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December 12, 2011

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Pharmaka, Philtres, and Pheromones: Getting High and Getting Off

m a p s • v o l u m e X I I n u m b e r 1 • s p r i n g 2 0 0 2 By Jonathan Ott, Director of Applied Psychonautics, Natural Products Co., Xalapa, Veracruz, México We've been told that with regard to seduction, "candy is dandy, but liquor is quicker," but in truth, rather, properly selected: "candy makes randy; liquor makes desire flicker;" or, as Shakespeare's porter said to Macduff: "[drink] provokes the desire but it takes away the performance." The wines and beers of antiquity, however, which were potent infusions of innumerable psychoactive plants often requiring dilution with water and in which alcohol served rather as preservative than inebriating active principle, had already in Shakespeare's day given way to straight alcoholic beverages, if anything augmented by the soporific and anerotic hops, Humulus lupulus. We know not the venereal verities of the archaic wines of mandrake, Mandragora officinarum (the famous aphrodisiac of the Biblical story of Leah and Rachel), nor of the genuine Pilsener beer, which gets its name, not from the place -- Pilsen -- but from Bilsenkraut, its original inebriating principle, Hyoscyamus niger or henbane, which contains visionary tropane alkaloids [Raetsch 1996; 1997]. It is still possible, albeit difficult, to obtain genuine absintheliqueur in Europe, a potent alcoholic libation fortified with extracts, or oil, of wormwood, Artemisia absinthium, which owes its psychoactivity to the volatile terpenoid thujone, which has left a lubricous legacy, at least in European art [Budavari et al. 1996; Conrad III 1988; Ott 1996]. An anonymous 16th-century Italian manuscript, Ricette magiche e afrodisiache [Pezzella 1978], gives special emphasis to philtres or love-potions, stimulants to venery, and points the way to a modern science of aphrobiology. One recipe, "for venereal pleasures," posits the preparation of a potent alcoholic extract of black truffles, Tuber melanosporum, which is concentrated and made into an electuary or comfit with sugar and amber. A second, "a venereal balsam for the impotent," confects in olive-oil large quantities of betel "nuts," Areca catechu, and oil of nutmeg (Myristica fragrans), with animal ingredients: ants, Spanish flies, civet and "oriental" musk (pheromone-rich, sexual-attractant secretions from the civet cat and the Asian musk deer). The third, "for he who cannot make use of women," consists of boli or pills made from the powder of dried Cannabis, moistened with "a good white wine." Here we see echoes of the use of alcohol and wine rather as solvents than as active principles in the composition of philtres, not to mention of the proper way to make truffle-candies, and I have chosen these three recipes of the 27 in the manuscript to highlight the most promising directions for a modern pharmacology of philtres: 1) phero- Pharmaka, Philtres, and Pheromones Getting High and Getting Off by Jonathan Ott, Director of Applied Psychonautics, Natural Products Co., Xalapa, Veracruz, Mexico mones (as exemplified by the truffle, amber[gris], plus ants and musks); 2) stimulants (betel nuts); and 3) visionary inebriants (Cannabis). I will examine hereunder each of these three categories of 16th-century Italian philtre-formulations in some detail. Pheromones, The Quintessence Of Philtres Although the truffle might seem out of place here, in fact it was shown in 1981 to be a potent source of androstenol, known since 1944 to be a component of boar-testes, and patented in the early 1970s for use in artificial insemination of sows [Maugh II 1982]. In 1974, androstenol was discovered to be a component of human male axillary perspiration, and later to stimulate sexual interest in human beings. Truffles are one especially rich source, which accounts for their "musky" aroma, and here they are compounded with "amber," in reality ambergris, a pheromone-rich secretion of sperm whales, Physeter catodon, like sperm-whale spermaceti, used in perfumery and cosmetics. These pheromonal ingredients lend verisimilitude to the first of our Italian philtreformulae, the second of which features musk, both of the civet cat (various species, family Viverridae) and the musk deer (Moschus moschiferus). Musks, likewise from the North American musk ox (Ovibos moschatus), derive their name via Latin and Greek, from the Sanskrit muska, "testicle, scrotum," and consist of oleaginous secretions of special glands that produce sex-attractant pheromones (pheromones are hormone-like substances acting