CYTOTRON - NEUROLOGICAL DISORDERS

CYTOTRON - NEUROLOGICAL DISORDERS

Rotational Field Quantum Magnetic Resonance–Fast Radio Burst (RFQMR-FRB) therapy represents a patented electromagnetic modulation technology that delivers circularly polarized radiofrequency bursts to interact with biological tissues at the quantum and cellular levels. This approach, implemented through the Cytotron system, is designed to modulate neuronal cell membrane potential and trigger molecular pathways that promote neuroprotection, neurogenesis, and synaptic repair without causing thermal or ionizing damage

Biophysical Basis

RFQMR-FRB is generated by Switching signals through rotating helical antennas synchronized with magnetic field modulators. The resulting rotational electromagnetic fields produce high-energy fast radio bursts (3 kHz – 300 MHz) characterized by circular polarization. When these fields interact with hydrogen nuclei and bound water molecules in neural tissue, they alter proton spin orientation and influence transmembrane potential (TMP). This modulation affects voltage-gated ion channels (VGICs), leading to a controlled influx of calcium ions (Ca²⁺)—a key secondary messenger in neuronal signaling. Consequently, RFQMR-FRB acts as an informational electromagnetic signal, initiating intracellular cascades responsible for neuronal activation and regeneration.

Molecular Mechanisms of Action

Key Signaling Pathways

Pathway Function Biological Outcome
Hsp70/Hsp90 Activation Chaperone-mediated cellular stress protection Reduces oxidative stress and misfolded protein accumulation
MAPK/ERK Pathway Mitogen-activated growth signaling Stimulates neuroprogenitor proliferation and differentiation
Ca²⁺/Calmodulin–CREB Pathway Calcium-dependent transcription activation Promotes synaptic plasticity, memory formation, and neurotrophic expression

Exposure to RFQMR-FRB induces the expression of multiple growth-associated proteins and neurotrophins, including Brain-Derived Neurotrophic Factor (BDNF), Nerve Growth Factor (NGF), Glial-Derived Neurotrophic Factor (GDNF), Vascular Endothelial Growth Factor (VEGF), Fibroblast Growth Factor 2 (FGF2), and Insulin-like Growth Factor 1 (IGF-1). These proteins collectively mediate neuroprotection, regeneration, and synaptic reorganization.

Therapeutic Mechanisms and Biological Outcomes

Mechanism Description Clinical Implication
Neuroprotection Reduction in apoptosis via Hsp70/90 activation and antioxidant signaling Slows neuronal loss in degenerative disorders (e.g., Parkinson’s, ALS)
Neurogenesis Induction of neuroprogenitor proliferation and differentiation Supports recovery post-stroke and in demyelinating conditions
Synaptic Repair Enhancement of BDNF/NGF-mediated synaptic connectivity Improves memory and cognitive performance
Vascular Regeneration VEGF-mediated angiogenesis in ischemic neural regions Promotes oxygenation and tissue repair

Safety and Biocompatibility

RFQMR-FRB therapy is designed to operate within non-ionizing and non-thermal electromagnetic parameters. No tissue heating or ionization occurs. It acts as a bio- informational modulator, not an ablative stimulus, and is safe for repetitive, localized, and long-term applications

Clinical Relevance and Future Directions

RFQMR-FRB introduces a biophysical and non-pharmacological strategy for managing Neurological disorders by activating the brain’s endogenous repair mechanisms. Potential applications include Neurodegenerative diseases (Parkinson’s disease, ALS, Alzheimer’s, Epilepsy, Multiple Sclerosis), Neurotraumatic conditions (stroke, traumatic brain injury, spinal cord injury), Neurodevlopmental disorders (Autism spectrum disorders, Attention deficit hypersensitivity disorder, intellectual disability) and Non-progressive Neurological disorders & Hypoxic Brain Injury (cerebral palsy, post-ischemic syndromes). Future research focuses on validating its quantum-biophysical interaction mechanisms and translational efficacy through molecular Neuroimaging and clinical Neurophysiological studies.

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