Nootropic
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It has been suggested that Cognitive enhancer be merged into this article. (Discuss) Proposed since February 2010. |
Nootropics (Template:Pron-en), also referred to as smart drugs, memory enhancers, and cognitive enhancers, are drugs, supplements, nutraceuticals, and functional foods that are purported to improve mental functions such as cognition, memory, intelligence, motivation, attention, and concentration.[1][2] The word nootropic was coined in 1972[3][4] by the Romanian Dr. Corneliu E. Giurgea, derived from the Greek words νους nous, or "mind," and τρέπειν trepein meaning "to bend/turn". Nootropics are thought to work by altering the availability of the brain's supply of neurochemicals (neurotransmitters, enzymes, and hormones), by improving the brain's oxygen supply, or by stimulating nerve growth. However the efficacy of nootropic substances, in most cases, has not been conclusively determined. This is complicated by the difficulty of defining and quantifying cognition and intelligence.
Nootropic vs. cognitive enhancer
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A nootropic is a cognitive enhancer that is neuroprotective or extremely nontoxic.
The term cognitive enhancer is not to be confused with the word "nootropic". Nootropics are by definition cognitive enhancers, but a cognitive enhancer is not necessarily a nootropic.
A cognitive enhancer is a substance that enhances concentration and memory. The first synthetic cognition enhancers to see widespread use were the amphetamines. The word "nootropic" has been abused by researchers who wish to promote a certain drug as side-effect free. The word was first coined by Corneliu E. Giurgea in 1972. He stated that nootropic drugs should have the following characteristics:[4]
- They should enhance learning and memory.
- They should enhance the resistance of learned behaviors/memories to conditions which tend to disrupt them (e.g. electroconvulsive shock, hypoxia).
- They should protect the brain against various physical or chemical injuries (e.g. barbiturates, scopalamine).
- They should increase the efficacy of the tonic cortical/subcortical control mechanisms.
- They should lack the usual pharmacology of other psychotropic drugs (e.g. sedation, motor stimulation) and possess very few side effects and extremely low toxicity.
- Note: section 5. of Giurgea's original definition has been gradually dropped[citation needed] by most researchers.
Availability and prevalence
At present, there are several drugs on the market that improve memory, concentration, planning, and reduce impulsive behavior. Many more are in different stages of development.[5] The most commonly used class of drug is stimulants.[6]
These drugs are used primarily to treat people with cognitive difficulties such as Alzheimer's disease, Parkinson's disease, and ADHD. However, more widespread use is being recommended by some researchers.[7] These drugs have a variety of human enhancement applications as well, and are marketed heavily on the internet. Nevertheless, intense marketing may not correlate with efficacy; while scientific studies support some of the claimed benefits, it is worth noting that many of the claims attributed to most nootropics have not been formally tested.
In academia, modafinil has been used to increase productivity, although its long-term effects have not been assessed in healthy individuals.[5] Stimulants such as methylphenidate are being used on college campuses, and by an increasingly younger group.[5] One survey found that 7% of students had used stimulants for a cognitive edge in the past year, and on some campuses the number is as high as 25%.[6]
Hazards
The main concern with pharmaceutical drugs is adverse effects, and these concerns apply to cognitive-enhancing drugs as well. Cognitive enhancers are often taken for the long-term when little data is available.[5]
Dr. Corneliu E. Giurgea originally coined the word nootropics for brain-enhancing drugs with very few side effects. Racetams are sometimes cited as an example of a nootropic with few effects and wide therapeutic window;[8] however, any substance ingested could produce harmful effects. An unapproved drug or dietary supplement does not have to have safety or efficacy approval before being sold.[9] (This mainly applies to the USA, but may not apply in the EU or elsewhere.)
Examples
The term "drug" here is used as a legal designation. Although some of the effects of these substances may be similar to others, only those substances that have shown cognitive effects are included.
