食入细孢Ceraceomyces tessulatus菌株BDM-X(琼脂)对小鼠非酒精性脂肪性肝炎的保护作用。

Hiroshi Suzuki, Kenichi Watanabe, Somasundaram Arumugam, Manoj Limbraj Yellurkar, Remya Sreedhar, Rejina Afrin, Hirohito Sone
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引用次数: 0

摘要

在发达国家,非酒精性脂肪性肝炎(NASH)正成为肝细胞癌(HCC)最常见的病因。氧化应激在脂肪变性引起的NASH的发病机制中起着重要作用;因此,新的治疗方法可能包括天然抗氧化剂。苔状Ceraceomyces tessulatus菌株担子菌-X(BDM-X)是一种新型食用菌,具有较强的抗氧化活性。本研究旨在研究C.tessulatus BDM-X在新型NASH-HCC小鼠模型中的肝脏保护作用。为了制备该动物模型,将2天大的C57BL/6J雄性幼崽暴露于低剂量链脲佐菌素(STZ);在4周龄时,他们被随机分为两组。NASH组(NASH)在14周大之前接受高脂肪饮食(HFD32);C.tessulatus BDM-X组(BDM-X)接受HFD32至10周龄,随后接受HFD32+20%BDM-X(饮食中每重量的重量百分比)至14周龄。未经STZ处理并喂食正常饮食的小鼠作为对照组。我们发现C.tessulatus BDM-X改善了NASH小鼠的血清转氨酶水平以及组织病理学特征,如脂肪变性、炎症灶和细胞周围纤维化。在NASH小鼠中,甾醇调节元件结合蛋白异构体SREBP-1和过氧化物酶体增殖物激活受体PPARα的肝脏蛋白表达显著增加。C.tessulatus BDM-X处理使两种蛋白质的表达正常化。我们的数据表明,C.tessulatus BDM-X可能保护NASH-HCC小鼠的肝脏免受脂肪生成的影响。
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Meal Ingestion of Ceraceomyces tessulatus Strain BDM-X (Agaricomycetes) Protects against Nonalcoholic Steatohepatitis in Mice.

Nonalcoholic steatohepatitis (NASH) is becoming the most common cause of hepatocellular carcinoma (HCC) in developed countries. Oxidative stress plays a major role in the pathogenesis of NASH due to steatosis; hence, novel therapeutic approaches might include natural antioxidants. Ceraceomyces tessulatus strain Basidiomycetes-X (BDM-X), a novel edible mushroom, possesses potent antioxidant activity. This study aimed to investigate the hepato-protective effect of C. tessulatus BDM-X in a novel NASH-HCC mouse model. To prepare this animal model, 2-day-old C57BL/6J male pups were exposed to low-dose streptozotocin (STZ); at 4 weeks of age, they were randomly divided into two groups. The NASH group (NASH) received a high-fat diet (HFD32) up to 14 weeks of age; the C. tessulatus BDM-X group (BDM-X) received HFD32 up to age 10 weeks, followed by HFD32 + 20% BDM-X (percent weight per weight in the diet) up to age 14 weeks. Mice not treated with STZ and fed a normal diet served as a control group. We found that C. tessulatus BDM-X improved serum aminotransferase levels as well as histopathological features such as steatosis, inflammatory foci, and pericellular fibrosis in NASH mice. Hepatic protein expression of sterol regulatory element binding protein isoform SREBP-1 and peroxisome proliferator-activated receptor PPARα was significantly increased in NASH mice. C. tessulatus BDM-X treatment normalized the expression of both proteins. Our data suggest that C. tessulatus BDM-X may protect the liver against lipogenesis in NASH-HCC mice.

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