Mad Mice & The Monte Carlo Method

Cultocracy note :

The basis of optogenetics is the genetic insertion of a fluorescent protein into a target cell group . The cell group can then be ‘activated’ by the application of an external light source , including infrared frequencies .

Similar effects can be produced by the insertion of metallic compound nano particles or modified D.N.A / R.N.A which are responsive to frequencies such as microwaves or other specific RF frequencies .

Individual tissue groups can be targeted using these methods , such as neuronal cells . Advanced targeting can insert modified D.N.A into the calcium signaling pathways in neuronal cells .

Rare Earth Metals have unique electromagnetic and luminescent properties . They are particularly suited to bio-sensing applications similar to optogenetics .

A recent article in ARS Technica described how a research team based at the Chinese Academy of Sciences have used optogenetics to stimulate the prefrontal cortex of a mouse brain to turn the mouse into an aggressive ‘super soldier’ .

The experiment used a standard ‘tube test’ where two mice are pitted against each other in a tube , the ‘winner’ mouse will always push the ‘loser’ mouse to the opposite end of the tube . In this particular experiment the dominant mouse is not necessarily the strongest , but is the most aggressive and tenacious because the section of the brain controlling aggression has been stimulated using light .

The experiment also suggested that the behaviour of a ‘winner’ mouse could be permanently altered to be more aggressive simply by stimulating the required brain region several times . Essentially the stimulated mouse brain undergoes a synaptic reconfiguration and aggression becomes hardwired into the mouse , forming a new ‘winner’ behaviour pattern . The mouse continues to win the tube test without the need for further external stimulation .

The research findings are not new . Similar research has found that optogenetic techniques can be used to inhibit pain , control reward seeking bahaviour and even ‘switch off’ the brain completely . You can safely assume that many other physiological & psychological functions guided by brain patterns have also been mapped in the same manner . You can also safely assume that optogenetic research is far more advanced than what is actually reported .

Like most bioscience the research can be used for therapeutic or diagnostic medical purposes . Or it can be subverted and used as a sophisticated tool of control which can map and therefore invoke a neural or biological process .

These findings could shine a new light (no pun intended) on the seemingly inexplicable ‘shootings’ and ‘random terror attacks’ that plague the modern world .


Is there a link between mind control technologies and ‘mass shootings’ ?


Optogenetics uses light sensitive molecules or proteins that are stimulated using a variety of visible or invisible light frequencies . The light sensitive molecules are genetically introduced to the targeted neuronal cells which are not light sensitive . The genetically modified neuronal cells can then be ‘activated’ using light to excite the modified neuronal cells which re-emit the light at a different wavelength . This process allows precision monitoring or control of the target cells .

The basic proteins used in optogenetics are called channelrhodopsins and are found in green algae where they function as photoreceptors .

A similar protein is the Green Fluorescent Proteins (GFP) which was was first extracted from a jellyfish , this original protein has since been further modified into several variants . Other fluorescent proteins are found in bacteria , specifically the small ultra red fluorescent protein (smURFP) which was cultivated from Cyanobacteria . Variants of the smURFP protein have been evolved which can covalently bond to biliverdin which is formed in the human body when red blood cells break down .

In biological terms a channelrhodopsin protein acts as a light-gated ion channel . When exposed to visible or IR light the protein opens allowing charged ions into the cells , this electrical charge causes the channelrhodopsin protein to fluoresce .


When a fluorescent protein is genetically spliced to a neuronal cell , visible or IR frequencies can ‘activate’ the modified neuronal cell . The cellular response is reversed when the light stimulation is stopped . In some cases the modified neuronal cell can also be ‘deactivated’ using a different wavelength of light .

Gene Delivery

Transgenic DNA needs to penetrate three biological barriers to successfully integrate itself into a cell . These are the cellular membrane , nuclear membrane and the chromosomal structure . There are a variety of methods for achieving gene transfer which can be classified into two broad groups , viral and non-viral .

Transfection introduces a foreign nucleic acid (D.N.A or R.N.A) to the target cells . The process uses chemical reagents to create a positively charged DNA / RNA complex or soup . This complex is then attracted to a negatively charged target cell , it then enters the cell and forms the new genetically modified hybrid cell .