especially between members of the same species, here in mating, thus being allomones, of benefit to the emitting species; they can also serve as kairomones, or of benefit to another, or a receiving species, who might exploit them as attractants to predation). Musks have a long and storied use in perfumery, again as sexattractants, and the discovery that androstenol appears to be a human sex-attractant pheromone has now led to its use in male colognes and after-shaves, often touted in skinmagazines as infallible female lures. Similarly, the masculine pheromone androstadienone is said to attract women; the female pheromone estratetraene, to attract men [Holden 1999]. I have known women who occasionally rub a bit of their own vaginal secretions behind their ears, when they feel the need of such "passion-perfume" to "inphiltrate" some man or other. This points to the urgent need for concerted research into our human pheromones, which of course militates against the absurd superstition of the Judaeo-Christian world, that human beings are not, after all, animals. But we do indeed, like all mammals, possess non-olfactory vomeronasal neuroreceptors believed to respond to pheromones, and encoded by some 100 genes in rodents [Hines 1997; Holy et al. 2000]. Interestingly, neural signals from the binding of pheromones to these receptors bypass those ordinary olfactory pathways, and possibly the so-called "higher cognitive centers" [Dorries 1997], and go thence to the amygdala and the hypothalamus, in the so-called midbrain, which separates the brain-stem from the cerebral cortex (connecting to an accessory [posterior] olfactory bulb attached to the cerebral cortex) [Keverne 1999]. As might be expected, both the amygdala and hypothalamus are thought to control our emotional responses. Human menstrual blood and other vaginal secretions were used as ingredients in philtres or "love-potions," believed to incite both love and lust [Birchler 1975; Mueller- Ebeling & Rätsch 1986]. There has been limited research of female human pheromones, but one such study of 50 healthy young women who wore special tampons showed their vaginal secretions contained an extensive complement of simple compounds like acetic, propanoic, and butanoic acids, which are called "copulins" [Michael et al. 1974]. These are known sex-attractant pheromones from the vaginal secretions of rhesus monkeys, which stimulate male sexual activity, and they also occur in such secretions of many other primate species. Interestingly, the levels of these human pheromones varied according to the menstrual cycle, being at their highest concentrations in the phase corresponding to maximum fertility. Philtres were employed to induce someone to fall in love, and were supposed to provoke so-called "love-sickness." Here in México, people especially fear toloache (Datura species) as such an amatory "toxin." Until the mediæval period, men were allegedly primary victims of "love-sickness," although more recently it became rather a supposititious female condition--as in the "hysteria" of the Freudians. There was even posited a so-called virus amatorium in menstrual blood, and even modern textbooks of gynæcology (such as the sixth edition of Geburtshilfe-gynäkologische Propädeutik und Untersuchungslehre, Leipzig, 1967) there survived belief in the existence of an infectious "menotoxin" in human menstrual blood! But to return now to the truffle: as Valentina P. and R. Gordon Wasson showed in their seminal book Mushrooms Russia and History (which, together with a pair of popular articles in 1957 launched the socalled "Psychedelic Age" [Wasson & Wasson 1957; R.G. Wasson 1957; V.P. Wasson 1957]), truffles were long known in Europe as stimulants to venery; indeed, they are known as "testicles" in various languages, such as the old Castillian turmas de tierra or criadillas de tierra, "Earth's testicles," and when the potato first appeared in Europe, it acquired that reputation of the truffle, inasmuch as unscrupulous vendors would pass-off lowly potatoes as truffles. As Agustín de Zárate noted in 1555: "the Indians consume some roots known as potatoes, which are of the form, and almost even of the taste, of turmas de tierra [truffles]." This then gave rise to the phrase "to truffle" or swindle someone, which survives today corrupted as "to trifle" --- thus the cad who "trifled" with a damsel's affections was symbolically giving her a potato, instead of a pheromonal truffle of audacious amatorious repute! Stimulants To Sexuality Our second archaic recipe compounds betel nuts with pheromone-rich musks. Betel is one of the world's most widely-used stimulants, taken as a masticatory, the