整个本体发生过程中阿片类受体信号传递:塑造神经和行为轨迹
Mary B Spodnick1, Shannon C McElderry1, Marvin R Diaz1
1Binghamton University, 4400 Vestal Parkway East, Binghamton, NY, USA.
Neuroscience and biobehavioral reviews
|February 2, 2025
概括
怀孕期间的阿片类药物暴露会通过改变关键的大脑信号通路,影响胎儿发育. 本综述研究了阿片类受体系统及其在神经发育中的作用,从受孕开始.
科学领域:
- 神经科学是一个神经科学.
- 发展生物学 发展生物学
- 药理学 药理学是指药理学的学科.
背景情况:
- 持续的阿片类药物危机增加了产前阿片类药物暴露.
- 对阿片类药物使用障碍的药物辅助治疗可能涉及产前暴露.
- 了解阿片类药物对胎儿发育的影响至关重要.
研究的目的:
- 审查Mu,Kappa和Delta阿片类受体系统的发展和功能.
- 突出这些系统在神经行为发展中的作用.
- 提出一种新的理解阿片类药物在发展中的监管功能.
主要方法:
- 关于阿片类药物信号的文献综述.
- 对阿片类受体本体发生和功能的分析.
- 检查受阿片类药物影响的神经发育过程.
主要成果:
- 阿片类受体系统是神经发育的组成部分.
- 外源性阿片类药物显著改变发育信号.
- 这些受体调节许多下游神经发育过程.
结论:
- 片受体系统是整个生命中神经发育的重要调节者.
- 需要一个范式的转变来认识到阿片类药物的广泛的监管作用.
- 对产前阿片类药物暴露影响的进一步研究是有必要的.
相关概念视频
Opioid Receptors: Overview
443
Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2,...
443
Analgesia and Pain Management
443
Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
443
Opioid Analgesics: Morphine and Other Natural Cogeners
168
Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
168
Drug Abuse and Addiction: Pharmacological Phenomena
432
Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not...
432
Opioid Analgesics: Synthetic and Semisynthetic Opioids
211
Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
211
Neurotransmitters
780
Neurotransmitters are essential chemical messengers within the nervous system, facilitating the communication between neurons. These chemical messengers, varying in function and effect, are critical for sustaining various aspects of neurological health and emotional well-being.
780