Electroporation uses an electric or laser pulse to disrupt the membrane of the target cells . This then allows a foreign nucleic acid to pass through the cell wall and form the new hybrid cell . The equipment used in electroporation is termed a ‘gene gun’ .

Transduction uses a virus or bacteria to introduce the foreign nucleic acid to the target cells also known as horizontal transfer . In this process a portion of the DNA / RNA in a virus is replaced with foreign DNA / RNA , the process takes advantage of the fact that a virus naturally incorporates certain portions of a hosts DNA in it’s natural cycle . The virus is then introduced to a subject where the virus inserts the foreign DNA into the target cells . Certain virus types such as adeno-associated virus (AAV) are perfectly suited for transduction in humans as they are not thought to cause any disease .

The transduction method can be further divided into generalized & specialized transduction .

Impalefection uses nano-fibres or nano-tubes which carry the foreign DNA / RNA . The nano-fibres attach themselves to a cell and then penetrate the cell wall , the DNA / RNA is then introduced to the target cells . Cell penetration can be enhanced by the application of electromagnetic radiation .

Each of the above methods of gene transfer has it’s advantages & disadvantages . Once gene transfer has occurred the genetic properties of the hybrid cell are inherited in future cell divisions .

Sleeping Beauty

In recent years the non-viral ‘Sleeping Beauty’ (SB) transposon system has been developed and is now considered a ‘safer’ and more efficient method for human subjects due to the accuracy in targeting specific tissue or cells.

The system consists of a transposon , a carefully matched transposase and the foreign DNA .

A transposon is a mobile segment of DNA that can replicate within the genome and is found in almost all living organisms , they are thought to constitute around 2-3% of the total human genome .

In simplistic terms the transposon can be visualized as a transporter carrying the foreign ‘DNA package’ which needs to be inserted into the DNA of biological tissue , such as the brain . The transposase is an enzyme which binds to the transposon & then homes in and ‘cuts out’ a section of target DNA . The ‘DNA package’ from the transposon is then ‘pasted’ into the gap in the target chromosome (DNA molecule) .


CRIPR (Clustered Regularly Interspersed Palindromic Repeats) is a relatively new gene editing technique which is very similar to the ‘Sleeping Beauty’ method . Just like the SB method , CRISPR uses an RNA molecule to ‘home in’ on a specific DNA sequence . Attached to the RNA molecule is an enzyme called Cas9 , this enzyme then ‘cuts out’ the required portion of DNA .

Unlike SB , CRISPR does not carry a DNA payload , which in SB is ‘pasted’ into the gap . In the CRISPR method the Cas9 enzyme can lie dormant at the ‘cut’ or gene gap , inhibiting or silencing gene expression . Alternatively a protein (for example a green fluorescent protein) can be attached to the dormant Cas9 enzyme , the enzyme can then act as ‘switch’ , activating the specific section of DNA where the Cas9 enzyme lies . In the case of an attached GFP protein the switch is activated by IR or NIR light .

Tissue / Brain Penetration & Interaction by infrared (IR) Laser

So we have now established how transgenic DNA can be introduced to neuronal tissue , the result being a subject that can potentially be stimulated by visible & IR light focused on the brain . But can IR or NIR (near infrared) light penetrate the skull and the brain tissue to activate the neuronal cells ?

In short , yes it can .

The penetration depth depends largely on the power , frequency & wavelength of the IR laser . Many low power infrared (or NIR lasers) cannot penetrate bone or skin tissue . Higher power lasers can penetrate the surface tissue but will damage the brain tissue . This problem is solved by rapidly pulsing the laser at specific wavelengths which can both penetrate surface tissue & not cause obvious damage to the underlying brain tissue .

The issue is further complicated by the fact that certain tissue types absorb light whilst other types scatter the light , the scattering effect can serve to increase the depth of tissue penetration as the reflected light spreads out . NIR light is weakly absorbed by most tissue and the scatter effect is prominent , allowing deeper tissue penetration than other light wavelengths . The near infrared window describes the optimum wavelengths at which light can penetrate tissue most effectively .