sliced or shredded fruits of the betel-palm being wrapped in aromatic leaves of the betle pepper, Piper betle, which has been smeared with a paste of a vegetable quicklime, and often the quid be seasoned with cloves and/or cardamoms and other spices, at times likewise with other drugs being added, such as opium and tobacco (and, at least during its glory days, also with cocaine). The major stimulating principle of betel is the alkaloid arecoline, which is one of the prototypical "smart drugs," shown to enhance learning [Sitaram et al. 1978]. In the Indian Ayurvedic system of medicine, betel is regarded to be an aphrodisiac [Raghavan & Baruah 1958]. Stimulants have singularly and collectively the reputation of potent aphrodisiacs; many act on the body's major stimulants system --- the adrenergic, responding to the hormone adrenaline and the neurotransmitter noradrenaline--also exerting dramatic effects on the neurotransmitter dopamine, key element of our so-called "pleasure-circuits" in the midbrain. The best-studied are the amphetamines, including the "psychedelic amphetamines" like Ecstasy or MDMA, and of course cocaine. Straight away one can dismiss MDMA as aphrodisiac--it belongs rather in the same class as alcohol, inasmuch as it "takes away the performance," as noted in a recent British book [Rudgley 1998]. The garden-variety amphetamines, on the other hand, richly deserve their concupiscent reputation, providing one does not exaggerate the dose. Not only do they dramatically heighten libido, but they have been used medically to reverse the depression of libido associated with the chronic use of some serotonineenhancing antidepressants--the "serotonergic" effect in general, while it may help to overcome depression, clearly depresses the sex-drive, which just might give the "patient" new cause for depression! Note, however, that the antidepressant drug nefazodone, Serzone® or Dutonin®, is known rather to enhance libido! Moreover, amphetamines can retard ejaculation in men and seem for many to enhance orgasmic pleasure; besides, they tend to raise blood-pressure, to which might accrue ancillary priapic benefits. The same can be said for cocaine; although again, excess doses may even depress male performance. Indeed, the plantsource of cocaine, the coca-leaf (Erythroxylum species) has a robust erotic reputation in its Andean home. As W.G. Mortimer noted in his 1901 classic History of Coca [Mortimer 1901], "The Peruvian Indians employ Coca to stimulate uterine contractions and regard it as a powerful aphrodisiac." He then went on to quote several contemporary authorities, who were adjudging its medical potentials before our modern era, blighted as it is with pharmacopathological nonsense: "Leopold Casper, of Berlin, considers Coca one of the best of genital tonics, and many modern observers concur in this opinion. Vecki says that cocaine internally to a man aged fifty-six invariably occasioned sexual excitement and cheerfulness." In fairness, it must also be said that he noted that homæopaths: "employ Coca in sexual excess, especially when dependent on onanism." I would say one "dependent on onanism" suffers rather from sexual dearth than excess, and this indeed serves as a valuable caveat regarding the dangers also of an insufficient dose of an aphrosidiac! As regards qat (Catha edulis), the stimulant-plant of Yemen and Ethiopia, the tender branches of which are chewed neat, and which contain the natural amphetamine cathinone and other stimulants: given that this was adopted as a drug in historical times, during the Moslem era, it is not surprising that there be little emphasis on aphrodisiacal effects in the scant literature. To be sure, like coffee after it (likewise adopted in comparatively recent times), and to avoid the general Islamic proscription of "intoxicants" (specifically alcohol, although this ban was extended to cover also traditional Arabian inebriants opium and hashish, but not the non-traditional tobacco), it became necessary to justify qat-use in the context of alertness for late-night Koranic study, for nocturnal prayers in the mosque, and the like. Although pharmacopuritans have disparaged qat-use as conducive to "sexual problems" (of course, for them, heightened libido is the primary such) and "spermatorrhea," or involuntary, non-orgasmic seminal emission, a recent careful study found that about a third of chronic male (but only about one in 20 of female) users reported aphrodisiacal properties, which were personally confirmed by the intrepid researcher, who found that qat-use both stimulated libido and enhanced sexual performance [Kennedy 1987]. Again, the dosage and