Amir Asadi, Ali Mandegary, Mostafa Pournamdari, Mahboobe Abbasi, Neda Mohamadi, Fariba Sharififar
{"title":"葫芦巴种子碱氯仿部分抗伤和抗氧化亚组分的生物活性引导分离","authors":"Amir Asadi, Ali Mandegary, Mostafa Pournamdari, Mahboobe Abbasi, Neda Mohamadi, Fariba Sharififar","doi":"10.2174/0115701808247887231110112551","DOIUrl":null,"url":null,"abstract":"Antinociceptive effect of fenugreek seeds (Trigonella foenum-graecum L.)\nhas been reported in different animal models in response to various chemical or thermal stimuli. In a\nrecent study, alkaline chloroform fraction (AKC) of this plant has exhibited the greatest analgesic\neffect.\n\n\n\nIn the present study, to isolate the active component(s) from the plant, the subfractions\nresulting from AKC column chromatography were evaluated in an animal model for anti-nociception\neffect.\n\n\n\nFrom the 17 separated fractions, 5 major fractions (F4, F6, F14, F15 and F16) were used for\nthe formalin test at three different doses (2.5, 5 10 mg/kg). Antioxidant activity of the most active\nsubfractions was studied too.\n\n\n\nSubsections F16 and F14 (5, 10 mg/kg) showed the greatest analgesic effect and reduced,\nwhich was similar to morphine and even stronger than morphine in some doses. The greatest antioxidant\nactivity was observed by F14 (radical inhibition percentage of 17.34± 0.14 in DPPH assay, reduction\npower percentage of 74.05±4.23 in RPA versus green tea (91.68± 3.04 and 97.59± 6.24 in\nDPPH assay and RPA test respectively). The absorbance of F14 was 0.25±0.11 in the FTC method in\ncomparison to ascorbic acid 10 μg/ml and 100 μg/ml (0.72±0.33 and 0.05±0.41 respectively).\n\n\n\nSeparated subfractions exhibited more antinociceptive effect than AKC fraction, so\nfurther separation can lead to the acquisition of antinociceptive compound (s), while AKC fraction\nwas found to be more potent antioxidant than separated sub-fractions in all three experiments. So,\nmost likely, the anti-nociception effect of subfractions might be achieved via other mechanisms than\nantioxidant activity. Based on phytochemical screening, AKC and all sub-fractions especially F14,\nF15 and F16 were positive for the presence of alkaloids and only F14 was positive for flavonoids.","PeriodicalId":18059,"journal":{"name":"Letters in Drug Design & Discovery","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bioactivity-guided Separation of Antinociceptive and Antioxidant Subfractions from Alkaline Chloroform Fraction of Fenugreek Seeds (Trigonella foenum-graecum L.) in an Animal Model\",\"authors\":\"Amir Asadi, Ali Mandegary, Mostafa Pournamdari, Mahboobe Abbasi, Neda Mohamadi, Fariba Sharififar\",\"doi\":\"10.2174/0115701808247887231110112551\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Antinociceptive effect of fenugreek seeds (Trigonella foenum-graecum L.)\\nhas been reported in different animal models in response to various chemical or thermal stimuli. In a\\nrecent study, alkaline chloroform fraction (AKC) of this plant has exhibited the greatest analgesic\\neffect.\\n\\n\\n\\nIn the present study, to isolate the active component(s) from the plant, the subfractions\\nresulting from AKC column chromatography were evaluated in an animal model for anti-nociception\\neffect.\\n\\n\\n\\nFrom the 17 separated fractions, 5 major fractions (F4, F6, F14, F15 and F16) were used for\\nthe formalin test at three different doses (2.5, 5 10 mg/kg). Antioxidant activity of the most active\\nsubfractions was studied too.\\n\\n\\n\\nSubsections F16 and F14 (5, 10 mg/kg) showed the greatest analgesic effect and reduced,\\nwhich was similar to morphine and even stronger than morphine in some doses. The greatest antioxidant\\nactivity was observed by F14 (radical inhibition percentage of 17.34± 0.14 in DPPH assay, reduction\\npower percentage of 74.05±4.23 in RPA versus green tea (91.68± 3.04 and 97.59± 6.24 in\\nDPPH assay and RPA test respectively). The absorbance of F14 was 0.25±0.11 in the FTC method in\\ncomparison to ascorbic acid 10 μg/ml and 100 μg/ml (0.72±0.33 and 0.05±0.41 respectively).\\n\\n\\n\\nSeparated subfractions exhibited more antinociceptive effect than AKC fraction, so\\nfurther separation can lead to the acquisition of antinociceptive compound (s), while AKC fraction\\nwas found to be more potent antioxidant than separated sub-fractions in all three experiments. So,\\nmost likely, the anti-nociception effect of subfractions might be achieved via other mechanisms than\\nantioxidant activity. Based on phytochemical screening, AKC and all sub-fractions especially F14,\\nF15 and F16 were positive for the presence of alkaloids and only F14 was positive for flavonoids.\",\"PeriodicalId\":18059,\"journal\":{\"name\":\"Letters in Drug Design & Discovery\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2023-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Letters in Drug Design & Discovery\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2174/0115701808247887231110112551\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Drug Design & Discovery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0115701808247887231110112551","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Bioactivity-guided Separation of Antinociceptive and Antioxidant Subfractions from Alkaline Chloroform Fraction of Fenugreek Seeds (Trigonella foenum-graecum L.) in an Animal Model
Antinociceptive effect of fenugreek seeds (Trigonella foenum-graecum L.)
has been reported in different animal models in response to various chemical or thermal stimuli. In a
recent study, alkaline chloroform fraction (AKC) of this plant has exhibited the greatest analgesic
effect.
In the present study, to isolate the active component(s) from the plant, the subfractions
resulting from AKC column chromatography were evaluated in an animal model for anti-nociception
effect.
From the 17 separated fractions, 5 major fractions (F4, F6, F14, F15 and F16) were used for
the formalin test at three different doses (2.5, 5 10 mg/kg). Antioxidant activity of the most active
subfractions was studied too.
Subsections F16 and F14 (5, 10 mg/kg) showed the greatest analgesic effect and reduced,
which was similar to morphine and even stronger than morphine in some doses. The greatest antioxidant
activity was observed by F14 (radical inhibition percentage of 17.34± 0.14 in DPPH assay, reduction
power percentage of 74.05±4.23 in RPA versus green tea (91.68± 3.04 and 97.59± 6.24 in
DPPH assay and RPA test respectively). The absorbance of F14 was 0.25±0.11 in the FTC method in
comparison to ascorbic acid 10 μg/ml and 100 μg/ml (0.72±0.33 and 0.05±0.41 respectively).
Separated subfractions exhibited more antinociceptive effect than AKC fraction, so
further separation can lead to the acquisition of antinociceptive compound (s), while AKC fraction
was found to be more potent antioxidant than separated sub-fractions in all three experiments. So,
most likely, the anti-nociception effect of subfractions might be achieved via other mechanisms than
antioxidant activity. Based on phytochemical screening, AKC and all sub-fractions especially F14,
F15 and F16 were positive for the presence of alkaloids and only F14 was positive for flavonoids.
期刊介绍:
Aims & Scope
Letters in Drug Design & Discovery publishes letters, mini-reviews, highlights and guest edited thematic issues in all areas of rational drug design and discovery including medicinal chemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, and structure-activity relationships. The emphasis is on publishing quality papers very rapidly by taking full advantage of latest Internet technology for both submission and review of manuscripts. The online journal is an essential reading to all pharmaceutical scientists involved in research in drug design and discovery.