System and method for treating inflammation
Described is a low voltage, pulsed electrical stimulation device for reducing inflammation in a subject, which can be useful in the treatment of concussions, traumatic brain injury, cancer, and so forth.
1. A device that determines a subject's level of inflammation following organ and/or tissue injury in the subject and then, in response to said determination, is programmed to provide at least one bioelectric signal to tissue of the subject so as to regulate expression of selected protein(s) by the tissue, so as to balance inflammation in the subject for organ and/or tissue healing and recovery in the subject, wherein the device comprises:
sensor(s) for determining the subject's level of inflammation;
a microprocessor that, based upon the subject's level of inflammation, is programmed to provide at least one bioelectric signal in order to balance inflammation in the subject; and
electrode(s) for applying bioelectric signal(s) to tissue of the subject,
wherein the applied bioelectric signal(s) influence expression of protein(s) in the tissue of the subject to which a bioelectric signal or signals is applied.
2. The device of claim 1 , wherein the device is programmed to produce bioelectric signals comprising at least each of the following:
a bioelectric signal of, within 15%, 100 mV, 50 Hz, square wave;
a bioelectric signal of 3 V, 10 Hz, square wave, and/or 20 V, 100 Hz, square wave;
a bioelectric signal of, within 15%, alternating high-frequency and medium-frequency signals, symmetric, biphasic, trapezoid pulses, with 400-μs pulse duration and 1.5/1-s ramp-up/ramp-down duration, respectively, and
a bioelectric signal of, within 15%, 3.5 V stimulation in 10 second bursts, one (1) burst every 30 seconds at a frequency of about 50 Hz.
3. A method of using the device of claim 2 to treat a subject with a concussion or other brain injury,
the method comprising:
applying the bioelectric signals to the subject's tissue.
4. The device of claim 1 , wherein the device is programmed to produce at least one bioelectric signal selected from the group consisting of
(a) within 15%, 3 mV with a frequency of about 22 Hz, and a current of about 1 mA, followed by 3 mA;
(b) a biphasic, continuous current of 10 μA at 50 Hz;
(c) 3 mV at 2/100 Hz, alternating frequency, with current of 3 mA, followed by 15 Hz, 1 Gauss EM field, consisting of 5-millisecond bursts with 5-microsecond pulses followed by 200 μs pulse duration at 30 Hz and with current amplitude of 140 mA;
(d) 20 V, 1 Hz with a pulse of 5 ms: and
any combination thereof.
5. A method of using the device of claim 4 in a subject to regenerate brain cells in the subject, the method comprising:
generating bioelectric signals from the device to upregulate the expression of a protein in the subject, wherein the protein is selected from the group consisting of insulin-like growth factor 1 (“IGF1”), tumor necrosis factor alpha (“TNF-α”), C—X—C motif chemokine 5 (“CXCL5”), and any combination thereof.
6. The method according to claim 5 , further comprising:
separately delivering to the subject stem cells and/or growth factors comprising any combination of IGF1, insulin-like growth factor 1 (“IGF1”), interleukin 6 (“IL-6”), interleukin 10 (“IL-10”), interleukin-1β(“IL-1β”), transforming growth factor-β(“TGFβ”), TNF-α, CXCL5, and any combination thereof.
7. The device of claim 1 , wherein the upregulation of expression of the selected protein(s) in the subject occurs without a diminishing effect over time.
8. A method of treating a subject suffering from a brain concussion or traumatic brain injury (“TBI”), the method comprising:
utilizing the device of claim 1 to treat the subject's brain by applying said bioelectric signal(s) to tissue of the subject.
9. The method according to claim 8 , comprising the application of bioelectric protein expression and/or release sequence(s) to the subject comprises:
from about five (5) to about forty (40) minutes, to increase IL-1β,
wherein the device then determines and adjusts the bioelectric protein expression signals to the subject's tissue for about five (5) minutes of an IL-1β inhibition shut off signal, and then from about five (5) to forty (40) minutes, a rise in TNF-α,
wherein the device then determines and adjusts the bioelectric protein expression signals to the subject's tissue for about five (5) minutes of TNF-α inhibition shut off signal, and then from about five (5) to forty (40) minutes rise in TGFβ, and
wherein the device then determines and adjusts the bioelectric protein expression signals to the subject's tissue for about five (5) minutes of a TGFβ inhibition shut off signal, and then about three (3) minutes of a rise in IL-10.
10. A method of using the device of claim 1 to treat a subject having heart failure, the method comprising:
delivering selected bioelectric protein expression and/or release signals to the subject so as to control protein expression and/or release of a protein or proteins selected from the group consisting of tumor necrosis factor alpha (“TNF-α”), vascular endothelial growth factor (“VEGF”), endothelial NOS (“eNOS”), SDF, C—X—C motif chemokine 5 (“CXCL5”), and any combination thereof to aid in the treatment of the subject's heart.
11. The method according to claim 10 , further comprising:
separately delivering to the subject a cocktail of regenerative agents comprising any combination of the following: stem cells, endothelial progenitor cells, selected exosomes, selected alkaloids, selected anti-inflammatory agents, nutrient hydrogel, organ specific matrix, selected growth factors, amniotic fluid, placenta fluid, cord blood, and embryonic sourced growth factors and cells.
12. A method of using the device of claim 1 in a subject's tissue to control expression and/or release of a protein, wherein the electrical signal stimulates the production of a protein selected from the group consisting of insulin-like growth factor 1 (“IGF1”), tumor necrosis factor alpha (“TNF-α”), C—X—C motif chemokine 5 (“CXCL5”), and any combination thereof.
13. A method of using the device of claim 1 to achieve a desired result in a subject, wherein the desired result is selected from the group consisting of brain regeneration, cognitive function brain improvement, treatment of brain stroke, treatment of traumatic injury, treatment of eye injury, and ear hearing regeneration.
14. The device of claim 1 , wherein the device is programmed to produce bioelectric signals comprising at least each of the following:
a bioelectric signal of, within 15%, a frequency of 50 Hz, square wave;
a bioelectric signal of 10 a frequency of Hz, square wave, and/or a frequency of 100 Hz, square wave;
a bioelectric signal of, within 15%, alternating high-frequency and medium-frequency signals, symmetric, biphasic, trapezoid pulses, with 400-μs pulse duration and 1.5/1-s ramp-up/ramp-down duration, respectively, and
a bioelectric signal of one (1) burst every 30 seconds at a frequency of about 50 Hz.
15. The device of claim 1 , wherein the device is programmed to produce at least one bioelectric signal selected from the group consisting of
(a) within 15%, a frequency of about 22 Hz;
(b) a biphasic, continuous current at a frequency of 50 Hz;
(c) a frequency of 2/100 Hz, alternating frequency, followed by a frequency of 15 Hz, 1 Gauss EM field, consisting of 5-millisecond bursts with 5-microsecond pulses followed by a frequency of 30 Hz and 200 μs pulse duration;
(d) a frequency of 1 Hz with a pulse of 5 ms: and
(e) any combination thereof.