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从樟芝菌丝体中分离得到的糖蛋白安络小皮伞素的肝脏保护生物活性。

Hepatoprotective bioactivity of the glycoprotein, antrodan, isolated from Antrodia cinnamomea mycelia.

作者信息

Ker Yaw-Bee, Peng Chiung-Chi, Chang Wan-Lin, Chyau Charng-Cherng, Peng Robert Y

机构信息

Department of Applied Food Technology, Hungkuang University, Taichung, Taiwan, ROC.

Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan, ROC.

出版信息

PLoS One. 2014 Apr 1;9(4):e93191. doi: 10.1371/journal.pone.0093191. eCollection 2014.

DOI:10.1371/journal.pone.0093191
PMID:24690763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3972158/
Abstract

Antrodan, a protein-bound polysaccharide isolated from Antrodia cinnamomea mycelia, was demonstrated to exhibit significant anti-inflammatory bioactivity in vitro. However, its role in hepatic injury in vivo still remains unclear. We hypothesized that antrodan may have beneficial hepatoprotective effects. To verify this, a lipopolysaccharide (LPS)-Sprague-Dawley rat model was used. Antrodan protected against liver damage by suppressing LPS-stimulated serum glutamine-oxaloacetic transaminase (GOT), glutamic-pyruvic transaminase (GPT), interleukin (IL)-6, hepatic thiobarbituric acid reactive substances (TBARS), nitric oxide (NO), inducible NO synthase (iNOS) and nuclear factor (NF)-κB, and by effectively alleviating the downregulated hepatic superoxide dismutase (SOD), catalase, and glutathione peroxidase (GSH-Px). Hematoxylin-eosin staining revealed that antrodan at a dosage of 40 mg/kg was able to alleviate LPS-induced liver damage to a normal status. In addition, we identified the partial main architectural backbone of antrodan to have a 1 → 3 linear β-glycosidic backbone of mannan linked by β-1 → 3 glucosidic branches. Conclusively, antrodan can potentially ameliorate liver damage in vivo by suppressing oxidative stress induced by LPS.

摘要

安络小皮伞菌多糖(Antrodan)是一种从樟芝菌丝体中分离得到的蛋白结合多糖,已证实在体外具有显著的抗炎生物活性。然而,其在体内肝损伤中的作用仍不清楚。我们推测安络小皮伞菌多糖可能具有有益的肝脏保护作用。为了验证这一点,使用了脂多糖(LPS)-斯普拉格-道利大鼠模型。安络小皮伞菌多糖通过抑制LPS刺激的血清谷草转氨酶(GOT)、谷丙转氨酶(GPT)、白细胞介素(IL)-6、肝硫代巴比妥酸反应性物质(TBARS)、一氧化氮(NO)、诱导型一氧化氮合酶(iNOS)和核因子(NF)-κB,以及有效缓解肝脏中超氧化物歧化酶(SOD)、过氧化氢酶和谷胱甘肽过氧化物酶(GSH-Px)的下调来保护肝脏免受损伤。苏木精-伊红染色显示,40mg/kg剂量的安络小皮伞菌多糖能够将LPS诱导的肝损伤减轻至正常状态。此外,我们确定安络小皮伞菌多糖的部分主要结构骨架具有由β-1→3糖苷分支连接的甘露聚糖1→3线性β-糖苷骨架。总之,安络小皮伞菌多糖可能通过抑制LPS诱导的氧化应激来改善体内肝损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/42f0478a4f9e/pone.0093191.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/b50dcf26af80/pone.0093191.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/58a430851db8/pone.0093191.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/3ffea3092396/pone.0093191.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/da25116bb5bc/pone.0093191.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/42f0478a4f9e/pone.0093191.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/b50dcf26af80/pone.0093191.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/58a430851db8/pone.0093191.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/3ffea3092396/pone.0093191.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/da25116bb5bc/pone.0093191.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3304/3972158/42f0478a4f9e/pone.0093191.g005.jpg

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