Razi Drug Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Pharmacology and Toxicology, School of Pharmacy, Iran University of Medical Sciences, Tehran, Iran.
Inflammopharmacology. 2024 Dec;32(6):3809-3824. doi: 10.1007/s10787-024-01574-0. Epub 2024 Sep 23.
Zhumeria majdae, a unique native plant of southern Iran, has been traditionally used to treat various health issues. Preclinical studies suggest its therapeutic potential for immunological and inflammatory disorders. This study investigates the effect of Z. majdae essential oil (ZMEO) on TNBS-induced colitis in rats, focusing on the NF-κB/p38 MAPK/Nrf-2 pathway.
Forty-eight male Wistar rats were used, with all groups except the sham group receiving a single intra-rectal dose of TNBS. Three different doses of ZMEO and also 1 mg/kg dexamethasone were administered orally for 2 weeks. Colon tissue was analyzed for ulcer index, histological changes, inflammatory cytokines, apoptotic factors, and levels of NF-κB, p38 MAPK, and Nrf-2.
GC-mass analysis identified 25 compounds with linalool (52.01%) and camphor (31.01%) as the major compounds in ZMEO. ZMEO ameliorated colon injuries, reduced ulcer index, and prevented the elevation of pro-inflammatory cytokines and pro-apoptotic proteins. It also increased the levels of IL-10 and Bcl-2 proteins. Furthermore, ZMEO decreased the expression of p-NF-κB and p38 MAPK while increasing the expression of pNrf-2.
ZMEO mitigates colon damage associated with IBD by suppressing inflammatory cytokines and pro-apoptotic proteins possibly through modulating the NF-κB/p38 MAPK/Nrf-2 signaling pathway.
朱美里亚·马贾代是伊朗南部特有的一种植物,传统上被用于治疗各种健康问题。临床前研究表明,其具有治疗免疫和炎症性疾病的潜力。本研究旨在探讨朱美里亚·马贾代精油(ZMEO)对大鼠三硝基苯磺酸(TNBS)诱导结肠炎的影响,重点关注 NF-κB/p38MAPK/Nrf-2 通路。
使用 48 只雄性 Wistar 大鼠,除假手术组外,所有组大鼠均接受单次直肠内 TNBS 给药。ZMEO 以三个不同剂量和 1mg/kg 地塞米松进行口服给药,持续 2 周。对结肠组织进行溃疡指数、组织学变化、炎症细胞因子、凋亡因子以及 NF-κB、p38MAPK 和 Nrf-2 水平的分析。
GC-质量分析鉴定出 ZMEO 中的 25 种化合物,其中芳樟醇(52.01%)和樟脑(31.01%)为主要成分。ZMEO 改善了结肠损伤,降低了溃疡指数,防止了促炎细胞因子和促凋亡蛋白的升高。它还增加了 IL-10 和 Bcl-2 蛋白的水平。此外,ZMEO 降低了 p-NF-κB 和 p38MAPK 的表达,同时增加了 pNrf-2 的表达。
ZMEO 通过抑制炎症细胞因子和促凋亡蛋白减轻与 IBD 相关的结肠损伤,其机制可能是通过调节 NF-κB/p38MAPK/Nrf-2 信号通路。