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莪术酮通过抑制氧化爆发和炎性细胞因子水平保护大鼠免受胶原诱导的关节炎。

Zerumbone Protects Rats from Collagen-Induced Arthritis by Inhibiting Oxidative Outbursts and Inflammatory Cytokine Levels.

作者信息

Alsaffar Rana M, Ali Aarif, Rashid Shahzada Mudasir, Ahmad Sheikh Bilal, Alkholifi Faisal K, Kawoosa Majid Shafi, Ahmad Sheikh Parvaiz, Rehman Muneeb U

机构信息

Department of Pharmacology & Toxicology, College of Pharmacy, Prince Sattam Bin Abdulaziz University, P.O. Box 173, Al-Kharj 11942, Saudi Arabia.

Division of Veterinary Biochemistry, Faculty of Veterinary Science and Animal Husbandry, SKUAST-Kashmir, Shuhama, Alusteng, Srinagar, Jammu and Kashmir 190006, India.

出版信息

ACS Omega. 2023 Jan 10;8(3):2982-2991. doi: 10.1021/acsomega.2c05749. eCollection 2023 Jan 24.

Abstract

Rheumatoid arthritis (RA) is an immunocompromised disorder characterized by a marked increase in the synthesis of inflammatory molecules that stimulates the destruction of bones and cartilage. The conventional treatment modalities for RA are associated with adverse side effects and lack sensitivity, suggesting an immediate demand for alternate beneficial therapeutic remedies. The current study sought to understand more about zerumbone's anti-inflammatory properties in diagnosing collagen-induced arthritis (CIA) in experimental animals. The current study observed that zerumbone reduced clinical severity in CIA-induced animals compared to healthy animals. Zerumbone administration significantly decreased ( < 0.001) the concentration of SOD, CAT, GR, and GSH in treatment groups. Zerumbone administration drove down significantly ( < 0.001) the concentration of inflammatory cytokine molecules. Zerumbone was effective in bringing significant changes in levels of MPO, NO, LDH, MMP-8, and ELA. The therapeutic potential of zerumbone was found to be associated with reduced joint destruction and restored normal histology in the cartilage and tissue. Adsorption, distribution, metabolism, excretion, and toxicity studies were used to determine the druglike properties of zerumbone. ProTox-II studies revealed that zerumbone did not possess toxic properties like hepatotoxicity, immunotoxicity, carcinogenicity, mutagenicity, and cytotoxicity. Therefore, the present study evaluated the therapeutic properties of zerumbone in CIA animal models.

摘要

类风湿性关节炎(RA)是一种免疫功能受损的疾病,其特征是炎症分子合成显著增加,刺激骨骼和软骨的破坏。RA的传统治疗方式伴有不良副作用且缺乏敏感性,这表明迫切需要其他有益的治疗方法。当前研究旨在更深入了解莪术酮在实验动物胶原诱导性关节炎(CIA)诊断中的抗炎特性。当前研究观察到,与健康动物相比,莪术酮降低了CIA诱导动物的临床严重程度。在治疗组中,莪术酮给药显著降低(<0.001)了超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽还原酶(GR)和谷胱甘肽(GSH)的浓度。莪术酮给药显著降低(<0.001)了炎性细胞因子分子的浓度。莪术酮有效地使髓过氧化物酶(MPO)、一氧化氮(NO)、乳酸脱氢酶(LDH)、基质金属蛋白酶-8(MMP-8)和弹性蛋白酶(ELA)水平发生显著变化。发现莪术酮的治疗潜力与减少关节破坏以及恢复软骨和组织的正常组织学有关。采用吸附、分布、代谢、排泄和毒性研究来确定莪术酮的类药物性质。ProTox-II研究表明,莪术酮不具有肝毒性、免疫毒性、致癌性、致突变性和细胞毒性等毒性特性。因此,本研究评估了莪术酮在CIA动物模型中的治疗特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0db4/9878628/bb1d6e6b4fb5/ao2c05749_0002.jpg

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