From: treon3verdery@gmail.com   
      
    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.   
      
      
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    * Origin: you cannot sedate... all the things you hate (1:229/2)