皮兰
四氢吡喃
甲醇
止痛药
衍生工具(金融)
化学
药理学
有机化学
医学
戒指(化学)
金融经济学
经济
作者
Gustavo Nunes de Santana Castro,Raquel do Nascimento de Souza,Alba Cenélia Matos da Silva,Roberto Laureano‐Melo,Wellington da Silva Côrtes,Saulo Luís Capim,Mário Luiz Araújo de Almeida Vasconcellos,Bruno Guimarães Marinho
出处
期刊:Anti-inflammatory & anti-allergy agents in medicinal chemistry
[Bentham Science Publishers]
日期:2024-02-27
卷期号:23 (2): 105-117
标识
DOI:10.2174/0118715230282982240202052127
摘要
Background: The development of analgesic and anti-inflammatory drugs plays a crucial role in modern medicine, aiming to alleviate pain and reduce inflammation in patients. Opioids and nonsteroidal anti-inflammatory drugs are groups of drugs conventionally used to treat pain and in-flammation, but a wide range of adverse effects and ineffectiveness in some pathological conditions leads us to search for new drugs with analgesic and anti-inflammatory properties. Objectives: In this regard, the authors intend to investigate the ((2s,6s)-6-ethyl-tetrahydro-2h-pyran-2-yl) methanol compound (LS20) on pain and acute inflammation. Methods: Male Swiss mice were evaluated using acetic acid-induced abdominal writhing, formalin, and tail-flick as models of nociceptive evaluation and edema paw, air pouch and cell culture as models of inflammatory evaluation besides the rotarod test for assessment of motor impairment. Results: The compound showed an effect on the acetic acid-induced abdominal writhing, formalin and tail-flick tests. Studying the mechanism of action, reversion of the antinociceptive effect of the compound was observed from previous intraperitoneal administration of selective and non-selective opioid antagonists on the tail flick test. In addition, the compound induced an antiedematogenic effect and reduced leukocyte migration and the production of pro-inflammatory cytokines in the air pouch model. LS20 was able to maintain cell viability, in addition to reducing cell production of TNF-α and IL-6. Conclusion: In summary, the LS20 compound presented an antinociceptive effect, demonstrating the participation of the opioid system and an anti-inflammatory effect related to the inhibition of pro-inflammatory cytokine production. The compound also demonstrated safety at the cellular level.
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