What can this tell me about myself?
I've been awake for two days. I can take caffeine and ephedrine no problem; but this causes super insomnia.
500mg Each morning
Posted 13 January 2016 - 08:45 AM
Posted 13 January 2016 - 05:02 PM
Posted 13 January 2016 - 09:28 PM
Posted 17 January 2016 - 06:47 AM
I have not found a dosage that gives me the benefits without the awful insomnia. It sucks. I've tried many of the other forms of ALCAR but insomnia always crops up.
Posted 18 January 2016 - 08:30 PM
Same here. ALCAR has always given me insomnia or shallow sleep. I've never been able to find a way to counteract this so its not worth taking unless I am willing to get the boost in cognitive performance for 1 day at the expense of throwing off my sleep and feeling like crap the next 1-2 days.
Posted 21 January 2016 - 10:52 PM
Strange but I never get insomnia from ALCAR and I didn't know you can get it. 1 gram each morning. Primaforce brand.
Posted 03 June 2016 - 04:17 PM
When I first took ALCAR it was definitely stimulating but now I take 500mg before bed with no problem at all.
Posted 03 June 2016 - 04:24 PM
What benefits do people get from it? I dont want studies. I want anecdotes.
Posted 03 June 2016 - 05:37 PM
more attentive, motivated, in the zone. better retention, improved clarity of thought, and tolerance to stress. an acidic, salty heartburn or backwash (if you consider that a benefit).
btw, 500mg with breakfast is a very small amount. try 250, and hopefully you can adjust and return to 500+
some people are just really sensitive to meds, and get insomnia from everything
Edited by gamesguru, 03 June 2016 - 05:40 PM.
Posted 04 June 2016 - 03:40 AM
Posted 04 June 2016 - 03:45 AM
ALCAR definitely gave me a "sharper" mind, meaning quicker thinking, more clarity of thought, better verbal fluency and alertness. I can usually take small 200mg doses for a few days, but if I continue beyond that the insomnia crops up and my brain won't shut off at night. Sleep becomes very shallow and unrestful.
Posted 04 June 2016 - 07:23 AM
This means you already have high mitochondrial metabolism.Guys if the answer is just lower the dose... I can do that.
I was hoping it would tell me something more about myself and what nootropics i need.
Edited by psychejunkie, 04 June 2016 - 07:29 AM.
Posted 04 June 2016 - 11:43 AM
Posted 04 June 2016 - 11:54 AM
if not on the thyroidism, consider bacopa. it boosts serotonin, which is the precursor to melatonin. also check your dietary melatonin, it wont improve nocturnal synthesis, but daytime levels will increase, and besides its role in sleep regulation, melatonin is very important antioxidant to the mitochondria even during daytime.
also consider ginger, a COX-2 inhibitor, as well as zinc, a cytochrome C oxidase inhibitor
Regulation of mitochondrial respiration and apoptosis through cell signaling: Cytochrome c oxidase and cytochrome c in ischemia/reperfusion injury and inflammation ☆
Maik Hüttemanna, b, , , Stefan Hellingc, Thomas H. Sandersond, f, Christopher Sinklera, Lobelia Samavatia, e, Gargi Mahapatraa, Ashwathy Varughesea, Guorong Lua, Jenney Liua, Rabia Ramzanf, Sebastian Vogtf, Lawrence I. Grossmana, b, Jeffrey W. Doana, Katrin Marcusc, Icksoo Leea (2012)Cytochrome c (Cytc) and cytochrome c oxidase (COX) catalyze the terminal reaction of the mitochondrial electron transport chain (ETC), the reduction of oxygen to water. This irreversible step is highly regulated, as indicated by the presence of tissue-specific and developmentally expressed isoforms, allosteric regulation, and reversible phosphorylations, which are found in both Cytc and COX. The crucial role of the ETC in health and disease is obvious since it, together with ATP synthase, provides the vast majority of cellular energy, which drives all cellular processes. However, under conditions of stress, the ETC generates reactive oxygen species (ROS), which cause cell damage and trigger death processes. We here discuss current knowledge of the regulation of Cytc and COX with a focus on cell signaling pathways, including cAMP/protein kinase A and tyrosine kinase signaling. Based on the crystal structures we highlight all identified phosphorylation sites on Cytc and COX, and we present a new phosphorylation site, Ser126 on COX subunit II. We conclude with a model that links cell signaling with the phosphorylation state of Cytc and COX. This in turn regulates their enzymatic activities, the mitochondrial membrane potential, and the production of ATP and ROS. Our model is discussed through two distinct human pathologies, acute inflammation as seen in sepsis, where phosphorylation leads to strong COX inhibition followed by energy depletion, and ischemia/reperfusion injury, where hyperactive ETC complexes generate pathologically high mitochondrial membrane potentials, leading to excessive ROS production. Although operating at opposite poles of the ETC activity spectrum, both conditions can lead to cell death through energy deprivation or ROS-triggered apoptosis.
Posted 04 June 2016 - 01:59 PM
I'm surprised to read all these stories because I feel nothing from ALCAR at all. I'm using Primaforce brand, pure powder in big 250g jar, doses from 500 to 1500mg. What brands are you using guys? Only one time when I felt a slight boost in energy from it was after a long and hard day when I was very very tired to that level when I started to feel depressed - I dosed 1.5g of ALCAR and my energy was restored.
Posted 05 June 2016 - 12:39 PM
also consider ginger, a COX-2 inhibitor, as well as zinc, a cytochrome C oxidase inhibitor
What form of zinc and at what dose would you suggest for help with mitochondrial function (such as Cytochrome C Oxidase)?
I have been wary of trying anything more than 20mg zinc because I vaguely recall zinc interacts with other nutrients and can cause their depletion.
Thanks for any info.
Posted 05 June 2016 - 04:52 PM
the fast phase requires 10microM, but let's assume even just 1 microM for the slow phase achieves 50-75% inhibition.
( 70kg man ) ( 65.3800 g/mol ) ( 1e-6 mol/kg ) = 0.0045766 g = 4.6mg, so 2microM or 9.2mg so also be easy and safe
i get it through diet, 5-6mg. ive heard zinc orortate is most bioavailable.
The slow phase is characterized by high affinity of the inhibitor for the enzyme: full inhibition can be achieved upon incubation of the solubilized oxidase for 24 h with zinc concentration as low as 2 microM.
Posted 07 June 2016 - 08:46 AM
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