Ya.Z. Grinberg. EFFECTIVENESS OF SCENAR THERAPY. PHYSIOLOGICAL ASPECTS
This article [1,2] discusses the peculiarities of SCENAR therapy
(SCENAR action) which sets it apart from other methods of electro-therapy.
The main area of focus was the difference between the SCENAR
signal and signals normally used in electro-therapy.
Therapeutic mechanisms have in general been observed in the
light of what is known in physiotherapy [3,4]. It has been found that due
to the fact that SCENAR action activates tissues in the somatic or autonomic
nervous system, it is possible to achieve a considerable therapeutic effect
compared with other methods of electro-therapy.
So how and by which physiological mechanisms is that effect
achieved? This paper aims to provide an answer to this question on the basis
of modern ideas about the functions, structure and chemical reactions involved
in providing the passage of excitation withinthe nervous system.
First, however, let us recall:
The peculiarities of SCENAR action [1,2]
1.High amplitude and, at the same time, non-damaging (short) action. [1,2]
2.Absence (or almost complete absence)of adaptation process. Due to biofeedback,
each new impulse differs from the previous one.
3.Neutralisation of the possible effect of accommodation (powerful first
peak of the action signal).
The methodological peculiarities in SCENAR therapy
1.Moving the device over the skin surface at the time of action.
2.Activation of numerous areas connected to the mass of nerve endings.
3.Choice of special zones (of small asymmetry, etc.)
SCENAR action applies electrical current on the skin surface.
The degree of excitation of the nerve tissue depends on the type of nerve fibres
that it consists of. According to classification by Gasser and Erlanger, there
are various types of nerve conductors [3] which differ by their diameters, speed
of action and presence of myelin cover. These are:
- Fibres of type A: A alpha (15-20;
90-120); A beta (10-15; 50-100); A gamma (5-10 ; 5-30); A sigma
(1-10; 5-30);
- Fibres of type B: (1-3; 3-15); and
- Fibres of type C: (0,5-1; 0,6-20).
The figures in brackets indicate the diameter is in mkm and
the speed of passage of an impulse in M/c. Of the fibres listed, type C are
non-myelinated.
It is known that C-fibres have a
high threshold of excitement. There is an existing rule (for the fibre), according
to which the value of the threshold of electrical excitation is in inverse proportion
to the diameter of the fibre. [6]
The force of currentrequired
to activate C-fibres should therefore be 15-40 times higher than for A alpha-fibres.
However, it should be noted that during the action, current from the electrode
flows through the tissues . The current should beproportional
to the volume of the conductor (all other conditions being equal) and at set
length to the square of the conductor. Thus, the force of current in
C-fibres should be 225-1600 times less than in A-fibres.Correspondingly,
the force of current necessary to excite C-fibres should be at a level equal
to the critical membranous potential, so as to keep the corresponding proportion:
- in this instance at most 16OO times higher. (A-fibres have a diameter of
equal to 20 mkm; that of C-fibres is 0.5 mkm).
It should be recalled here that the SCENAR generates
a high amplitude current impulse. Accordingly, the potential for exciting thin
fibres, including C-fibres, is considerably higher than with other methods of
electro-therapy.
Quantity correlation between the fibres mentioned is also essential.
To give a few examples [7,8]:
The cranial cervical sympathetic node has been the subject
of considerable study. The following shows numbers of nerve cells found :
- in rats : 42,OOO
- in guinea-pigs: 16,OOO
- in cats : 1OO,OOO
- in man : 911,OOO nerve cells
Of all the types of fibres, 80% relate to sensory fibres, particularly
in cats. 20% of fibres are myelinated and the rest – i.e. C-type fibres – are
thin, non-myelinated, with a diameter of 1-2 mkm.
In the study of celiac nerves in cats, it was established that
out of approximately 13,500 fibres, nearly ll,000 were non-myelinated. The
presence of B-afferents was discovered which were small in diameter and had
a correspondingly high threshold of excitement. B-fibres and also pelvic nerves
were discovered in the parasympathetic vagus.The quantity of C-fibres
in these nerve tracts was, 90% and 50% respectively. Hence thin, non-myelinated
or weakly-myelinated fibres make up the biggest part of the main nerve tracts.
