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The Effects of Statins on Neurotransmission and Their Neuroprotective Role in Neurological and Psychiatric Disorders.

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TLDR
A review of the literature describing the impacts of statins on dopamine, serotonin, acetylcholine, and glutamate neurotransmission, as well as their neuroprotective role is presented in this paper.
Abstract
Statins are among the most widely used drug classes in the world. Apart from their basic mechanism of action, which is lowering cholesterol levels, many pleiotropic effects have been described so far, such as anti-inflammatory and antiatherosclerotic effects. A growing number of scientific reports have proven that these drugs have a beneficial effect on the functioning of the nervous system. The first reports proving that lipid-lowering therapy can influence the development of neurological and psychiatric diseases appeared in the 1990s. Despite numerous studies about the mechanisms by which statins may affect the functioning of the central nervous system (CNS), there are still no clear data explaining this effect. Most studies have focused on the metabolic effects of this group of drugs, however authors have also described the pleiotropic effects of statins, pointing to their probable impact on the neurotransmitter system and neuroprotective effects. The aim of this paper was to review the literature describing the impacts of statins on dopamine, serotonin, acetylcholine, and glutamate neurotransmission, as well as their neuroprotective role. This paper focuses on the mechanisms by which statins affect neurotransmission, as well as on their impacts on neurological and psychiatric diseases such as Parkinson’s disease (PD), Alzheimer’s disease (AD), vascular dementia (VD), stroke, and depression. The pleiotropic effects of statin usage could potentially open floodgates for research in these treatment domains, catching the attention of researchers and clinicians across the globe.

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Dyslipidemia in age-related macular degeneration

TL;DR: In this paper , the authors highlight the evidence that supports a role for altered lipid metabolism in AMD and provide their perspective regarding the remaining questions that need to be addressed before lipid-based therapies can emerge for specific cohorts of AMD patients.
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Statins in depression: a repurposed medical treatment can provide novel insights in mental health

TL;DR: In this article , a narrative review summarises relevant findings from translational studies implicating many interconnected neurobiological and neuropsychological, cardiovascular, endocrine-metabolic, and immunological mechanisms by which statins could influence mood.
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Atorvastatin ameliorates depressive behaviors via regulation of α7nAChR expression by PI3K/Akt-BDNF pathway in mice.

TL;DR: Wang et al. as mentioned in this paper investigated the effect of AV treatment on depressive behaviors and showed that AV treatment had antidepressant-like effect in physiological conditions and antidepressant effect in depressive state which depended on α7 nicotinic acetylcholine receptor (α7nAChR) expression in the ventral hippocampus (vHPC), but not α4β2 nicotinically acetyl choline receptor expression in vHPC, nor the α7n AChR and α 4β2nAchR expression in dorsal hippocampus (dHPC).
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The effects of statin monotherapy on depressive symptoms: A systematic review and meta-analysis

TL;DR: This paper conducted a literature search of randomised controlled trials using any statin monotherapy versus any control condition for depressive symptoms and concluded that statins may not have intrinsic antidepressant properties, but may be useful for the management of depression in add-on to antidepressants.
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Pathophysiological role of 27-hydroxycholesterol in human diseases

TL;DR: A recent review summarizes the pathophysiological relevance of 27-hydroxycholesterol (27-OHC) in various tissues, with a special discussion on their functions in human diseases as discussed by the authors .
References
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Journal ArticleDOI

Glutamate as a Neurotransmitter in the Brain: Review of Physiology and Pathology

TL;DR: Endogenous glutamate, by activating NMDA, AMPA or mGluR1 receptors, may contribute to the brain damage occurring acutely after status epilepticus, cerebral ischemia or traumatic brain injury, and may also contribute to chronic neurodegeneration in such disorders as amyotrophic lateral sclerosis and Huntington's chorea.
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Decreased prevalence of Alzheimer disease associated with 3-hydroxy-3-methyglutaryl coenzyme A reductase inhibitors.

TL;DR: There is a lower prevalence of diagnosed probable AD in patients taking 2 different 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors-lovastatin and pravastatin, which warrants further study.
Journal ArticleDOI

Central cholinergic systems and cognition

TL;DR: Evidence is presented that the nucleus basalis-neocortical cholinergic system contributes greatly to visual attentional function, but not to mnemonic processes per se, and it is suggested that nucleus basali-amygdala cholinerential projections have a role in the retention of affective conditioning while brainstem cholinery projections to the thalamus and midbrain dopamine neurons affect basic arousal processes.
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NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders

TL;DR: An emerging concept is that activity-dependent, bidirectional regulation of NMDAR trafficking provides a dynamic and potentially powerful mechanism for the regulation of synaptic efficacy and remodelling, which, if dysregulated, can contribute to neuropsychiatric disorders such as cocaine addiction, Alzheimer's disease and schizophrenia.
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How statin drug affects the body?

The paper discusses the pleiotropic effects of statins, including their impact on neurotransmitter systems and neuroprotective effects, but does not provide a specific explanation of how statin drugs affect the body.