Vitamins and Supplements
- B Vitamins - May influence cognitive function through their effect on methylation and homocysteine levels, as excess homocysteine has been associated with cognitive impairment and the B vitamins work to reduce homocysteine.[10] A systematic review of trials found "little evidence of a beneficial impact" from supplements on cognitive function later in life. However, although epidemiological evidence shows an association, two studies did not find B vitamin supplementation improves cognitive function, and another which found an association was criticized.[11] A systematic review of trials found "little evidence of a beneficial impact" from supplements on cognitive function later in life.[12]
- Omega-3 - Linked to the maintenance brain function[citation needed]. A study done in Norway[citation needed], demonstrated a potential link between Omega-3 consumption during pregnancy and child intelligence test scores.[13]
- Caffeine - Shown to increase alertness, performance and in some studies memory.[14] Children and adults who consume low doses of caffeine showed increase alertness, yet a higher dose was needed to improve performance.[15] Caffeine has also been shown to have more of an effect on improving cognitive performance and sustaining attention in older adults[citation needed]. Chronic pretreatment of caffeine in animals has shown to reduce ischaemic brain damage, in addition to reducing the risk of Parkinson’s disease [citation needed].
- Isoflavones - may be related to cognitive function.[16]
Racetams
The word nootropic was coined upon discovery of the effects of piracetam, developed in the 1960s.[17] Although piracetam is the most commonly taken nootropic,[17] there are many relatives in the family that have different potencies and side effects. Other common racetams include pramiracetam, oxiracetam, and aniracetam. There is no generally-accepted mechanism for racetams. In general, they show no affinity for the most important receptors, although modulation of most important central neurotransmitters, including acetylcholine and glutamate, have been reported.[18] Although aniracetam and nebracetam show affinity for muscarinic receptors, only nefiracetam shows it at the nanomolar range. Racetams have been called "pharmacologically safe" drugs.[8]
Other substances sometimes classified as nootropics include hydergine, vinpocetine, bifemelane, huperzine A (cholinergic activator below), and dimethylaminoethanol (DMAE).[8]
Stimulants
Stimulants are often seen as smart drugs, but may be more accurately termed productivity enhancers. Some stimulants can enhance cognition and memory in some people, but cause psychosis in others.[citation needed] They generally have a very substantial side-effect profile and are not considered classical "nootropic" drugs. These typically improve concentration and a few areas of cognitive performance, but only while the drug is still in the blood. Some scientists recommend widespread use of stimulants such as methylphenidate and amphetamines by the general population to increase brain power.[6][19]
- Amphetamines
- Amphetamine (Adderall, Dexedrine) - adrenergic, dopaminergic
- Lisdexamfetamine (Vyvanse) - adrenergic, dopaminergic
(It must be noted, however, that amphetamines have high potential to act as neurotoxins to dopaminergic and serotonergic neurons, particularly after chronic usage.[20] Therefore, their effectiveness as nootropics are highly limited.)
- Adrenergics
- Atomoxetine - Norepinephrine reuptake inhibitor; approved for ADHD
- Reboxetine - Norepinephrine reuptake inhibitor; approved in Europe for clinical depression but may also be used off-label to treat ADHD
- Synephrine (found in Bitter orange) - agonist at α1 adrenergic receptors
- Cholinergics
- Eugeroics ("Wakefulness Enhancers") - unproven primary mechanisms but proven efficacy
- Xanthines - reduces fatigue perception
Dopaminergics
Dopaminergics are substances that affect the neurotransmitter dopamine or the components of the nervous system that use dopamine. Attributable effects of dopamine are enhancement of attention, alertness, and antioxidant activity. Dopamine is the primary activity of stimulants like methylphenidate (Ritalin) or amphetamine. Dopaminergic nootropics include dopamine synthesis precursors, dopamine reuptake inhibitors, monoamine oxidase inhibitors, and other compounds:
- Metabolic precursors - raise levels
- L-Phenylalanine - purported cognitive improvement
- L-Tyrosine (or N-Acetyl-L-Tyrosine, more bioavailable form) - purported cognitive improvement
- L-DOPA (L-3,4-dihydroxyphenylalanine) - precursor to catecholamines (dopamine); neurotoxic effects documented[21][22][23]
- Biopterin - A rare vitamin (coenzyme) that is synthesized in the pineal gland[24] & crucial to the biosynthesis of dopamine
- Pyridoxal-phosphate (or PLP, pyridoxal-5'-phosphate, P5P, active form of Vitamin B6) - plays a role in the conversion of L-DOPA into dopamine (via the enzyme aromatic L-amino acid decarboxylase).
