A method for improving the efficiency of sodium-potassium pumps through bioresonance driving

Abstract

The present invention provides a method for improving the efficiency of a sodium-potassium pump through bioresonance drive, comprising: obtaining the membrane potential of a nerve cell region and constructing an ion distribution model; generating electromagnetic radiation on the nerve cells using far-infrared rays, thereby changing the membrane potential to generate a resonant membrane potential; and driving the sodium-potassium pump to move according to the resonant membrane potential. This method can cure and improve the prognosis of cardiovascular disease. FIR can be used to combat inflammation and protect cells from damage. FIR can be used to maintain cells in hemodialysis patients. FIR can be used to enhance sleep. The present method can also be used to inhibit tumor growth. Finally, FIR therapy can promote neural repair.

Description

Technical Field

[0001] The present invention relates to the field of biological cell technology, and in particular to a method for improving the working efficiency of a sodium-potassium pump through biological resonance driving. Background Art

[0002] The human body is composed of approximately 60 trillion cells, which are the fundamental structural and functional units of life. Cells are the fundamental unit of biological structure and function. Human tissues and organs are composed of individual cells, and all functions are performed by the cells. Abnormal cell activity or function can lead to illness. Besides genetic problems, the primary cause of abnormal cell function is the "sodium-potassium pump" (also known as the sodium-potassium-ATPase, Na+ / K+-ATPase).

[0003] Normal cell function requires the transfer of electrons through the sodium-potassium pump. This transfer of electrons creates ion channels for sodium and potassium ions to enter and exit the cell. This mechanism has the following effects:

[0004] 1. Maintain a low Na+ and high K+ intracellular environment;

[0005] 2. Maintain osmotic balance and maintain the body characteristics of cells.

[0006] 3. Maintaining the resting potential of the cell membrane. In other words, whether the sodium-potassium pump can function normally is crucial to the health of cells and the human body.

[0007] However, although there are devices and methods for cell repair through electromagnetic fields in the prior art, most of the prior art only performs single cell therapy, and one device and one method can only treat one disease, which is very restrictive. Summary of the Invention

[0008] The present invention provides a method for improving the working efficiency of a sodium-potassium pump through bioresonance driving, so as to solve the problem that although there are devices and methods for cell repair through electromagnetic fields in the prior art, most of the prior art only perform single cell therapy, and one device and one method can only treat one disease, which is very restrictive.

[0009] A method for improving the working efficiency of a sodium-potassium pump through bioresonance driving, comprising:

[0010] Obtain the membrane potential of the nerve cell region and construct an ion distribution model;

[0011] generating electromagnetic radiation on the nerve cells by far infrared rays, and changing the membrane potential to generate a resonant membrane potential;

[0012] The sodium potassium pump is driven to move according to the resonant membrane potential.

[0013] In one embodiment of the present invention, the method further comprises:

[0014] Obtain a grayscale image of the nerve cell area;

[0015] N potential grayscale curves of the nerve cells are extracted according to the grayscale image, wherein:

[0016] The nerve cell region is composed of N nerve cell potential curves, where N is an integer greater than 1;

[0017] The shape of the nerve cell potential curve is linear, and the potential of each nerve cell in the nerve cell potential curve is different;

[0018] Each of the potential grayscale curves corresponds to a nerve cell potential curve, and the potential grayscale curve reflects the grayscale change of the nerve cell potential curve along the radial direction;

[0019] superimposing the potential grayscale curve to obtain an accumulated grayscale curve of the nerve cell potential curve;

[0020] Detecting the peak of the cumulative grayscale curve, wherein

[0021] The peak of the accumulated grayscale curve corresponds to the ion distribution state in the nerve cell region.

[0022] In one embodiment of the present invention, the obtaining of the membrane potential of the nerve cell region and the construction of the ion distribution model include:

[0023] Step 1: Construct a membrane potential model:

[0024] Obtaining an ion potential distribution sequence according to the ion distribution state;

[0025] According to the ion potential distribution sequence, the maximum coverage range of the ion potential is set to build an ion rectangular distribution model; wherein,

[0026] The potential of each ion in the ion rectangular distribution model is marked with a potential;

[0027] generating a membrane potential model according to the potential annotation;

[0028] Step 2: Construct an ion distribution model:

[0029] extracting all potential distribution information according to the membrane potential model;

[0030] According to the potential distribution information, different ions are connected according to distance to form a tree diagram;

[0031] Based on the dendrogram, an ion distribution model is generated using the overall distribution.

