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Channelopathies influence on neurotransmitters monitorable by real time in situ voltammetry, a review and research proposal

Francesco Crespi

Biology Department, GSK, Verona, Italy

E-mail : aa

DOI: 10.15761/MCA.1000128

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Introduction

Channels are pores and through them ions flow across the cell membrane and depolarize or hyperpolarize the cell. They open in response to voltage changes or binding of a chemical messenger, such as a neurotransmitter (i.e. ligand-gated ion channels).
Biochemically, channels are specialized membrane macro-molecular protein complexes divided into distinct protein units called sub-units. Each sub-unit has a specific function and is encoded by a different gene. These proteins play heterogeneous physiological roles such as impulse generation and propagation, synaptic transmission and plasticity, hormonal secretion, hearth rhythm, blood pressure regulation, salt-water balance, cell proliferation and survival. Thus, defects in ion channels function may cause diverse and severe diseases collectively known as channelization [1,2]. They include diabetes, migraine, ataxia, epilepsy, autism, intramuscular, psychiatric, degenerative, renal, lung and cardiovascular diseases. The cause of such diseases may be congenital (mutations in the encoding genes) or acquired (ire. originating from autoimmune attacks) [3-5].

In particular, link between altered activity of the serotonin system and migraine, ataxia, epilepsy and autism have been proposed.

Migraine

is a chronic episodic disorder that has been linked to abnormalities in serotonin signaling and abnormal function of a synaptic voltage-gated calcium channel: CACNA1A. More precisely, a low condition of the serotonergic (serotonin, 5-HT) system from the brain-stem raphe nucleus has been implicated in the activation of the trigeminovascular nociceptive pathway [6]. In parallel, it has been reported that the brain-specific P/Q-type Ca2+channel gene CACNA1A acts as a pivotal player in the pathogenesis of migraine [7] and that transgenic expression of human CACNA1A can suppress the lethargic and serotonin-deficient phenotypes of unc-2 mutant animals, therefore proposing that CACNA1A function might affect the levels of serotonin, a neurotransmitter known to be important in migraine [8] and in particular in Familial hemiplegic migraine (FHM). This is the rare Mendelian dominant form of migraine which is more prevalent in mono-zygotic twins than dizygotic ones. Numerous genetic abnormalities, especially in the genes encoding membrane transport proteins, ion pumps and channels such as CACNA1A, ATP1A2, SCN1A are likely to be involved in this migraine type. Motor weakness and/or paralysis are the symptoms of diagnosis [9].

Ataxia

Ataxia is a non-specific clinical condition characterized by dysfunction of the areas of the nervous system that control movement, such as the cerebellum [10].

A possible link between cerebellar ataxia and the metabolism of serotonin has been proposed as anti-ataxic effect of buspirone hydrochloride, a serotoninergic 5-hydroxytryptamine1A (5-HT1A) agonist, in a homogenous group of patients characterized by the same well-defined single condition i.e. cerebellary cortical atrophy has been reported [11]. Accordingly, it has been observed that 5-hydroxytryptophan, serotonin precursor, is more effective than placebo improving neurological symptoms in patients with Friedreich ataxia (FA) [12]. FA is an autosomal recessive genetic illness responsible for progressive damage to the nervous system in the spinal cord, in particular of sensory neurons basal for leading muscle motion of the arms and legs via link with the cerebellum [13].

Epilepsy and Autism

Epilepsy is a crucial medical complication that evolves in subjects with autism [14].

Anomalous cortical development in both autism and forms of epilepsy has been observed. It is known that serotonin plays an essential neurotrophic function during brain development and in both these diseases altered serotonergic functions have been detected [15].

Imaging data and analysis of tissue of epileptic patients, as well as studies in animal models provide evidence that endogenous serotonin (5-HT), the activity of its receptors and pharmaceuticals with serotonin agonist and/or antagonist properties play a significant role in the pathogenesis of epilepsies [16]. On the other hand, a role for altered metabolism of the serotonin precursor, tryptophan, in both epilepsy and autism has been proposed [15].

Psychiatric

Anxiety disorders, depression, eating disorders are psychiatric diseases in which serotonin is directly involved [17].

In particular, the Selective Serotonin Reuptake Inhibitors (SSRIs) have emerged as a major therapeutic advance in psychopharmacology. SSRIs have demonstrated efficacy and tolerability in the treatment of obsessive-compulsive disorder (OCD). They have been found to be effective in the treatment for social anxiety disorder both in reducing total levels of social anxiety and in improving overall clinical condition. Benefits for anorexia nervosa are also observed. SSRIs should also be considered as one of the first-line drugs in the treatment of depression [18].

In addition to the success of pharmacological treatment with SSRIs OCD appeared to be treatable with atypical antipsychotic drugs [19].

Furthermore, the co-existence of serotonergic and dopaminergic dysfunction in the same homogeneous group of drug-naive OCD patients has been monitored [20] therefore proposing complex molecular mechanisms of OCD. This suggests that both the central serotonergic and dopaminergic systems are involved in the pathophysiology of the disorder. Indeed, in randomized, double-blind, controlled trials evaluating the efficacy of the norepinephrine-dopamine reuptake inhibitor (NDRI) bupropion versus SSRIs for treatment of depression in adults it appeared that bupropion and SSRIs have similar effectiveness [21].

Additionally, dopamine is implicated in Parkinson's disease (PD), which is marked by progressive degeneration of midbrain dopaminergic neurons [22,23] and dopamine agonists are being used increasingly as first-line treatment for Parkinson's disease [24].

Various investigations implicate ion channel functions and acetylcholine (Ach) as well as ACh receptors in the development of Alzheimer's disease (AD) [4,25,26].

Finally, functional changes in ion channel activity induced by reactive oxygen species (ROS) and reactive nitrogen species such as nitric oxide (NO) might occur during the aging process [27] and association between rat neutrophil membrane depolarization and NO-dependent free radical generation has been shown [28].

Research proposal

Serotonin, dopamine, Ach, NO are neurotransmitters that can be monitored in vivo in situ and in real time by voltammetry [29-32]. Therefore, it seems possible to propose to couple such electrochemical methodology with the 'classic" in vitro methodologies described in the various references cited above for a parallel analysis of the channelopathies that are involving such neurotransmitters. The “classic” in vitro analyses together with voltammetric in vivo, in situ and in real time studies will probably permit a better understanding of their implication in all these diseases and possibly open up new in view for novel therapeutic approaches.

References

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Editorial Information

Editor-in-Chief

Article Type

Review Article

Publication history

Received: January21, 2018
Accepted: January 25, 2018
Published: January 26, 2018

Copyright

©2018 Crespi F.This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Crespi F (2018) Channelopathies influence on neurotransmittersmonitorable by real time in situ voltammetry, a review andresearch proposal. Med Clin Arch 2: DOI: 10.15761/MCA.1000128

Corresponding author

Francesco Crespi

Biology Department, GSK, Verona, Italy

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