Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Neuroscience, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Metab Brain Dis. 2023 Apr;38(4):1421-1432. doi: 10.1007/s11011-023-01190-x. Epub 2023 Feb 22.
Neuropathic pain is a subtype of chronic pain characterized by a primary lesion or dysfunction of the peripheral or central nervous system. The current pain management of neuropathic pain is inadequate and needs new medications.
We studied the effects of 14 days of intraperitoneal ellagic acid (EA) and gabapentin administration in a rat model of neuropathic pain induced by chronic constriction injury (CCI) of the right sciatic nerve.
Rats were divided into six groups: (1) control, (2) CCI, (3) CCI + EA (50 mg/kg), 4) CCI + EA (100 mg/kg), 5) CCI + gabapentin (100 mg/kg), and 6) CCI + EA (100 mg/kg) + gabapentin (100 mg/kg). Behavioral tests, including mechanical allodynia, cold allodynia, and thermal hyperalgesia, were conducted on days - 1(pre-operation), 7, and 14 post-CCI. In addition, at day 14 post-CCI, spinal cord segments were collected to measure the expression of inflammatory markers, including tumor necrosis factor-alpha (TNF-α), nitric oxide (NO), and oxidative stress markers, including malondialdehyde (MDA) and thiol.
CCI increased mechanical allodynia, cold allodynia, and thermal hyperalgesia in rats which were reduced by treatment with EA (50 or 100 mg/kg), gabapentin, or their combination. CCI increased TNF-α, NO, and MDA levels and decreased thiol content in the spinal cord, which all were reverted by administration of EA (50 or 100 mg/kg), gabapentin, or their combination.
This is the first report on ellagic acid's ameliorative effect in rats' CCI-induced neuropathic pain. This effect can be attributed to its anti-oxidative and anti-inflammatory, thus making it potentially useful as an adjuvant to conventional treatment.
神经病理性疼痛是一种慢性疼痛,其特征为外周或中枢神经系统的原发性损伤或功能障碍。目前神经病理性疼痛的治疗效果并不理想,需要新的药物。
我们研究了腹腔内鞣花酸(EA)和加巴喷丁给药 14 天对慢性缩窄性坐骨神经损伤(CCI)诱导的神经病理性疼痛大鼠模型的影响。
将大鼠分为六组:(1)对照组,(2)CCI 组,(3)CCI+EA(50mg/kg)组,(4)CCI+EA(100mg/kg)组,(5)CCI+加巴喷丁(100mg/kg)组,和(6)CCI+EA(100mg/kg)+加巴喷丁(100mg/kg)组。在 CCI 后第-1 天(术前)、第 7 天和第 14 天进行行为学测试,包括机械性痛觉过敏、冷感觉过敏和热痛觉过敏。此外,在 CCI 后第 14 天,收集脊髓节段以测量炎症标志物的表达,包括肿瘤坏死因子-α(TNF-α)、一氧化氮(NO)和氧化应激标志物,包括丙二醛(MDA)和巯基。
CCI 增加了大鼠的机械性痛觉过敏、冷感觉过敏和热痛觉过敏,而 EA(50 或 100mg/kg)、加巴喷丁或两者联合治疗可减轻这些症状。CCI 增加了脊髓中 TNF-α、NO 和 MDA 水平,并降低了巯基含量,而 EA(50 或 100mg/kg)、加巴喷丁或两者联合治疗可逆转这些变化。
这是鞣花酸对大鼠 CCI 诱导的神经病理性疼痛的改善作用的首次报道。这种作用可能归因于其抗氧化和抗炎作用,因此它可能对常规治疗有辅助作用。