Foudah Ahmed I, Alqarni Mohammed H, Devi Sushma, Singh Akanksha, Alam Aftab, Alam Pravej, Singh Sima
College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia.
Guru Nanak Institute, Hema Majra Road, Mullana, Ambala, India.
Front Pharmacol. 2022 Aug 11;13:895079. doi: 10.3389/fphar.2022.895079. eCollection 2022.
Chronic neuropathy is a common and debilitating problem that poses a significant challenge to health care worldwide. Natural compounds have received considerable attention as potential sources of new drugs for the treatment of neuropsychiatric pain. Catechin is a well-known novel flavonoid with several therapeutic properties, notably in neurodegenerative diseases. The current study is designed to investigate the role of catechin in neuroprotective activity in the chronic constriction injury (CCI) model. Apparently, healthy adult male Sprague-Dawley rats weighing 160-190 g (8 weeks old) were selected and grouped into the following: sham (distilled water), CCI group (CCI), standard [CCI + pregabalin (10 mg/kg, p.o.)], and test catechin [CCI + catechin (50 and 100 μg/kg p.o.)] for 28 days. Behavioral, thermal, and mechanical changes were evaluated. The results showed that mechanical allodynia and thermal hyperalgesia were reduced in the catechin-treated group when compared with the CCI group. In addition, the relationship between the analgesic effect of catechin and the expressions of TNF-α, IL-6, and IL-β was established. The results showed that catechin reversed the signs of neuropathic pain. It also decreased the levels of TNF-α, IL-6, and IL-β in the rat brain. Therefore, the results suggested that catechin has promising potential in the treatment and management of neuropathic pain by decreasing the levels of NF-κβ-regulated inflammatory cytokines in the chronic constriction injury model.
慢性神经病变是一个常见且使人衰弱的问题,给全球医疗保健带来了重大挑战。天然化合物作为治疗神经精神性疼痛的新药潜在来源受到了广泛关注。儿茶素是一种著名的新型黄酮类化合物,具有多种治疗特性,尤其是在神经退行性疾病方面。本研究旨在探讨儿茶素在慢性压迫损伤(CCI)模型中的神经保护活性作用。显然,选择体重160 - 190克(8周龄)的健康成年雄性Sprague-Dawley大鼠,并将其分为以下几组:假手术组(蒸馏水)、CCI组(CCI)、标准组[CCI + 普瑞巴林(10毫克/千克,口服)]和儿茶素测试组[CCI + 儿茶素(50和100微克/千克,口服)],持续28天。评估行为、热和机械变化。结果表明,与CCI组相比,儿茶素治疗组的机械性异常性疼痛和热痛觉过敏有所减轻。此外,还建立了儿茶素镇痛作用与TNF-α、IL-6和IL-β表达之间的关系。结果表明,儿茶素逆转了神经性疼痛的体征。它还降低了大鼠脑中TNF-α、IL-6和IL-β的水平。因此,结果表明儿茶素通过降低慢性压迫损伤模型中NF-κβ调节的炎性细胞因子水平,在神经性疼痛的治疗和管理方面具有广阔的潜力。