Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Mar 12:5:10.
doi: 10.1186/1750-1326-5-10.

Antidepressants are a rational complementary therapy for the treatment of Alzheimer's disease

Affiliations

Antidepressants are a rational complementary therapy for the treatment of Alzheimer's disease

Marwa Aboukhatwa et al. Mol Neurodegener. .

Abstract

There is a high prevalence rate (30-50%) of Alzheimer's disease (AD) and depression comorbidity. Depression can be a risk factor for the development of AD or it can be developed secondary to the neurodegenerative process. There are numerous documented diagnosis and treatment challenges for the patients who suffer comorbidity between these two diseases. Meta analysis studies have provided evidence for the safety and efficacy of antidepressants in treatment of depression in AD patients. Preclinical and clinical studies show the positive role of chronic administration of selective serotonin reuptake inhibitor (SSRI) antidepressants in hindering the progression of the AD and improving patient performance. A number of clinical studies suggest a beneficial role of combinatorial therapies that pair antidepressants with FDA approved AD drugs. Preclinical studies also demonstrate a favorable effect of natural antidepressants for AD patients. Based on the preclinical studies there are a number of plausible antidepressants effects that may modulate the progression of AD. These effects include an increase in neurogenesis, improvement in learning and memory, elevation in the levels of neurotrophic factors and pCREB and a reduction of amyloid peptide burden. Based on this preclinical and clinical evidence, antidepressants represent a rational complimentary strategy for the treatment of AD patients with depression comorbidity.

PubMed Disclaimer

Figures

Figure 1
Figure 1
A: Represents examples of non-selective monoamine reuptake inhibitor (NSRI) antidepressants. B: Represents examples of selective nor epinephrine reuptake inhibitor (SNRI) antidepressants. C: Represents examples of selective serotonin reuptake inhibitor (SSRI) antidepressants. D: Represents examples of Monoamine oxidase inhibitor (MAOI) antidepressants. E: Represents examples of atypical antidepressants. All the structures are downloaded from PubChem Substance http://pubchem.ncbi.nlm.nih.gov/.
Figure 2
Figure 2
Summary of different actions of antidepressants that can modulate the pathological features of Alzheimer's disease.

Similar articles

Cited by

References

    1. Berton O, Nestler EJ. New approaches to antidepressant drug discovery: beyond monoamines. Nature reviews. Neuroscience. 2006;7(2):137–151. doi: 10.1038/nrn1846. - DOI - PubMed
    1. Thase ME, Nierenberg AA, Keller MB, Panagides J. Group RPS. Efficacy of mirtazapine for prevention of depressive relapse: a placebo-controlled double-blind trial of recently remitted high-risk patients. The Journal of clinical psychiatry. 2001;62(10):782–788. - PubMed
    1. Thompson C. Onset of action of antidepressants: results of different analyses. Human psychopharmacology. 2002;17(Suppl 1):S27–32. doi: 10.1002/hup.386. - DOI - PubMed
    1. Pacher P, Kecskemeti V. Trends in the development of new antidepressants. Is there a light at the end of the tunnel? Current medicinal chemistry. 2004;11(7):925–943. doi: 10.2174/0929867043455594. - DOI - PMC - PubMed
    1. Glassman AH. Cardiovascular effects of tricyclic antidepressants. Annual Review of Medicine. 1984;35:503–511. doi: 10.1146/annurev.me.35.020184.002443. - DOI - PubMed

LinkOut - more resources