[0032] In one embodiment of the present invention, the method further comprises:

[0033] Determining the low vibration frequency of the sodium-potassium pump according to the ion distribution model;

[0034] Determining, based on the low frequency, a target high frequency that drives the low frequency to resonate;

[0035] According to the target high vibration frequency, set the driving parameters of the infrared emission device;

[0036] emitting far infrared rays according to the driving parameters to form electromagnetic waves;

[0037] The electromagnetic wave is used as an energy radiation source to form an electromagnetic field, and the target high frequency is generated through the electromagnetic field.

[0038] In one embodiment of the present invention, the method further comprises:

[0039] determining a target micron frequency band of the electromagnetic wave according to the target high vibration frequency;

[0040] in,

[0041] The electromagnetic waves include: a low-frequency micrometer band of invisible light, a visible light micrometer band, and a high-frequency micrometer band of invisible light;

[0042] Determining the infrared micron frequency band of the infrared emitting device according to the target micron frequency band;

[0043] The driving parameters of the infrared emitting device are determined according to the infrared micron frequency band.

[0044] In one embodiment of the present invention, the method further comprises:

[0045] According to the nerve cell area, the disease type is determined; wherein,

[0046] The disease types include: cellular inflammation, tumors, cardiovascular disease and nerve cell damage;

[0047] According to the disease type, determining a corresponding type of long-range infrared light;

[0048] According to the remote infrared light, resonance radiation treatment is performed on the disease of the disease type.

[0049] In one embodiment of the present invention, the method further comprises:

[0050] one or more sensors configured to receive one or more bioelectric signals of sodium potassium pump displacement in a region of a nerve cell;

[0051] a stimulation generator configured to deliver an electromagnetic field to the region of nerve cells; and

[0052] The control circuit is configured as follows:

[0053] controlling the stimulation generator to transmit infrared light at a plurality of different resonance frequencies to the nerve cell region;

[0054] Identifying a bioelectric resonance response of a nerve cell region to the infrared light, wherein the bioelectric resonance response is identified based on an oscillation parameter of the one or more bioelectric signals, and the bioelectric resonance response indicates a resonant frequency of the nerve cell region to one of a plurality of stimulation frequencies;

[0055] According to the control frequency, the infrared emitting device is controlled to use the set resonance frequency to drive the displacement of the sodium potassium pump.

[0056] In one embodiment of the present invention, the method further comprises:

[0057] Detecting the real-time membrane potential of the nerve cell area, determining the real-time voltage signal frequency, adjusting the voltage of the infrared emitting device according to the voltage signal frequency, and generating a standard voltage for marking the electromagnetic field;

[0058] Detect electromagnetic oscillations in the nerve cell area and determine the generated pulsed electric field;

[0059] Converting the frequency of the pulsed electric field into a damped pulsed electric field frequency that matches the specific frequency of a biological body;

[0060] Bioresonance is achieved by the frequency of the damped pulse electric field and the original low frequency of the cell region.

[0061] In one embodiment of the present invention, the method further comprises:

[0062] generating a light detection device in the region of the nerve cells;

[0063] Obtain the light signal intensity value of each cell in the nerve cell; wherein,

[0064] The light signal intensity value includes a fluorescence intensity value and a scattered light intensity value;

[0065] According to the distribution characteristics of the light signal intensity values ​​of each cell, characteristic parameters of the nerve cell are obtained, wherein:

[0066] The characteristic parameters include position characteristic parameters;

[0067] The position characteristic parameter is used to characterize the distribution form of the optical signal intensity value of each cell of the nerve cell;

[0068] When the characteristic parameter satisfies the unique determination condition of the sodium-potassium pump, the displacement of the sodium-potassium pump is controlled.

