WO2017076324A1 - Method and system for overcoming drug addiction by using electromagnetic field to modulate brain excitation region - Google Patents

Abstract

Provided are a method and system for using hypnosis to induce a brain to enter a deep sleep pattern so as to cause the quantity of dopamine receptors (15) of a brain cell to increase rapidly to the level it was at prior to drug addiction (the quantity of normal dopamine receptors (15) of the brain cell) and thereby overcome the drug addiction, comprising using an electromagnetic field (18) to modulate the sleep excitation region (7) of the brain (1), causing the brain (1) to change from an awake pattern to a sleep pattern, and also comprising using or producing the effect of the electromagnetic field (18) on the sleep excitation region (7) of the brain (1), inducing the sleep excitation region (7) to increase excitation and thereby suppress the waking excitation region (4) of the brain (1); thus the inhibitory effect of the waking excitation region (4) of the brain (1) on the thalamic reticular nucleus (41) is suppressed and blocked, inducing the thalamic reticular nucleus (41) to release a sleep hormone to the excitation regions of the whole brain and causing the brain (1) to change from an awake pattern to a sleep pattern; also comprised is monitoring the degree to which the drug addiction flares up so as to control the start of the hypnosis effect, and further comprised is measuring the depth of sleep to automatically start, stop, and restart the hypnosis effect in order to maintain a desired or set depth of sleep during a process of hypnosis to overcome drug addiction.

Description

Method and system for modulating brain excitation zone with electromagnetic field to realize drug addiction

[Technical Field]

The present invention provides a method and system for modulating the sleep excitatory region of the brain with an electromagnetic field to achieve drug addiction by hypnosis.

【Background technique】

Drug addiction is an urgent problem in modern people's lives. At present, the common methods of drug addiction are mainly natural withdrawal, drug withdrawal, and non-drug withdrawal. These three methods have not achieved a good drug addiction effect, and it takes a long time. In the process of drug addiction, it often brings great physical and mental damage to the drug addict.

[Summary of the Invention]

Dopamine is a stimulant of the brain. When the brain is in a normal state, the amount of FosB in the nucleus accumbens is a normal amount. The amount of dopamine sent to the various excitatory regions of the brain through the nucleus accumbens is normal, and the dopamine on each cell in the brain is normal. The number of receiving ports is also normal. When taking drugs, the amount of FosB in the nucleus accumbens greatly exceeds the normal amount. The nucleus accumbens rapidly releases dopamine in a short time and greatly exceeds the normal amount. Dopamine in the brain that receives more than its tolerance will be damaged by excessive excitement. . In this case, each brain cell will reduce its own number of dopamine receptors based on its own protective mechanism (permanently shutting down a certain number of dopamine receptors). When the drug has been used, the cells in the brain are unable to receive a sufficient amount of dopamine due to the reduced amount of dopamine receptors in the normal release of dopamine, and thus cannot be normally excited, resulting in various drug addiction symptoms (including: Pain, trembling, and sweating, etc.) In this case, if the drug is inhaled again, the symptoms of drug addiction will be temporarily relieved, but since the number of dopamine receptors in the brain cells is reduced, the brain cells are excited to inhale more drugs. Inhaling more drugs will further reduce the number of dopamine receptors in the brain cells, and the drug addiction will become more serious. Therefore, from the fundamental point of brain physiology, quit drug addiction is to make each brain cell re-growth according to its original normal amount based on a large number of dopamine receptors that have their own protective mechanism. The necessary conditions for this re-growth, except that no further drug use is allowed, is the condition that each brain cell can re-grow its own dopamine receptor in the original normal amount. At present, the common methods of drug addiction such as natural withdrawal, drug withdrawal, and non-drug withdrawal do not fully provide these necessary conditions, so they can not achieve good drug addiction effects, and take a long time, in the process of drug addiction, It often causes great physical and mental damage to the drug addict.

