Yamabushitake

Yamabushitake, known as the Lion's Mane Mushroom, is a dietary mushroom that can be supplement. It appears to be a promising cognitive enhancer, and can boost the potency of the immune system and inflammation as well

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Also Known As

Hericium erinaceus, Lion's Mane, Monkey's Head, Houtou (infrequent)


Things to Note

  • As the water soluble extract seems to be less potent than other fractions, it may be best to take Yamabushitake with meals if in supplemental form
  • If itchy skin occurs, this may be related to an increase in Nerve Growth Factor[1] and unless accompanied by signs of allergy should be benign

The only human study currently used a dose of 1g (96%) Yamabushitake extract, three times a day (totaling 3g)

It may be best to take Yamabushitake with meals.


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The Human Effect Matrix looks at human studies (excluding animal/petri-dish studies) to tell you what effect Yamabushitake has in your body, and how strong these effects are.
GradeLevel of Evidence
ARobust research conducted with repeated double blind clinical trials
BMultiple studies where at least two are double-blind and placebo controlled
CSingle double blind study or multiple cohort studies
DUncontrolled or observational studies only
Level of Evidence
EffectChange
Magnitude of Effect Size
Scientific ConsensusComments
CCognition

Minor

An improvement in cognition has been seen in older adults with cognitive decline; no evidence to support usage in youth at this moment in time

CAnxiety

Minor

Decreases in anxiety noted, this may be secondary to menopausal symptom reduction

CDepression

Minor

Decrease in depressive symptoms has been noted, which may be secondary to attenuating menopausal symptoms

CSymptoms of Menopause

Minor

A reduction in menopausal symptoms has been noted with yamabushitake consumption

CSleep Quality

No significant effects on sleep quality


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Table of Contents:


Edit1. Sources and Composition

Yamabushitake is a mushroom that grows on old or dead broadleaf trees, and is consumed in Japan and China without harmful effects.[2]

1.1. Composition

The mushroom Yamabushitake (Hericium erinaceus) contains:

  • Hericenones A and C through H[3][4][5]

  • Erinacines, A through I[6][2]

  • Sialic-acid binding lectin[7]

  • Sterols, such as ergosterol and beta-sitosterol.[8]

  • Polysaccharides, named HEF-P and belonging to the beta-glucan family; which can be broken down into four polysaccharides[9][10][11] The percentage of polysaccharides in the fruiting bodies seems to be around 20%, with 18.59% found with an ethanol extraction.[11][12]

The total phenolic content of Yamabushitake appears to be in the range of 10.20 ± 2.25mg GAE/g[13] with the hot water extract, which appears to be up to 5-fold higher than oven cooked levels () and either methanolic or freeze-dried fruit bodies.[14]


Edit2. Interactions with Neurology

2.1. Neurotrophic Growth Factor (NGF)

Yamabushitake has been shown in vitro to increase the mRNA expression for Nerve-Growth Factor in astrocytes, a neuronal protein important in neurogenesis and cognitive decline, as well as preserving and organizing cholinergic neurons.[2] Secretion of NGF from astrocytes was also increased in vitro with Yamabushitake at 100ug/mL, although benefits were dose dependent (this concentration hit statistical significance).

Isolated hericinones failed to increase NGF, and NGF appeared to be increased through JNK signalling pathways to ultimately phosphorylate c-Fos.[2] The Erinacines or other compounds are thought to be the agent that increases NGF production and secretion in vivo. at 5% of the diet.[2]

Through the above mechanisms, Yamabushitake appears to protect rats against cognitive decline caused by β-amyloid pigmentation at the same 5% of the diet seen previously.[15]

2.2. General Neuroprotection

An analogue of the Hericenones, called 3-hydroxyhericenone, has been implicated in preserving neurons from death induced by endoplasmic reticulum stress.[5] This mechanism of action is also seen with various benzene compounds in Yamabushitake.[16]

It has also been shown, in vitro, to enhance myelination (production of myelin sheath) of neurons, which may be downstream of NGF.[17]

2.3. Cognition

One human study using 3g of 98% Yamabushitake powder (in capsule form) showed significantly improvements on a rating scale of dementia in persons suffering from general cognitive decline.[18] The supplement increased cognition relative to control, and the degree of improvement increased with time; however, 4 weeks after cessation saw the start of a decline back to normal despite still being significantly elevated above control.[18]

Anxiety and Depressive symptoms have also been reduced in humans fed 2g of Yamabushitake, via cookies, over the course of 4 weeks.[19] There was a significant difference between groups on the measurements of concentration and irritability, favoring the Yamabushitake group.[19]


