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      중추신경계에서 포공영의 항염증작용에 관한 연구 = Studies on the anti-inflammatory action of Taraxacum officinale extract in central nervous system

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      https://www.riss.kr/link?id=A19720310

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      Substance P(SP) can stimulate production of tumor necrosis factor-α(TNF-α) from astrocytes stimulated with lipopolysaccharide(LPS). The objective of the current study was to determine the effect of Taraxacum officinale(TO) on the production of TNF-α from primary cultures of rat astrocytes. TO(100 & 1000㎍/ml) significantly inhibited the TNF-α production by astrocytes stimulated with LPS and SP. Interleukin-1(IL-1) has been shown to elevate TNF-α production from LPS-stimulated astrocytes while having no effect on astrocytes in the absence of LPS. We therefore examined whether IL-1 mediated inhibition of TNF-α production from primary astrocytes by TO. Treatment of TO(100 and 1000㎍/ml) to astrocytes stimulated with both LPS and substance P decreased IL-1 production significantly. Moreover, the production of TNF-α by LPS and substance P in astrocytes was progressively inhibited with increasing amount of IL-1 neutralizing antibody. These results suggest that TO may inhibit TNF-α production by inhibiting IL-1 production and that TO has an antiinflammatory activity in the central nervous system.
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      Substance P(SP) can stimulate production of tumor necrosis factor-α(TNF-α) from astrocytes stimulated with lipopolysaccharide(LPS). The objective of the current study was to determine the effect of Taraxacum officinale(TO) on the production of TNF-�...

      Substance P(SP) can stimulate production of tumor necrosis factor-α(TNF-α) from astrocytes stimulated with lipopolysaccharide(LPS). The objective of the current study was to determine the effect of Taraxacum officinale(TO) on the production of TNF-α from primary cultures of rat astrocytes. TO(100 & 1000㎍/ml) significantly inhibited the TNF-α production by astrocytes stimulated with LPS and SP. Interleukin-1(IL-1) has been shown to elevate TNF-α production from LPS-stimulated astrocytes while having no effect on astrocytes in the absence of LPS. We therefore examined whether IL-1 mediated inhibition of TNF-α production from primary astrocytes by TO. Treatment of TO(100 and 1000㎍/ml) to astrocytes stimulated with both LPS and substance P decreased IL-1 production significantly. Moreover, the production of TNF-α by LPS and substance P in astrocytes was progressively inhibited with increasing amount of IL-1 neutralizing antibody. These results suggest that TO may inhibit TNF-α production by inhibiting IL-1 production and that TO has an antiinflammatory activity in the central nervous system.

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