Immunomodulating activities of water extract from xanthium strumarium 2

  • Moon, Eun-Yi (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology) ;
  • Park, Seung-Yong (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology) ;
  • Ahn, Mee-Ja (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology) ;
  • Ahn, Jong-Woong (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology) ;
  • Zee, Ok-Pyo (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology) ;
  • Park, Eun-kyue (Laboratories of Pharmacology and Natural Products, Korea Research Institute of Chemical Technology)
  • Published : 1991.09.01

Abstract

One of water and/or methanol extracts from 14 herbal deugs which were screened using murine splenocytes showed immunosuppressive activities previously. After water extract from Xanthium strumarium was treated with chloroform. $100 \mu{g/ml}$ of water layer (XS-WCI) has very strong immunosimulating activities tested by $^3H$-thmidine incorporation (control as $100 \mu{g/ml}$, 26345 cpm was 69515 cpm). MLR also appears to be simulated strongly (control vs $100 \mu{g/ml}$, 4962 cpm vs 78688 cpm). When $100 \mu{g/ml}$ of XS-WCI and $0.8 \mu{g/ml}$ of concanavalin a (ConA) were added. more $^3H$-thymidine were incorporated significantly, compared with $0.8 \mu{g/ml}$ of ConA only. In contrast with ConA. results from $5 \mu{/ml}$ of lipopolysaccharide (LPS) and $100 \mu{g/ml}$ of XS-WCI were not different. compared with $5\mu{/ml}$of LPS only. These results indicated the responses of XS-WCI to B cell and T cell may be different. XS-WCI was injected intraperitoneally (10 mg/kg. 50mg/kg/ 100 mg/kg) for 4 days or 10 days and tested secretion of IgM or IgG by direct and indirect hemolytic plaque-forming cell assays, respectively. Numbers of hemolytic plaques for both IgM and IgG were increased significantly. Especially, secretion of IgGs was increased more than 10 times. After administration of XS-WCI for 7 days (50 mg/kg. 100 mg/kg) splenomegaly deu to graft vs host reaction was observed. Human lymhocytes separated from whole blood by Ficoll-Hypaque method were also proliferated after treatment of $10 \mu{g/ml}$ and $50 \mu{g/ml}$ of XS-WCI. As seen in murine lymphocytes, human lymphocyte proliferation was increased synergistically after treatment with both of XS-WCI and phytohemagglutinin (PHA). It appears that XS-WCI may have potential immunosimulating activities and that it remains to be purified further for isolation of active components.

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