Fujita H, Ogawa K, Ikuzawa M, Muto S, Matsuki M, Nakajima S, Shimamura M, Togawa M, Yoshikumi C, Kawai Y
Gan To Kagaku Ryoho. 1986 Aug;13(8):2653-7.
The effects of PSK on hepatic drug-metabolizing enzymes were investigated using Sarcoma 180-bearing and non-tumor-bearing ICR mice. PSK, an immunomodulator, has been commonly used in combination with tegafur for post-operative adjuvant chemotherapy. Tegafur is a typical masked compound transformed into 5-FU by the hepatic drug-metabolizing enzyme P-450. It has been reported that immunostimulants such as BCG and anaerobic Corynebacterium suppress the drug metabolism. PSK and Propionibacterium acnes were administered to mice inoculated s.c. with Sarcoma 180. It was demonstrated that Propionibacterium acnes had an effect of inhibiting these enzymatic activities, especially the amount of P-450 and cytochrome b5 and aminopyrine demethylation. On the other hand, PSK had no influence on the drug-metabolizing enzymes. Propionibacterium acnes was shown to decrease the 5-FU level in organs and sera of mice given FT-207 orally. By contrast, PSK showed no difference in 5-FU level compared to controls, indicating that PSK had no inhibitory effect on the activation of FT-207 by hepatic drug-metabolizing enzymes.
使用接种肉瘤180的和未接种肿瘤的ICR小鼠研究了PSK对肝脏药物代谢酶的影响。PSK是一种免疫调节剂,通常与替加氟联合用于术后辅助化疗。替加氟是一种典型的前体药物,通过肝脏药物代谢酶P-450转化为5-氟尿嘧啶。据报道,诸如卡介苗和厌氧棒状杆菌等免疫刺激剂会抑制药物代谢。将PSK和痤疮丙酸杆菌给予皮下接种肉瘤180的小鼠。结果表明,痤疮丙酸杆菌具有抑制这些酶活性的作用,尤其是P-450、细胞色素b5的量以及氨基比林去甲基化。另一方面,PSK对药物代谢酶没有影响。已表明痤疮丙酸杆菌可降低口服FT-207的小鼠器官和血清中的5-氟尿嘧啶水平。相比之下,与对照组相比,PSK在5-氟尿嘧啶水平上没有差异,表明PSK对肝脏药物代谢酶激活FT-207没有抑制作用。