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首页> 外文期刊>The American Journal of Chinese Medicine >Inhibition of Urinary Bladder Carcinogenesis by Aqueous Extract of Sclerotia of Polyporus umbellatus Fries and Polyporus Polysaccharide
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Inhibition of Urinary Bladder Carcinogenesis by Aqueous Extract of Sclerotia of Polyporus umbellatus Fries and Polyporus Polysaccharide

机译:猪Poly薯条菌核菌水提物和猪por多糖对膀胱膀胱癌变的抑制作用

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摘要

The study aimed to evaluate inhibition effect of sclerotia of Polyporus umbellatus Fries aqueous extract (SPUE) and polyporus polysaccharide (PPS) on bladder cancer, then to measure their effect on mRNA expression of glutathione S-transferase π (GSTPi) and NAD(P)H:quinone oxidoreductase 1 (NQO1) in female Fischer-344 rats model. The model rats were induced by N-butyl-N-(4-hydroxybutyl)-nitrosamine (BBN) for a period of 8 weeks and saccharin for 12 weeks. SPUE (50 mg/kg, 250 mg/kg, 500 mg/kg) and PPS (28 mg/kg) were orally administrated to the model rats during the whole study. Compared to the control group, a more preventive effect of SPUE and PPS treatment on bladder cancer was discovered, higher mRNA upregulation of GSTpi and NQO1 was seen in the treatment group. Furthermore, the GSTPi and NQO1 mRNA upregulated level in the low-dose group (SPUE 50 mg/kg) was at maximum. In brief, SPUE and PPS are highly effective in inhibiting bladder carcinogenesis in rats, which may be associatedwith upregulation of GSTPi and NQO1 in the bladder.
机译:该研究旨在评估猪Poly水泡提​​取物(SPUE)和猪por多糖(PPS)的菌核对膀胱癌的抑制作用,然后测定其对谷胱甘肽S-转移酶π(GSTPi)和NAD(P)mRNA表达的影响。雌性Fischer-344大鼠模型中的H:醌氧化还原酶1(NQO1)。用N-丁基-N-(4-羟丁基)-亚硝胺(BBN)诱导模型大鼠,持续8周,糖精诱导12周。在整个研究过程中,将SPUE(50 mg / kg,250 mg / kg,500 mg / kg)和PPS(28 mg / kg)口服给予模型大鼠。与对照组相比,SPUE和PPS治疗对膀胱癌的预防作用更强,治疗组中GSTpi和NQO1的mRNA上调更高。此外,低剂量组(SPUE 50 mg / kg)的GSTPi和NQO1 mRNA上调水平最大。简而言之,SPUE和PPS在抑制大鼠膀胱癌发生中非常有效,这可能与膀胱中GSTPi和NQO1的上调有关。

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