scholarly journals Antitumor, Anti-inflammatory and Antiallergic Effects of Agaricus blazei Mushroom Extract and the Related Medicinal Basidiomycetes Mushrooms, Hericium erinaceus and Grifola frondosa: A Review of Preclinical and Clinical Studies

Nutrients ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1339 ◽  
Author(s):  
Geir Hetland ◽  
Jon-Magnus Tangen ◽  
Faiza Mahmood ◽  
Mohammad Reza Mirlashari ◽  
Lise Sofie Haug Nissen-Meyer ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Gut Microbiota ◽  
Clinical Findings ◽  
Grifola Frondosa ◽  
Special Focus ◽  
Agaricus Blazei ◽  
Antitumor Effects ◽  
Medicinal Mushrooms ◽  
Hericium Erinaceus ◽  
Anti Inflammatory

Since the 1980s, medicinal effects have been documented in scientific studies with the related Basidiomycota mushrooms Agaricus blazei Murill (AbM), Hericium erinaceus (HE) and Grifola frondosa (GF) from Brazilian and Eastern traditional medicine. Special focus has been on their antitumor effects, but the mushrooms’ anti-inflammatory and antiallergic properties have also been investigated. The antitumor mechanisms were either direct tumor attack, e.g., apoptosis and metastatic suppression, or indirect defense, e.g., inhibited tumor neovascularization and T helper cell (Th) 1 immune response. The anti-inflammatory mechanisms were a reduction in proinflammatory cytokines, oxidative stress and changed gut microbiota, and the antiallergic mechanism was amelioration of a skewed Th1/Th2 balance. Since a predominant Th2 milieu is also found in cancer, which quite often is caused by a local chronic inflammation, the three conditions—tumor, inflammation and allergy—seem to be linked. Further mechanisms for HE were increased nerve and beneficial gut microbiota growth, and oxidative stress regulation. The medicinal mushrooms AbM, HE and GF appear to be safe, and can, in fact, increase longevity in animal models, possibly due to reduced tumorigenesis and oxidation. This article reviews preclinical and clinical findings with these mushrooms and the mechanisms behind them.

Gut microbiota metabolite urolithin B attenuates intestinal immunity function through regulation of oxidative stress and inflammatory signaling in aging mice

2021 ◽  
Author(s):  
Peng Chen ◽  
Fuchao Chen ◽  
lei jiexin ◽  
Benhong Zhou
Keyword(s):  
Oxidative Stress ◽  
Gut Microbiota ◽  
Intestinal Immunity ◽  
Inflammatory Signaling ◽  
Anti Inflammatory ◽  
Immunity Function ◽  
Urolithin B

Urolithin B (Uro B), one of the major subcategories of urolithins (microbiota metabolites) found in various tissues after ellagitannin consumption, has been shown to possess antioxidant and anti-inflammatory effects. The...

scholarly journals Cytotoxicity Effect of Agaricus blazei, Grifola frondosa and Hericium erinaceus Used in Traditional Medicine

2014 ◽  
Vol 5 (1) ◽  
pp. 27-30
Author(s):  
N. Nur Shahirah ◽  
M.Y. Farida Zuraina ◽  
R. Nor Fadilah ◽  
C.F. Suziana Zaila ◽  
L. Florinsiah ◽  
...  
Keyword(s):  
Traditional Medicine ◽  
Grifola Frondosa ◽  
Agaricus Blazei ◽  
Hericium Erinaceus

scholarly journals Picroside II Improves Severe Acute Pancreatitis-Induced Intestinal Barrier Injury by Inactivating Oxidative and Inflammatory TLR4-Dependent PI3K/AKT/NF-κB Signaling and Improving Gut Microbiota