Let us take a further look at the modern concept of chemical
passage. The basis for this was established at the beginning of the 20th
century. It was demonstrated that the passage of the signal in the neuro-effector
connections was due to the release of acetylcholine or adrenaline in the nerve
endings. Up to the l950’s, two groups of chemical compounds were known as neuromediators
(NM), namely:
-amines : acetylcholine (AC), noradrenaline (NA), adrenaline, dopamine,
serotonin; and
-amino acids : glicin, glutamin, asparginate acid and gamma-aminobutyric
acid.
A third group of neuromediators (purine/neucleitides) was discovered
in the l960’s.
In the mid-l950’s, it was suggested that a peptide – compound
P (CP) - had a role of neuromediator. Since then, neuropeptides (NP) have been
established as the most numerous group of neuromediators. The co-existence of
the representatives of various groups of compounds was traced in the same neurones
of the central and peripheral nervous systems [9] i.e. - a few classical NM,
classical NM + NP. Purines were subsequently added to this combination.
In the context of the subject under discussion, we above all
are interested in the properties that can influence the therapy. The bioactive
properties of the classical NM are widely known [3,6]. We will therefore focus
to the properties of NP.
Table 1 [9,10] sets out the most general characteristics of
the bioactivity of neuropeptides.
The following are the abbreviations used for neuropeptides
(NP) :
CCK – choliecystokinin;
VIP – vasoactive intestinal peptide;
ACTH – adrenal-corticotrophin;
CGRP – Ca-gene relative peptide.
Analysis of the table shows that each of the NP represented
(or group of NP) does not completely match the bioactivities listed but has
a clearly expressed specific property or complex of properties. Some physiological
functions are under control of not only one but a whole range of NP, where each
NP has evolved into a “package of programmes” for triggering or modulating a
certain set of functions. NP, together with the other humor regulators, form
a functional continuity (or continuum) assuring compatibility of biological
activities.
Table
2 sets out a list of given functions on which neuropeptides have their main
influence. At this point, it makes sense to move from the notion of NP to the
notion of regulative peptide (RP), which is used as a synonym when referring
to given properties of NP. The concept of RP [9] is slightly wider, as a whole
range of RP is produced by neurones. Persistence in the search for peptide-producing
neurones (previously considered to be non-neurones) has in many cases been rewarded
with success. The next important peculiarity of NP is its long life span in
the liquids of the organism. If the average duration of the effective concentration
of AC is split seconds (l0-2), for catecholamines, serotonin, histamine
and GABA from 10-1
to 5 seconds, then for small peptides it will be tens of minutes and, for medium
and large peptides, tens of hours.
Another peculiarity of the NP which differentiates it from regular
NM is the fact that its breakdown is not just a simple act of decomposition
of the regulator but the creation, or synthesis, of a new bioactive compound.
The end activity of the chemical compounds resulting from the cascade reaction
breakown of the original NP, differs from the activity of the starting NP and
this is a valuable difference: the formation of complex chains and cascades
is taking place. Each of the peptides studied demonstrated the ability to induce
certain other NP to appear in the blood and interstitial liquor of the organism.
Each of the peptides mentioned, in turn, is capable of the same inducing effect.
The long-lasting effects of NP with a short life-span may be explained by the
existence of such regulative chains.
It seems logical, therefore, that the likelihood of chains
and cascades appearing essentially increases if the dosage of NP exceeds a certain
threshold, i.e. when the effective dose of NP is being released.
Distant effect is a logical continuation of the aforementioned
peculiarities (formation and duration of the complex chains and cascades).
NP come from the synapse area and act on the less remote receptors. The majority
of NP is recognized as regulators, transferred by blood and/or CSLiquid in any
area of the organism. For some distantly-acting NP, special carrier-proteins
are described, which stabilise them in the process of transportation. With
distant action of NP, the ability of the NP to induce the release of other NP
is an important property.
The next important property of NP, which differentiates them
from regular NP, is connected to their high numbers and therefore to the possibility
of many new functional combinations in the synapse and intersynapsis interactions.
Finally, it should be noted that exhaustive study of each NP
always leads to the discovery of its action on the genome activity. The triggering
or increase of the activity of given genes under the influence of NM, especially
RP, is an typical process. The process can even be caused by the mediators,
whose action is so short and seems to be focused on quick synaptic reactions.
To sum up. There are biologically-active compounds
in the organism consisting basically of RP. Together with other humor regulators,
they ensure compatible biological activity. RP are characterised by their ability
to create complex regulative chains and cascades, their long life-span, their
distant effect and action on the genome activity.
