Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Opioid Analgesics: Synthetic and Semisynthetic Opioids01:15

Opioid Analgesics: Synthetic and Semisynthetic Opioids

336
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...
336
Opioid Analgesics: Morphine and Other Natural Cogeners01:20

Opioid Analgesics: Morphine and Other Natural Cogeners

293
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...
293
Analgesia and Pain Management01:25

Analgesia and Pain Management

660
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...
660
Opioid Receptors: Overview01:22

Opioid Receptors: Overview

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

Drugs Affecting GI Tract Motility: Opioids as Antidiarrheal Agents

247
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...
247
Pain01:20

Pain

503
Pain serves as a critical warning signal that alerts the body to potential or actual harm. When mechanical pressure on the skin is intense, such as from a sharp pinch, the sensation transitions from touch to pain. Similarly, extreme temperatures, like a hot pot handle, convert the sensation of heat into pain. Pain can also result from overstimulation of other senses, such as blinding light, loud noise, or the intense heat from habañero peppers. This ability to sense pain is essential for...
503

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Reactive arthritis: the convoluted history of Reiter's disease.

Inflammopharmacology·2023
Same author

Salsalate: a pleotropic anti-inflammatory drug in the treatment of diabetes, obesity, and metabolic diseases.

Inflammopharmacology·2023
Same author

John Alexander Mullin (1835-1899): The Canadian Physician who first described Osler's Nodes.

Inflammopharmacology·2023
Same author

Medical aspects of the tour by Martin Martin (c 1660-1719) of the Western and Northern Islands of Scotland, Circa 1695.

Inflammopharmacology·2023
Same author

The illness of William Soutar (1898-1943).

Inflammopharmacology·2023
Same author

Spondyloarthropathies and arthritis post-infection: a historical perspective.

Inflammopharmacology·2023
Same journal

Agomelatine for Sjögren's syndrome: a study on its therapeutic effects and mechanisms.

Inflammopharmacology·2026
Same journal

Neuropathic pain in traumatic brain injury: consequences, mechanisms, and therapeutic avenues.

Inflammopharmacology·2026
Same journal

REJENERA<sup>©</sup>, a multi-component bioflavonoid-based formula, alleviates osteoarthritis and provides chondroprotection by regulating the NLRP3-TXNIP-iNOS axis and inflammation: a comparative study with olive leaf nutraceuticals and ibuprofen.

Inflammopharmacology·2026
Same journal

Therapeutic evaluation of myricetin in experimental arthritis: modulation of inflammatory signaling and oxidative stress pathways.

Inflammopharmacology·2026
Same journal

Cortistatin as a pleiotropic regulator of neuroimmune and inflammatory pathways in experimental disease: a scoping review of preclinical evidence.

Inflammopharmacology·2026
Same journal

Clemastine ameliorates ulcerative colitis-induced cognitive impairment by restoring PI3K/Akt/GSK-3β signaling and suppressing ferroptosis.

Inflammopharmacology·2026
查看所有相关文章

相关实验视频

Updated: Jul 20, 2025

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
07:23

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities

Published on: July 29, 2014

33.4K

麻醉类止痛药是一种药物.

W Watson Buchanan1, K D Rainsford2, Colin A Kean3

  • 1Department of Medicine, McMaster University, Hamilton, ON, L8P 1H6, Canada.

Inflammopharmacology
|July 29, 2023
PubMed
概括
此摘要是机器生成的。

片是一种片.

关键词:
编码因 (Codeine) 是一种蛋白质.这是海洛因.吗啡是一种吗啡.麻醉药物 麻醉药物 麻醉药物 麻醉药物片是一种片.疼痛 疼痛 疼痛 疼痛

更多相关视频

Intracranial Pharmacotherapy and Pain Assays in Rodents
02:26

Intracranial Pharmacotherapy and Pain Assays in Rodents

Published on: April 9, 2019

5.3K
The Sciatic Nerve Cuffing Model of Neuropathic Pain in Mice
07:09

The Sciatic Nerve Cuffing Model of Neuropathic Pain in Mice

Published on: July 16, 2014

48.3K

相关实验视频

Last Updated: Jul 20, 2025

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
07:23

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities

Published on: July 29, 2014

33.4K
Intracranial Pharmacotherapy and Pain Assays in Rodents
02:26

Intracranial Pharmacotherapy and Pain Assays in Rodents

Published on: April 9, 2019

5.3K
The Sciatic Nerve Cuffing Model of Neuropathic Pain in Mice
07:09

The Sciatic Nerve Cuffing Model of Neuropathic Pain in Mice

Published on: July 16, 2014

48.3K

科学领域:

  • 药理学 药理学是指药理学的学科.
  • 医学史 医学史 医学史

背景情况:

  • 片的历史使用可以追溯到古代文明.
  • 亚述人,埃及人和罗马人已经记录了片衍生产品.

研究的目的:

  • 追踪片衍生物的历史使用和科学隔离.
  • 突出阿片类药物的治疗价值和成潜力.

主要方法:

  • 关于片使用的历史文献综述.
  • 关于与吗啡分离相关的关键科学发现的文件.

主要成果:

  • 片的使用可以追溯到古代历史,像阿维琴纳,帕拉塞尔索斯和莎士比亚这样的人物.
  • 吗啡是在19世纪初由德罗尼和塞尔图尔纳分离出来的.
  • 在1800年代中期,阿片类药物成为一个重要的成问题.

结论:

  • 片衍生物在治疗疼痛方面具有显著的治疗价值.
  • 历史上的使用和科学进步揭示了阿片类药物的双重性质,即它们既是有益的物质,又是成的物质.