[0069] In one embodiment of the present invention, the method further comprises:

[0070] According to the distribution of the light signal intensity values ​​of each nerve cell in the nerve cell area, a reference light signal intensity value is determined; wherein,

[0071] The reference light signal intensity value includes a fluorescence intensity value and / or a scattered light intensity value;

[0072] Determining a value range of the optical signal intensity value when the sodium-potassium pump is displaced according to the reference optical signal intensity value;

[0073] The nerve cells whose light signal intensity values ​​are within the value range are counted to obtain the number of the nerve cells, determine the number of sodium-potassium pumps when the sodium-potassium pumps are displaced, and monitor whether all the sodium-potassium pumps are displaced.

[0074] The beneficial effects of the present invention lie in the following: The present invention predetermines the membrane potential of the area to be treated, namely the nerve cell region, and then determines the internal ion distribution. This method determines the potential of any ion, not just the Na+ ion, to better determine the overall potential and generate an effective electromagnetic field. The present invention then drives an infrared emitting device to generate electromagnetic radiation, which generates a high-frequency electromagnetic field. This high-frequency electromagnetic field drives the original low-frequency electromagnetic field in the nerve cell region to undergo bioresonance, thereby controlling the displacement of the sodium-potassium pump. The chemical nature of the sodium-potassium pump is the sodium-potassium ATPase on the cell membrane. It releases energy by consuming one ATP molecule, pumping out three sodium ions and in two potassium ions against the electrochemical gradient. The sodium-potassium pump functions to maintain the uneven ion distribution of high potassium inside the membrane and high sodium outside. Under normal circumstances, if there is an ion concentration difference between the two sides of the membrane, a certain electrochemical potential energy exists, causing ions to flow from the high-concentration side to the low-concentration side. To maintain this concentration difference, the electrochemical potential energy must be overcome, which requires ATP consumption to provide energy. For example, it's like water automatically flows from high to low because of gravitational potential energy. To overcome this energy and allow water to flow from low to high, additional energy is needed to drive it, such as light energy, electrochemical gradient energy, and other external energy drives. Therefore, the present invention uses external energy drive of the electromagnetic field to control the magnetic waves centered on the energy radiation source to form an electromagnetic field. The field energy can drive the sodium and potassium ions in the field through resonance, with high frequency driving low frequency. This drive is more efficient than ordinary light energy and electrochemical gradient energy drives. The method of the present invention can cure and improve the prognosis of cardiovascular diseases. FIR can be used to fight inflammation and protect cells from damage. FIR can be used to maintain cells in hemodialysis patients. FIR can be used to enhance sleep. The method of the present invention can inhibit tumor growth. Finally, the FIR therapy of the present invention can also promote nerve repair.

[0075] Other features and advantages of the present invention will be described in the following description, and in part will become apparent from the description, or will be understood by practicing the present invention. The purpose and other advantages of the present invention can be realized and obtained by the structures particularly pointed out in the written description and the accompanying drawings.

[0076] The technical solution of the present invention is further described in detail below through the accompanying drawings and embodiments. BRIEF DESCRIPTION OF THE DRAWINGS

[0077] The accompanying drawings are used to provide a further understanding of the present invention and constitute a part of the specification. Together with the embodiments of the present invention, they are used to explain the present invention and do not constitute a limitation of the present invention. In the accompanying drawings:

[0078] Figure 1This is a flow chart of a method for improving the working efficiency of a sodium-potassium pump through bioresonance driving in an embodiment of the present invention;

[0079] Figure 2 This is the published range of the frequencies of different light rays according to the embodiments of the present invention. DETAILED DESCRIPTION

[0080] The preferred embodiments of the present invention are described below with reference to the accompanying drawings. It should be understood that the preferred embodiments described herein are only used to illustrate and explain the present invention, and are not used to limit the present invention.

[0081] As attached Figure 1 As shown, a method for improving the working efficiency of a sodium-potassium pump by bioresonance driving comprises:

[0082] Obtain the membrane potential of the nerve cell region and construct an ion distribution model;

[0083] generating electromagnetic radiation on the nerve cells by far infrared rays, and changing the membrane potential to generate a resonant membrane potential;

[0084] The sodium potassium pump is driven to move according to the resonant membrane potential.