- Reuptake inhibitors - stabilize/improve levels
- Amineptine - mild stimulant
- Methylphenidate - stimulant approved for ADHD; strong DAT inhibiton
- Bupropion - atypical antidepressant; moderate DAT inhibiton
- MAO-B inhibitors - prevent breakdown
- Selegiline - Mild stimulant; irreversible
- Rasagiline - Mild stimulant; irreversible
- Rhodiola Rosea - Adaptogenic herb; reversible[25]
- Dopamine agonists
- Ropinirole - Agonist at D2, D3, and D4 receptors
- Pramipexole - Agonist at D2, D3 and D4 receptors
- Others
- Mucuna pruriens (Velvet Bean) - Natural source for L-DOPA
- Modafinil - purported dopaminergic activity
- Yohimbe - purported dopaminergic activity (possibly though antagonism at Alpha-2 adrenergic receptors)[citation needed]
Memory enhancement
Memory can come from many different processes, but is dependent on the ability to store and recall information.
Cholinergics
Cholinergics are substances that affect the neurotransmitter acetylcholine or the components of the nervous system that use acetylcholine. Acetylcholine is a facilitator of memory formation. Increasing the availability of this neurotransmitter in the brain may improve these functions. Cholinergic nootropics include acetylcholine precursors and cofactors, and acetylcholinesterase inhibitors:
- Precursors
- Choline - precursor of acetylcholine and phosphatidylcholine
- DMAE - precursor of acetylcholine
- Meclofenoxate - probable precursor of acetylcholine, approved for Dementia and Alzheimer's
- Alpha-GPC - thought to be the only cholinergic to deliver choline to the brain across the Blood-brain barrier, it is sold under its chemical name.
- Cofactors
- Acetylcarnitine - amino acid that functions in acetylcholine production by donating the acetyl portion to the acetylcholine molecule
- Vitamin B5 - cofactor in the conversion of choline into acetylcholine
- Acetylcholinesterase inhibitors
- Galantamine
- Lycoris radiata (Red Spider Lily) - natural source for Galantamine
- Huperzine A - also shown to act as an NMDA antagonist & appears to increase nerve growth factor levels in rats.[26]
- Donepezil
- Rosemary
- Sage
- Reuptake inhibitors and enchancers
- Coluracetam - choline uptake enhancer
- Agonists
GABA blockers
The GABAA α5 receptor site has recently displayed memory improvements when inverse agonized.
- α5IA - α5 inverse agonist
- Suritozole - α5 partial inverse agonist
Glutamate activators
The AMPA transmitter and the AMPA receptors are currently being researched, and there are signs that significant memory improvement and possible alertness enhancement may occur when agonized. The drug class for AMPA system modulation is called Ampakines. Although there are many Ampakines currently in-research, those mentioned here are significantly notable, and/or show reasonable signs of coming to market.
Some racetams have shown this activity, such as aniracetam
- CX-717 - Going through FDA approval for memory-impairing illnesses
- IDRA-21 - believed to improve memory by significantly enhancing long-term potentiation but used only in animals - incredibly potent
- LY-503,430 - Being developed for Parkinson's but showing increase in BDNF, specifically in areas of memory and higher cognitive skills
cAMP
Cyclic adenosine monophosphate is a secondary messenger that, if increased, has shown memory improvements. One common method is by decreasing the activity of phosphodiesterase-4, an enzyme that breaks down cAMP. Typical effects include wakefulness and memory enhancement.
- Propentofylline - nonselective phosphodiesterase inhibitor with some neuroenhancement
- Rolipram - PDE4 inhibitor, shows alertness enhancement, long term memory improvement and neuroprotection
- Mesembrine - PDE4-inhibitor with possible serotonergic activity
Other
α2A receptors are concentrated heavily in the prefrontal cortex and the locus coeruleus, with the potential to improve attention abilities via modulating post-synaptic α2A receptors in the prefrontal cortex.[27]
- Guanfacine is an α2A receptor agonist, FDA approved for and frequently used to treat ADHD symptoms.[2][3] Studies have shown guanfacine to strengthen working memory, reduce distractibility, improve response inhibition, increase regional cerebral blood flow, reduce locomotor hyperactivity, and improve attentional control in animal models, as well as enhance memory function in humans.[28]
Serotonergics
Serotonin is a neurotransmitter with various effects on mood and possible effects on neurogenesis. Serotonergics are substances that affect the neurotransmitter serotonin or the components of the nervous system that use serotonin. Serotonergic nootropics include serotonin precursors and cofactors, and serotonin reuptake inhibitors:
- Precursors
- 5-HTP - precursor (intermediate between tryptophan and serotonin)
- Tryptophan - essential amino acid precursor
- Cofactors
- Pyridoxal-phosphate (or PLP, pyridoxal-5'-phosphate, P5P, active form of Vitamin B6) - plays a role in the conversion of 5-HTP into serotonin (via the enzyme aromatic L-amino acid decarboxylase).[29][30]
- Reuptake inhibitors
- SSRIs - Class of antidepressants that increase active serotonin levels by inhibiting its reuptake. Have also been shown to promote Neurogenesis in the hippocampus.