ancillary health-factors may account for the 20% of male and 10% of female users who rather reported anaphrodisiacal effects. Of the caffeine-containing stimulants, it is the African cola-nut (Cola nitida), which has the strongest reputation as an aphrodisiac. Cola, of course, was ingeniously combined by a Georgia pharmacist with coca-leaves to yield the original Coca-Cola®, that brilliant, non-alcoholic "temperance" beverage which however, along with its host of imitators, was later to be denounced as being causative of the "Coca- Cola fiends" (largely African-American, of course), given to raping white women; to be used as a pretext to proscribe the free-sale of coca and cocaine in the United States in 1914. Coffee (roasted seeds of Coffea species), tea (fermented leaves of Camellia sinensis) and guaraná (seeds of Paullinia cupana) are alike caffeine-containing stimulants with some renown as aphrodisiacs [Rätsch 1997], whereas the caffeine-rich guayusa-leaves (Ilex guayusa) are used in Ecuador against female sterility, and in Argentina the related yerba mate (Ilex paraguariensis) is closely associated with romantic intrigue, judging by the number of mate-sayings used to intimate or reject coquetry. Another African aphrodisiac of wide repute is eboka or iboga, the root of Tabernanthe iboga, which contains the visionary stimulant ibogaine [Pope 1967; Shulgin & Shulgin 1997]. I would be remiss should I fail to mention here that other great African aphrodisiac, chemically related to eboka, yohimbe or the bark of Corynanthe johimbe, which contains yohimbine, an alkaloid that has been shown dramatically to enhance sexual motivation in male rats [Clark et al. 1984]; and has been used to treat "erectile dysfunction" [Pittler 1998]. My brief survey of stimulant aphrodisiacs would be incomplete were I to fail to include that most famous lovedrug of all time, chocolate or cacao, from the seeds of Theobroma cacao. As I detailed in my book on the subject [Ott 1985], when the Spanish conquistadores first reached the palace of Aztec ruler Moctezuma II, they were astonished to find the royal coffers filled, not with gold, but with cacaobeans, and that the emperor took no other beverage than his cacao-potion, cacáhautl, particularly when he would repair to his harem [Díaz del Castillo 1976]! Pharmacopuritans denounced chocolate early on as an "inflamer of passions," and indeed, its major alkaloid, theobromine (there are only minor amounts of the related xanthine, caffeine), proved to be a potent aphrodisiac in hornets, their drones even copulating with moribund queens [Ishay & Paniry 1979]! Although I should point out I have yet seen no evidence of such dramatic "inphiltration" in the human species, nonetheless chocolate is the love-drug, being packaged in heartshaped boxes for St. Valentine's Day gifts to a sweetheart, and theobromine, like love, is a potent cardiac stimulant, its effects akin to the quickening pulse of amorous excitement. Chocolate also contains minute levels of anandamide, which is our natural neurochemical whose receptor the THC from marijuana activates [di Tomasso et al. 1996], and Moctezuma's cacáhuatl was "spiked" with all manner of stimulant and visionary plants, which may help account for its reputation as an aphrodisiac [Ott 1985; 1996]. Compounded with the appropriate ingredients, not for nothing might they be known as "chocolate truffles!" Philtrum Psychopticum, Or Visionary Venery Our excursus among the erotic electuaries, philtry potions and pubic pomades now brings us to the truly heroic medicines, the "Psychoptica" or entheogens, in which direction points our third classic recipe, for the bhang-boli or pot-pills. Cannabis or marijuana, of course, has long been tarred with a licentious brush, but there are many who attest to its place on Aphrodite's altar. In my experience, unlike many of the pharmaka we have examined, where the emphasis in on male performance (for which alone I can personally vouch), Cannabis would seem to be a bisexual stimulant. In my case, I find its effects to be rather too debilitating in general to be of much use in this regard, more enervating than erotic, but many women I have known are effusively enthusiastic about its aphrodisiacal amatory attributes. In the pages of Playboy magazine [Leary 1966], Timothy Leary described LSD as being: "the most powerful aphrodisiac ever discovered," noting also that the LSD-state was to ordinary, waking consciousness as that state was to deep sleep. (I don't know about anybody else, but that had been enough for me--being a bored, 17-year-old high-schooler in the dreariest of suburbs, I began at once assiduously to seek