2020 ◽  
Vol 2020 ◽  
pp. 1-12 ◽  
Author(s):  
Xuehua Piao ◽  
Baohai Liu ◽  
Xiaodan Sui ◽  
Shuangdi Li ◽  
Wei Niu ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Acute Pancreatitis ◽  
Gut Microbiota ◽  
Severe Acute Pancreatitis ◽  
Rat Model ◽  
Intestinal Barrier ◽  
Oxidative Stress Marker ◽  
Inflammatory Signaling ◽  
Picroside Ii ◽  
Anti Inflammatory

Background. Picroside II exerts anti-inflammatory and antidiarrheal effects for treating the diseases associated with oxidative injury. However, its function on pancreatitis-induced intestinal barrier injury remains unclear. Hypothesis/Purpose. We hypothesized that picroside II will have protective effects against pancreatitis-induced intestinal barrier injury by affecting oxidative and inflammatory signaling (Toll-like receptor 4- (TLR4-) dependent phosphatidylinositol 3-kinase (PI3K), protein kinase B (AKT), and nuclear factor kappa B (NF-κB)). Study Design and Methods. A Sprague-Dawley (SD) rat model with severe acute pancreatitis (SAP) was induced via the injection of sodium taurocholate (4% wt/vol; 1 mL/kg). All rats were divided into 3 groups: sham (CG), SAP-induced intestinal barrier injury (MG), and picroside II (PG) groups. Intestinal barrier injury was assessed by scanning electron microscopy (SEM), hematoxylin and eosin staining, and pathological scores. We measured the levels of pancreatitis biomarkers (amylase and lipase), oxidative and inflammatory signaling (TLR4-dependent PI3K/AKT/NF-κB), oxidative stress marker (superoxidase dismutase (SOD), catalase (CAT), glutathione peroxidases (GPx), and malondialdehyde), and inflammatory markers (tumor necrosis factor α (TNFα), interleukin- (IL-) 1, IL-6, and IL-10) in serum and/or gut tissues. Gut microbiota composition in feces was measured by using 16S rRNA sequencing. Results. SEM showed that intestinal barrier injury was caused with the loss of intestinal villi and mitochondria destruction, and pathological scores were increased in the MG group. The levels of amylase, lipase, malondialdehyde, TNFα, IL-1, IL-6, TLR4, PI3K, AKT, and NF-κB were increased, and the levels of SOD, GPx, CAT, and IL-10 was reduced in the MG group when compared with CG group (P<0.05). Picroside II treatment inhibited the symptoms in the MG group and showed antioxidant and anti-inflammatory activities. The serum levels of picroside II had strong correlation with the levels of inflammatory and oxidative stress biomarkers (P<0.05). Picroside II treatment increased the proportion of Lactobacillus and Prevotella and decreased the proportion of Helicobacter and Escherichia_Shigella in the model. Conclusions. Picroside II improved the SAP-induced intestinal barrier injury in the rat model by inactivating oxidant and inflammatory signaling and improving gut microbiota.

Auxiliary antitumor effects of fungal proteins from Hericium erinaceus by target on the gut microbiota

2020 ◽  
Vol 85 (6) ◽  
pp. 1872-1890
Author(s):  
Dongdong Wang ◽  
Xiangxiang Zhu ◽  
Xiaocui Tang ◽  
Hongye Li ◽  
Xie Yizhen ◽  
...  
Keyword(s):  
Gut Microbiota ◽  
Antitumor Effects ◽  
Hericium Erinaceus

scholarly journals Effects of Rich-Polyphenols Extract of Dendrobium loddigesii on Anti-Diabetic, Anti-Inflammatory, Anti-Oxidant, and Gut Microbiota Modulation in db/db Mice

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3245 ◽  
Author(s):  
Xue-Wen Li ◽  
Hui-Ping Chen ◽  
Ying-Yan He ◽  
Wei-Li Chen ◽  
Jian-Wen Chen ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Gut Microbiota ◽  
Relative Abundance ◽  
High Throughput Sequencing ◽  
Chinese Herb ◽  
Intestinal Flora ◽  
Stress Index ◽  
Rrna Gene ◽  
Tnf Α ◽  
Anti Inflammatory

