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Today there is still
no scientific answer to why and how epileptic seizures emerge and what
determines the duration between two seizures. This article provides fundamental
answers to these following conditions: 1) Outer etiological factors urge
abnormal genes to produce a macro biophysical physiological distress by
neuronal webs connectivity loop leading to; 2) Physical change in neuronal
membrane in vulnerable ion channels sizes, blocking information flow through of
extra- and intra-cellular liquids of neuronal membrane ceasing to function
leading to; 3) Transform a given membrane into electrostatic templates, on
which the ionic sedimentation rate (ISR) deposit ionic pileup due to
speed-related body's physical ranges (BOR), to shift the membrane electric bio-impedance
level, raising thereby the seizure threshold level leading to; 4) Extra
accumulation of ISR reaching seizure threshold, to begin ionic leaking into
non-specific neuronal routes leading to; 5) Single or combined sensory or motor
arousal of an epileptogenic aura leading to; 6) accelerating ISR phenomenon
with an avalanche-like electric-like discharge, to resemble an extra cranial
ECT-like power source discharging the cortex under decerebration phenomena with
loss of conscious leading to a tonic attack and after partial recovery by motor
cortex to originate clonic attacks leading to; 7) The end of the ictal period
to fall into short-term sleep with lucid post-ictal period thereafter. The
interim periods hold personal predisposition to external stressors and internal
physiological distresses with repeated epileptic cycles.
Keywords: Epileptic seizures, Pre-ictal, Post-ictal, Aura, Bio-impedance
Abbreviations: CES: Cranial Electrical Stimulation; ISR:
Ionic Sedimentation Rate; BOR: Body's Physical Ranges; ECT: Electroshock
Therapy; NEP's: Neuronal Electrical Pathways; THD: Transient Homeostatic
De-regulation
BACKGROUND
Trauma, tumors, degeneration, infection, vascular changes, stress and others may originate a complex of macro biophysical physiological distress leading to a chain reaction of biophysical changes across affected neuronal webs connectivity to profoundly influence upon various cortical neuronal sites functional conditions. Epilepsy as a functional disorder may stay silently for whatever individual period in a pre-ictal state. Many years ago, the author made a pilot project based on three successive hypotheses: a) An electroshock therapy (ECT) and epilepsy share a common denominator. b) An external electrical current source feeds ECT producing an epileptic-like manifestation, and an equipotent electro-epileptogenic source of an inner electrostatic field gradually develop and induce real epileptic seizures and c. electrical bio-impedance level at electrostatic foci region fall beneath healthy and other morbidities measured non-invasively over scalp regions by an electrical bio-impedance analyzer. The latter adopted the International classification of EEG 10 to 20 montage of 24 EEG electrodes providing 276 points of measurements on the scalp with a harmless 5 mA current and of 80 kHz of high with schizophrenia with positive signs, another subgroup of frequency, injected during 10 ms for each pair of electrodes [1-3] The small research sample presented by 16 patients 21 patient with negative signs and the third group of 19 with epilepsy (post psychotic behavior) and a subgroup of 16 healthy volunteers. Together this small sample composed of 74 patients that evidenced the hypotheses, feasibility of the method and safety of the performance. Regretfully, for lack of finances the startup failed to keep on investigations. Research screening on epilepsy [4-6] had not advanced the answers on how and why epileptic seizures automatically run around cycles. The aim of this two-page article is to present an epileptic loop operating in seven successive stages from one post-ictal to the next ictal periods and to raise a highly probability that CES is capable monitoring epilepsy cycles with a portable device to be introduced in nearby future research.
Etiology of epilepsy
Inborn or acquired abnormal genetic mutation under macro
neuro-biophysical physiological deregulated body operational ranges (BOR) rely
on physical velocity law automatically navigating the uncontrollable ionic
sedimentation rate (ISR) to piling-up within the epileptogenic foci to reach
its seizure threshold level. An epileptic-induced neuronal algorithmic loop in
operation empowers pre-and post-ictal intervals. The aim of this short
presentation is to highlight all three stages: the aura, ictal and post-ictal
periods.
Rational for an epileptic-induced neuronal
algorithmic loop in operation
An abnormal neuronal loop must contain in parallel operating an array of
neuronal electrical pathways (NEP's) composing of at least one row of ion
channels physically getting deform under an ongoing exposure to stress-inducing
macro biophysical physiological distress. This abnormal neuronal loop is
presented below.
Abnormal
conditions preceding the aura
The electrical pre-epileptogenic sources
appear in some neuronal ion membrane channels to raise their thresholds above
action potentials, temporarily blocking up the ion channels leading the
formation of ionic templates. A gradual raise in ISR reaches the pre-seizure
level to begin with leaking into non-harmed NEP's conveying sensory information
to an already established non specialized working memory centers to decode a
give sensory informative aura (scent, parastesias, taste, vision, hearing,
emotion or some combinations of them).
Abnormal
conditions for an ictal period
Experience aura accelerates BOR velocity
in a unit of time increasing thereby ISR deposit of ions arising to the
threshold level creating an aura with a farther avalanche-like paroxysmal
kindling. The last in its first phase resolute in tonic seizures and in the
second phase in clonic seizures. Gradually to subside into some somnolence with
a further full clear conscious awakening into a post-ictal state.
CONCLUSION
All stages, pre-ictal, aura, ictal and
post-ictal hold individually defined periods. In order to control epilepsy, the
expert must presently delay and sustain the ISR in a non-piling pattern. Our
previous pilot project showed that our electrical bio-impedance analyzer with
induced safe and noninvasive electrical units to the scalp of a patient's head
of micro-milliamps', high frequency and during 60 ms was able to precisely
dilute in the topographical brain region with the underlying electrostatic
epileptogenic source to prevent and control epileptic seizures. Maybe it is
possible with electrical bio-impedance portable devices to teach patients for
self-control to prove it in the future.
1. Naisberg Y, Avnon M, Weizman A, Cohen A
(1996) Estimating brain homeostatic derangement by bio impedance technology. In
conference Proceedings. The 26th Israeli Conference on Mechanical Engineering.
Technion City: Haifa, pp: 76-86.
2. Naisberg Y (2007) Diagnosis, treatment and
research of mental disorder. USPTO Patent Number: 7239919.
3. Naisberg Y (2009) Diagnosis, treatment and
research of brain disorders. USPTO Patent Number: 7610095.
4. Maguire J, Salpekar JA (2013) Stress,
seizures and hypothalamic-pituitary-adrenal axis targets for the treatment of
epilepsy. Epilepsy Behav 26: 352-362.
5. Heinrichs SC, Seyfried TN (2006) Behavioral
seizure correlates in animal models of epilepsy: A road map for assay
selection, data interpretation and the search for causal mechanisms. Epilepsy
Behav 8: 5-38.
6. Friedman AR, Cacheaux LP, Ivens S, Kaufer D
(2011) Elucidating the complex interactions between stress and epileptogenic
pathways. Cardiovasc Psychiatr Neurol 2011: 461263.
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