Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad 45000, Pakistan.
Rural Health Centre, Head RajkanYazman, Bahawalpur 63236, Pakistan.
Molecules. 2022 Aug 2;27(15):4926. doi: 10.3390/molecules27154926.
The current study explored the effects of natural compounds, berbamine, bergapten, and carveol on paclitaxel-associated neuroinflammatory pain. Berbamine, an alkaloid obtained from been previously researched for anticancer and anti-inflammatory potential. Bergapten is 5-methoxsalenpsoralen previously investigated in cancer, vitiligo, and psoriasis. Carveol obtained from caraway is a component of essential oil. The neuropathic pain model was induced by administering 2 mg/kg of paclitaxel (PTX) every other day for a week. After the final PTX injection, a behavioral analysis was conducted, and subsequently, tissue was collected for molecular analysis. Berbamine, bergapten, and carveol treatment attenuated thermal hypersensitivity, improved latency of falling, normalized the changes in body weight, and increased the threshold for pain sensation. The drugs increased the protective glutathione (GSH) and glutathione S-transferase (GST) levels in the sciatic nerve and spinal cord while lowering inducible nitric oxide synthase (iNOS) and lipid peroxidase (LPO). Hematoxylin and eosin (H and E) and immunohistochemistry (IHC) examinations confirmed that the medication reversed the abnormal alterations. The aforementioned natural substances inhibited cyclooxygenase-2 (COX-2), tumor necrosis factor-alpha (TNF-α), and nuclear factor kappa B (NF-κb) overexpression, as evidenced by enzyme-linked immunosorbant assay (ELISA) and Western blot and hence provide neuroprotection in chronic constriction damage.
本研究探讨了天然化合物小檗胺、佛手柑内酯和香芹酚对紫杉醇相关神经炎性疼痛的影响。小檗胺是一种从黄连中提取的生物碱,先前研究表明其具有抗癌和抗炎潜力。佛手柑内酯是 5-甲氧基补骨脂素,先前研究用于癌症、白癜风和银屑病。香芹酚是从葛缕子中提取的,是精油的成分。神经病理性疼痛模型通过每隔一天给予 2 毫克/千克紫杉醇(PTX)诱导,持续一周。最后一次 PTX 注射后,进行行为分析,随后收集组织进行分子分析。小檗胺、佛手柑内酯和香芹酚治疗减轻了热敏感性,提高了跌倒潜伏期,使体重变化正常化,并增加了疼痛感觉的阈值。这些药物增加了坐骨神经和脊髓中保护性谷胱甘肽(GSH)和谷胱甘肽 S-转移酶(GST)的水平,同时降低了诱导型一氧化氮合酶(iNOS)和脂质过氧化物(LPO)的水平。苏木精和伊红(H&E)和免疫组织化学(IHC)检查证实,药物逆转了异常改变。上述天然物质抑制环氧化酶-2(COX-2)、肿瘤坏死因子-α(TNF-α)和核因子 kappa B(NF-κb)的过度表达,这一点通过酶联免疫吸附测定(ELISA)和 Western blot 得到证实,从而在慢性缩窄性损伤中提供神经保护。