Gammoh Omar Salem, Qnais Esam, Bseiso Yousra, Alrosan Khaled, Alqudah Abdelrahim
Clinical Pharmacy and Pharmacy Practice, Yarmouk University, Irbid, Jordan.
Department of Biology and Biotechnology, Faculty of Science, The Hashemite University, Zarqa, Jordan.
Heliyon. 2023 Mar 1;9(3):e14185. doi: 10.1016/j.heliyon.2023.e14185. eCollection 2023 Mar.
Pain is a common undertreated worldwide complaint. The need to explore the antinociceptive potential of alternative herbal products is essential. Although used as a mild sedative, limited evidence focused on the potential antinociceptive effect of valerian and hops combination. The present study was carried out to evaluate the in vivo anti-nociceptive effect of the valerian-hops combination to justify its use as an effective and safe analgesic agent. Anti-nociceptive effects of valerian-hops combination (50, 100, and 200 mg/kg) were assessed in swiss albino mice for performing the acetic acid-induced writhing test, the paw licking test using formalin, the paw licking test using glutamate, and the tail immersion test. The effects were compared to those of diclofenac or morphine in the presence or absence of the opioid receptor antagonist naloxone. Valerian-hops" extract of 100 and 200 mg/kg demonstrated a significant reduction in the number of writhing episodes induced by acetic acid compared to the control (p < 0.05), a significant reduction in the licking number at doses of 100 and 200 mg/kg in the late phase formalin-induced paw licking, significantly reduced the number of lickings after glutamate injection compared to control (p < 0.05). And significantly increased pain reaction after 60 and 90 min of tail immersion test, this effect was opposed by naloxone treatment. The valerian-hops combination produced a significant antinociceptive effect that involved the opioid system. Further studies are required to fully uncover the underlying active constituents and their mechanisms.
疼痛是一种在全球范围内普遍未得到充分治疗的病症。探索替代草药产品的抗伤害感受潜力至关重要。尽管缬草和啤酒花组合被用作轻度镇静剂,但针对其潜在抗伤害感受作用的证据有限。本研究旨在评估缬草 - 啤酒花组合的体内抗伤害感受作用,以证明其作为一种有效且安全的镇痛剂的用途。在瑞士白化小鼠中评估了缬草 - 啤酒花组合(50、100和200毫克/千克)的抗伤害感受作用,以进行醋酸诱导的扭体试验、福尔马林致痛舔足试验、谷氨酸致痛舔足试验以及热板试验。在存在或不存在阿片受体拮抗剂纳洛酮的情况下,将这些作用与双氯芬酸或吗啡的作用进行了比较。与对照组相比,100和200毫克/千克的缬草 - 啤酒花提取物在醋酸诱导的扭体发作次数上有显著减少(p < 0.05),在福尔马林诱导的舔足试验后期,100和200毫克/千克剂量下的舔足次数显著减少,与对照组相比,谷氨酸注射后的舔足次数显著减少(p < 0.05)。在热板试验60和90分钟后,疼痛反应显著增加,纳洛酮处理可对抗这种作用。缬草 - 啤酒花组合产生了显著的抗伤害感受作用,涉及阿片系统。需要进一步研究以充分揭示其潜在的活性成分及其作用机制。