The last question to be cleared up is related to the localisation
of NP. The short answer to this question is: NP are present in all parts of
the central and peripheral nervous system, somatic and autonomic. (Refer to
the list of various NP that co-exist with each other [9]) cerebral pons, cerebrum,
cortex of hemispheres, striatum, cerebro-spinal ganglions, parasympathetic neurones,
sympathetic neurones, enthral ganglions, spinal cord, peripheral vegetative
nerves, retina cells, preganglion sympathetic nerves, hypocampus formation,
medullar of the adrenal glands, hypothalamus hypocampus, cerebral trunk, olivo-cochlear
neurones, suture nucleus, blue macular, primal afferent neurones.)
Let us examine the modern idea
of chemical reactions involved in the passage of excitation in the peripheral
autonomic reflex [7] .The main mediator in the pre-ganglion sympathetic
and parasympathetic structures is AC. In the post-ganglion, AC prevails in
the parasympathetic structures and NA in the sympathetic. In the post-ganglion
sympathetic pathways, together with adrenergic cells, there is a certain
quantity of cells which are choilinergic. Classical mediators, as mentioned
earlier, exist in combination with various peptides. These are: vasopressin
(VP), CHRP, Bom/HRP, VIP, SOM, pancreatic peptide (PP), RFLH, NT, neurotensin
A (AT), galonino-like peptide (GAL), petid-gystidin-siolicin (PGI), gastroliberin
(GLB), ENK, CCK, NPU and others.
It is always a surprise to researchers
studying the distribution of visceral fibres innervating the internal organs
(vagus, celiac, pelvic nerves) to find that there is a prevalence of sensory
fibres over motor fibres [8]. In the vagus nerve, the ratio is 9:1; in the
celiac nerve – 3:1 and in the pelvic nerve – 1:1. The efferent sensory fibres
transfer information about the condition of an object and create their own local
control for the object. In response to adequate stimulation or irritation by
electrical current, bioactive compounds are released (mainly RP) which act specifically
on the surrounding tissue and beyond, as follows from the above. The process
of effective regulation by sensory endings is seen especially clearly in regulation
of the immune process, the inflammatory trophic process, healing of wounds [7]
and in regulation of the gastro-intestinal mechanism, where ulcer formation
is prevented [8].
Traditionally, neurosecrete cells
were studied mainly through the hypothalamo-hypofisis-adrenal connections.
Today, it is clear that large quantities of neuosecrete cells are spread around
the various parts of the nervous system and their activity is closely connected
to the production of the peptide regulators.
Based on these explanations, let
us look at some postulates and reports received on the practical effects of
SCENAR therapy.
SCENAR
treats everything. (Ref also “The Principle
of Universality “ [4]).
This statement very often makes medical
doctors and scientists wary when first faced with the device and treatment method.
Results from SCENAR therapists (at present the device is being used by medical
doctors in over 30 specialities), publications of compilations of SCENAR therapy,
multiple trials, including trials at five departments of I.M.Sechenev MMA (ref.
Supplement to the second compilation) have, to a considerable degree, served
to reassure them.
The main
modality of SCENAR therapy. This phenomenon is explained as follows:
Due to the peculiarity of its action,
SCENAR activates thin peptide-containing fibres to a higher degree than other
methods of influence. This enables the effective dosage of RP to be created
and, consequently, RP with other humoral factors which are also subjected to
the essential influence of RP, thus creating a regulator continuum - i.e. a
full set of biological activities which are capable of managing practically
any disease.
There are numerous publications describing
the influence of RP on regulation of vessel tone [7], heart rhythm [11], respiratory
system [13], degree of epileptic activity [14], integrative brain action [15]
and pain mechanism [16] (see below).
SCENAR
– regulator. This statement is repeatedly corroborated by practice. Regardless
of the direction of the disease (a characteristic example: hypertonia – hypotonia),
the same zones of action are used for the therapy. This is natural, as SCENAR
only activates the release of regulative peptides stored in the body and which,
as a result of genetic programming , substantiates
the therapy. In common electrotherapy this, as a rule, cannot be achieved
due to limitations connected to its peculiarity [1] and also bearing in mind
the main functions of the afferent fibres of the A-type which are involved in
high-speed transference of chemical supply. NP are not suited as chemical mediators
to the process of transferring the impulse to A-type fibres endings [8]. Therefore,
when they are activated - which is a characteristic of the common methods of
electrotherapy - the likelihood of peptic chains and cascades appearing is small,
compared to SCENAR therapy.
