I noticed that while taking a lot of nootropics at a time, I would forget the neurotransmitter serotonin. I knew it because I'd want to cry for no reason. Choline uptake, as well as preventing Acetylcholine break down, means less methylation for dopamine and serotonin. Since I always take things for dopamine (ranging from MAOi's to CNS stims), serotonin was neglected completely sometimes.
Bacopa fixed that. I started taking 500mg of Bacopin® powder before bed. It made me much calmer during the day as well as clearer, too. Plus, it increases serotonin creation and transport, which offsets the negative effects of Huperzine A which I take every now and then.
Bacopa Raises Serotonin Levels & Decreases Dopamine Levels (http://www.ncbi.nlm....pubmed/21129470):
There are studies out there that say that Bacopa increases dopamine levels... (http://www.ncbi.nlm....pubmed/17321089) is one, for example, but this is a restorative action against acute stress and chronic unpredictable stress (poore rats...) which would make it an adaptogen. However, I and the study agrees that this is most likely due to anti-oxidant activity, which is an indirect way to raise monoamine levels and only effective under stressful conditions.AIM OF THE STUDY:
To examine the effect of Bacopa monniera leaf ethanolic extract (BMEE) on the serotonergic system of postnatal rats with reference to learning and memory.
MATERIALS AND METHODS:
From postnatal day (PND)-15-29, rats were treated with BMEE (40 mg/kg BW+0.5% gum acacia) by oral gavage. Behavioural tests (Y-maze, hole-board and passive avoidance) were used to evaluate their learning (PND-32-37) and retention of memory (PND-47-53). Effect of BMEE on neurotransmitter system was analyzed by ELISA and semi-quantitative polymerase chain reaction (PCR).
RESULTS:
Oral administration of BMEE improved learning and retention of memory significantly in all behavioural tasks. Following BMEE treatment, the level of serotonin (5-HT) increased while dopamine (DA) decreased significantly. We also found variation in the level of acetylcholine (ACh). However, no significant changes were observed in the level of ACh and glutamate (Glu). The level of 5-HT was significantly elevated up to PND-37 and was then restored to normal level on PND-53. Interestingly, concomitant up-regulation was recorded in the mRNA expression of serotonin synthesizing enzyme tryptophan hydroxylase-2 (TPH2) and serotonin transporter (SERT) on PND-29 and PND-37, which was restored on PND-53.
CONCLUSIONS:
The results suggest that BMEE treatment significantly enhances the learning and retention of memory in postnatal rats possibly through regulating the expression of TPH2, 5-HT metabolism and transport.
This morning I woke up with a lot of energy. I made my supplement cocktail (500mg Tyrosine, 500mg of ALCAR, 1.15mg Methylene Blue, 1g Choline Bitartate, 25mg DMAA, Lemonade Powder) and only finished a quarter of it before I had to stop. I was beginning to get jittery and got some jaw clenching like on Concerta. This is highly unusual. I've had this morning cocktail for a week and nothing more than a raise in heart rate accompanied it.
I had good sleep... really deep sleep. I usually take 150mg Picamilon (which has 300mcg of Huperzine A) and 500mg Bacopin® powder before bed. I don't need either to sleep, but I've found I couldn't take them during the day. Using them, my sleep is fast onset, but I need less of it and usually begin vivid dreaming at around 7 hours into sleep. Last night I didn't take either, and I'm wondering if it's the lack of Bacopa or Picamilon (or combo?) that caused my morning cocktail to kick me in the jaw. I hope it's the Picamilon because I never particularly cared for it, but if it is the Bacopa, I have to find a different antifungal for my tinea versicolor and another way of balancing serotonin.
Anyone have any experience with stopping Bacopa or Picamilon?
Edited by devinthayer, 24 July 2011 - 02:11 PM.