Recent studies have shown that NIR lasers operating at a power level of 10-15w and at a wavelength of 800-1000nm can penetrate brain tissue to a depth of around 3cm or more . Although these figures relate to a therapeutic laser operating in close range to the subject .

Optical probes

The penetration depth into biological tissue can be greatly enhanced by the surgical surgical insertion of optical probes , which function in much the same way as fiber-optic cables . The polymer probes are flexible and mimic natural tissue , therefore allowing D.N.A to be fused to the probe .

The probes can also be dosed with modified D.N.A proteins such as GFP , which react to a certain frequency or chemical compound . Furthermore , modified proteins bonded to the hydrogel can be engineered to release certain natural biological proteins when stimulated , the released proteins could then alter or accelerate a natural bodily response . Genetic markers in the human body that produce a hormonal response could be replicated using this method .

The probes can also be used to monitor cellular activity and emit light when faced with a particular metabolic response . For example a probe could be bonded to genetically modified receptors which are activated when the calcium signaling pathways between individual neurons are activated .

Neural probes could further be placed under an opaque surgically implanted ‘skull cap’ which would allow light to enter the cranium directly for the stimulation of neural cells .


In the example shown on the left a small hole is made in the skull and then ‘patched’ with a small disc of nano formed zirconia , allowing a directed beam to be targeted at a specific region of the brain . A small array of implanted discs would allow access to the major sensory regions of the brain .


Other slightly more sophisticated probes allow light activation , gene delivery and also the monitoring of a biological response at the cellular level .


An array of these probes could be used to activate a region of the brain and read the resulting neural signal . These arrays are often termed scaffolds .

When attached to a computer running software that is able to decode the invoked neural firing patterns , the probes could literally read your mind .

Quantum Dots

Hydrogel can also be loaded with quantum dots (QD’s) .

QD’s have semiconducting properties and can be ‘tuned’ so that they react to a specific frequency .


Lit up like a Christmas Tree

QD’s can be bonded to the hydrogel along with other biological enzymes . The enzymes can be genetically engineered to activate when faced with a specific metabolic reaction , the enzyme then starts a domino effect which causes the QD to fluoresce . For example , an enzyme that reacts with calcium could detect the calcium signaling of a firing neuron , this then causes the QD to fluoresce , thereby creating a pattern of neural activity that can be transmitted to the hydrogel probe .



Magnetic nano particles can also be fused to the hydrogel along with QD’s . The magnetic particles can be activated by an external electromagnetic frequency which causes the QD’s to fluoresce , which in turn activates the modified enzymes , which in turn causes the synthetic firing of neuronal cells .

Another domino effect .


Mind the Terahertz Gap

Terahertz (THz) frequencies , also known as submillimeter waves or T-Rays , occupy the gap on the electromagnetic spectrum between microwaves and infrared light . Terahertz frequencies seem to share both the optical properties of light and the wavelike properties of low frequency RF waves .


Electromagnetic Spectrum

A few facts about THz waves :

  • Unlike X-rays , T-rays are non-ionizing which means that they are considered less harmful to biological tissue .
  • Just like X-rays , T-rays can be used for biological imaging .
  • T-rays are absorbed by the Earth’s atmosphere , including fog and clouds .
  • T-rays can penetrate many common materials such as clothing , wood , masonry , plastic and ceramics . The penetration depth of T-rays is generally less than microwaves .
  • T-rays can penetrate biological tissue to a depth of only a few millimeters .
  • T-rays can be absorbed by biological proteins and many other materials .
  • T-rays are easily absorbed by a liquid such as water .
  • Electrons in semiconductors resonate at THz frequencies .
  • Carbon nano tubes can be formed to both absorb and emit THz frequencies .
  • Graphene and THz frequencies have been described as the future of electronic communications .
  • Biological proteins and D.N.A vibrate at THz frequencies in the picosecond range . This vibration is thought to form part of the process of cellular communication and also facilitates cellular interaction with other compounds .


  • Specific proteins , D.N.A and other compounds are thought to have their own unique ‘THz fingerprint’ at which they vibrate . In fact most objects and materials are known to emit faint T-rays .
  • The application of a THz wavelength to a protein , which matches the THz ‘fingerprint’ of the protein , can enhance the reaction rate of the protein . Theoretically this could speed up a specific biological process , depending on which proteins are targeted .


