The localized acetylcholine, dopamine, and epinepherine, as well as cortical homonculus of those areas reduction of gaba activity and adenosine build up could cause much larger amplitude of sensual feeling at the hips, buttocks, and thighs, causing
greater sexual and recreational dance pleasure. These may also cause nongenital pillow humping like orgasms even during partner sex, which is also supported and amplified this way. Sexual hip and thigh movements from thrusting to bouncing while woman on
top riding are brain chemistry adjustable to be 200-300% stronger and more vigorous, increasing sexual pleasure intensity at mover, simultaneous movers, and receivers of the stronger sustained thrusting and riding/bouncing motions. Along with the
cortical homonculus the cerebellum, brainstem, and pelvic ganglion could be superactivated by a new localized sex enjoyment and performance drug that causes female hip lifts to meet more intense and possibly faster male thrusting. A variety of brain
localization drug activity areas are published, and are written at my paper notes. A new one is laser or thz beam illuminating specific brain areas. Everywhere that gets illuminated undergoes a drug or docking site epithelial capillary attachment
reaction like michael reaction keratin attaching henna, this attaches a beneficial peptide like epithalon dimer to the capillaries in that specific brain area. Then, aptamer peptides that glom to epithalon dimer, where those glomming aptamers are
attached to a neuron modulating drug concentrate at just those physical areas of the brain with the highly localized epithalon dimers on them. The peptide aptamer is attached to the active drug with an enzymatically degradeable linker so that it is
gradually released to diffuse into its nearby highly localized brain area. Photoacoustic tomography seems to be modifiable to make photoacoustic brain stimulation, with a 2012 resolution of 1 mm or less through monkey skull, and a 2012ish resolution of
about 2.5 mm through human skull. 1-2.5 mm brain area localization, smaller than some 2020Ad fMRI voxels is made possible with photoacoustic cofocalization or overlapping intersecting light sheets outside the head. Photoacoustic brain localization could
be improved by using THz radiation which easily passes through hair. A THz responsive michael reaction epithalon dimer docksite making drug is likely possible. A thz fiber optic cap can then install the dockingsite ultra high localization drugs. To
increase the the resolution of the 2012ish 2.5 mm through the human skull technology, metamaterial superlensing can produce an activity beam about 1/10th the size of a wavelength of light, Thz radiation, or acoustics. That order of magnitude might make
250 micrometer voxel brain drug activation size from the modification of the published through the skull 2.5 mm technology. As an experience the user would put a Thz active swim cap on their head, once, for 7-11 minutes and snort or drink liposomal
docksite generating drug. More than one docksite, perhaps hundreds of different brain localizations, from a single swim cap Thz treatment. Then, noting the described sex drug, anytime the person felt like being a better sex partner and having a more
pleasurable sexual experience they could take oral liposome or somethingsome aptamer to epithalon moiety drugs, or perhaps snort them to have enhanced sexual attributes from 3-14 days before the next dose. A depot drug airjection of the brain localized
docksite sex drug could last decades or even centuries. (If 1 gram of localized brain tissue is dosed then that is 1/70k the usual oral amount of a drug, or 360 years of drug activity with 100-200 mg airjected depot drug). This docksite building laser/
thz procedure can also increase wellness and longevity when treating cardiovascular disease and cancer. To prevent heart attacks and angina and strokes install a plurality of docking sites for anticholesterol drugs right on top or artery narrowing
cholesterol plaque lumps. No bone between various angles of heart and chest surface makes 3-7 micrometer sized docksites easy to make. After the docksites are produced the person can take anticholesterol drugs with an enzymatically degradeable link to
the docksite glomming peptide aptamer. Similarly to terminate oncocytes at tumors with minimal risk of metasteses use beamed photoacoustics to internally cauterize the entire tumor, raster scanning the cyte termination beam terminates all the tumor
tissue. Another anticancer approach that reduces unwell feelings and risk of cancer spread is to cauterize all the arterioles and capillaries feeding the tumor, and create a layer of minimized oxygen and food passing scar tissue around the tumor, causing
tumor cells to expire from lack of nutrients. As a side thing, injecting highly deliquescent potassiumPCA NaPCA or better into a tumor pulls all the water out of tumor cells to liquefy the PCA. Doing that to a tumor may terminate it osmotically, and at a
laser/thz encapsulated tumor the PCA absorbs all the water. The technology of through the skin laser/Thz photoacoustic cofocal or intersecting light or 3D light shapes to multicentimeter depths makes this function.