The present invention provides methods and systems for modulating the sleep excitatory region of the brain with an electromagnetic field to achieve detoxification by hypnosis and controlling continued deep sleep.

In the present invention, drug addiction is achieved by hypnotizing and controlling continuous deep sleep to restore the growth of the dopamine receptor of the brain cells to a normal amount in deep sleep mode. Hypnosis and control continue deep sleep to accelerate the growth of dopamine receptors in brain cells in deep sleep mode, It also relieves the symptoms of drug addiction.

In the present invention, hypnosis is achieved by generating an electromagnetic field, modulating the sleep excitatory region of the brain, enhancing excitement, and allowing the brain to enter a deep sleep mode.

In the present invention, hypnosis and control of continuous deep sleep are achieved by a sleep depth monitor and a hypnotist. Among them, the sleep depth monitor detects the drug addiction attack status of the drug addict and activates the hypnotist to let the drug user's brain enter the deep sleep mode, and detects the depth of sleep to control the hypnotist to maintain the deep sleep mode of the brain, so that the dopamine receptor of the brain cell Accelerated growth in deep sleep mode returns to normal levels to achieve addiction.

[Description of the Drawings]

Figure 1 shows four parts of the brain associated with the present invention: the midbrain ventral tegmental area (VTA), the forebrain medial bundle, the nucleus accumbens, and the dopamine receptor, in which the brain is in a normal state.

Figure 2 shows the four parts of the brain associated with the present invention: the midbrain ventral tegmental area (VTA), the forebrain medial bundle, the nucleus accumbens, the dopamine receptor, and the relationship between the brain in a drug-taking state.

Fig. 3 shows the principle of drug addiction related to the present invention, that is, the relationship between the ventral tegmental area (VTA) of the midbrain, the medial forebrain bundle, the nucleus accumbens, and the dopamine receptor in the detoxification state of the brain.

Figure 4 shows the interrelationship of the brain's four excitatory regions (driving excitatory regions, sleep excitatory regions, thalamus, and awakening excitatory regions) in the awake mode associated with the present invention.

Figure 5 shows the interrelationship of the brain's four excitatory regions (driving excitatory regions, sleep excitatory regions, thalamus, and waking excitatory regions) in deep sleep mode associated with the present invention.

Fig. 6 shows the use of an electromagnetic field in the present invention to modulate the sleep excitatory region of the brain, so that the excitement is increased, so that the brain shifts from the awake mode to the deep sleep mode to achieve drug addiction through hypnosis.

Fig. 7 shows the pulsed electromagnetic field of the present invention modulating the sleep excitatory region of the brain to enhance excitement, so that the brain shifts from the awake mode to the deep sleep mode to achieve drug addiction through hypnosis.

FIG. 8 shows that the electromagnetic field driving power source of the present invention drives an antenna to generate an electromagnetic field to the brain, and by modulating the sleep excitatory region of the brain to enhance the excitement, the brain shifts from the awake mode to the deep sleep mode to realize drug addiction through hypnosis.

Figure 9 shows a hardware addiction instrument hardware system of the present invention.

Figure 10 shows a bedside/pillow addiction addiction apparatus of the present invention.

Figure 11 shows a forehead addiction addiction apparatus of the present invention.

Figure 12 shows a horizontal addiction addiction apparatus of the present invention.

Figure 13 shows a sitting addiction addiction apparatus of the present invention.

 【detailed description】

As shown in Fig. 1, when the brain 1 is in a normal state, the amount of FosB in the nucleus accumbens 14 belongs to a normal amount, and the dopamine produced in the ventral tegmental region (VTA) 13 of the midbrain passes through the forebrain inner bundle 16 and passes through the volt The nuclear 14 is released to the whole brain, and the amount that passes through the nucleus nucleus 14 is normal, and the dopamine receiving port 15 on each cell in the brain 1 is normally received.

