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. 2018 May 21;2018:5802634. doi: 10.1155/2018/5802634

Table 2.

The beneficial activities of H. erinaceus mycelium and its active components on age-associated cognitive change and early dementia.

Material studied (dose used) In vivo models Effects Reference
Erinacine A Normal Wistar rats Enhanced NGF and catecholamine secretion in the LC and hippocampus after intragastric dosing erinacine A at 8 mg/kg body weight [18]

Erinacine A-enriched mycelia and erinacine A Ischemic stroke in Sprague-Dawley rats (1) Mycelia at 50 and 300 mg/kg body weight reduced infarcted volume in cortex and subcortex of transient stroke rats
(2) Erinacine A at 1, 5, and 10 mg/kg body weight reduced levels of proinflammatory cytokines such as iNOS, IL-1β, IL-6, and TNF-α in the serum of transient stroke rats
[24]

Erinacine A-enriched mycelia APPswe/PS1dE9 transgenic mice (1) Mycelia at 300 mg/kg body weight reduced amyloid plaque burden in the area including the cerebral cortex and hippocampus
(2) Increased NGF/proNGF ratio and promoted hippocampal neurogenesis
(3) Restored nesting behavior
[43]

Erinacine A
Erinacine S
APPswe/PS1dE9 transgenic mice (1) Both compounds at 30 mg/kg body weight reduced amyloid plaque burden in the cerebral cortex
(2) Increased the level of IDE in the cortex by 130.5 ± 68.9% and 141.1 ± 63.7%, respectively
[20]

Erinacine A-enriched mycelia MPTP-induced neurotoxicity in C57BL/6 mice (1) Treatment at 10.76 and 21.52 mg/day elevated dopamine, NGF, and GSH levels
(2) Reduced motor dysfunction
(3) Reduced dopaminergic neurons apoptosis in the striatum and substantia nigra
[39]

Mycelia ethanolic extract C57BL/6 mice (1) Treatment at 2000 mg/kg body weight blocked the rise in [Ca2+] induced by ATP
(2) Increased the latency in tail-flick and paw-lifting times exposed to a thermal stimulus
[50]

Erinacine A-enriched mycelium Restraint stress induced depression in ICR mice (1) Treatment at 200 and 400 mg/kg body weight increased dopamine and serotonin levels
(2) Increased BDNF, TrκB, and PI3K expressions in the hippocampus
(3) Reduced IL-6 and TNF-α levels
(4) Reduced the immobility time in the tail suspension test and forced swimming test, as well as decreased the number of entries and the time spent in the open arm
[47]