NMN or NR with a blood brain barrier passing moiety, which could be as simple as an acetyl or diacetyl could benefit cognitive ability even raising g (like IQ). Enteric coated pills could be tested at volunteers, and a longevity increase study with mice
could measure longevity increase, if any. A high dose potency version could have enhanced transport to mitochondria with a triphenylphosphonium moiety.

PQQ contains a triphenylpolyphosphonium (TPP) group, causing it to have preferential transport to mitochondria. NMN or NR or NAD with a TPP moiety could preferentially concentrate at mitochondria, strongly increasing dose potency and benefit. The TPP
group could be attached with an enzymatically deggradable linker.

Brain scans and voluntarily taking on the brain localization and neurotransmitter activity of exemplarary 9.9th percentile of subjective well being (happiness) mentally well and being at 99.9th percentile of g, cognitive ability, who are voluntarily
employed who enjoy their work, are 9.99th percentile of light triad psychometric scores, and have had 3 children who they love. Find these exemplarary persons and have them wear a portable brain scanner for a month (the lightest wear-anywhere brain
scanner ive read about is one for mice that weighs near 2.59 grams, so a human version might be 100 grams, or with technology improvements 8-16 grams), during that month about 40 environments, actions, states of mind, live conversation topics, computer
use reactions, and benefits and challenges occur per 24 hours, so 1240 microevents and situations per month, many of which are highly similar. As a beneficial voluntary mental illness treatment the mentally ill could take photonically/Thz activated
neurotransmitter drugs and wear a headband or circlet that illuminates specific brain areas to activate the drugs such that the mentally ill person's brain duplicates-approximates the brain activation of an exemplarary person. This could be measured to
verify improvement of quality of life and reduction or removal of mental illness symptoms like depression, voices, visuals, delusions, paranoia, and apathetic negative symptoms of schizophrenia. Most people are well. Mentally well people could wear a
circlet or headband and take the photonically/Thz activated neurotransmitter drugs to try out, learn from, and utilize exemplary persons brain chemistry patterns, improving partner, work, children, happiness, propensity to light triad feelings, thoughts,
beliefs and behaviors. From utilizing exemplary persons brain area activation chemistry they could even know they were benefitting their childrens future from the cumulative effect of raising them well. Notably, a plurality of different exemplary persons
would be recorded, and software synthesized super-exemplary brain area chemistry simulations provide a wide range of different, but all beneficial brain area chemistry exemplars.

At circlets and headbands that scan the brain and activate brain area localized drugs, THz terahertz radiation may be advantageous as i think it sees through hair, just like it sees through garments and it may also be unchanged by passing through scalp
hair. Possibly any engineer or technologist would improve photonic/Thz brain imaging, drug activation, brain localization by utilizing numerous circa 2016-2020AD technologies; wikipedia ghost imaging, negative refractive index metamaterial subwavelength
focusing and light shape making, synthetic aperture/refractor computer directed volumetric holography, spectroscopy of deuterated neurotransmitter drugs IDs their amount, activity, location, and products, EEG waves considered as tens of thousands or
hundreds of thousands of separately computer correlateable hyperspectral components, resolution heightening front, mid, and deep brain laser produced focusing reticles produced as veticle line looking sequences and 2D lined circles on the walls of
capillaries, the blood brain barrier, and vessels like arterioles a size up from capillaries

It could be that unpoppable except at the liver electrically conductive liposomes could have color or polarization change with electrical field liquid crystals in them, or electroactive quantum dots in them, noting that each liposome could contain its
own reference voltage silver zinc ion or metal concentrations across an onion layer liposome, or a miniature onion somethingsome inside a much bigger liposomal bag. Photonic brain scanning and spectroscopy could then do a thing like an all brain volume
or area of interest highly detailed 3D electroencephalograph, and computers could record it changing with thought and feeling processes

4 times antipsychotic drug concentration just at the brains audio processing areas could voluntarily and beneficially get rid of the mental illness sourced voices people hear

wikipedia ghost imaging of .25 mm aperture, a series of 2020 photonic voxels

An epigenetic drug that permanantly, but reversibly amplifies intelligence (g like iq) and improves memory is acetylation of arginine vasopressin production and receptor genes, such as those found at arginine vasopressin neurons. Also, viewed as a
network, there may be physiochemicals and receptors that previously decreased arginine vasopressin response. These can be epigenetically reduced with hypermethylation of their genes. RNA drugs are among numerous possible epigenetic drugs to do this.

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