As shown in Fig. 2, in the case of drug abuse, the amount of FosB in the nucleus 14 in the brain 1 greatly exceeds the normal amount, and the nucleus 14 increases the excitability, and the dopamine produced by the ventral tegmental area (VTA) 13 of the midbrain passes. After the forebrain bundle 16 is passed, the whole brain is rapidly released through the nucleus accumbens 14 in a short time to greatly exceed the normal amount of dopamine. Since each cell in the brain is damaged by excessive excitement when it receives an excessive amount of dopamine, each brain cell will reduce its own number of dopamine receptors based on its own protective mechanism (permanently shutting down a certain number of dopamine receptors). ). After the drug has been used, when dopamine is released in normal amounts, the cells in the brain are unable to receive sufficient dopamine due to the reduced number of dopamine receptors. Therefore, it is not possible to be normally excited, and various symptoms of drug addiction (including pain, trembling, sweating, etc.) occur.

Figure 3 shows the principle of drug addiction in the present invention, which is to hypnotize and control the continuous deep sleep to accelerate the growth of the number of dopamine receptors in the brain cells in the deep sleep mode to the number before the drug use, thereby quit the drug addiction. As a result, the amount of FosB in the nucleus accumbens 14 is normal, so the amount of dopamine produced by the ventral tegmental area (VTA) 13 of the midbrain, after passing through the forebrain inner bundle 16, passes through the nucleus nucleus 14 to the whole brain. Returning to normal, the dopamine receiving port 15 of each brain cell receives a normal amount of dopamine and is normally excited.

As shown in Fig. 4, when the brain 1 is awake, the driving excitation zone 2 drives the electric signal or the standby electrical signal 5 first through the thalamus 3, and then passes through the awake excitation zone 4 (including: the blue plaque nucleus LC, the dorsal lateral nucleus) LDT, foot bridge nucleus PPT), sleep excitatory zone 7 (including: ventral lateral preoptic area VLPO), which is then transmitted to any muscle 8 of the body by driving nerve 6, which can be detected from muscle 8 by detector electrode 17 of the monitor To.

As shown in Fig. 5, when the brain 1 transitions from the awake mode to the sleep mode, the sleep excitement zone 7 increases the excitement, and the excitement of the rejuvenation zone 4 is suppressed by the channel 9 until the excitement frequency of the rejuvenation zone 4 is reduced to zero. Thus, the driving electric signal or the standby electric signal 5 is blocked from waking up the exciting zone 4, causing the driving electric signal or the standby electric signal 5 in the driving nerve 6 to also tend to zero, indicating that the drug addiction symptom disappears and the brain has entered the deep sleep mode.

Figure 6 shows a method and system of the present invention for modulating the sleep excitatory zone 7 of the brain 1 with an electromagnetic field for hypnosis to achieve drug addiction. The content includes applying the electromagnetic field 18 to the brain 1, modulating the sleep excitatory zone 7 of the brain 1, increasing the excitement of the sleep excitatory zone 7, and effectively suppressing the rejuvenation zone 4, due to the resuscitation zone 4 through the channel 27 to the thalamic reticulate The inhibition of nuclear 41 is blocked, and the thalamic reticular nucleus 41 is increased. As a result, the sleep hormone is released in the whole brain through the channel 28, so that the brain 1 enters a deep sleep mode, and the number of dopamine receptors in the brain cells is rapidly increased to return to normal, thereby realizing Drug addiction through hypnosis. The electromagnetic field can be any electromagnetic field, including an electromagnetic field of any frequency, an electromagnetic field of any waveform, a pulsed electromagnetic field of any duty cycle, any electromagnetic field with a modulation frequency, and an electromagnetic field of any intensity; also includes naturally occurring electromagnetic fields and artificially generated electromagnetic fields.