[0085] In the above technical solution, the membrane potential of the area to be treated, namely the nerve cell region, is pre-determined, and the internal ion distribution is determined. This method determines the potential of any ion, not just the Na+ ion, to better determine the overall potential and generate an effective electromagnetic field. The method then drives an infrared emitting device to generate electromagnetic radiation, which generates a high-frequency electromagnetic field. This high-frequency electromagnetic field drives the original low-frequency electromagnetic field in the nerve cell region to undergo bioresonance, thereby controlling the displacement of the sodium-potassium pump. The chemical nature of the sodium-potassium pump is the sodium-potassium ATPase on the cell membrane. It releases energy by consuming one ATP molecule, pumping out three sodium ions and in two potassium ions against the electrochemical gradient. The sodium-potassium pump's function is to maintain the uneven ion distribution of high potassium inside the membrane and high sodium outside. Under normal circumstances, if there is an ion concentration difference between the two sides of the membrane, a certain electrochemical potential energy exists, causing ions to flow from the high-concentration side to the low-concentration side. To maintain this concentration difference, the electrochemical potential energy must be overcome, which requires ATP consumption to provide energy. For example, it's like water automatically flows from high to low because of gravitational potential energy. To overcome this energy and allow water to flow from low to high, additional energy is needed to drive it, such as light energy, electrochemical gradient energy, and other external energy drives. Therefore, the present invention uses external energy drive of the electromagnetic field to control the magnetic waves centered on the energy radiation source to form an electromagnetic field. The field energy can drive the sodium and potassium ions in the field through resonance, with high frequency driving low frequency. This drive is more efficient than ordinary light energy and electrochemical gradient energy drives. The method of the present invention can cure and improve the prognosis of cardiovascular diseases. FIR can be used to fight inflammation and protect cells from damage. FIR can be used to maintain cells in hemodialysis patients. FIR can be used to enhance sleep. The method of the present invention can inhibit tumor growth. Finally, the FIR therapy of the present invention can also promote nerve repair.

[0086] In one embodiment of the present invention, the method further comprises:

[0087] Obtain a grayscale image of the nerve cell area;

[0088] N potential grayscale curves of the nerve cells are extracted according to the grayscale image, wherein:

[0089] The nerve cell region is composed of N nerve cell potential curves, where N is an integer greater than 1; the N potential grayscale curves correspond to the diseased nerve cells, and then the diseased condition of the nerve cells can be judged.

[0090] The shape of the nerve cell potential curve is linear, and the potential of each nerve cell in the nerve cell potential curve is different;

[0091] Each of the potential grayscale curves corresponds to a nerve cell potential curve, and the potential grayscale curve reflects the grayscale change of the nerve cell potential curve along the radial direction;

[0092] superimposing the potential grayscale curve to obtain an accumulated grayscale curve of the nerve cell potential curve;

[0093] Detecting the peak of the cumulative grayscale curve, wherein

[0094] The peak of the accumulated grayscale curve corresponds to the ion distribution state in the nerve cell region.

[0095] In the above technical solution, the present invention uses a grayscale image to sort the potential curves of different ions from high to low to generate a potential curve. The distribution of ions with different potentials can be judged through this curve. Through the distribution of ions with different potentials, it is determined which areas of the nerve cells have high potentials and high ion concentrations. Thus, through the distribution of peaks, it is determined which areas have severe lesions, so as to better perform resonance treatment.

[0096] In one embodiment of the present invention, the obtaining of the membrane potential of the nerve cell region and the construction of the ion distribution model include:

[0097] Step 1: Construct a membrane potential model:

[0098] Obtaining an ion potential distribution sequence according to the ion distribution state;

[0099] According to the ion potential distribution sequence, the maximum coverage range of the ion potential is set to build an ion rectangular distribution model; wherein,

[0100] The potential of each ion in the ion rectangular distribution model is marked with a potential;

[0101] generating a membrane potential model according to the potential annotation;

[0102] Step 2: Construct an ion distribution model:

[0103] extracting all potential distribution information according to the membrane potential model;

[0104] According to the potential distribution information, different ions are connected according to distance to form a tree diagram;

[0105] Based on the dendrogram, an ion distribution model is generated using the overall distribution.

[0106] In the above technical solution, the present invention controls membrane potential and ion distribution in two ways. In this process, the present invention first generates a membrane potential model by using the distribution of ion potentials in a potential annotation manner. When the ions are distributed, a dendrogram based on ions is generated based on the distance between ions, and the ion distribution model is determined by the dendrogram.