LSD!) Leary, then well on his path from professor to proselyte, continued: "[S]ex under LSD becomes miraculously enhanced and intensified. I don't mean that it simply generates genital energy. It doesn't automatically produce a longer erection. Rather, it increases your sensitivity a thousand percent. [...] In a carefully prepared, loving LSD session, a woman will inevitably have several hundred orgasms." If that sounds too good to be true, it is--no woman I have ever spoken to has had the good fortune to experience any suchlike "carefully prepared LSD session!" Noting that by that time he had had 311 "psychedelic sessions" and had made love "every time I've taken" LSD, Leary twice evaded the interviewer's questions regarding the number of orgasms a man might expect under the lubricous influence of LSD! But Leary had clearly hit at least one nail squarely on the head, and by the following year there were pulp-novels aplenty, exposing The Sexual Paradise of LSD, LSD Lusters (both 1967) and the 1969 Acid Party, among others, all festooned with concupiscent cover-art. There had already appeared Thelma Moss' pseudonymous (as Constance Newland) account of her having been cured of her frigidity via LSD-psychotherapy [Newland 1962], one of many testimonials to the curative virtues of this uniquely-potent entheogen. The comments that follow apply likewise to the visionary familiars of LSD, such as psilocybine and the mushrooms that contain it (species of Psilocybe and other genera), mescaline (from peyotl, Lophophora williamsii, San Pedro, Trichocereus species, and others) and n,n-dimethyltryptamine or DMT (from some ayahuasca-brews and related South American entheogens). In my opinion, LSD has by far the best erotic possibilities of the class, since it is generally free of physical side-effects, apart from exerting an amphetamine- like stimulation, at 1% of the dose! Like the amphetamines, LSD can work aphrodisiacal wonders, and can certainly exert solid erectile effects on men, but as is the case with many other aspects of its pharmacology, this is captive to "set and setting" (expectation and milieu). As Grinspoon and Bakalar noted in their unbiased review Psychedelic Drugs Reconsidered [Grinspoon & Bakalar 1979]: "The basic rule, for stronger psychedelic drugs as for marihuana, is that they heighten sexual interest and enjoyment only when the user is already inclined that way. They are anything but a stimulus to indiscriminate activity. Nevertheless, if temperaments, mood, and circumstances are right, they can produce an extraordinary intensification, prolongation, and elaboration of sexual experience, as they can for almost any experience. [...] But psychedelic drugs are not a reliable way to increase sexual pleasure any more than to achieve other emotional states. They not only enhance sexuality but transform it, often to the point where it becomes hardly recognizable; and they can be as powerfully anaphrodisiac as aphrodisiac. In the varying moods of the drug trip, intense sexual desire may suddenly turn into equally intense disgust or fear, or it may be transcended in a feeling of all-embracing cosmic love that makes mere sexual pleasure seem trivial or irrelevant." [emphasis mine] Although I have never experienced intense sexual desire transmogrifying into disgust or fear, for me the rule has been that the immoderately-prolonged nature of LSD-time in general causes that desire to be transcended before the particular sexual act is consummated or willfully brought to closure. I can recall episodes when some titillating tete a tete mysteriously transmogrified into something else; then abruptly, an eternity later, one or the other might remember: hey, what happened, weren't we making love? To my mind, the true erotic potential of LSD and allied Psychoptica is to ease a mutual attraction into the sexual realm, rapidly to enable people to become better acquainted, in an emotionally-opened way, which applies equally to MDMA. Having spoken to innumerable people about their entheogenic experiences, I would have to say that very rarely does the subject of eroticism ever come up, and it is rather in the scope of "pale religious letchery," to borrow Blake's phrase, in the paranoid, propagandistic fantasies of the pharmacopuritans, that the priapic potentials of LSD and its congeners loom large, so to speak. Moreover, in the traditional world, and with the exception of Cannabis, whose use can be seen clearly in Indian erotic paintings, as well as in association with the Tantric arts, it must be said that the emphasis is far more upon spiritual ecstasy (literally, separating the soul from the body--sex, eating, much light