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口服紫锥菊(美洲草药)对AKR/J小鼠中重组白血病病毒引起的自发性白血病发病率的影响。

Effects of oral administration of Echinacea purpurea (American herb) on incidence of spontaneous leukemia caused by recombinant leukemia viruses in AKR/J mice.

作者信息

Hayashi I, Ohotsuki M, Suzuki I, Watanabe T

机构信息

Department of Clinical Nutrition, Suzuka University of Medical Science.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 2001 Feb;24(1):10-20. doi: 10.2177/jsci.24.10.

DOI:10.2177/jsci.24.10
PMID:11280896
Abstract

Four-week-old female AKR/J mice were given oral doses of powdered leaves from Echinacea purpurea three times weekly for 8 weeks (7.5 mg/mouse/week): controls received phosphate-buffered saline. Mean survival age of experimental AKR/J mice treated with the E. purpurea preparation was significantly prolonged and enlargement of thymic lymphoma in experimental mice was significantly suppressed compared with controls. In normal 3-week-old female AKR/J mice, mortality from thymic lymphoma was delayed markedly after injection into the thymus of cell-free extract of thymus from the experimental 28-week-old female AKR/J mice that received the oral E. purpurea preparation was injected directly into the thymus. Proliferation of endogenous recombinant murine leukemia viruses (MuLV) in the thymus was markedly inhibited after the first oral administration of the E. purpurea preparation as compared with untreated controls (final age, 28 weeks). Production of endogenous interferon (IFN)-gamma in AKR/J mice was also effectively augmented by the oral treatment with the E. purpurea preparation, however, the production of other cytokines such as tumor necrosis factor (TNF)-alpha and interleukin (IL)-12 was minimal. These results suggest that this suppressive effects on spontaneously occurring leukemia caused by endogenous recombinant MuLV in female AKR/J mice may depend on enhancement of nonspecific immune or cellular immune systems (or of both) by the E. purpurea preparation.

摘要

对4周龄雌性AKR/J小鼠每周口服三次紫锥菊叶粉,持续8周(7.5毫克/只/周):对照组给予磷酸盐缓冲盐水。与对照组相比,用紫锥菊制剂处理的实验性AKR/J小鼠的平均存活年龄显著延长,实验小鼠胸腺淋巴瘤的肿大也得到显著抑制。在正常3周龄雌性AKR/J小鼠中,将接受口服紫锥菊制剂的28周龄雌性实验性AKR/J小鼠的胸腺无细胞提取物直接注射到胸腺后,胸腺淋巴瘤的死亡率明显延迟。与未处理的对照组(终龄28周)相比,首次口服紫锥菊制剂后,胸腺中内源性重组鼠白血病病毒(MuLV)的增殖受到明显抑制。口服紫锥菊制剂也有效增强了AKR/J小鼠内源性干扰素(IFN)-γ的产生,然而,其他细胞因子如肿瘤坏死因子(TNF)-α和白细胞介素(IL)-12的产生极少。这些结果表明,紫锥菊制剂对雌性AKR/J小鼠内源性重组MuLV引起的自发性白血病的抑制作用可能取决于其对非特异性免疫或细胞免疫系统(或两者)的增强作用。

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