摘要
慢性疼痛是一种多方面复杂的疾病,可分为躯体性疼痛、内脏性疼痛和神经性疼痛。虽然阿片类药物和非甾体类抗炎药物会引起镇痛并起作用。在治疗慢性疼痛时,其效用受到副作用、滥用潜力和对其止痛作用的耐受性的影响。所以,寻找替代的止痛药其疗效好,副作用小,是一种很有前途的食欲系统。食欲素-A和-B仅在下丘脑外侧区表达,与I有关。喂养、睡眠/觉醒周期、心血管功能、激素分泌、癫痫发作和疼痛调节。摘要食欲素肽及其受体被认为是一种新的发展前景。SiC药物。在实验研究中,食欲肽诱导的镇痛效果与吗啡相当。此外,有证据表明,食欲素受体1和2参与了对两者的反应。压力刺激和疼痛。因此,直接和间接激活食欲能系统是一种新的治疗方法来控制疼痛。本文将回顾最近和重要的研究成果。描述食欲素在疼痛调节中的作用。
关键词: 神经肽,食欲素,次生质,疼痛,食欲素受体,神经病理性疼痛。
Current Medicinal Chemistry
Title:The Orexinergic (Hypocretin) System and Nociception: An Update to Supraspinal Mechanisms
Volume: 25 Issue: 32
关键词: 神经肽,食欲素,次生质,疼痛,食欲素受体,神经病理性疼痛。
摘要: Chronic pain is a multifaceted and complex condition that is divided into somatic, visceral, and neuropathic pain. Although opioids and nonsteroidal anti-inflammatory drugs cause analgesia and are effective in the treatment of chronic pain, their utility is hampered by side effects, abuse potential, and development of tolerance to their pain-relieving effects. So, finding alternative analgesics with good efficacy and low side effects is of great interest and the orexinergic system is a potential candidate. Orexin-A and -B are exclusively expressed in the lateral hypothalamus and are involved in the feeding, sleep/wake cycle, cardiovascular function, hormone secretion, seizure, and pain modulation. Orexin peptides and their receptors have been proposed as opportunities for developing analgesic drugs. In experimental studies, orexin peptides induce analgesia that is comparable to morphine. Furthermore, there is evidence that orexin receptors 1 and 2 participate in responsiveness to both stressful stimuli and pain. Thus, direct and indirect activation of the orexinergic system is a new therapeutic approach to pain control. This article will review the most recent and important studies describing the role of orexins in pain modulation.
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Cite this article as:
The Orexinergic (Hypocretin) System and Nociception: An Update to Supraspinal Mechanisms, Current Medicinal Chemistry 2018; 25 (32) . https://dx.doi.org/10.2174/0929867324666170529072554
DOI https://dx.doi.org/10.2174/0929867324666170529072554 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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