Antinociceptive, anti-inflammatory, and antiophidic potential of Punica granatum leaves extract and fraction: an in vitro and in vivo evaluation.

IF 5.3 2区 医学 Q2 IMMUNOLOGY
Janaina Carla Barbosa Machado, Joyce Cristina da Silva, Wêndeo Kennedy Costa, Márcia Vanusa da Silva, Alisson Macário de Oliveria, Alessandra Daniele-Silva, Adriana Marina E Silva Parente, Sarah de Sousa Ferreira, Diana Pontes da Silva, Manoela Torres-Rêgo, Felipe França Cavalcanti, Matheus de Freitas Fernandes-Pedrosa, Magda Rhayanny Assunção Ferreira, Luiz Alberto Lira Soares
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引用次数: 0

Abstract

Punica granatum (Punicaceae) is a shrub with a worldwide distribution that has been used in folk medicine for the treatment of inflammatory disorders. The study investigated the therapeutic potential of spray-dried hydroethanolic extract (SDE) and spray-dried ethyl acetate fraction (EAF) from Punica granatum leaves in models of pain, inflammation, and snakebite envenomation. Phytochemical analysis highlighted the presence of polyphenols, particularly luteolin and hydrolysable tannins in SDE, and a significant concentration of flavonoids in EAF. Both samples demonstrated safety in murine fibroblast cultures, exhibiting no toxicity at concentrations up to 250 µg/mL. In vivo, EAF (25 mg/kg) showed remarkable peripheral antinociceptive activity, reducing abdominal writhings by 88.0%, comparable to morphine (87.0%), and superior to indomethacin (72.0%). In the formalin test, EAF reduced neurogenic and inflammatory pain by 80.9% and 87.3%, respectively, while SDE (200 mg/kg) reduced writhings by 76.7% and inflammatory pain by 57.1%. In the tail immersion test, both extracts increased latency time, confirming central antinociceptive effects. SDE and EAF also reduced carrageenan-induced edema and leukocyte migration by over 70%. In vitro, both samples completely inhibited the proteolytic and hyaluronidase activities of Bothrops brazili and Bothrops leucurus venoms and strongly inhibited PLA₂ activity. Notably, in vivo administration of SDE and EAF significantly reduced B. leucurus-induced paw edema and myeloperoxidase activity by up to 85.5%. These findings reinforce the traditional use of P. granatum leaves and provide the first report of their in vivo analgesic and antiophidic potential, supporting the role of their rich phenolic composition in modulating inflammatory and venom-induced responses.

石榴叶提取物和部分的抗伤、抗炎和抗蛇作用:体外和体内评价。
石榴属灌木(石榴科)是一种灌木与世界各地的分布,已被用于民间医学治疗炎症性疾病。研究了石榴叶喷雾干燥氢乙醇提取物(SDE)和喷雾干燥乙酸乙酯提取物(EAF)在疼痛、炎症和蛇咬中毒模型中的治疗潜力。植物化学分析表明,SDE中存在多酚类物质,特别是木犀草素和可水解单宁,而EAF中存在大量黄酮类物质。两种样品在小鼠成纤维细胞培养中均表现出安全性,浓度高达250 μ g/mL时无毒性。在体内,EAF (25 mg/kg)表现出显著的外周抗疼痛活性,减少腹部扭动88.0%,与吗啡(87.0%)相当,优于吲哚美辛(72.0%)。在福尔马林试验中,EAF分别减轻了80.9%和87.3%的神经源性和炎症性疼痛,而SDE (200 mg/kg)减轻了76.7%的扭动和57.1%的炎症性疼痛。在尾浸试验中,两种提取物均增加了潜伏期,证实了中枢抗伤害感受作用。SDE和EAF还能减少卡拉胶诱导的水肿和白细胞迁移70%以上。在体外,两种样品均能完全抑制巴西肉虱和白肉虱毒液的蛋白水解酶和透明质酸酶活性,并强烈抑制PLA 2活性。值得注意的是,体内给药SDE和EAF可显著降低白弧菌诱导的足跖水肿和髓过氧化物酶活性高达85.5%。这些发现加强了传统的使用石榴叶,并提供了其体内镇痛和抗蛇毒作用的首次报道,支持其丰富的酚类成分在调节炎症和毒液诱导反应中的作用。
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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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