Fig. 7 shows a method and system for activating a drug addiction zone 7 by pulsing an electromagnetic field 10 to modulate a sleep excitement zone of the brain. The pulsed electromagnetic field 10 is applied to the brain 1 to modulate the sleep excitatory zone 7 of the brain, so that the excitement of the sleep excitatory zone 7 is increased (including the increase of the excitatory frequency and the excitatory intensity), effectively suppressing the rejuvenation zone 4, due to wake up In the excitatory zone 4, the inhibition of the thalamic reticular nucleus 41 through the channel 27 is blocked, and the thalamic reticular nucleus 41 is increased in excitement. As a result, the sleep hormone is released in the whole brain through the channel 28, and the brain 1 enters the deep sleep mode. The number of dopamine receptors rapidly increased to return to normal in deep sleep mode, thereby achieving drug addiction through hypnosis.

Fig. 8 shows a method and system for drug addiction according to the present invention, which is mainly composed of an electromagnetic field driving power source 12 and an antenna 11. In this method, the electromagnetic field driving power source 12 drives the antenna 11 to generate an electromagnetic field for the brain 1, and by modulating the sleep excitation region 7 of the brain 1, it enhances the excitement (including the increase of the excitation frequency and the enhancement of the excitation intensity), and effectively suppresses Sudden Excitement Zone 4, due to the inhibition of the thalamic reticular nucleus 41 through the channel 27 by the wake-up zone 4, the thalamic reticular nucleus 41 is increased, and the sleep hormone is released through the channel 28 throughout the brain, thereby allowing the brain 1 to enter the depth. Sleep mode. The number of dopamine receptors rapidly increased to return to normal in deep sleep mode, thereby achieving drug addiction through hypnosis. In the present invention, the distance of the antenna 11 from the brain 1 is fixed (static) or time-varying (dynamic) during the action of the electromagnetic field on the sleep excitatory region of the brain. The electromagnetic field can be one or more.

Figure 9 shows the hardware system of a drug addiction device of the present invention. It mainly includes hypnotist body and monitor. Hypnotism consists of a system that uses electromagnetic fields to modulate the brain's sleep excitatory region to shift the brain from a wake-up mode to a deep sleep mode, consisting primarily of one or more electromagnetic field generation and emission systems to enhance the excitement of the brain's sleep-excited region. , the brain is normally transferred from the awake mode to the deep sleep mode.

Specifically, the hypnotic body includes a signal source 19, a first-stage power amplifier module 20, a secondary power amplifier module 21, a driving power module 22, a microcontroller 23, a voltage regulator source module 24, a battery 25, a charging module 26, and an antenna 11. The monitor includes a control system 44 for the hypnotist, a monitoring system 45, an operational display system 47, and an antenna 46).

In the system, the operation display system 47 of the monitor receives the input detoxification management parameter manipulation monitoring system 45 (through the detection electrode 17, Figure 4) to detect the degree of drug addiction and the depth of sleep, when the degree of drug addiction is higher than a critical value. When the sleep depth is less than a threshold, the control system 44 sends an enable signal to the hypnotist through the antenna 46. After receiving the signal through the antenna 43, the receiving module 42 transmits the information to the microcontroller 23, and the microcontroller 23 sends out the signal. The signal of the hypnotist is turned on, the high frequency electric signal is sent by the signal source 19, amplified by the first power amplifier module 20, amplified by the second power amplifier module 21, and then input to the antenna 11, and the desired modulation brain 1 sleep is generated by the antenna 11. The electromagnetic field in the excited area. When the degree of drug addiction is below a critical value or the depth of sleep is greater than a critical value, the control system 44 sends a shutdown signal to the hypnotist via the antenna 46, and after receiving the signal, the receiving module 42 transmits the information to the microcontroller. 23. The hypnosis device is turned off by the microcontroller 23. During the entire sleep process, the monitoring system 45 of the monitor is always in the state of monitoring control until the sleep time reaches the input parameter requirement. After brain 1 enters deep sleep mode, the number of dopamine receptors in brain cells rapidly grows back to normal in deep sleep mode, achieving drug addiction through hypnosis.

