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Opioid Analgesics: Synthetic and Semisynthetic Opioids01:15

Opioid Analgesics: Synthetic and Semisynthetic Opioids

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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...
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Opioid Receptors: Overview01:22

Opioid Receptors: Overview

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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,...
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Opioid Analgesics: Morphine and Other Natural Cogeners01:20

Opioid Analgesics: Morphine and Other Natural Cogeners

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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...
1.0K
Drugs Affecting GI Tract Motility: Opioids as Antidiarrheal Agents01:17

Drugs Affecting GI Tract Motility: Opioids as Antidiarrheal Agents

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Diarrhea, a condition marked by frequent loose or watery bowel movements, can be triggered by multiple factors such as viral or bacterial infections, food intolerances, anxiety, medications, and digestive disorders. Symptoms may include abdominal pain, bloating, nausea, and cramping. Severe or prolonged diarrhea can lead to complications like electrolyte imbalances, malnutrition, and dehydration if left untreated.
Opioids, widely used antidiarrheal agents, mitigate diarrhea by slowing down...
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Epigenetic Regulation01:46

Epigenetic Regulation

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Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
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GTPases and their Regulation02:14

GTPases and their Regulation

9.9K
Guanine nucleotide-binding proteins (G-proteins), also known as GTPases, are a superfamily of proteins that regulate many cellular processes, such as cell signaling, vesicular transport, and the regulation of cell shape and motility. Mutation or dysfunction of these proteins can lead to disease. There are around 40,000 known G-proteins that can broadly be classified into two groups ‒  small G-proteins consisting of a single domain and large multi-domain G-proteins.
Large G-proteins,...
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Updated: Feb 7, 2026

Comprehensive Profiling of Dopamine Regulation in Substantia Nigra and Ventral Tegmental Area
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Comprehensive Profiling of Dopamine Regulation in Substantia Nigra and Ventral Tegmental Area

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腹部状周神经网络调节阿片类药物复发

Margareth Nogueira, Giuseppe Giannotti, Carley N Miller

    bioRxiv : the preprint server for biology
    |February 6, 2026
    PubMed
    概括
    此摘要是机器生成的。

    腹部皮 (VP) 中的周围神经网络 (PNN) 驱动阿片类药物寻找. 准VPPNN可能为阿片类药物使用障碍和复发提供新的治疗方法.

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    科学领域:

    • 神经科学是一个神经科学.
    • 分子生物学分子生物学
    • 成研究 研究成研究

    背景情况:

    • 阿片类药物使用障碍是全球重要的健康问题.
    • 腹腔 (VP) 神经活动影响阿片类药物奖励和复发.
    • 在VP中的帕尔瓦胺 (PV) 神经元与药物复发有关.
    • 围神经网络 (PNN) 围绕着PV神经元,调节它们的活性和可塑性.

    研究的目的:

    • 为了研究PNN在VP帕瓦蛋白 (PV) 神经元中的作用.
    • 为了确定VP中的PNN是否因阿片类药物暴露而改变.
    • 检查PNN对阿片类药物寻求行为和复发的影响.

    主要方法:

    • 雄性和雌性小鼠的海洛因自我管理.
    • 在VP中评估PNN密度.
    • 使用冠状腺酶ABC的PNN酶降解.
    • VP PV神经元的电生理记录.
    • 对VP PV神经元活动的化学基因操纵.
    • 测量Fos表达作为神经元活动的标志物.

    主要成果:

    • 自用海洛因增加了VP中的PNN密度.
    • 氏丁酶ABC治疗可以防止诱导寻找海洛因的诱因.
    • VP PNN 枯竭减少了 VP PV 神经元的刺激性,并增强了抑制性输入.
    • 在复发期间,PNN耗尽减少了VP PV神经元中的Fos表达.
    • 对VP PV神经元的化学遗传激活挽救了PNN枯竭的抑制作用.

    结论:

    • VP PV神经元及其相关PNN对寻找阿片类药物至关重要.
    • PNN调节VP PV神经元的神经生理学.
    • 准VPPNN代表了阿片类药物使用障碍的潜在治疗策略.
    • 在神经可塑性中PNN的作用表明了成治疗的治疗潜力.