The hydroalcoholic extract of the leaves of red mombin (Spondias purpurea L.) is more effective in accelerating ulcer healing than preventing them in rodents.

IF 5.3 2区 医学 Q2 IMMUNOLOGY
Ruan Kaio Silva Nunes, Bruna Longo, Caio Henrique Willrich, Levy Mota da Silva, Luísa Santiago, Thiago Farias de Queiroz Silva, Lucas Matheus Lessa de Olinda, Layla Francielle Pereira, Heloisa Immianovsky Eisendecker, José Roberto Santin, Larissa Benvenutti, Luiza Felipim Corsi, Bianca Priscila Miranda, Hydima Julião Cóta, Larissa Venzon, Tauani Caroline Santos França, Max Vidal-Gutiérrez, Zuleide Maria Ignacio, Walter Antônio Roman-Junior, Luísa Mota da Silva
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引用次数: 0

Abstract

This study evaluated the anti-ulcer effects of the hydroalcoholic extract from the leaves of Spondias purpurea L. (SPHE). The gastroprotection was assessed using acidified ethanol-induced gastric ulcer in mice given orally with the vehicle, carbenoxolone (200 mg/kg), or SPHE (10-1.000 mg/kg). The extract's healing activity was evaluated using acetic acid-induced ulcers in rats treated with vehicle, omeprazole (20 mg/kg), or SPHE (3-300 mg/kg). Histological and biochemical analyses were done in ulcerated tissue from both models. SPHE antisecretory action was tested in pylorus-ligated rats. The in vitro antioxidant potential was assessed using the DPPH test; its cytotoxicity and proliferative effects were measured in L929 cells. Mass spectrometry analysis was used to determine the extract's chemical profile and the quantification of phenolic compounds in the extract was performed in LCMS. SPHE induced gastroprotection at a dose of 1.000 mg/kg, and this effect was lost in mice treated with NEM, indomethacin, or yohimbine but not L-NAME. SPHE improves the healing of acetic acid-induced ulcers by 69.5% and 83.7% at 10 and 30 mg/kg, respectively. The microscopic examination confirms the healing effect of SPHE. SPHE enhanced PAS-stained mucins, SOD, and GST activities while decreasing MPO activity, and MDA levels in ulcerated mucosa, and scavenged DPPH radicals but did not change the gastric acid secretion. SPHE showed no cytotoxicity and favored fibroblast proliferation. The presence of hibiscus acid, hydroxy citric acid, hibiscus acid glycoside, ellagic acid, and the flavonoids quercetin and rutin were confirmed and quercetin, caffeic acid, p-coumaric acid, gallic acid, and epigallocatechin were quantified. Therefore, SPHE accumulated chemicals with higher gastric healing potential mediated by gastric protective features, specifically antioxidant resources, mucus barrier, and cell proliferation.

红芒豆(Spondias purpurea L.)叶子的水酒精提取物在加速溃疡愈合方面比在啮齿类动物中预防溃疡愈合更有效。
研究了紫花Spondias purpurea L. (SPHE)叶水醇提取物的抗溃疡作用。用酸化乙醇诱导的小鼠胃溃疡来评估胃保护作用,同时给药,卡贝诺洛酮(200 mg/kg)或SPHE (10-1.000 mg/kg)。以醋酸致溃疡大鼠为实验对象,分别用对照物、奥美拉唑(20mg /kg)或SPHE (3- 300mg /kg)治疗,评价该提取物的愈合活性。对两种模型的溃疡组织进行组织学和生化分析。在幽门结扎大鼠中检测了SPHE的抗分泌作用。采用DPPH法测定其体外抗氧化能力;在L929细胞中测定其细胞毒性和增殖作用。质谱法测定提取物的化学成分,LCMS法测定提取物中酚类化合物的含量。SPHE在剂量为1.000 mg/kg时诱导胃保护,在用NEM、吲哚美辛或育亨宾治疗的小鼠中,这种作用消失,但L-NAME没有。在10和30 mg/kg剂量下,SPHE对乙酸致溃疡愈合的促进作用分别为69.5%和83.7%。显微镜检查证实了SPHE的愈合效果。SPHE增强了pas染色的粘蛋白、SOD和GST活性,降低了溃疡黏膜的MPO活性和MDA水平,清除了DPPH自由基,但没有改变胃酸分泌。SPHE无细胞毒性,有利于成纤维细胞增殖。测定了木槿酸、羟基柠檬酸、木槿酸苷、鞣花酸、黄酮类化合物槲皮素和芦丁的含量,并测定了槲皮素、咖啡酸、对香豆酸、没食子酸和表没食子儿茶素的含量。因此,SPHE积累的化学物质具有更高的胃愈合潜力,这是由胃的保护功能介导的,特别是抗氧化资源、粘液屏障和细胞增殖。
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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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