探索拉法辛对慢性疼痛的影响:情绪变化和疼痛调节网络
Yaseen Awad-Igbaria1, Saher Abu-Ata1, Yara Nakhleh-Francis2
1Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel; Research Institute of Galilee Medical Center, Nahariya, Israel.
Neuropharmacology
|November 20, 2023
概括
诱发性 (PV) 涉及到大脑基因表达的情绪和疼痛中心的变化. 文拉法辛治疗通过调节这些神经炎症和神经可塑性通路来减少部疼痛和焦虑.
科学领域:
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
- 遗传学 是一个遗传学.
背景情况:
- 诱发性 (PV) 是一种复杂的疼痛状况,病因不明.
- 拉法辛等氨酸-上腺素再吸收抑制剂 (SNRIs) 显示出在管理部疼痛方面的潜力,这表明中枢神经系统的参与.
研究的目的:
- 在PV的动物模型中研究调节情绪,压力和疼痛的大脑区域的基因表达改变.
- 在这个模型中评估venlafaxine的止痛和抗焦虑作用.
主要方法:
- 在桃体 (Amg),中间前额叶皮质 (mPFC) 和带水管周灰质 (PAG) 中进行基因表达分析,这些基因表达分析来自诱导性疼痛的老鼠.
- 行为测试来评估类似焦虑的行为和部过敏.
- 用文拉法辛 (37.5 mg/kg) 治疗一个月.
主要成果:
- 慢性部疼痛与AMG,mPFC和PAG中与神经元活动和神经炎症相关的基因表达增加有关.
- 在Amg和mPFC中观察到GABA和血清素合成/再吸收基因的变化.
- 文拉法辛治疗显著降低了阴道过敏和焦虑,并调节了脑部关键区域的基因表达.
结论:
- Vulvar过敏可能与调节情绪,压力和疼痛的大脑区域的基因表达变化有关,有助于中心敏感和焦虑.
- 文拉法辛在动物PV模型中显示出显著的止痛和抗焦虑作用,可能是通过增强血清激素和上腺素的活性.
更多相关视频
相关概念视频
Antidepressant Drugs: Tricyclics, SSRIs, and SNRIs
403
Tricyclic Antidepressants (TCAs), including Desipramine (Norpramin), Imipramine (Tofranil), Clomipramine (Anafranil), and Amitriptyline (Elavil), inhibit serotonin and norepinephrine reuptake and also block other receptors. They are used for depression, pain conditions, and insomnia. Common adverse effects include anticholinergic effects, sedation, orthostatic hypotension, and weight gain. They have a narrow therapeutic window and so require plasma-level monitoring. Abrupt discontinuation can...
403
Antidepressant Drugs: MAOIs and Other Agents
248
Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
248
Analgesia and Pain Management
632
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...
632
Drugs for Treatment of Diarrhea-Predominant IBS
183
Diarrhea-predominant irritable bowel syndrome (IBS-D) is a subtype of IBS characterized primarily by frequent, loose, or watery stools, abdominal pain, and abdominal discomfort. Therapeutic approaches to managing IBS-D include dietary changes, stress management techniques, and pharmaceutical interventions.
Two specific drugs used in the treatment are alosetron (Lotronex) and eluxadoline (Viberzi). Alosetron, a 5-HT3 antagonist, works by slowing the movement of stools in the gut, reducing bowel...
Two specific drugs used in the treatment are alosetron (Lotronex) and eluxadoline (Viberzi). Alosetron, a 5-HT3 antagonist, works by slowing the movement of stools in the gut, reducing bowel...
183
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists
269
Serotonin, a crucial neurotransmitter synthesized by enterochromaffin cells, plays a cardinal role in regulating gastrointestinal (GI) motility. With over 90% of the body's total serotonin in the GI tract, its influence on digestive processes is profound. Serotonin is swiftly released upon various stimuli, such as food boluses or certain drugs, triggering intrinsic sensory neurons in the myenteric plexus and extrinsic vagal and spinal sensory neurons. This leads to the activation of the...
269
Drugs Affecting Neurotransmitter Release or Uptake
1.1K
Certain drugs can affect how neurotransmitters called catecholamines, are released or taken back up in the adrenergic neuron. They can have different effects on the body's sympathetic transmission. Reserpine, a natural compound found in the Rauwolfia shrub, blocks a transporter called vesicular monoamine transporter (VMAT), which leads to a buildup of catecholamines in the cell and reduces sympathetic transmission. Another drug called guanethidine works in multiple ways, including blocking...
1.1K