[0107] In one embodiment of the present invention, the method further comprises:

[0108] Determining the low vibration frequency of the sodium-potassium pump according to the ion distribution model;

[0109] Determining, based on the low frequency, a target high frequency that drives the low frequency to resonate;

[0110] According to the target high vibration frequency, set the driving parameters of the infrared emission device;

[0111] emitting far infrared rays according to the driving parameters to form electromagnetic waves;

[0112] The electromagnetic wave is used as an energy radiation source to form an electromagnetic field, and the target high frequency is generated through the electromagnetic field.

[0113] In the above technical solution, because the technical principle of the present invention is that high frequency drives low frequency, the present invention determines what the high frequency should be by first determining the low frequency, and then determines the target high frequency by controlling the infrared emitting device to form the corresponding electromagnetic wave, and generates the target high frequency through the electromagnetic field formed by the electromagnetic wave.

[0114] In one embodiment of the present invention, the method further comprises:

[0115] determining a target micron frequency band of the electromagnetic wave according to the target high vibration frequency;

[0116] in,

[0117] The electromagnetic waves include: a low-frequency micrometer band of invisible light, a visible light micrometer band, and a high-frequency micrometer band of invisible light;

[0118] Determining the infrared micron frequency band of the infrared emitting device according to the target micron frequency band;

[0119] The driving parameters of the infrared emitting device are determined according to the infrared micron frequency band.

[0120] In the above technical solution: In the prior art, the present invention needs to determine the high frequency in three different light rays in order to generate the target high frequency. Figure 2 As shown, attached Figure 2Represents all regions within the solar electromagnetic belt. There are many high- and low-frequency waves, such as X-rays and ultraviolet rays, which are harmful to the human body. However, there are also essential light waves between 8 and 14 microns, also known as "vital light waves." The energy band near 9 to 10 microns is most beneficial to human physiological functions. Biomolecules and cells generate electromagnetic radiation in the far infrared (FIR) range. Interactions between electromagnetic radiation and living cells can alter cell membrane potential and mitochondrial metabolism. Photons with quantum energy levels between 12.4 meV and 1.7 eV fall within the FIR range and are absorbed by the vibrational energy levels of bonds within molecules.

[0121] In one embodiment of the present invention, the method further comprises:

[0122] According to the nerve cell area, the disease type is determined; wherein,

[0123] The disease types include: cellular inflammation, tumors, cardiovascular disease and nerve cell damage;

[0124] According to the disease type, determining a corresponding type of long-range infrared light;

[0125] According to the remote infrared light, resonance radiation treatment is performed on the disease of the disease type.

[0126] In the above technical solution: the present invention will first determine what frequency optical fiber will be used to treat different types of diseases. After determining the type of disease, the maximum and minimum thresholds of the frequency of the remote infrared device will be set, and then the remote infrared optical fiber will be notified to perform resonance radiation therapy.

[0127] In one embodiment of the present invention, the method further comprises:

[0128] one or more sensors configured to receive one or more bioelectric signals of sodium potassium pump displacement in a region of a nerve cell;

[0129] a stimulation generator configured to deliver an electromagnetic field to the region of nerve cells; and

[0130] The control circuit is configured as follows:

[0131] controlling the stimulation generator to transmit infrared light at a plurality of different resonance frequencies to the nerve cell region;

[0132] Identifying a bioelectric resonance response of a nerve cell region to the infrared light, wherein the bioelectric resonance response is identified based on an oscillation parameter of the one or more bioelectric signals, and the bioelectric resonance response indicates a resonant frequency of the nerve cell region to one of a plurality of stimulation frequencies;

[0133] According to the control frequency, the infrared emitting device is controlled to use the set resonance frequency to drive the displacement of the sodium potassium pump.

[0134] In the above technical solution, during the process of controlling the displacement of the sodium-potassium pump and performing bioresonance, the present invention will judge the state of the bioelectric signal and whether there is feedback through the bioresonance response. The feedback from the nerve cells will determine whether the sodium-potassium pump has been displaced, because the potential will change during the displacement of the sodium-potassium pump.

