蒿草和莪术提取物复方制剂对骨关节炎大鼠模型的抗炎活性。

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Sri Ningsih, Kurnia Agustini, Susi Kusumaningrum, Nisrina Firdausi, Agung Eru Wibowo, Julham Efendi, Ngatinem Ngatinem, Agus Himawan Subiantoro, Suparjo Suparjo, Catherine Catherine, Nasal Auni Rabbina, Anton Bahtiar, Rini Damayanti, KyuJong Lee
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引用次数: 0

摘要

本研究旨在评估蒿属植物和莪术(AC)提取物复方制剂在碘乙酸钠(MIA)诱导的骨关节炎(OA)大鼠模型中的抗炎活性。给 OA 大鼠口服 AC(240、480 和 960 毫克/千克体重)三周。对照组和模型组包括分别用双氯芬酸钠和载体治疗的 OA 大鼠。与模型组相比,经 AC 处理的大鼠的水肿体积明显减少(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory activity of the combination Ardisia humilis Vahl. and Curcuma xanthorrhiza Roxb. extract on an osteoarthritis rat model.

This study aimed to evaluate the anti-inflammatory activity of the combination of Ardisia humilis Vahl. and Curcuma xanthorrhiza Roxb. (AC) extract in monosodium iodoacetate (MIA)-induced osteoarthritis (OA) rat model. AC was administered orally to OA rats (240, 480, and 960 mg/kg bw) for three weeks. The control and model groups comprised OA rats treated with diclofenac sodium and carrier, respectively. AC-treated rats exhibited a significant reduction in oedema volume compared to those of the model group (p < 0.05). Notably, AC, at 960 mg/kg bw, significantly decreased inflammatory cytokines TNF-α and IL-1β, along with matrix metalloproteinase-9 (MMP-9) levels compared to those of the model group (p < 0.05). AC's attenuation of OA progression was also observed through haematoxylin and eosin (H&E) and Safranin O-fast green analysis. A phytochemical study showed AC contained phenolic, flavonoid, curcumin, demethoxycurcumin, and bisdemethoxycurcumin compounds. This study concludes that AC alleviated OA progression through anti-inflammatory effects and depressed MMP-9 levels.

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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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