At first glance it would seem that infrared , THz and other similar bands of the electromagnetic spectrum are useful in biosensing applications , but only at close range because the frequencies are absorbed or attenuated by atmospheric effects and have low penetration depths in biological tissue .

This is not entirely true .




Cultocracy note :

Debris in above diagram = Human Target


Source : Advanced Concepts Team, European Space Agency

Advanced tunable laser systems have now been developed . The beams can be directed using filament propagation which acts as a waveguide . The system can be enhanced with atmospheric compounds . An ‘atmospheric lens’ can also be created using charged particle beams , the ‘lens’ that is created can be used to converge or diverge a separate laser beam .


Do you think that deep state organisations would never conduct covert testing on random human targets ?

Do you think that advances in genetics are being tested only on mice and rats and would never be tested on targeted individuals ?

Do you think that nano technology and genetics will never replace traditional military hardware ?

Do you think that slavery and control of individuals has been abolished ?

Do you think that a large underground network of research and development facilities are a myth ?

Do you think that the technology does not exist and is far from being developed ?

Think again .

The military corporate complex is at the forefront of the development of the technology described in this article .

 Coming soon : Mad Mice & the Monte Carlo Method – Part 2

Related :


  1. Scientists Turn Docile Mice Into Super Aggressive Alphas With Brain Stimulation
  2. A brain implant turns “loser” mice into aggressive fighters
  3. Pain Inhibition by Optogenetic Activation of Specific Anterior Cingulate Cortical Neurons
  4. ‘Optogenetics’ used to control reward-seeking behavior
  5. Optogenetics and Deep Brain Stimulation Neurotechnologies (PDF)
  6. Near-infrared light penetration profile in the rodent brain (PDF)
  7. Pulsed infrared light alters neural activity in rat somatosensory cortex in vivo (PDF)
  8. Optogenetics: controlling brain cells with lasers
  9. AI , Genetics & Eugenics
  10. Nano Fibres , Bacteria , D.N.A manipulation , Epigenetics


  1. Fluorescent protein-based calcium integrators (patent)
  2. Label-free tetra-modal molecular imaging of living cells with CARS, SHG, THG and TSFG
  3. Channelrhodopsin
  4. Near-infrared fluorophores for biomedical imaging



  1. Wireless Optofluidic Systems for Programmable In Vivo Pharmacology and Optogenetics
  2. Using lasers and carbon nanotubes to look inside living brains
  3. Through Skull Fluorescence Imaging of the Brain in a New Near-Infrared Window (PDF)
  4. Futuristic brain probe allows for wireless control of neurons
  5. Wireless Optofluidic Systems for Programmable In Vivo Pharmacology and Optogenetics
  6. Brain probe of the future allows scientists to wirelessly deliver drugs and control neurons
  7. Spin-Based Broadband Terahertz Radiation from Topological Insulators


  1. Pulsed Laser Tissue Interaction
  2. Laser-Tissue Interactions (PDF)
  3. Near-infrared photonic energy penetration: can infrared phototherapy effectively reach the human brain?
  4. Laser Penetration NASA (PDF)
  5. Lockheed Martin To Showcase Aculight Laser Products And Capabilities
  6. New record achieved in terahertz pulse generation


  1. TeraHz heterodyne system for bio-imaging
  2. Scanning Terahertz Heterodyne Imaging Systems


  1. The Sleeping Beauty transposon system: a non-viral vector for gene therapy
  2. Sleeping Beauty Transposons
  3. Sleeping Beauty Transposition: Biology and Applications for Molecular Therapy
  4. Efficient Sleeping Beauty DNA Transposition From DNA Minicircles


  1. Bose–Einstein condensation (network theory)
  2. Quantum coherent-like state observed in a biological protein for the first time
  3. Weak, strong, and coherent regimes of Fröhlich condensation and their applications to terahertz medicine and quantum consciousness
  4. Terahertz radiation induces non-thermal structural changes associated with Fröhlich condensation
This entry was posted in Health, Mind Control, Psychotronic Warfare, State Surveillance & Control, Targeted Individuals, Uncategorized. Bookmark the permalink.

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