Duration: 45min
Programm Access Link:
https://www.epemf.app/digestive-system/c/12

Weight Loss – GLP-1 Resonance Energetics Collection

What this is

The GLP-1 Peptide Harmonic Energetics Collection translates the vibrational backbone of therapeutic GLP-1 peptides into structured resonance fields. Each program is derived from canonical peptide vibrational bands measured in terahertz, then octave-reduced into audible and subharmonic ranges for entrainment with headphones, coils, PEMF mats, vibroacoustic systems, or TENS.

Rather than treating these molecules as chemical agents, this approach interprets their biochemical vibrational signatures—Amide A, I, II, III, side-chain motions, and lipid modifications—as coherent sound and field expressions.

Also known as

  • Native GLP-1 (7–36) amide
  • Semaglutide (Ozempic, Wegovy, Rybelsus)
  • Liraglutide (Victoza, Saxenda)
  • Tirzepatide (Mounjaro, Zepbound)
  • Dulaglutide (Trulicity)
  • Exenatide (Byetta, Bydureon)

How we calculated these

  • Canonical peptide bands – using standard IR/Raman ranges for peptide backbones and side chains.
  • Conversion to THz – each wavenumber was converted into terahertz frequency.
  • Subharmonic reduction – frequencies divided down into audible & body-resonant bands (<20 kHz, <500 Hz).
  • Molecule-specific notes – lipidation intensifies CH₂ stretches; Dulaglutide broadens peaks.

1. Native GLP-1 (7–36 amide)

  • Biology: Endogenous peptide hormone released by the gut in response to food. Stimulates insulin secretion, slows gastric emptying, and reduces appetite.
  • Structure: A 30-amino acid peptide, non-lipidated.
  • Spectroscopy: Vibrational backbone dominated by Amide I (C=O stretch), Amide II (N–H bend + C–N stretch), and Amide A (N–H stretch).
  • Energetic relevance: Serves as the reference baseline, with lower CH₂ intensity due to lack of fatty modifications.

2. Semaglutide

  • Biology: A synthetic GLP-1 analogue with C18 fatty acid chain attached for albumin binding, increasing half-life to ~7 days. Used clinically as Ozempic, Wegovy, Rybelsus.
  • Structure: Lipidated peptide, nearly identical to liraglutide with stronger CH₂ signatures.
  • Spectroscopy: C–H stretches (2850–3000 cm⁻¹, ~85–90 THz) are stronger due to lipid chain.
  • Energetic relevance: Resonance programs show enhanced side-band energy in the aliphatic C–H regions, making its vibrational field “heavier” and more persistent.

3. Liraglutide

  • Biology: Another lipidated GLP-1 analogue, half-life ~13 hours, marketed as Victoza and Saxenda.
  • Structure: Similar fatty acid modification to Semaglutide, but shorter effect window.
  • Spectroscopy: Same canonical amide modes, but broadened slightly due to lipid tail dynamics.
  • Energetic relevance: Falls between Semaglutide and native GLP-1, bridging subtle flexibility with enhanced CH₂ expression.

4. Tirzepatide

  • Biology: A dual incretin agonist, activating both GIP and GLP-1 receptors. Marketed as Mounjaro and Zepbound.
  • Structure: Lipidated peptide with extended sequence; strong CH₂ intensity.
  • Spectroscopy: Shares canonical bands, but dual-receptor design influences secondary structure, giving slightly broadened Amide I/II bands.
  • Energetic relevance: Richest vibrational palette due to dual-binding orientation—seen as more complex resonance layering.

5. Exenatide

  • Biology: Derived from the saliva of the Gila monster, structurally distinct but GLP-1 mimetic. Shorter half-life, marketed as Byetta and Bydureon.
  • Structure: Non-lipidated peptide, different sequence.
  • Spectroscopy: Canonical amide modes, minor shifts from sequence variation.
  • Energetic relevance: Leaner resonance profile, less dense CH₂ vibration, making it a “lighter” harmonic field.

6. Dulaglutide

  • Biology: A GLP-1 analogue fused to an IgG4 Fc fragment, giving a very long half-life (~4–5 days). Marketed as Trulicity.
  • Structure: Large fusion protein, heavy, more complex vibrational spread.
  • Spectroscopy: Broader peaks in low-frequency collective modes (0.6–6.0 THz).
  • Energetic relevance: Expansive resonance, with less sharp modes and more diffuse harmonics.