- Sceletium tortuosum - active constituent mesembrine shown to act as a potent SSRI[31] and PDE4 inhibitor
- Hypericum perforatum - inhibits reuptake of serotonin (as well as Norepinephrine, Dopamine, GABA and Glutamate) via activation of TRPC6
- MAO-A inhibitors
- Reuptake enhancers
- Tianeptine - paradoxical antidepressant, improves mood and reduces anxiety
Anti-depression, adaptogenic (antistress), and mood stabilization
Stress, depression, and depressed mood negatively affect cognitive performance.[citation needed] It is reasoned that counteracting and preventing depression and stress may be an effective nootropic strategy.[citation needed] The term adaptogen applies to most herbal anti-stress claims.[citation needed]
The substances below may not have been mentioned earlier on the page:
- Beta blockers - reduce somatic symptoms of anxiety [citation needed]
- Lemon Balm - displays adaptogen properties. Has also shown to possess GABA transaminase inhibitor properties [citation needed]
- Passion Flower - possible MAOI and neurotransmitter reuptake activity [citation needed]
- Rhodiola Rosea - adaptogen; possible MAOI activity [citation needed]
- St John's Wort - herbal SSRI that has been approved (in Europe) to treat mild depression [citation needed]
- Ginseng (including Siberian ginseng) - adaptogenic effects shown [citation needed]
- Sutherlandia frutescens - possible anti-inflammatory reducing pain from those illnesses [citation needed]
- Kava - anxiolytic herb [citation needed]
- Tea - contains many different adaptogens [citation needed]
- Theanine - GABAergic activity producing relaxation, also increases brain serotonin and dopamine levels [citation needed]
- Grape seed extract - has shown some efficacy in reducing bodily stress [citation needed]
- Adafenoxate - possible anxiolytic effect [citation needed]
- Valerian - possible anxiolytic effect through agonism at GABA-A receptors [citation needed]
- Butea frondosa - possible anxiolytic effect[39]
- Gotu Kola - adaptogen and anxiolytic [citation needed]
- Foti - adaptogen; possible MAOI activity [citation needed]
- Berberine - alkaloid, found in various herbs, with antidepressant properties; acts as a sigma receptor agonist; also shown to act as a mild tyrosine hydroxylase inhibitor [citation needed]
Blood flow and metabolic function
Brain function is dependent on many basic processes such as the usage of ATP, removal of waste, and intake of new materials. Improving blood flow or altering these processes can benefit brain function. Vasodilators mentioned are only those which have shown, at minimum, probable mental enhancement.
- Blessed Thistle - increases blood circulation, improving memory.
- Coenzyme q-10 - antioxidant; increases oxygen usage by mitochondria.
- Creatine - protects ATP during transport.
- Lipoic acid - improves oxygen usage and antioxidant recycling, possibly improving memory.
- Pyritinol - Drug. Similar to B vitamin Pyridoxine.
- Picamilon - GABA activity and blood flow improver.
- Ginkgo biloba - vasodilator; it has also been shown to act as a negative allosteric modulator of GABA-A receptors, and as an antagonist at GABAA-rho receptors (formerly known as GABA-C receptors)
- Vinpocetine - increases blood circulation (vasodilator) and metabolism in the brain; also shown to inhibit voltage-sensitive Na+ channels. However, through a similar mechanism to reserpine, Vinpocetine may temporarily deplete the monoamines serotonin, dopamine and norepinephrine by inhibiting VMAT, thus preventing them from reaching the synapse.[40] Vinpocetine may therefore induce or exasperate depressive symptoms as an adverse effect.
