Similar to TrkA receptors, stimulation of TrkB receptors sets in motion many of the pathways responsible for the process of neuroplasticity. Furthermore, erinacine A also interacts with monoamine neurotransmitters, such as norepinephrine which plays a major role in memory consolidation, focus and mood. Taken together, it is clear to see why erinacine A has been held in such high regard, because it has an incredibly comprehensive effect on cognitive function and mood!
While ErinaMAX is currently only standardized for erinacine A, it will also contain other erinacines. We are still working hard on developing reference standards for the other erinacines, and in the future this will allow us to enhance the scope of our analytical chemistry. Having more erinacine reference standards on hand, will also allow us to perfect our extraction methodologies in order to create both full spectrum and targeted lion’s mane mycelium extracts! One of the other erinacines we are very interested in, is erinacine S. This erinacine has a very unique mechanism of action, and affects neuroplasticity via a pathway we had been previously unaware of. Erinacine S leads to the accumulation of two steroid hormones, pregnenolone and progesterone, in neural tissue. These two steroid hormones have a significant effect on neuroplasticity. Thus, by enhancing the levels of pregnenolone and progesterone in neural tissue, erinacine S produces a very unique neuroplasticity enhancing effect. Within the context of the NGF and BDNF modulating effects of erinacine A, it is clear to see why this novel effect of erinacine S is very exciting, lots of possible synergies!
Speaking of synergies, in our opinion one of the most interesting applications of Erinamax is in combination with our lion’s mane fruiting body offerings, especially our more nootropic focused lion’s mane 8:1 extract. This is due to the fact that the bioactives compounds within the lion’s mane fruiting bodies, such as the hericenones, can enhance the effects of NGF. Thus, combining hericenones with erinacine A which boost NGF synthesis, will yield the most comprehensive NGF focused effects.
Besides the cognitive benefits, Erinamax will also provide some very interesting effects for overall nerve health, specifically for nerve pain. Due to the fact that NGF is involved in the regeneration of damaged nerves, boosting NGF synthesis with Erinamax can have a beneficial effect on overall nerve function. This can lead to a pain management effect, especially in those who are experiencing nerve related pain. The pain management effects of Erinamax are likely to be further amplified by one of the other erinacines that should be in Erinamax, erinacine E. Erinacine E is a mild agonist at the kappa opioid receptor, which can produce robust pain management effects. The one downside with kappa opioid agonism, is that at high levels, it can induce a negative mood state. However, during our beta-testing we did not notice a negative mood state. In terms of kappa opioid agonism, Erinamax felt less pronounced than matrine which is a fairly significant kappa opioid agonist. Erinamax likewise also does not have as pronounced of a pain management effect when compared to matrine. However, in combination with its NGF modulating effects, Erinamax does have a very unique pain management effect for nerve related pain!
Subjectively, the effects of Erinamax are very different in comparison to our lion’s mane fruiting body offerings. The fruiting body offerings are more gentle, and take a little bit longer to produce their beneficial effects. With Erinamax, the effects are noticeable much more quickly. For example, on our Erinamax podcast Erika felt the effects of Erinamax kick in after about 30 minutes. On the other hand, she did not feel major acute effects with the lion’s mane 1:1 and 8:1. Within our beta-testing rounds, the acuteness of Erinamax also stood out for various participants. Now that Erinamax has been out for a week, we have also read a few reddit reports indicating rapid acute effects.