or noise, tend to anchor one's consciousness in the body, militating against ecstasy), whether this be used for self-actualization or more commonly for shamanic healing, than on any potential aphrodisiacal virtues. On the other hand, we are dealing today with the degenerated remnants of archaic traditions, often corrupted by Christianity, and we know but little of the potential breadth of use-modalities in antiquity. In Mesoamerica, there survives rather extensive documentation of "the Age of Entheogens" [Ott 1995] from the time of the conquest a half-millennium ago, which tells us that the entheogens enjoyed ludible, as well as medicinal, sacred and ceremonial roles. To my knowledge there is no specific mention of entheogens as aphrodisiacs, with the exception of the famous case of the cacahuatl-potion of Moctezuma, but the arrogant Spaniards, who evidently did not deign to sample them in any context, could hardly have been aware of such, had it existed, which I think quite likely. There is, however, one class of entheogen that merits special mention here: the Caribbean and South American visionary snuffs ñopo/cohoba and cebíl (prepared from seeds of Anadenanthera peregrina and A. colubrina var. Cebil), whose psychoptic principle is bufotenine, a positional isomer of psilocine, the true active principle of the psilocybian mushrooms [Ott 2001a; 2001b]. As the accompanying photograph of a classic Taíno cemí (zemí) indicates (these are wooden or stone anthropomorphic tables, the flat upper-surface of which was used to array "lines" of the cohoba-snuff), the erotic essence of this entheogen hardly took a back-seat in that long-lost culture. These cemí-artifacts have been found on all four large islands in the Greater Antilles, and their association with the snuff was documented at first-hand by Ramón Pané, left by Columbus on Hispaniola to study the Taíno [Pané 1974; Torres 1998]. Bufotenine provoked circulatory crises when unethically injected intravenously into convicts and mental "patients" (non-convict prisoners) in the United States, and turned their faces the color of an "eggplant" [Fabing & Hawkins 1956; Ott 1996; Turner & Merlis 1959]. Bufotenine is dimethyl-serotonine, and of the many visionary tryptamines (LSD, psilocybine, DMT, etc.) is the closest to serotonine--all are thought to act primarily via serotonine-receptors in the brain. But there are also serotonine-receptors in the vascular system, which accounts for its name: sero, "blood[pressure]," tonine "toning." That bufotenine injected into the bloodstream would cause facial lividity suggests the compound can also bring blood to the penis and indeed, after one particularly intense session of snuffing bufotenine-rich cebíl-seeds in Argentina, I experienced an impressive priapism when I repaired to my lodging. Regrettably, I was totally alone at that moment, and so had no other recourse than "onanism" (note to any homæopaths: I was already chewing coca to beat the band!). Cebíl may well prove to be that much sought-after "herbal Viagra®." While on the subject of bufotenine, a few words about toads (Bufo species, from which the compound gets its name) are in order. Toads being marathon-copulators, some species of which breed en masse in ponds, it is natural that they came to symbolize fertility and venery, and indeed toads figure prominently as ingredients in philtres [Morgan 1995; Wasson & Wasson 1957]. The toad parotoid-gland secretions (technically not venoms, 'though commonly called that) often contain bufotenine, which was first isolated from secretions of Bufo vulgaris in 1920 [Ott 1996]. On the other hand, these toad-secretions contain various toxic compounds, especially cardiotoxic steroids, which would seem to overwhelm bufotenine toxicologically, as this is generally present in relatively modest amounts. Nevertheless, dried Bufosecretion is used in traditional Chinese medicine, under the name Ch'an-su, and similar preparations were used to treat cardiac insufficiency before the introduction of Digitalis extracts. One use of Ch'an-su is as a so-called "love-stone"-- small cubes of the dried secretion are sold as aphrodisiacs, to be moistened and rubbed on the penis to prolong erections, which is thought to involve local anæsthesia, rather than any vascular actions of bufotenine, although this has been detected in the "love-stones." Recently, however, at least four toad-titillators in New York died after they had ingested this product, which likewise contained toxic amounts of cardioactive steroids! There also exist reports of people smoking these toad-preparations, as a supposititious psychoactive drug [Chamakura 1994]. In the famous