Nerve growth stimulation and brain cell protection
Nerves are necessary to the foundation of brain communication and their degeneracy, underperformance, or lacking can have disastrous results on brain functions. Antioxidants may prevent oxidative stress and cell death, therefore exerting a neuroprotective effect.
- Idebenone - antioxidant [citation needed]
- Melatonin - antioxidant [citation needed]
- Glutathione - chief antioxidant [citation needed]
- Acetylcarnitine (Acetyl-L-Carnitine Arginate or Hydrochloride) - neuroprotective [citation needed]
- Inositol - implicated in memory function, deficit linked to some psychiatric illnesses. It has shown to be particularly efficacious in OCD patients
- Anticonvulsants inhibit seizure related brain malfunction if a person has seizures [citation needed]
- Phosphatidylserine - possible membrane stabilizer [citation needed]
- Lion's Mane Mushroom - Stimulated myelination in an in vitro experiment[41] and stimulated nerve growth factor in an in vitro experiment with human astrocytoma cells.[42] Also improved cognitive ability, in a double-blind, parallel-group, placebo-controlled trial.[43]
- SAM-e (S-Adenosyl methionine) - crucial for cellular regeneration (fuels DNA methylation[44]), also involved with the biosynthesis of dopamine & serotonin. [citation needed]
- Acetylcysteine (L-cysteine) - precursor to antioxidant glutathione [citation needed]
- Apoaequorin (Calcium-binding protein) (CaBP) - (Prevagen®) neuroprotective[citation needed]
- Uncaria tomentosa (Cat's Claw) - in an in vitro experiment with rats, Cat's Claw (PTI-00703™), was shown to inhibit the formation of brain beta amyloid deposits[45][46]
- (Dopamine enhancers) - dopamine is an antioxidant and can enhance dendrite extension [citation needed]
Direct hormones
These are hormones that have activity not necessarily attributable to another specific chemical interaction, but have shown effectiveness. Only specific nootropic effects are stated.
- Vasopressin - memory hormone that improves both memory encoding and recall
- Pregnenolone - increases neurogenesis
- Orexin - Significant wakefulness promoter
Secondary enhancers
These are substances which by themselves may not improve brain function, but may have benefits for those lacking them (in the case of hormones) or may alter the balance of neurotransmitters.
- DHEA - Precursor to Estrogen and Testosterone
Unknown enhancement
Other agents purported to have nootropic effects but which do not (yet) have attributable mechanisms or clinically significant effects (but may upon refinement of administration) are mentioned here.
Nootropics with proven or purported benefits:
- Bacopa monniera - shown to possess adaptogenic properties; enhances memory and concentration.[47] Folk use in Ayurvedic medicine purports "enhancement of curiosity".
- Brahmi rasayana - improved learning and memory in mice.[48]
- Fipexide - drug for Dementia
- Gerovital H3 - famous anti-aging mixture, most effects disproven, but some mind enhancement shown
- Sulbutiamine - fat soluble vitamin B1 derivative. When sulbutiamine was administered to mice, they performed better on operant conditioning tests[49] and object recognition tests.[50]
- Royal Jelly - Increases brain cell growth and diversity, only proven in-vitro, improbable in-vivo
- Curcumin - Significant in-vitro activity, but in-vivo activity is limited by low bioavailability
Other nootropics
These substances have been linked to better cognitive function, but may not be the cause. See correlation does not imply causation
- Alcohol - Moderate drinkers tend to have better cognitive function than both abstainers and heavy drinkers.[51][52][53][54][55][56]
See also
Brain and neurology
Areas of potential improvement from nootropic drugs
Health
Cognitive enhancement without drugs or supplements
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External links
- "A Pandora's box full of smart drugs" by Ann Robinson (The Guardian: February 23, 2010)
- Greely H, Sahakian B, Harris J; et al. (2008). "Towards responsible use of cognitive-enhancing drugs by the healthy". Nature. 456 (7223): 702–5. doi:10.1038/456702a. PMID 19060880.
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ignored (help)CS1 maint: multiple names: authors list (link) - "Brain Gain: The underground world of “neuroenhancing” drugs" by Margaret Talbot (The New Yorker: April 27, 2009)
- Business Week Online - "I Can't Remember" September 1, 2003 at Business Week
- List of Nootropic drugs at Erowid