生物活性 | |||
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描述 | Peimine is a natural compound with good anti-inflammatory effects in vivo. Peimine (0-25 mg/L) significantly inhibited tumor necrosis factor (TNF)-α, interleukin (IL)-6, IL-1β, and increased IL-10 production. Furthermore, peimine significantly inhibited the phosphorylation of p38, ERK and c-jun N-terminal kinase (JNK) as well as decreased p65 and IκB[3]. Moreover, peimine reduced MAPKs (Mitogen-activated protein kinases) phosphorylation and the nuclear NF-κB expression in PMACI-induced HMC-1(human mast cell). Peimine decreased PCA (Passive cutaneous anaphylaxis) reactions in rats as well[4]. Peimine increased the systemic exposure of paeoniflorin through inhibiting the activity of CYP3A4 and P-gp[5]. The intestinal absorption of peimine across Caco-2 cell monolayers involves active transport and that peimine is a substrate of P-gp[6]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.32mL 0.46mL 0.23mL |
11.58mL 2.32mL 1.16mL |
23.17mL 4.63mL 2.32mL |
参考文献 |
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