Edit3. Interaction with injury

3.1. Nerve injury

In one study conducted in rats, Yamabushitake water extract was able to promote neuronal regrowth after crushing injury. Rats that had a gluteal nerve damaged (purposefully) during surgery were able to walk better after ingestion of water containing the extract of the fruits.[20] Two doses used in this study were 10 or 20mL per kg bodyweight daily, but the exact mg or mmol dose was not recorded; the two doses, however, did not differ between each other.[20] This was conducted as a follow-up to an in vitro study suggesting neuronal growth from Yamabushitake, which showed no toxic symptoms.[21]

3.2. Topical Injury

Yamabushitake is associated with increasing the rate of repair of flesh wounds when the water extract is applied to the wound.[22]


Edit4. Inflammation

4.1. Anti-inflammatory reactions

Yamabushitake extract appears to have anti-inflammatory properties by reducing the inflammatory response from macrophages induced by LPS.[23] It decreased nuclear translocation of nF-kB and c-Jun N-terminal kinase in a dose dependent manner, with the chloroform fraction being more potent than the ethanol or water fractions.[23]

In a study on rats in which wounds had the water extract of Yamabushitake added to them, healing rate was accelerated and less immune cells were found in the wound.[22]

4.2. Pro-inflammatory reactions

An isolated polysaccharide, HEF-AP Fr II (of the beta-glucan family) has been shown in vitro to enhance a macrophages actions by potentiating the amount of NO release, and TNF-a as well as IL-b release.[11] These studies were done with incubation at 1000ug/mL, and the molecular mass appears to be a mere 13kDa.[11]

Additionally, Yamabushitake extract appears to stimulate production of macrophages and T cells in vitro.[24]

These results suggest that Yamabushitake may stimulate the immune system and modulate the signals sent out by immune cells; however, a lack of studies limit conclusions.


Edit5. Interactions with Cardiovascular Health

5.1. Blood

Hericenone B has been shown to exert anti-platelet actions by inhibiting signalling from collagen through α2/β1 to release arachidonic acid; the mechanism appears to be potent but specific in tested rabbits.[25]

Additionally, Yamabushitake appears to be an ACE inhibitor and may reduce blood pressure. However, it was shown to be less potent than other mushrooms such as Ganoderma Lucidum[13] The IC50 value of this reaction was 0.580+/-0.023.[13]


Edit6. Interactions with Obesity and Fat Metabolism

An upregulation of PPARa mRNA was not noted and its agonism was not noted in vitro, but the downstream protein mRNA such as Acad1, Srebf1, and Slc27a1 (amongst others) were significantly elevated.[26]

Body weight gain was attenuated in the groups fed Yamabushitake at 2g/100g dietary intake, by 30% in the hot water extract group and 42.4% in the ethanolic extract group.[26] With significant differences in hepatic and mesenteric adipose build-up, but not epididymal tissue.[26]

A lowering of Triglyceride levels was also noted, with more benefits seen in the ethanol extract (89.3mg/dl) compared to the hot water extract (112.7mg/dl) at a dose of 2g per 100g dietary intake, with control at 122.5mg/dl.[26] A similar trend was noted in the liver TG stores in regards to the previous study, and another study using an isolated compound (exo-polymer) in Yamabushitake noted drastic lowering LDL by 45.4% and increasing of HDL by 31.1%, in addition to lesser artherogenic markers in rats. These results were dose dependent, with the most drastic seen at 200mg/kg but some improvements seen at 50mg/kg.[27] These drastic reductions in lipoproteins, however, were seen with the mushroom's mycelium and not the fruiting body which many other studies use.[27]


Edit7. Safety and Toxicity

Toxicology studies in rats suggest that doses up to 5g/kg bodyweight are safe in rats when given as MUNOPHIL, which is a combination of Yamabushitake and Panax Ginseng.[28] The percentage of this compound by weight that is Yamabushitake was not listed.

There has been one case study of a 63 year old man who suffered acute respiratory failure, and the excess lymphocytes in his lungs showed high reactivity to Yamabushitake daily for 4 months in dosages commonly bought.[29] The connection between the two, when rated, is seen as a 'probably' connection.[30]