In the system, the monitoring system 45 in the monitor detects the depth of sleep by using a direct detection method or an indirect detection method to detect the degree of inhibition of the excitatory region of the brain 1 in the sleep excitatory region of the brain 1 to increase the degree of inhibition during excitation. 1 sleep depth. The sleep depth of Brain 1 refers to the measure of the degree of sleep in the process of transitioning from the awake mode to the deep sleep mode of the brain 1, and is expressed by the percentage of reduction in which the awake excitation zone is suppressed to reduce the excitement, and thus the sleep depth can be divided into several levels. . The detection of the degree of inhibition of the wake-up zone of the brain by the sleep excitatory zone is achieved by detecting the decrease in the intensity of the drive electrical signal or the standby electrical signal emitted by the brain-driven excitation zone received by any muscle of the body; the monitoring system is mainly It consists of one or more electrodes attached to the skin near the muscles, a signal acquisition circuit, a signal storage module, a signal transmission module, a system control module, and a battery. The monitoring system also includes a strap provided with a locking mechanism, the signal acquisition circuitry being disposed on the strap.

The monitoring system 45 in the monitor detects the degree of drug addiction by direct detection or indirect detection by detecting the degree of excitement of the brain 1 excitatory area exceeding normal. The degree of excitement of detecting the excitatory area of the brain beyond the normal level is achieved by detecting the increase in the intensity of the driving electrical signal or the standby electrical signal emitted by the brain-driven excitatory region received by any muscle of the body. In terms of percentages above normal excitement, the degree of drug addiction can be divided into several levels. The critical value of the degree of drug addiction (the monitor according to the threshold indicates that the drug addicts start a hypnosis drug addiction treatment course) can be zero or greater than zero.

Through the above hardware system of drug addiction addiction instrument, a hypnosis drug addiction management method and treatment course can be realized, which mainly includes: 1 monitor detects the degree of drug addiction of the drug addicts, and when the degree of drug addiction is higher than a critical value, the prompt The drug addicts start a hypnosis addiction treatment and automatically set the hypnotic control parameters according to the degree of drug addiction, including the length of the treatment; 2 detect the sleep depth of the brain, when the sleep depth is less than a critical value, the monitor automatically controls The hypnotist is turned on; 3 when the degree of drug addiction is at a critical value or when the depth of sleep is greater than a critical value, the monitor controls the hypnotist to be turned off, continues to detect and the degree of drug addiction is higher than a critical value or the depth of sleep is less than one The hysteresis is re-opened at the critical value; 4 when the treatment reaches the set time, the monitor controls the hypnosis to be turned off to complete a hypnosis addiction treatment course.

The critical value of the degree of drug addiction can be zero or greater than zero. The critical value of the depth of sleep (when the depth of sleep is below this threshold, the hypnosis is turned on, and when the depth of sleep is higher than this threshold, the hypnosis is turned off) is set according to the effect of the hypnosis addiction effect.

The monitor can touch any muscle on the body and detect the driving signals from the driving excitatory area of the muscle upper brain, for example, it can be worn on a person's wrist.

Figure 10 shows a bedside/pillow addiction addiction apparatus of the present invention, which is mainly composed of a structural frame 30 and a body 29 which is rotatably coupled to the body 29. The bedside/pillow type of addiction addiction device comprises two uses: 1 rotating the body 29 relative to the structural frame 30, forming an angle of approximately 90° with the structural frame 30, placing the structural frame 30 under the pillow, at which time the body 29 At an angle of 90° to the bed surface, when the switch of the bedside/pillow type drug addiction device is turned on, the body 29 generates an electromagnetic field from the top of the head to the sleep excitement area of the brain to modulate the sleep excitement area of the brain and enhance its excitement. The brain enters deep sleep mode. The number of dopamine receptors rapidly increased to normal in deep sleep mode, achieving drug addiction through hypnosis; 2 the body 29 and the structural frame 30 were closed and placed under the pillow, when the bedside/pillow detoxification device When the switch is turned on, the body 29 generates an electromagnetic field from the back of the head to the sleep excitation zone of the brain to modulate the sleep excitement zone of the brain, enhance its excitement, and enter the deep sleep mode. The number of dopamine receptors rapidly increased to return to normal in deep sleep mode, achieving drug addiction through hypnosis. The bedside/pillow addiction addiction device also includes a monitor worn on a part of the person (such as a wrist) to detect the degree of drug addiction and depth of sleep and to control the opening and closing of the body.