Treatment
of children is better. Practice has time and again corroborated this statement. It is relatively
simple to explain in the light of the above. Myelinisation of fibres is complete
by the age of 11/2 – 2 years. The quantity of endocrine
cells in the foetus and neonate is considerably higher than in adults.
Here, I would like to mention the
successful experience of SCENAR use in the treatment of respiratory asphyxia
in neonates, practically with a single touch of the device. This took place
at the 2nd City Hospital in Tanganrog. It is known that more than
10 RP synthesize in the neuroendrocrine cells of the lungs [12].
False,
true SCENAR complications. It is characteristic
that, following treatment of osteochondrosis, for example, women unexpectedly
become pregnant. There have been numerous positive results in the treatment
of infertility. The explanation for this effect is obvious, as 30 NM take part
in the functioning of the reproductive system [13]. They also provide a chemical
structure for an autonomic reflex [7]. Here, I should also make a reference
to the effect of the distant properties of RP.
Absence
of contra-indications. This statement claims
that SCENAR therapy is different from other methods of electrotherapy [1] which,
to a great extent, can be ascertained from the reaction of the organism to the
introduction of RP.
It is known that the pharmacological
(physiological) effect depends on the functional status of the system being
tested. When introducing moderate dosages of RP into a “normally”-functioning
organism, i.e. in equally balanced relations, the exogenous factor will be subject
to intensive influence and these peptides will be destroyed, in order to conserve
homeostasis. In pathological conditions, the opposite is true: balanced relations
between chemical and physiological systems, cells, tissues and the organism
are disrupted. The links which are susceptible to the corrective action of
the regulator, are revealed.
Pain-killing
effect. The success of SCENAR action in
analgesia is well known (ref. [18]). According to the existing concept [16],
regulation of pain sensation in the organism is based on the mechanism of interaction
between nociceptive and anti-nociceptive endogenous systems. They form a functionalvariable pain threshold. Both these systems have a
multiple chemically- heterogeneous make-up, and both have in their basis neuro-chemical
reactions. Some of the reactions are called peptide-ergic reactions. Besides
opioid peptides, there is: neurotensin, AT-2, CHRP, SP, BOM, SOM, CCK and others
involved in the mechanism regulating pain sensation. Peptic mechanisms possess
a certain selectivity, confirmed by the activity of extremely small dosages
of certain peptides. The pain sensitivity mechanisms occur through interaction
of the functions of various peptides. As mentioned earlier, it is clear to
see how complicated it is to develop medical drugs for anaesthesia. The optimal
solution can only provided by the organism itself, which only needs a little
help.
The experience acquired from the
application of SCENAR therapy shows that this treatment tackles all three tasks
involved in combating pain:
- anaesthesia without a change in
the general pain sensation;
- therapy; and
- reduction in intake of narcotic
drugs (refusal of these).
Participation of the peptic mechanisms
in this process confirms, from the effect of the increase of pain (aggravation),
the obvious improvement of the functional condition (via aggravation to recovery).
A patient expresses anxiety and the SCENAR therapist endeavours to persuade
him/her to hang on. This effect promotes essential progress in the distribution
of RP. The restoration of the function occurs against a background of change
in the RP which are responsible for anaesthesia, which consequently leads to
an increase in pain sensitivity.
When treating
one disease – cures another as well. This is a phenomenon familiar to all SCENAR therapists and is easily
explained as follows: a regular continuum of biological activity and distant
effect of RP. Positive results achieved after a single SCENAR session [17]
are connected to the long duration of RP and their ability to form new biological
compounds on decomposition.
Quick effect,
acceleration of recovery. (Ref. Reply from
I.M.Sechenev MMA, compilation 2). Fast action of RP (different from that of
steroid hormones) is due to activation of earlier synthesised ferments and proteins
[15]. This property is used in certain peptic drugs for the correction of functions
in extreme conditions.
Let us list briefly some of the SCENAR
“fairy tales”:
- Restoration of the reproductive
function;
- Treatment of a brain tumour by
action on the appendages (uterine or epididymis): distant property of RP;
- Treatment of ileus.
