Evidence map›Paper›PMID 42834214›Full record

ReviewReviews of physiology, biochemistry and pharmacology2027

AA in Brain-Memory, Dementia, Depression, Anxiety, Alzheimer's Disease, Affective and Psychiatric Disorders, and Coronary Heart Disease (CHD).

Undurti N Das

Abstract readReview
PubMed Publisher
In one paragraph

Review in Reviews of physiology, biochemistry and pharmacology, 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Undurti N DasUND Life Sciences, Battle Ground, WA, USA. undurti@lipidworld.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human brain is rich in AA and DHA, which are crucial for normal brain growth and development and memory. They form a major structural component of neurons of the cerebral cortex and photoreceptor cells in the retina. AA and DHA support synaptic plasticity and contribute to efficient neurotransmission. Adequate amounts of AA and DHA support neuronal growth and the formation of new synapses and thus are crucial for memory and cognitive function.Depression, anxiety, schizophrenia, and other neurological diseases occur more frequently in those with coronary heart disease (CHD) and vice versa. Transient depression and anxious mood can trigger acute cardiac events and fatal arrhythmias. Serotonin and catecholamines play a significant role in depression and anxiety and are known to activate platelets, which increases the risk of cardiovascular events. Both serotonin and catecholamines modulate inflammation, while levels of pro-inflammatory cytokines are elevated in anxiety and depression and other psychiatric conditions and CHD. Depression, anxiety, and CHD involve altered essential fatty acid metabolism, particularly of AA and DHA, whose metabolites can inhibit platelet activation, suppress inflammation, and enhance acetylcholine levels. Acetylcholine, in turn, regulates the concentrations of serotonin and catecholamines. Acetylcholine and catecholamines have a modulatory influence on inflammation. Exercise is anti-inflammatory in nature, by virtue of its ability to enhance the formation of anti-inflammatory lipoxin A4, resolvins, protectin, and maresins and suppress pro-inflammatory cytokines IL-6 and TNF-α. AA and DHA enhance acetylcholine release and augment the formation of endothelial nitric oxide (NO). These results imply that anxiety, depression, and CHD are low-grade systemic inflammatory conditions that could benefit from the administration of appropriate amounts of AA and DHA. Risk factors for CHD such as obesity, type 2 diabetes mellitus, dyslipidemia, and atherosclerosis are all considered pro-inflammatory conditions.Since both neuropsychiatric conditions and recovery from CHD need the generation of new neurons and myocardial cells respectively that need to get integrated to the existing cells/tissues, it is proposed that a combination of brain-derived neurotrophic factor (BDNF) (that is needed for neuronal cells to survive), growth hormone (GH) (needed for growth of the newly generated neurons and myocardial cells), resolvins/lipoxins/protectins/maresins (needed to suppress inflammation and enhance wound healing), retinoic acid (needed for vertebrate development), and 1,4-DPCA that inhibits the excessive deposition of collagen and an inducer of formation of new blood vessels (angiogenesis) may be of significant benefit both in the prevention and management of neuropsychiatric conditions and CHD and their associated conditions such as obesity, diabetes mellitus, dyslipidemia, and atherosclerosis.

Indexed as

BrainCoronary DiseaseMemoryMental DisordersAlzheimer DiseaseAnimalsAnxietyDementiaDepressionHumansAnxietyCoronary heart diseaseDepressionNeuropsychiatric conditionsSchizophrenia

Identifiers

PMID42834214

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.