[0135] In one embodiment of the present invention, the method further comprises:

[0136] Detecting the real-time membrane potential of the nerve cell area, determining the real-time voltage signal frequency, adjusting the voltage of the infrared emitting device according to the voltage signal frequency, and generating a standard voltage for marking the electromagnetic field;

[0137] Detect electromagnetic oscillations in the nerve cell area and determine the generated pulsed electric field;

[0138] Converting the frequency of the pulsed electric field into a damped pulsed electric field frequency that matches the specific frequency of a biological body;

[0139] Bioresonance is achieved by the frequency of the damped pulse electric field and the original low frequency of the cell region.

[0140] In one embodiment of the present invention, the method further comprises:

[0141] generating a light detection device in the region of the nerve cells;

[0142] Obtain the light signal intensity value of each cell in the nerve cell; wherein,

[0143] The light signal intensity value includes a fluorescence intensity value and a scattered light intensity value;

[0144] According to the distribution characteristics of the light signal intensity values ​​of each cell, characteristic parameters of the nerve cell are obtained, wherein:

[0145] The characteristic parameters include position characteristic parameters;

[0146] The position characteristic parameter is used to characterize the distribution form of the optical signal intensity value of each cell of the nerve cell;

[0147] When the characteristic parameter satisfies the unique determination condition of the sodium-potassium pump, the displacement of the sodium-potassium pump is controlled.

[0148] In the above technical solution, we will use a light detection device to determine the fluorescence intensity and scattered light intensity of nerve cells. The light intensity of cells is also a way to detect the state of nerve cells. Through this characteristic parameter, the present invention can determine the aggregation state of nerve cells through light detection, thereby monitoring the displacement of the sodium-potassium pump.

[0149] In one embodiment of the present invention, the method further comprises:

[0150] According to the distribution of the light signal intensity values ​​of each nerve cell in the nerve cell area, a reference light signal intensity value is determined; wherein,

[0151] The reference light signal intensity value includes a fluorescence intensity value and / or a scattered light intensity value;

[0152] Determining a value range of the optical signal intensity value when the sodium-potassium pump is displaced according to the reference optical signal intensity value;

[0153] The nerve cells whose light signal intensity values ​​are within the value range are counted to obtain the number of the nerve cells, determine the number of sodium-potassium pumps when the sodium-potassium pumps are displaced, and monitor whether all the sodium-potassium pumps are displaced.

[0154] In the above technical solution, when controlling the displacement of the sodium-potassium pumps, we need to monitor whether all the sodium-potassium pumps are displaced. If some sodium-potassium pumps are not displaced, it means that the distribution of the electromagnetic field is uneven. Therefore, the present invention provides a supervision method to monitor whether all the sodium-potassium pumps are displaced.

[0155] Obviously, those skilled in the art may make various changes and modifications to the present invention without departing from the spirit and scope of the present invention. Thus, if such changes and modifications fall within the scope of the claims and their equivalents, the present invention is intended to include such changes and modifications.

Claims

1. A method for improving the efficiency of a sodium-potassium pump by bioresonance driving, wherein the method is for non-disease treatment purposes, characterized in that: include: Obtain the membrane potential of the nerve cell region and construct an ion distribution model; generating electromagnetic radiation on the nerve cells by far infrared rays, and changing the membrane potential to generate a resonant membrane potential; driving the sodium-potassium pump to move according to the resonant membrane potential; The method further comprises: Obtain a grayscale image of the nerve cell area; N potential grayscale curves of the nerve cells are extracted according to the grayscale image, wherein: The nerve cell region is composed of N nerve cell potential curves, where N is an integer greater than 1; The shape of the nerve cell potential curve is linear, and the potential of each nerve cell in the nerve cell potential curve is different; Each of the potential grayscale curves corresponds to one of the nerve cell potential curves, and the potential grayscale curve reflects the grayscale change of the nerve cell potential curve along the radial direction; superimposing the potential grayscale curve to obtain an accumulated grayscale curve of the nerve cell potential curve; Detecting the peak of the cumulative grayscale curve, wherein The peak of the accumulated grayscale curve corresponds to the ion distribution state in the nerve cell region; The obtaining of the membrane potential of the nerve cell region and the construction of the ion distribution model include: Step 1: Construct a membrane potential model: Obtaining an ion potential distribution sequence according to the ion distribution state; According to the ion potential distribution sequence, the maximum coverage range of the ion potential is set to build an ion rectangular distribution model; wherein, The potential of each ion in the ion rectangular distribution model is marked with a potential; generating a membrane potential model according to the potential annotation; Step 2: Construct an ion distribution model: extracting all potential distribution information according to the membrane potential model; According to the potential distribution information, different ions are connected by distance to form a dendrogram; generating an ion distribution model using the overall distribution according to the dendrogram; The method further comprises: Determining the low vibration frequency of the sodium-potassium pump according to the ion distribution model; Determining, based on the low frequency, a target high frequency that drives the low frequency to resonate; According to the target high vibration frequency, set the driving parameters of the infrared emission device; emitting far infrared rays according to the driving parameters to form electromagnetic waves; The electromagnetic wave is used as an energy radiation source to form an electromagnetic field, and the target high frequency is generated through the electromagnetic field.