Figure 11 shows a forehead type addiction addiction apparatus of the present invention, which is mainly composed of a structural frame 35 and a body 34. In use, the person lies on a bed or chair, adjusts the structural frame 35, so that the body 34 is located just above the brain 1. When the forehead type drug addiction device is turned on, the body 34 generates an electromagnetic field from the forebrain to the sleep excitatory region of the brain 1. To modulate the sleep excitement zone of brain 1 and increase its excitement, brain 1 enters a deep sleep mode. The number of dopamine receptors rapidly increased to return to normal in deep sleep mode, achieving drug addiction through hypnosis. The structural frame 35 mainly has the following functions: 1 supporting the body 34 and making the body 34 properly fit the forehead of the head during use to achieve the most effective generation of the electromagnetic field and acting on the sleep excitation zone of the brain 1; 2 adjusting the body 34 The position and position of the sleep excitation zone that causes the electromagnetic field to act on the brain can be from the left side of the head, the right side or the top to the sleep excitatory area of the brain, or any combination of the above orientations simultaneously or at different times to the sleep excitatory area of the brain For ease of use and best results; 3 fixed anywhere on the bed, bedside, bedroom or detox room. The forehead addiction addiction device also includes a monitor worn on a part of the person (e.g., wrist) to detect the degree of drug addiction and depth of sleep and to control the opening and closing of the body 34.

Figure 12 shows a horizontal detoxification addiction apparatus of the present invention, which is mainly composed of a multi-function structural frame 32 and a body 31. When in use, the person lies on the bed 33, adjusts the multi-function structure frame 32, and places the body 31 above the forebrain. When the horizontal detoxification addiction device is turned on, the body 31 sleeps from the forebrain to the brain. The electromagnetic field is generated to modulate the sleep excitatory area of the brain, enhance its excitement, and the brain enters a deep sleep mode. The number of dopamine receptors rapidly increases and returns to normal in deep sleep mode, achieving drug addiction through hypnosis.

Figure 13 shows a sitting addiction addiction apparatus of the present invention. It is mainly composed of a chair 36, a body 37 and a fixing device. When in use, the person sits on the chair 36 so that the body 37 is located just behind the brain. When the sitting detoxification device is turned on, the body 37 generates an electromagnetic field from the hindbrain to the sleep excitatory region of the brain to modulate the sleep excitatory region of the brain. Increase their excitement and brain into deep sleep mode. The number of dopamine receptors rapidly increased to return to normal in deep sleep mode, achieving drug addiction through hypnosis. The fixture 38 secures the hand of the person to limit the movement of the hand, and the fixture 39 secures the foot of the person to limit the movement of the foot. The chair 36 is a multi-position bracket, wherein the chair 36 is adjustable, and when adjusted to its sitting position, the hypnosis device allows the user to sit and sleep; when adjusted to the sleeping position, the hypnotist Allows the user to fall asleep normally. The sitting addiction addiction device also includes a monitor that fits the muscles or skin of a certain part of the person (such as the wrist) to detect the degree of drug addiction and the depth of sleep and control the opening and closing of the body.

The technical features of the above-described embodiments may be arbitrarily combined. For the sake of brevity of description, all possible combinations of the technical features in the above embodiments are not described. However, as long as there is no contradiction between the combinations of these technical features, All should be considered as the scope of this manual.

