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王一菱,陈迪,吴景兰.三七总皂甙抗炎和镇痛作用及其机理探讨[J].中国中西医结合杂志,1994,(1):35-36,5,6
三七总皂甙抗炎和镇痛作用及其机理探讨
Effects and Mechanism of Total Saponins of Panax Notoginseng on Anti-Inflammation and Analgesia
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DOI:
中文关键词:  三七总皂甙  电针  纳洛酮  痛阈  细胞免疫
英文关键词:total saponins of Panax notoginseng  electroacupuncture  naloxone  pain threshold  cellular immunity
基金项目:
作者单位
王一菱 河南医科大学组胚教研室 
陈迪 河南医科大学生物教研室 
吴景兰 河南医科大学组胚教研室 
摘要点击次数: 1595
全文下载次数: 1002
中文摘要:
      本研究通过建立炎症动物模型,应用三七总皂甙(TSPN)、电针(EA)进行治疗,并用纳洛酮(Nx)阻断两者作用,用组织化学的方法对TSPN和EA的效应进行比较。结果可见痛阈(PT)在TSPN组、EA组和EA加TSPN组均显著提高,且硝基蓝四氮唑试验(NBT)阳性的多形核白细胞(PMN)和醋酸萘酚酯酶(ANAE)的点型亚群计数均明显增加,以上的全部效应均被纳洛酮部分阻断;TSPN组与Nx组腹腔肥大细胞脱颗粒率无明显差异。由此可见,TSPN与EA效应相似,具有明显的抗炎镇痛及免疫调整作用。这提示三七总皂甙可能是阿片样肽受体的激动剂而不具有成瘾副作用。
英文摘要:
      In this study the effects of total saponins of Panax notoginseng(TSPN)and electroacupuncture(EA)were compared.Liquid paraffin was intraperitoneally injected (0.1ml/mouse)to establish the animal model with inflammation.The mice were randomly divided into 4 groups with different treatments for 7 days:EA group,TSPN group(100mg.kg intraperitoneal administration),Naloxone(Nx)plus TSPN group and EA plus TSPN group.The pain threshold was measured by a detector(EQ-9E)and the nitroblue tetrazolium test(NBT)for polymorphonuclear neutrophil(PMN)bacteriocidal activity and the α-naphthyl acetate esterase(ANAE)histochemical staining for detection of the focal pattern lymphocyte subpopulation and the toluidine blue histochemical staining for detection of degranulation rate peritoneal mast cells were performed.The results showed that in TSPN,EA and EA plus TSPN group the pain threshold was elevated significantly,the enumeration of NBTpositive PMN and the ANAE-F lymphocyte subpopulation was enhanced.All the above effocts could be partially inhibited by naloxone.Between TSPN group and Nx group the degranulation rate of peritoneal mast cells had no significant difference.Since the TSPN and EA have similar effects e.g.anti-inflammatory,analgesic and immunomodulatory action,it suggested that the TSPN might be somewhat agonist of the opioid like peptide receptor without addiction side reactions.
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