Chemical composition and studying the possible neuroprotective effect of iridoids-rich fraction from Pentas lanceolata leaves using rotenone model of Parkinson's disease in mice.

IF 4.6 2区 医学 Q2 IMMUNOLOGY Inflammopharmacology Pub Date : 2024-12-01 Epub Date: 2024-07-04 DOI:10.1007/s10787-024-01509-9
Ahmed H Afifi, Heba-Tollah M Sweelam, Marwa E El-Shamarka, Hisham A Orban, Wessam H Elesawy, Maki Nagata, Kuniyoshi Shimizu, Howaida I Abd-Alla
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Abstract

Parkinsonism is an age-related neurodegenerative illness that affects motor coordination leading to loss of dopaminergic neurons. Many medications are used for the treatment of Parkinson's disease but are only symptomatic and have a limited effect on the progression of this ailment. Therefore, bioactive compounds which derived from plants have been examined for their ability to improve the neuronal damage and cell death happened in parkinsonian patients. In this study the iridoids-rich fraction isolated from Pentas lanceolata (PIRF) leaves was investigated for its phytoconstituents. Seven iridoids (1-7) and one flavonol diglycoside (8) were isolated, and their chemical structures were achieved by 1H and 13C nuclear magnetic resonance and ESI-MS spectral data. Compound 1 (6β,7β-epoxy-8-epi-splendoside) and 5 (gaertneroside) were isolated for the first time from Pentas genus as well as compound 8 (kaempferol-3-O-robinobioside). The current study aims to investigate the possible anti-parkinsonian effect of PIRF using a rotenone model of Parkinsonism in mice. Behavioural tests (wirehanging, stair and wooden-walking tests) were done to examine the motor coordination in mice after treatment. Biochemical and histopathological examinations for brain striatum in different groups were also evaluated. Results revealed that rotenone-treated mice had poor motor functions described by depletion of dopamine and Ach levels, a significant increase in proinflammatory cytokines, IL-1B, TNF-α and Mcp-1 and oxidative biomarkers with subsequent reduction in antioxidant mediators. Disorganization of striatum, degenerated neurocytes, slight vacuolation, shrunken neurons with pyknotic nuclei and apoptotic cells are displayed by histopathological examinations. Treatment with PIRF ameliorates the neurodegeneration-induced by rotenone in the brain of mice. The anti-parkinsonian effect of PIRF could be attributed to their bioactive constituents of iridoids.

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利用小鼠帕金森病的鱼藤酮模型,研究五加科植物叶片中富含虹彩类物质的化学成分及其可能的神经保护作用。
帕金森病是一种与年龄有关的神经退行性疾病,会影响运动协调,导致多巴胺能神经元的丧失。许多药物被用于治疗帕金森病,但这些药物只能对症下药,对该疾病的进展影响有限。因此,人们开始研究从植物中提取的生物活性化合物是否能够改善帕金森病患者神经元损伤和细胞死亡的情况。本研究对从五加科植物(Pentas lanceolata,PIRF)叶片中分离出的富含鸢尾样成分的植物成分进行了研究。通过 1H、13C 核磁共振和 ESI-MS 光谱数据,分离出了七种鸢尾类化合物(1-7)和一种黄酮醇二糖苷(8),并确定了它们的化学结构。化合物 1(6β,7β-环氧-8-epi-splendoside)和化合物 5(gaertneroside)以及化合物 8(山柰酚-3-O-芦宾糖苷)是首次从五角枫属植物中分离出来。目前的研究旨在利用小鼠帕金森病的鱼藤酮模型,研究 PIRF 可能具有的抗帕金森作用。研究人员进行了行为测试(悬挂钢丝、爬楼梯和走木桩测试),以检查治疗后小鼠的运动协调性。此外,还对不同组别的大脑纹状体进行了生化和组织病理学检查。结果显示,鱼藤酮处理的小鼠运动功能较差,表现为多巴胺和 Ach 水平下降,促炎细胞因子、IL-1B、TNF-α 和 Mcp-1 以及氧化生物标志物显著增加,抗氧化介质随之减少。组织病理学检查显示,纹状体紊乱、神经细胞变性、轻微空泡化、神经元萎缩、核分裂和细胞凋亡。使用 PIRF 可改善鱼藤酮诱导的小鼠脑神经变性。PIRF 的抗帕金森效应可归因于其生物活性成分鸢尾酮。
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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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Chemical composition and studying the possible neuroprotective effect of iridoids-rich fraction from Pentas lanceolata leaves using rotenone model of Parkinson's disease in mice. Neuroprotective efficiency of celecoxib vesicular bilosomes for the management of lipopolysaccharide-induced Alzheimer in mice employing 23 full factorial design. Protective effect of freeze-dried extract of Persicaria bistorta Samp. on acetic acid-induced colitis model in rats: Involvement of nitric oxide and opioid system. Combinatorial intervention with dental pulp stem cells and sulfasalazine in a rat model of ulcerative colitis. Genetic proxies for therapy of insulin drug targets and risk of osteoarthritis: a drug-target Mendelian randomization analysis.
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