经科学是一个神经科学.
- 精神病学是一个精神病学.
- 药理学 药理学是指药理学的学科.
背景情况:
- 精神病药物开发在评估神经生物学影响和患者分层方面面临着挑战.
- 需要可靠的方法来量化药理干预对神经回路的影响.
研究的目的:
- 审查测量大脑电路调节的现有和新兴方法.
- 突出这些工具在精神病药物开发中的潜力.
主要方法:
- 关于过去,现在和新兴技术的文献评论.
- 分析用于捕捉大脑电路调制结果的工具.
主要成果:
- 有几种方法可以捕捉调节大脑电路的影响.
- 这些方法在药物开发中变得越来越可行.
结论:
- 评估神经回路变化的验证工具对于精神病药物发现至关重要.
- 现场已经准备好在临床试验中实施这些先进的方法.
相关概念视频
Ligand-gated Ion Channels
11.4K
Ligand-gated ion channels are transmembrane proteins with a channel for ions to pass through and a binding site for a ligand. The channel opens only when a ligand attaches to the binding site.
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that...
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that...
11.4K
Neurochemical Transmission: Sites of Drug Action
3.5K
Neurochemical transmission, the conduction of electrical impulses between neurons mediated by neurotransmitters, plays a vital role in various physiological processes. Autonomic drugs exert their effects by modulating neurotransmission within the autonomic nervous system. For instance, drugs such as hemicholinium block the precursor uptake necessary for synthesizing acetylcholine, an essential autonomic neurotransmitter. Following synthesis, neurotransmitters are stored in vesicles. Metyrosine...
3.5K
Drugs Affecting Neurotransmitter Release or Uptake
1.8K
Certain drugs can affect how neurotransmitters called catecholamines, are released or taken back up in the adrenergic neuron. They can have different effects on the body's sympathetic transmission. Reserpine, a natural compound found in the Rauwolfia shrub, blocks a transporter called vesicular monoamine transporter (VMAT), which leads to a buildup of catecholamines in the cell and reduces sympathetic transmission. Another drug called guanethidine works in multiple ways, including blocking...
1.8K
Drugs Affecting Neurotransmitter Synthesis
2.5K
Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase,...
2.5K