References

  1. Tanaka A, Matsuda H. Expression of nerve growth factor in itchy skins of atopic NC/NgaTnd mice. J Vet Med Sci. (2005)
  2. Mori K, et al. Nerve growth factor-inducing activity of Hericium erinaceus in 1321N1 human astrocytoma cells. Biol Pharm Bull. (2008)
  3. Yaoita Y, Danbara K, Kikuchi M. Two new aromatic compounds from Hericium erinaceum (BULL.: FR.) PERS(1). Chem Pharm Bull (Tokyo). (2005)
  4. Chromans, hericenones F, G and H from the mushroom Hericium erinaceum
  5. Ueda K, et al. An endoplasmic reticulum (ER) stress-suppressive compound and its analogues from the mushroom Hericium erinaceum. Bioorg Med Chem. (2008)
  6. Erinacines E, F, and G, stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum
  7. A sialic acid-binding lectin from the mushroom Hericium erinaceum
  8. Li JL, et al. A comparative study on sterols of ethanol extract and water extract from Hericium erinaceus. Zhongguo Zhong Yao Za Zhi. (2001)
  9. Mizuno T, et al. Antitumor-active polysaccharides isolated from the fruiting body of Hericium erinaceum, an edible and medicinal mushroom called yamabushitake or houtou. Biosci Biotechnol Biochem. (1992)
  10. Xu H, et al. Chemical analysis of Hericium erinaceum polysaccharides and effect of the polysaccharides on derma antioxidant enzymes, MMP-1 and TIMP-1 activities. Int J Biol Macromol. (2010)
  11. Lee JS, et al. Study of macrophage activation and structural characteristics of purified polysaccharides from the fruiting body of Hericium erinaceus. J Microbiol Biotechnol. (2009)
  12. Dong Q, Jia LM, Fang JN. A beta-D-glucan isolated from the fruiting bodies of Hericium erinaceus and its aqueous conformation. Carbohydr Res. (2006)
  13. Abdullah N, et al. Evaluation of Selected Culinary-Medicinal Mushrooms for Antioxidant and ACE Inhibitory Activities. Evid Based Complement Alternat Med. (2012)
  14. Effects of cultivation techniques and processing on antimicrobial and antioxidant activities of Hericium erinaceus ( Bull .: Fr .) Pers . Extracts
  15. Mori K, et al. Effects of Hericium erinaceus on amyloid β(25-35) peptide-induced learning and memory deficits in mice. Biomed Res. (2011)
  16. Ueda K, et al. Endoplasmic reticulum (ER) stress-suppressive compounds from scrap cultivation beds of the mushroom Hericium erinaceum. Biosci Biotechnol Biochem. (2009)
  17. Kolotushkina EV, et al. The influence of Hericium erinaceus extract on myelination process in vitro. Fiziol Zh. (2003)
  18. Mori K, et al. Improving effects of the mushroom Yamabushitake (Hericium erinaceus) on mild cognitive impairment: a double-blind placebo-controlled clinical trial. Phytother Res. (2009)
  19. Nagano M, et al. Reduction of depression and anxiety by 4 weeks Hericium erinaceus intake. Biomed Res. (2010)
  20. Wong KH, et al. Peripheral Nerve Regeneration Following Crush Injury to Rat Peroneal Nerve by Aqueous Extract of Medicinal Mushroom Hericium erinaceus (Bull.: Fr) Pers. (Aphyllophoromycetideae). Evid Based Complement Alternat Med. (2011)
  21. Activity of Aqueous Extracts of Lion's Mane Mushroom Hericium erinaceus (Bull.: Fr.) Pers. (Aphyllophoromycetideae) on the Neural Cell Line NG108-15
  22. Abdulla MA, et al. Potential activity of aqueous extract of culinary-medicinal Lion's Mane mushroom, Hericium erinaceus (Bull.: Fr.) Pers. (Aphyllophoromycetideae) in accelerating wound healing in rats. Int J Med Mushrooms. (2011)
  23. Kim YO, et al. Hericium erinaceus suppresses LPS-induced pro-inflammation gene activation in RAW264.7 macrophages. Immunopharmacol Immunotoxicol. (2011)
  24. Wang JC, et al. Antitumor and immunoenhancing activities of polysaccharide from culture broth of Hericium spp. Kaohsiung J Med Sci. (2001)
  25. Mori K, et al. Inhibitory effect of hericenone B from Hericium erinaceus on collagen-induced platelet aggregation. Phytomedicine. (2010)
  26. Hiwatashi K, et al. Yamabushitake mushroom (Hericium erinaceus) improved lipid metabolism in mice fed a high-fat diet. Biosci Biotechnol Biochem. (2010)
  27. Yang BK, Park JB, Song CH. Hypolipidemic effect of an Exo-biopolymer produced from a submerged mycelial culture of Hericium erinaceus. Biosci Biotechnol Biochem. (2003)
  28. Park ID, et al. Toxicological study on MUNOPHIL, water extract of Panax ginseng and Hericium erinaceum in rats. J Acupunct Meridian Stud. (2008)
  29. Nakatsugawa M, et al. Hericium erinaceum (yamabushitake) extract-induced acute respiratory distress syndrome monitored by serum surfactant proteins. Intern Med. (2003)
  30. A method for estimating the probability of adverse drug reactions

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