载薯蓣皂苷纳米颗粒对Wistar大鼠Freund佐剂性多关节炎的改善作用机械的研究。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Hamna Mehmood, Ammara Saleem, Muhammad Furqan Akhtar, Aisha Mobashar
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引用次数: 0

摘要

目前的研究旨在合成负载薯蓣皂苷纳米颗粒(DNPs),为佐剂诱导的多发性关节炎提供一种替代的安全治疗方法。采用壳聚糖生物聚合物制备了DNPs,并对其进行了表征。还进行了急性毒性研究,并利用生物制剂获得了急性抗炎潜力。除正常对照组外,其余各组左后爪均于第1天注射弗氏佐剂0.15 ml进行免疫接种,观察其抗关节炎作用。从第8-28天开始口服DNPs 5- 20mg /kg和地奥明20mg /kg和甲氨蝶呤。x射线衍射结果表明,纳米颗粒粒径为223 nm,电势2.9 Mv,多视差指数> 0.7,扫描电镜显示为球形,x射线衍射显示为非晶态。与疾病对照相反,DNPs剂量依赖性地改善了关节炎评分、疼痛、足跖肿胀和体重。DNPs和游离药物显著恢复了治疗动物的血液参数、氧化状态和神经递质水平,这是组织组织学检查所证明的。DNPs和游离药物治疗可显著下调关节炎动物环氧合酶-2、白细胞介素(IL)-6、TNF-α、NF-κβ的表达,升高IL-4、IL-10的表达。DNP 20 mg/kg对地臭米和甲氨蝶呤处理的动物显示出显著的抗关节炎、抗炎和抗伤害作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amelioration of Freund's adjuvant-induced polyarthritis by Diosmin-loaded nanoparticles in Wistar rats; a mechanistic study.

The current study aims to synthesize diosmin-loaded nanoparticles (DNPs) to make available an alternative safe treatment for adjuvant-induced polyarthritis. DNPs were formulated using chitosan biopolymer and characterized. Acute toxicity study was also performed and acute anti-inflammatory potential was accessed using phologistic agents. For anti-arthritic potential, disease was inoculated by injecting 0.15-ml Freund's adjuvant at day 1 to all groups except normal control in left hind paw. Therapy using DNPs at 5-20 mg/kg and diosmin 20 mg/kg and methotrexate was started from day 8-28 orally. The DNPs of size 223 nm, potential 2.9 Mv, polydisparity index > 0.7 and spherical shape particles as revealed by scanning electron microscopy and amorphous nature were revealed by X-ray diffraction. DNPs dose dependently ameliorated arthritic scoring, pain, paw swelling and body weight in contrary to disease control. DNPs and free drug restored significantly altered blood parameters, oxidation status and neurotransmitters level in treated animals as evident by histologic examination of tissues. Treatment with DNPs and free drug profoundly downregulated the expression of cyclooxygenase-2, interleukin (IL)-6, TNF-α, NF-κβ and increased IL-4 and IL-10 in arthritic animals. DNP 20 mg/kg revealed noteworthy anti-arthritic, anti-inflammatory and anti-nociceptive potential in counter to diosmin and methotrexate treated animals.

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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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