Arunporn Itharat, Pun Thongmee, Krit Piwngam, Janjira Inprasit, Sunita Makchuchit, Pranporn Kuropakornpong, Neal M Davies
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Lastly, rat models with ethyl phenylpropionate (EPP)-induced ear edema and carrageenan-induced paw edema were utilized to assess anti-inflammatory activity.</p><p><strong>Findings/results: </strong>LAMP possessed potent inhibitory effects on NO, PGE2, and TNF-α production with IC50 values of 24.90 ± 0.86, 4.77 ± 0.03, and 35.01 ± 2.61 µg/mL, respectively. In addition, LAMP extract demonstrated stable biological activity, anti-inflammatory effects, and phytochemical content stability under stress conditions. Additionally, 0.5%, 1%, and 2% w/v LAMP significantly inhibited EPP-induced rat ear edema over time equivalent to 5% w/v phenylbutazone. LAMP at 180, 375, and 750 mg/kg also considerably reduced carrageenan-induced rat paw edema 2 h after carrageenan administration compared to phenylbutazone at 250 mg/kg.</p><p><strong>Conclusion and implications: </strong>LAMP has anti-inflammatory activity by inhibiting PGE2 formation. These findings are consistent with the efficacy and traditional use of the LAMP remedy in treating inflammatory diseases.</p>","PeriodicalId":21075,"journal":{"name":"Research in Pharmaceutical Sciences","volume":"19 6","pages":"683-697"},"PeriodicalIF":2.1000,"publicationDate":"2024-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11792718/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>In vitro</i> and <i>in vivo</i> evaluation of anti-inflammatory activities of ethanol extract from Lom-Am-Ma-Pruek remedy for pain relief.\",\"authors\":\"Arunporn Itharat, Pun Thongmee, Krit Piwngam, Janjira Inprasit, Sunita Makchuchit, Pranporn Kuropakornpong, Neal M Davies\",\"doi\":\"10.4103/RPS.RPS_26_24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and purpose: </strong>Lom-Am-Ma-Pruek (LAMP) remedy has been used in Thai traditional medicine to relieve pain associated with the inflammatory process. The anti-inflammatory activity and bioactivity of LAMP in an animal model have not been previously investigated. We evaluated the <i>in-vitro</i> and <i>in-vivo</i> anti-inflammatory activity of LAMP ethanol extract.</p><p><strong>Experimental approach: </strong>The anti-inflammatory activity of LAMP and its plant ingredients were investigated on lipopolysaccharide-stimulated NO, PGE2, and TNF-α release from RAW264.7 cells. Furthermore, the stability of LAMP under biological and chemical accelerated conditions was evaluated using the Griess reaction assay and HPLC. Lastly, rat models with ethyl phenylpropionate (EPP)-induced ear edema and carrageenan-induced paw edema were utilized to assess anti-inflammatory activity.</p><p><strong>Findings/results: </strong>LAMP possessed potent inhibitory effects on NO, PGE2, and TNF-α production with IC50 values of 24.90 ± 0.86, 4.77 ± 0.03, and 35.01 ± 2.61 µg/mL, respectively. 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引用次数: 0
摘要
背景和目的:lomam - ma - pruek (LAMP)疗法在泰国传统医学中用于缓解炎症过程相关的疼痛。LAMP在动物模型中的抗炎活性和生物活性尚未被研究。我们评估了LAMP乙醇提取物的体外和体内抗炎活性。实验方法:研究LAMP及其植物成分对脂多糖刺激RAW264.7细胞释放NO、PGE2和TNF-α的抗炎活性。采用Griess反应法和高效液相色谱法对LAMP在生物和化学加速条件下的稳定性进行了评价。最后,采用苯基丙酸乙酯(EPP)诱导的大鼠耳水肿和卡拉胶诱导的大鼠足水肿模型来评估抗炎活性。结果:LAMP对NO、PGE2和TNF-α的产生有较强的抑制作用,IC50值分别为24.90±0.86、4.77±0.03和35.01±2.61µg/mL。此外,LAMP提取物在逆境条件下表现出稳定的生物活性、抗炎作用和植物化学成分的稳定性。此外,0.5%、1%和2% w/v的LAMP可显著抑制epp诱导的大鼠耳部水肿,其作用相当于5% w/v的苯丁酮。与苯基丁酮(250 mg/kg)相比,180、375和750 mg/kg的LAMP也显著减少了卡拉胶诱导的大鼠足部水肿。结论及意义:LAMP通过抑制PGE2的形成具有抗炎作用。这些发现与LAMP治疗炎症性疾病的疗效和传统用法一致。
In vitro and in vivo evaluation of anti-inflammatory activities of ethanol extract from Lom-Am-Ma-Pruek remedy for pain relief.
Background and purpose: Lom-Am-Ma-Pruek (LAMP) remedy has been used in Thai traditional medicine to relieve pain associated with the inflammatory process. The anti-inflammatory activity and bioactivity of LAMP in an animal model have not been previously investigated. We evaluated the in-vitro and in-vivo anti-inflammatory activity of LAMP ethanol extract.
Experimental approach: The anti-inflammatory activity of LAMP and its plant ingredients were investigated on lipopolysaccharide-stimulated NO, PGE2, and TNF-α release from RAW264.7 cells. Furthermore, the stability of LAMP under biological and chemical accelerated conditions was evaluated using the Griess reaction assay and HPLC. Lastly, rat models with ethyl phenylpropionate (EPP)-induced ear edema and carrageenan-induced paw edema were utilized to assess anti-inflammatory activity.
Findings/results: LAMP possessed potent inhibitory effects on NO, PGE2, and TNF-α production with IC50 values of 24.90 ± 0.86, 4.77 ± 0.03, and 35.01 ± 2.61 µg/mL, respectively. In addition, LAMP extract demonstrated stable biological activity, anti-inflammatory effects, and phytochemical content stability under stress conditions. Additionally, 0.5%, 1%, and 2% w/v LAMP significantly inhibited EPP-induced rat ear edema over time equivalent to 5% w/v phenylbutazone. LAMP at 180, 375, and 750 mg/kg also considerably reduced carrageenan-induced rat paw edema 2 h after carrageenan administration compared to phenylbutazone at 250 mg/kg.
Conclusion and implications: LAMP has anti-inflammatory activity by inhibiting PGE2 formation. These findings are consistent with the efficacy and traditional use of the LAMP remedy in treating inflammatory diseases.
期刊介绍:
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