Dendrobium is a traditional Chinese herb with anti-diabetic effects and has diverse bibenzyls as well as phenanthrenes. Little is known about Dendrobium polyphenols anti-diabetic activities, so, a rich-polyphenols extract of D. loddigesii (DJP) was used for treatment of diabetic db/db mice; the serum biochemical index and tissue appearance were evaluated. In order to gain an insight into the anti-diabetic mechanism, the oxidative stress index, tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and gut microbiota modulation were determined by ELISA, immunohistochemistry or high throughput sequencing 16S rRNA gene. The results revealed that DJP had the effects to decrease the blood glucose, body weight, low density lipoprotein cholesterol (LDL-C) levels and increase insulin (INS) level in the mice. DJP improved the mice fatty liver and diabetic nephropathy. DJP showed the anti-oxidative abilities to reduce the malondialdehyde (MDA) level and increase the contents of superoxide dismutase (SOD), catalase (CAT) as well as glutathione (GSH). DJP exerted the anti-inflammatory effects of decreasing expression of IL-6 and TNF-α. After treatment of DJP, the intestinal flora balance of the mice was ameliorated, increasing Bacteroidetes to Firmicutes ratios as well as the relative abundance of Prevotella/Akkermansia and reducing the relative abundance of S24-7/Rikenella/Escherichia coli. The function’s prediction of gut microbiota indicated that the microbial compositions involved carbohydrate metabolism or lipid metabolism were changed. This study revealed for the first time that DJP improves the mice symptoms of diabetes and complications, which might be due to the effects that DJP induced the decrease of inflammation as well as oxidative stress and improvement of intestinal flora balance.

scholarly journals Antioxidant and Anti-Inflammatory Effects of Crocin Ameliorate Doxorubicin-Induced Nephrotoxicity in Rats

2021 ◽  
Vol 2021 ◽  
pp. 1-12
Author(s):  
Mona A. Hussain ◽  
Noha M. Abogresha ◽  
Ghada AbdelKader ◽  
Ranya Hassan ◽  
Eman Z. Abdelaziz ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Kidney Function ◽  
Underlying Mechanism ◽  
Control Group ◽  
Protective Effects ◽  
Antitumor Effects ◽  
Anthracycline Antibiotics ◽  
Anti Inflammatory ◽  
Doxorubicin Group ◽  
Factor Α

Doxorubicin is a drug that belongs to the anthracycline antibiotics. Nephrotoxicity is one of the serious side effects of doxorubicin treatment. Crocin, which is one of the most bioactive components of saffron, has antioxidant, anti-inflammatory, and antitumor effects. The current study was aimed at investigating the possible protective effects of crocin against doxorubicin-induced nephrotoxicity to elucidate the underlying mechanism of this effect. The study included four groups, six rats in each group: normal control, crocin control, doxorubicin, and crocin/doxorubicin. Doxorubicin and crocin/doxorubicin groups received intraperitoneal injections of doxorubicin (3.5 mg/kg twice weekly for 3 weeks). Rats in the crocin control group and the crocin/doxorubicin group were treated with intraperitoneal injections of crocin (100 mg/kg body weight per day) for 3 weeks. Biomarkers of kidney function and oxidative stress as well as the abundance of mRNA for nuclear factor-κβ and inducible nitric oxide synthase were evaluated. In addition, the abundance of cyclooxygenase 2 and tumor necrosis factor α immunoreactivity was evaluated. Crocin treatment had renoprotective effects manifested by significant improvement in kidney function as well as a reduction in the abundance of biomarkers of oxidative stress markers and inflammatory mediators. In conclusion, crocin has a protective effect against doxorubicin-induced nephrotoxicity in rats by serving as an antioxidant and attenuating the expression of NF-κB, iNOS, COX2, and TNFα.

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