Genil Dantas de Oliveira , Mariana França de Moraes , Magna Maria Lima Araújo , Dilma Maria de Brito Melo Trovão , José Iranildo Miranda de Melo , Wêndeo Kennedy Costa , Maria Tereza dos Santos Correia , Alisson Macário de Oliveira , Samuel Paulo Cibulski , Harley da Silva Alves
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Despite ethnopharmacological reports, there is currently a lack of evidence about its chemical composition, toxicity and pharmacological effects.</div></div><div><h3>Aim of the study</h3><div>This study aimed to investigate the chemical composition of the aqueous extract of <em>D. emetocathartica</em> stems (DEAQ), evaluate its acute oral toxicity, mutagenicity and its anti-inflammatory profile in mice.</div></div><div><h3>Material and methods</h3><div>The DEAQ chemical composition was evaluated through HPLC-MS/MS. Acute oral toxicity was assessed for 14 days after the oral administration of DEAQ in a single dose of 2000 mg kg<sup>−1</sup>. The mutagenic assessment was carried out through micronucleus test in mice. The DEAQ anti-inflammatory activity was evaluated at doses of 25, 50 and 100 mg kg<sup>−1</sup> throught models of carrageenan-induced paw edema, peritonitis and air pouch.</div></div><div><h3>Results</h3><div>Using HPLC-MS/MS the cayaponoside D<sub>2</sub> was identified as the most abundant compound in DEAQ. Oral DEAQ administration showed no signs of toxicity or mutagenicity. All tested DEAQ doses had anti-edematogenic effects, decreased the migration of total leukocytes and neutrophils and decreased the levels of TNF-α and IL-1β.</div></div><div><h3>Conclusions</h3><div>The <em>in vivo</em> tests results indicated that DEAQ showed strong anti-inflammatory activity, with possible cayaponoside D<sub>2</sub> involvement, highlighting the absence of toxicity and genotoxicity for the dose and route used. Furthermore, the study provides chemical and pharmacological evidences about the therapeutic use of <em>D. emetocathartica</em> in folk medicine.</div></div>","PeriodicalId":15761,"journal":{"name":"Journal of ethnopharmacology","volume":"345 ","pages":"Article 119534"},"PeriodicalIF":5.4000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-inflammatory and non-toxic effects of Doyerea emetocathartica aqueous extract in mice\",\"authors\":\"Genil Dantas de Oliveira , Mariana França de Moraes , Magna Maria Lima Araújo , Dilma Maria de Brito Melo Trovão , José Iranildo Miranda de Melo , Wêndeo Kennedy Costa , Maria Tereza dos Santos Correia , Alisson Macário de Oliveira , Samuel Paulo Cibulski , Harley da Silva Alves\",\"doi\":\"10.1016/j.jep.2025.119534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Ethnopharmacological relevance</h3><div><em>Doyerea emetocathartica</em> is a Cucurbitaceae known as ''cabeça de negro'' and used by North-eastern Brazil and South-eastern Mexico communities to treat rheumatism, inflammation and pain. 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The DEAQ anti-inflammatory activity was evaluated at doses of 25, 50 and 100 mg kg<sup>−1</sup> throught models of carrageenan-induced paw edema, peritonitis and air pouch.</div></div><div><h3>Results</h3><div>Using HPLC-MS/MS the cayaponoside D<sub>2</sub> was identified as the most abundant compound in DEAQ. Oral DEAQ administration showed no signs of toxicity or mutagenicity. All tested DEAQ doses had anti-edematogenic effects, decreased the migration of total leukocytes and neutrophils and decreased the levels of TNF-α and IL-1β.</div></div><div><h3>Conclusions</h3><div>The <em>in vivo</em> tests results indicated that DEAQ showed strong anti-inflammatory activity, with possible cayaponoside D<sub>2</sub> involvement, highlighting the absence of toxicity and genotoxicity for the dose and route used. 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引用次数: 0
摘要
民族药物学相关性:Doyerea emetocathtica是葫芦科的一种,被称为“cabea de negro”,被巴西东北部和墨西哥东南部社区用于治疗风湿病、炎症和疼痛。尽管有民族药理学报道,但目前缺乏关于其化学成分,毒性和药理作用的证据。研究目的:研究吐痰草茎水提物(DEAQ)的化学成分,评价其对小鼠的急性口服毒性、致突变性和抗炎作用。材料与方法:采用HPLC-MS/MS法测定DEAQ的化学成分。以2000 mg kg-1单剂量口服DEAQ后14天进行急性口服毒性评估。通过小鼠微核试验进行了致突变性评价。在25、50和100 mg kg-1剂量下,通过卡拉胶诱导的足跖水肿、腹膜炎和气袋模型评估DEAQ的抗炎活性。结果:HPLC-MS/MS鉴定出DEAQ中含量最高的化合物为山麻子皂苷D2。口服DEAQ无毒性或致突变性迹象。所有测试的DEAQ剂量均具有抗致水肿作用,减少总白细胞和中性粒细胞的迁移,降低TNF-α和IL-1β的水平。结论:体内试验结果表明DEAQ具有很强的抗炎活性,可能与cayaponoside D2有关,强调使用剂量和途径没有毒性和遗传毒性。此外,本研究还为吐痰菌在民间医学中的治疗作用提供了化学和药理学依据。
Anti-inflammatory and non-toxic effects of Doyerea emetocathartica aqueous extract in mice
Ethnopharmacological relevance
Doyerea emetocathartica is a Cucurbitaceae known as ''cabeça de negro'' and used by North-eastern Brazil and South-eastern Mexico communities to treat rheumatism, inflammation and pain. Despite ethnopharmacological reports, there is currently a lack of evidence about its chemical composition, toxicity and pharmacological effects.
Aim of the study
This study aimed to investigate the chemical composition of the aqueous extract of D. emetocathartica stems (DEAQ), evaluate its acute oral toxicity, mutagenicity and its anti-inflammatory profile in mice.
Material and methods
The DEAQ chemical composition was evaluated through HPLC-MS/MS. Acute oral toxicity was assessed for 14 days after the oral administration of DEAQ in a single dose of 2000 mg kg−1. The mutagenic assessment was carried out through micronucleus test in mice. The DEAQ anti-inflammatory activity was evaluated at doses of 25, 50 and 100 mg kg−1 throught models of carrageenan-induced paw edema, peritonitis and air pouch.
Results
Using HPLC-MS/MS the cayaponoside D2 was identified as the most abundant compound in DEAQ. Oral DEAQ administration showed no signs of toxicity or mutagenicity. All tested DEAQ doses had anti-edematogenic effects, decreased the migration of total leukocytes and neutrophils and decreased the levels of TNF-α and IL-1β.
Conclusions
The in vivo tests results indicated that DEAQ showed strong anti-inflammatory activity, with possible cayaponoside D2 involvement, highlighting the absence of toxicity and genotoxicity for the dose and route used. Furthermore, the study provides chemical and pharmacological evidences about the therapeutic use of D. emetocathartica in folk medicine.
期刊介绍:
The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.