The above-described embodiments are merely illustrative of several embodiments of the present invention, and the description thereof is more specific and detailed, but is not to be construed as limiting the scope of the invention. It should be noted that a number of variations and modifications may be made by those skilled in the art without departing from the spirit and scope of the invention. Therefore, the scope of the invention should be determined by the appended claims.

Claims (18)

A method of achieving drug addiction by hypnotizing the brain into a deep sleep mode to promote the rapid increase of the number of dopamine receptors in the brain cells to the level before the formation of drug addiction, including modulating the brain's sleep excitatory region with electromagnetic fields to wake up the brain The method of transferring the model into the deep sleep mode also includes utilizing or generating an electromagnetic field to act on the sleep excitatory region of the brain, thereby promoting the excitement of the sleep excitatory region, thereby suppressing the excitatory region of the brain, and thereby retracing the thalamus by blocking the excitatory region of the brain. The inhibitory effect of the nucleus promotes the release of sleep hormones from the reticular nucleus of the thalamus to the excitatory regions of the whole brain, and shifts the brain from the awake mode to the deep sleep mode. It also includes monitoring the degree of drug addiction to control the onset of hypnosis and includes detecting sleep. Depth automatically starts, stops, and resumes hypnosis to maintain the desired or set depth of sleep during a hypnosis addiction process. In claim 1, the electromagnetic field is any electromagnetic field, including an electromagnetic field of any frequency, an electromagnetic field of any waveform, a pulsed electromagnetic field of any duty cycle, any electromagnetic field having a modulation frequency, and an electromagnetic field of any intensity; also includes naturally occurring electromagnetic fields and artificial The electromagnetic field generated. In claim 1, the excitement of the sleep excitement zone includes an increase in the frequency of excitement and an increase in excitability. In claim 1, the electromagnetic field acts on the sleep excitatory region of the brain to be dynamic or static; the direction and position of the electromagnetic field acting on the sleep excitatory region of the brain mainly includes sleep excitatory regions from the hindbrain to the brain, and sleep from the head to the brain. Excitatory area, from the front of the head to the sleep excitement area of the brain, from the left or right side of the head to the sleep excitement area of the brain, or any combination of the above orientations to the sleep excitement area of the brain at the same time or at different times. In claim 1, the electromagnetic field utilized or generated to cause the sleep excitatory region to increase excitement in the sleep excitatory region of the brain such that the brain normally transitions from the awake mode to the deep sleep mode is one or more electromagnetic fields. In claim 1, the method for achieving drug addiction by hypnotizing the brain into a deep sleep mode to promote the rapid increase of the number of dopamine receptors in the brain cells to the level before the formation of drug addiction includes a hypnosis drug addiction management method and treatment, mainly Contains: 1 monitor detects the degree of drug addiction in drug addicts. When the degree of drug addiction is higher than a critical value, it prompts the drug addict to start a hypnosis drug addiction treatment and automatically set hypnosis control according to the degree of drug addiction. Parameters, including the length of time of the treatment; 2 detecting the depth of sleep of the brain, when the depth of sleep is less than a critical value, the monitor automatically controls the hypnosis to open; 3 when the degree of drug addiction is at a critical value or the depth of sleep is greater than one At the critical value, the monitor controls the hypnosis to be turned off, continues to detect, and controls the hypnotist to re-open when the degree of drug addiction is above a critical value or the depth of sleep is less than a critical value; 4 when the treatment reaches the set time, monitoring The instrument controls the hypnosis to close to complete a hypnosis drug addiction treatment. In claim 6, the degree of drug addiction is measured by the degree of excitement of the brain's wake-up zone over normal excitement, expressed as a percentage of normal excitement, and the degree of drug addiction can be divided into several levels; The critical value of the degree can be zero or greater than zero. In claim 6, the depth of sleep