Essential influence of CCK, BOM, VIP on the secretion of the grastro-intestinal
tract (ref. [19] in this compilation);
- Emergency effects (ref above: fast
effects);
- Reversal of Growth retardation. CCK stimulates excretion
of the growth hormone;
- Reversal ofMental development retardation. Essential stimulation
of VAZ, ACTH and alphamelanotropin on ability to study and memory;
- Correction of disturbance in motor activity and tactile
sensitivity. Effective application of the device in this case follows from
analysis of the table.
- There are positive cases of treatment
of epilepsy. It is know that black substance, neuromediators and peptidergic
systems of the brain halt epileptic activity [14].
In conclusion,
let us examine to what extent certain SCENAR techniques correspond to what has
been stated.
- Action on the projection of the
lesion of the injury. In this case, distant effects occur more quickly and
a fast therapeutic effect can be expected to take place in practice.
- Action on the three pathways, 6
points, collar zone, projection of the gastro-intestinal tract, active points
and zones activates a great number of nerve cells containing practically the
whole range of RP, leads to the desired effect.
The fact that
SCENAR therapy is based on the mechanisms of peptide activation makes it possible
to look upon the system “organism-device” as a generator of Regulative Peptides.
Reference
1. Grinberg Ya.Z. SCENAR therapy: the effectiveness from the point
of view of methods of electrotherapy. SCENAR therapy and SCENAR expertise.
Compilation of articles, issue 2, p 18-33. Tangarog, 1996.
2, Grinberg Ya.Z. Question of the substantiation of the effectiveness
of SCENAR therapy. SCENAR therapy and SCENAR expertise. Compilation of articles,
issue 3, p.17-23. Tangarog, 1997.
3. Bogolubov V.M., Ponomarento G.N. General physiotherapy. M.;
compilation 1996 – 480 pp.
5. Gorfinkel Yu.V. Theoretical and practical basis for the increase
in effectiveness of SCENAR therapy. SCENAR therapy and SCENAR expertise. Compilation
of articles, issue 2.
6.
Nozdrachev A.D. Physiology of the
nervous system. L.: “Medicine”, 19238, p.296.
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(visceral) reflex. Usp.physiol. science, 1996, v.27, No.2, p.28-60.
8. Nozdrachev A.D. Axon-reflex.
New point of view in the old area.
I.M.Sechenev Physiol.magazine, 1992, v.11, p.135-142.
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passage. Results of science and technique. Ser. “Physiology of humans and animals”,
v.34, 1988, p. 183.
10. Ashmarin
I.P., Obuchova M.F. Content of regulative peptides in the brain cortex and
their central activity. M. “Highest nervous activity”, v.35, No.2, p. 211-221.
11. Osadchyi O.E., Pokrovskyi V.M. Peptidergic mechanism in the
parasympathetic regulation of the cardiac rhythm. UFN, v.24, No.3, 1993, p. 71-85.
12. Belyakov N.A., Solovieva I.E., Meshkova M.E. Regulative
peptides in the lung. UFN,
v.23, No.2, 1992, p.74-87.
13. Babichev V.N. Neuroendocrine regulation of the secretion of gonadotrophins and prolactin
and the role of neuromediators in it. UFN, v.26, No.2, 1995, p.44-59.
14. Shandra A.A., Godlevskyi L.S.,
Tkachenko I.V., Servetskyi K.L. The
role of black substance in mechanisms stopping epileptic activity. UFN,
v.26, No.2, 1996, p.90-102.
15. Malyshenko N.M., Popv N.S. Hormones and neuropeptides in the integrative processes. UFN,
v.21, No.2, 1990, p.94-106.
16. Kaluzhnyi L.P., Heterogeneity of nociceptive and anti-nociceptive
peptic mechanisms and their correlation with the genesis of pain. UFN,
v.21, No.4, p.68-84.
17. Zavitaev
Y.A. SCENAR examples of single SCENAR application. SCENAR therapy and SCENAR
expertise. Compilation of articles, issue 2,c.81-82. Tangarog 1996
19.Lyashedko P.P. Usage of bio-regulative electrostimulation in the treatment
of complications in the gastro-intestinal tract in patients suffering from sever
multiple-injury. SCENAR therapy and SCENAR expertise. Compilation of articles,
issue 4, 1998.
In the table, the following abbreviations are used :
Table to be inserted…
…
CE Complex effect that cannot be generalised or simplistically
explained;
Blank areas indicate the absence
of data [or] absence of interpretation of the results.
(NB Harry: please note that the top line of
the table with all the abbreviations is missing)