2. The method for improving the working efficiency of a sodium-potassium pump by bioresonance driving according to claim 1, characterized in that: The method further comprises: determining a target micron frequency band of the electromagnetic wave according to the target high vibration frequency; in, The electromagnetic waves include: a low-frequency micrometer band of invisible light, a visible light micrometer band, and a high-frequency micrometer band of invisible light; Determining the infrared micron frequency band of the infrared emitting device according to the target micron frequency band; The driving parameters of the infrared emitting device are determined according to the infrared micron frequency band.

3. The method for improving the working efficiency of a sodium-potassium pump by bioresonance driving according to claim 1, characterized in that: The method further comprises: one or more sensors configured to receive one or more bioelectric signals of sodium potassium pump displacement in a region of a nerve cell; a stimulation generator configured to deliver an electromagnetic field to the region of nerve cells; and The control circuit is configured as follows: controlling the stimulation generator to transmit infrared light at a plurality of different resonance frequencies to the nerve cell region; Identifying a bioelectric resonance response of a nerve cell region to the infrared light, wherein the bioelectric resonance response is identified based on an oscillation parameter of the one or more bioelectric signals, and the bioelectric resonance response indicates a resonant frequency of the nerve cell region to one of a plurality of stimulation frequencies; According to the resonance frequency, the infrared emitting device is controlled to use the set resonance frequency to drive the displacement of the sodium-potassium pump.

4. The method for improving the working efficiency of a sodium-potassium pump by bioresonance driving according to claim 1, characterized in that: The method further comprises: Detecting the real-time membrane potential of the nerve cell area, determining the real-time voltage signal frequency, adjusting the voltage of the infrared emitting device according to the voltage signal frequency, and generating a standard voltage for marking the electromagnetic field; Detect electromagnetic oscillations in the nerve cell area and determine the generated pulsed electric field; Converting the frequency of the pulsed electric field into a damped pulsed electric field frequency that matches the specific frequency of a biological body; Bioresonance is achieved by the frequency of the damped pulse electric field and the original low frequency of the cell region.

5. The method for improving the working efficiency of a sodium-potassium pump by bioresonance driving according to claim 1, characterized in that: The method further comprises: generating a light detection device in the region of the nerve cells; Obtain the light signal intensity value of each cell in the nerve cell; wherein, The light signal intensity value includes a fluorescence intensity value and a scattered light intensity value; According to the distribution characteristics of the light signal intensity values ​​of each cell, characteristic parameters of the nerve cell are obtained, wherein: The characteristic parameters include position characteristic parameters; The position characteristic parameter is used to characterize the distribution form of the optical signal intensity value of each cell of the nerve cell; When the position characteristic parameter satisfies the unique determination condition of the sodium-potassium pump, the displacement of the sodium-potassium pump is controlled.

6. The method for improving the working efficiency of a sodium-potassium pump by bioresonance driving according to claim 5, characterized in that: The method further comprises: According to the distribution of the light signal intensity values ​​of each nerve cell in the nerve cell area, a reference light signal intensity value is determined; wherein, The reference light signal intensity value includes a fluorescence intensity value and / or a scattered light intensity value; Determining a value range of the optical signal intensity value when the sodium-potassium pump is displaced according to the reference optical signal intensity value; The nerve cells whose light signal intensity values ​​are within the value range are counted to obtain the number of the nerve cells, determine the number of sodium-potassium pumps when the sodium-potassium pumps are displaced, and monitor whether all the sodium-potassium pumps are displaced.

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