• Title/Summary/Keyword: Killkyungtang

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Cytotoxic Activity of the Medicinal Formula Kilkyungtang and Two Modified Kilkyungtangs against Cultured Tumor Cells in Vitro. II (생약복합제제 길경탕 및 가미길경탕의 항암효과 (제 2 보))

  • Kim, Sung-Hoon;Park, Kyung-Sik;Ryu, Shi-Yong
    • Korean Journal of Pharmacognosy
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    • v.27 no.1
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    • pp.42-46
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    • 1996
  • The medicinal formula, Kilkyungtang (KKT) and two modified Kilkyungtangs (KKT-1 and KKT-2), which were supplemented by the additional crude drug, Houttuyniae herba (KKT-1), and Oldenlandiae diffusae herba (KKT-2) to KKT, had been applied widely as decoctions for the treatment of malignant tumors. Cytotoxic activities against two tumor cell lines, A549 and $B16-F_0$ were investigated. However, none of them were found to exhibit significant cytotoxicity upon tested tumor cells below the concentration of $1000{\mu}g/ml$. However, cytotoxic activities of three reputed antitumor agents, i.e., mitomycin C (MMC), cisplatin (CPT) and 5-fluorouracil (5-FU) was significantly potentiated by the combined treatment of them with KKT, KKT-1 and KKT-2 respectively, especially against A549 (human non small cell lung adenocarcinoma), in vitro.

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Antitumor Activity of the Medicinal Formula Kilkyungtang and Two Modified Kilkyungtangs in Vivo. I (생약복합제제 길경탕 및 가미길경탕의 항암효과 (제 1 보))

  • Kim, Sung-Hoon;Park, Kyung-Sik;Ryu, Shi-Yong
    • Korean Journal of Pharmacognosy
    • /
    • v.27 no.1
    • /
    • pp.37-41
    • /
    • 1996
  • The prescription, Kilkyungtang (KKT), which originally consists of twelve kinds of medicinal plant materials and was used as a decoction for the treatment of malignant tumors and two modified Kilkyungtangs (KKT-1 and KKT-2), supplemented by the additional crude drug to KKT (KKT-1:Houttuyniae herba, and KKT-2:Oldenlandiae diffusae herba) were investigated on their antitumoral properties, in vivo respectively. All KKTs were found to exhibit significant life time-prolonging effects when they were administered orally to Sarcoma-180 bearing ICR mice for 7 days. (ILS was estimated as 20% in KKT, 42% in KKT-1 and 57% in KKT-2). A profound lessening of tumor weights was also observed when KKTs were administered to $B16-F_0$ bearing C57B/6 mice.

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