相关实验视频
Updated: Sep 10, 2025

09:36
Murine Orchiectomy and Ovariectomy to Reduce Sex Hormone Production
Published on: November 17, 2023
10.3K
甲在经过切除术的马群中的止痛和胃肠道作用
Natalya Maldonado Moreno1, Júlia Alves Moreira1, Luiza Araujo De Oliveira1
1Department of Clinical and Veterinary Surgery, Veterinary School, Universidade Federal de Minas Gerais, UFMG, Belo Horizonte 31270-901, MG, Brazil.
Animals : an open access journal from MDPI
|August 28, 2025
概括
甲与acepromazine和detomidine (ADM) 结合,在马中提供有效的止痛药,只有轻微的胃肠道效应. 这种治疗疼痛的策略可以改善术后护理,而不会造成显著的低运动.
科学领域:
- 兽医麻醉学
- 马的疼痛治疗方法
背景情况:
- 马的阿片类药物使用受到中枢神经系统的刺激和肠道运动的减少的限制.
- 建议使用多种方法,以对动物进行最佳的术后疼痛控制.
研究的目的:
- 评估甲,阿塞普罗玛和德托米丁 (ADM) 对马的生理变量,肠道运动,胃张张和面部疼痛的影响.
- 评估ADM协议的安全性和有效性,以治疗马的疼痛.
主要方法:
- 19匹健康的马被分为两组:ADM (阿西普罗玛,德托米丁,甲) 和ADS (阿西普罗玛,德托米丁,盐水).
- 在施用前和施用后的多个时间点评估了生理变量,肠移动性,胃膨胀和马脸部疼痛 (EQUUS- FAP).
- 统计分析包括ANOVA,曼-惠特尼和德宾测试.
主要成果:
- 两组患者的肠机动性在服药后1 - 2小时下降,但在6 - 8小时后恢复到基线.
- 在ADM组中,胃膨胀在几个时间点更为明显.
- 在ADM组2,4和6小时后,EQUUS- FAP得分明显较低,这表明有效的止痛作用.
结论:
- 该ADM协议提供化学克制和止痛药在马.
- 这种方案可能是一个可行的选择来治疗马的外科手术疼痛,而不会造成显著的低运动性.
相关概念视频
Opioid Analgesics: Synthetic and Semisynthetic Opioids
421
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...
421
Drugs Affecting GI Tract Motility: Opioids as Antidiarrheal Agents
323
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...
Opioids, widely used antidiarrheal agents, mitigate diarrhea by slowing down...
323
Analgesia and Pain Management
788
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...
788
Opioid Analgesics: Morphine and Other Natural Cogeners
361
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...
361
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents
595
The gastric mucosa produces prostaglandins E2 (PGE2) and prostacyclin (PGI2), crucial in maintaining gastric health. They exert cytoprotective effects, including increasing bicarbonate secretion, releasing protective mucin, reducing gastric acid output, and preventing harmful vasoconstriction. These effects are mediated through various receptors, such as EP1, EP2, EP3, and EP4.
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
595