of the brain refers to a measure of the degree of sleep in the process of transitioning from a wake-up mode to a deep sleep mode, and the percentage of decrease in excitement is suppressed by the wake-up excitatory zone, and the sleep depth is divided into Several levels; the critical value of sleep depth is set according to the hypnotic addiction effect requirements. A system for achieving drug addiction by hypnotizing the brain into a deep sleep mode to promote the rapid increase in the number of dopamine receptors in the brain cells to the level before the formation of drug addiction, mainly by one or more hypnotic devices and one or more monitors Composition, wherein the monitor detects the degree of drug addiction and controls the hypnotist to enable the brain of the drug addict to enter a deep sleep mode and detect and maintain a deep sleep mode of the brain, so that the dopamine receptor of the brain cell accelerates growth in deep sleep mode Revert to normal levels to achieve addiction. In claim 9, the hypnotist comprises a system for modulating the sleep excitatory region of the brain with an electromagnetic field to shift the brain from the awake mode to the deep sleep mode, consisting primarily of one or more electromagnetic field generation and emission systems for enhancing the brain. The excitement of the sleep-exciting area makes the brain normally transition from a wake-up mode to a deep sleep mode. In claim 10, the hypnotic device is mainly composed of a body of different sizes and different shapes for generating the electromagnetic field and a structural frame supporting the body, the body comprising an antenna, a primary or multi-stage power amplifier module, a signal source, and a driving power module. The voltage regulator source module, the microcontroller, the charging module, the battery, the receiving module and the outer casing, the structural frame is a horizontal structural frame (including: bed type, pillow type, forehead type) or a sitting structure frame. In claim 11, the structural frame is a headboard/pillow structural frame, and includes a bracket foldably disposed with the body, so that the hypnotheraposcope is used as a bedside hypnosis device when opened, placed on the bedside and The pillows face the head of the sleeper and produce an electromagnetic field that modulates the brain's sleep-exciting area, and when closed, can be placed under the pillow as a pillow-type hypnosis. In claim 11, the structural frame is a pillow, the body is placed in the pillow, or the body is placed under the pillow. In claim 11, the structural frame is fixed to the head of the bed to support the body; the structural frame is used for: 1 supporting the body and properly fitting the forehead of the head during use to achieve the most efficient generation and emission of the electromagnetic field. Increase the excitement of the brain's sleep excitement zone; 2 adjust the position of the body for ease of use; 3 fix it anywhere on the bed, bedside or bedroom. In claim 11, the structural frame is a multi-position bracket, wherein the multi-position bracket is adjustable, and when adjusted to its sitting position, the hypnosis device allows the user to sit and sleep; when adjusted to The hypnotist allows the user to lie down and sleep normally while lying down. In claim 9, the monitor is mainly composed of a monitoring system for the wake-up zone, a control system for the hypnotizer, and an operation display system, wherein the degree of inhibition of the sleep-excited region of the brain to the wake-up zone is determined. Detecting the reduction in the intensity of the drive electrical signal or standby electrical signal from the driving excitation zone of the brain received by any muscle in the body; the monitoring system is primarily attached to one or more skins attached to the muscles The electrode, the signal acquisition circuit, the signal storage module, the signal transmission module, the system control module, and the battery are composed. In claim 16, detecting the degree of drug addiction is achieved by detecting an increase in the intensity of a driving electrical signal or a standby electrical signal emitted by a brain-driven excitatory region received by any muscle of the body. In claim 16 or 17, the monitoring system includes a strap provided with a locking mechanism, the signal acquisition circuit being disposed on the strap to detect driving power generated by the driving excitation zone of the brain received by any muscle of the body. The amount of decrease or increase in the intensity of the signal or standby electrical signal to detect the degree of inhibition of the wake-up zone of the brain or to detect the excitement of the wake-up zone exceeds normal, thereby measuring the depth of sleep or the degree of drug addiction.