» Articles » PMID: 34298984

Norepinephrine May Oppose Other Neuromodulators to Impact Alzheimer's Disease

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2021 Jul 24
PMID 34298984
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

While much of biomedical research since the middle of the twentieth century has focused on molecular pathways inside the cell, there is increasing evidence that extracellular signaling pathways are also critically important in health and disease. The neuromodulators norepinephrine (NE), serotonin (5-hydroxytryptamine, 5HT), dopamine (DA), acetylcholine (ACH), and melatonin (MT) are extracellular signaling molecules that are distributed throughout the brain and modulate many disease processes. The effects of these five neuromodulators on Alzheimer's disease (AD) are briefly examined in this paper, and it is hypothesized that each of the five molecules has a u-shaped (or Janus-faced) dose-response curve, wherein too little or too much signaling is pathological in AD and possibly other diseases. In particular it is suggested that NE is largely functionally opposed to 5HT, ACH, MT, and possibly DA in AD. In this scenario, physiological "balance" between the noradrenergic tone and that of the other three or four modulators is most healthy. If NE is largely functionally opposed to other prominent neuromodulators in AD, this may suggest novel combinations of pharmacological agents to counteract this disease. It is also suggested that the of cases of AD and possibly other diseases involve an excess of noradrenergic tone and a collective deficit of the other four modulators.

Citing Articles

Future Therapeutic Strategies for Alzheimer's Disease: Focus on Behavioral and Psychological Symptoms.

Kwon K, Kim H, Han S, Shin C Int J Mol Sci. 2024; 25(21).

PMID: 39518892 PMC: 11547068. DOI: 10.3390/ijms252111338.


Pathogenesis of (smoking-related) non-communicable diseases-Evidence for a common underlying pathophysiological pattern.

Kopp W Front Physiol. 2023; 13:1037750.

PMID: 36589440 PMC: 9798240. DOI: 10.3389/fphys.2022.1037750.

References
1.
Pepeu G, Giovannini M . The fate of the brain cholinergic neurons in neurodegenerative diseases. Brain Res. 2017; 1670:173-184. DOI: 10.1016/j.brainres.2017.06.023. View

2.
Weinshenker D . Long Road to Ruin: Noradrenergic Dysfunction in Neurodegenerative Disease. Trends Neurosci. 2018; 41(4):211-223. PMC: 5878728. DOI: 10.1016/j.tins.2018.01.010. View

3.
Schultz W, Dickinson A . Neuronal coding of prediction errors. Annu Rev Neurosci. 2000; 23:473-500. DOI: 10.1146/annurev.neuro.23.1.473. View

4.
Kelly J, Dodd J, Dingledine R . Acetylcholine as an excitatory and inhibitory transmitter in the mammalian central nervous system. Prog Brain Res. 1979; 49:253-66. DOI: 10.1016/S0079-6123(08)64638-5. View

5.
Arnsten A . Catecholamine and second messenger influences on prefrontal cortical networks of "representational knowledge": a rational bridge between genetics and the symptoms of mental illness. Cereb Cortex. 2007; 17 Suppl 1:i6-15. DOI: 10.1093/cercor/bhm033. View