Comparative vibrational data (THz ranges)

Program structure

  • Amide III: 11.0 min (warmup + focused block)
  • Amide II: 10.0 min
  • Amide I: 10.0 min
  • Amide A: 12.5 min (focused + cooldown)
  • Transitions (sweeps): 1.5 min

Advanced Subharmonic & Usage Data

The following table shows the calculated subharmonic frequencies, isotope sensitivities, binaural offsets, and recommended audio delivery types for each peptide and vibrational mode.

MoleculeModeWavenumber (cm⁻¹)Subharmonic Frequency (Hz) ≤20kOctaves ReducedLow Subharmonic Frequency (Hz) ≤500Low Octaves ReducedIsotope-sensitive atomsIsotopic panning (L/R)Binaural/beat offset (Hz)HeadphonesCoilTENSVibroacousticPEMF Mat
Native GLP-1Amide A330011517.1433359.9138H→D; 15N minorL light • R heavy1–3Sine; fades; AMSine/triangle burstsBiphasic PRFSine / 40–80 HzSine bursts
Native GLP-1Amide I164311468.2832358.3837¹³C/¹⁸O C=OL light • R heavy0.5–2Sine; fadesSine/triangle burstsBiphasic PRFSine / 40–80 HzSine bursts
SemaglutideC–H stretch290010121.1333316.2938H→D C–H→C–DL light • R heavy1–3Sine; fadesSine/triangle burstsBiphasic PRFSine / 40–80 HzSine bursts
TirzepatideC=O side171011935.9532373.0037¹³C/¹⁸O carbonylL light • R heavy0.5–2Sine; fadesSine/triangle burstsBiphasic PRFSine / 40–80 HzSine bursts
DulaglutideAmide I164011447.3432357.7337¹³C/¹⁸O C=OL light • R heavy0.5–2Sine; fadesSine/triangle burstsBiphasic PRFSine / 40–80 HzSine bursts

What Tirzepatide biologically does

Tirzepatide is a dual incretin peptide acting on GLP-1 and GIP receptors. It supports appetite regulation, insulin response, slower gastric emptying, satiety, and weight control. Formulations include Mounjaro and Zepbound.

What it includes

  • Amide A – N–H stretch (H/D substitution sensitive)
  • Amide I – C=O stretch (¹³C/¹⁸O sensitive)
  • Amide II – N–H bend + C–N stretch
  • Amide III – Mixed C–N/N–H backbone motions
  • C–H stretches – lipid side bands
  • C=O side chains – isotope sensitive

Who is this for?

  • Individuals seeking calm satiety and fewer cravings
  • Mindful eating practitioners
  • Digestive harmony and energy rhythm support
  • Meditators exploring peptide resonance
  • PEMF, coil, mat, or vibroacoustic users

Why this program is unique

  • Expanded palette – multiple Amide + side modes
  • Bass mapping – tied to molecular fingerprint
  • Isotopic awareness – H→D, ¹³C, ¹⁵N, ¹⁸O built-in
  • Cross-platform – headphones, coils, mats, vibro, TENS
  • Flow structure – warmup, blocks, sweeps, cooldown

Potential benefits

  • Encourages inner satiety and balanced food choices
  • Supports digestive calm and smooth energy flow
  • Deepens relaxation and body awareness
  • Enhances PEMF, coil, and vibroacoustic practices
  • Provides a unique vibrational echo of GLP-1 peptide biology

Instructions

  • Headphones – Over-ear, wired, comfortable volume
  • Schedule – Up to 3 × 45 min sessions/day or loop at night
  • Grounding – Always 2–5 minutes before/after with breathing & hydration

Use with the Imprinter

  1. Place water or an object on the plate while track plays
  2. Store charged items in copper or Faraday bags
  3. Metatronic Flower of Life Dual Frequency Imprinter

Use with iTorus coils

  1. Position coil near abdomen or midline
  2. Low to moderate drive
  3. iTorus i2 | iTorus i5

Use with PEMF Mat

  1. Lie on the mat while track plays
  2. One 45 min session recommended (extend into sleep if desired)
  3. Vortex 6 PEMF Mat

Use with TENS

  1. Apply 4 pads in a 2×2 grid on abdomen/lower back
  2. Keep intensity comfortable; avoid chest, neck, head

More useful tips

  • Hydrate before and after (minerals optional)
  • Journal sensations for awareness
  • Pair with slow breathing: 5 sec inhale / 5 sec exhale
Disclaimer: This program is an experimental vibrational wellness audio. It is not medical advice and does not diagnose, treat, cure, or prevent disease. Do not use with implanted medical devices. If pregnant, epileptic, or under clinical care, consult your provider before use. Always listen at comfortable levels and stop if discomfort occurs.