potion-brewing scene of Shakespeare's Macbeth, his three "weird sisters" give the toad pride of place in their cauldron: "Toad, that under cold stone / Days and nights hast thirty-one / Swelter'd venom sleeping got / Boil thou first i' the charmed pot." There is some evidence for the use of toads in European witches' philtres, as well as in the so-called "flying ointments," as also their addition as fortificants to American chicha beers, but we have at present insufficient data to speculate on relevant pharmacology, either psychoptic or aphrodisiac. Several artistic representations point to an erotic dimension of the ointments, which did contain known visionary plants, such as belladonna (Atropa belladonna), henbane (Hyoscyamus niger), mandrake (Mandragora officinarum) and thornapple (Datura stramonium) [Hansen 1978; Müller-Ebeling et al. 1998], all of which contain psychoptic tropane alkaloids, such as scopolamine, hyoscyamine and atropine [Ott 1996]. Indeed, in a famous bioassay experiment, the Spanish physician Andrés de Laguna "managed to obtain a good cannister-full" of a "flying ointment" which he "used to anoint from head to toe the wife of the hangman" of Metz, who promptly fell into a profound sleep for 36 hours! When she came to her senses, she was distraught at having been awakened "from all the pleasures and delights of the world," and told her husband with a sly smile: "know that I have made you a cuckhold, and with a lover younger and better than you" [Gómez Fernández 1999]! Toad-secretions or oneirogenic aphrodisiacs anyone? --- I prefer conscious concupiscence! An Erotic Epilogue Laurence Sterne showed the keenest of poetic intuition in his riotous farce, The Life & Opinions of Tristram Shandy, Gentleman, that "Cock and a Bull" story, "and one of the best of its kind, I ever heard," when he included the learned Hafen Slawkenbergius' tale, in which Nosarians and prodigious Noses take the place of priapic Penises [Sterne 1935]. For in matters erotic, it is clear to me that the nose knows, and we would do well to remember that our sexual centers are not in the cerebral cortex but in that reptilian rhinencephalon or "smell brain." Indeed, the best sexual connections I have ever experienced have been with women that not only were not exemplary of my particular ideal of female allure, but with whom I had all manner of fundamental incompatibilities; cultural, (anti-) religious, socioeconomic and intellectual-- indeed, the only compatibility evident to me was a fabulous fit between pheromones and receptors which, not surprisingly, tends to be mutual. In one particularly memorable case, I could not be for too long within a meter or two of the woman--even fully clothed, in a crowded office--without getting a persistent erection, which I usually had to conceal with my backpack. In somewhat over a year, essentially all we did together was have animalistic sex, and if we had managed to sate our amatory appetites, which generally required some hours, we basically just got in each other's way! Conversely, alas, some of the best overall compatibilities I have known with women have tended to be sexually ordinary. It is clear to me that the pathway to a science of aphrochemistry leads via research on human sex-attractant pheromones, and that most potent philtre will likely be some erotic effluvium, a sort of "amorous aromatherapy," rather than a pill, puff or powder; mayhap a pheromonal pessary for women, philtry pomade for men. This direction was pointed to by Patrick Sueskind, in his interesting novel The Perfume, at the climax of which his antihero Grenouille ("frog," which should rather be Crapaud, "toad") is about to be executed for the murder of numerous women, when he uncorks the bottle of perfume he had made from the erotic essences of their bodies, for which purpose he had slain them, so unleashing a frenetic orgy in the crowd of morbid spectators! It is evident that pheromones, indeed olfaction itself, are not operative in all human beings. Many people are effectively anosmic, and 72% of the roughly 1000 human genes associated with olfactory receptors are non-functional (pseudogenes), as well as all of the human genes which have been correlated with putative pheromonal receptors. Moreover, anatomical studies of 564 adults found that 70% lacked the vomeronasal organ, which was present bilaterally in merely 8%, unilaterally in the remaining 22% [Keverne 1999]. Even stranger, it has been said that in those human beings possessing a vomeronasal organ, this invariably lacks effective neuronal connections! This I do not believe, at least in my own case, and there are surely those Grenouille among us, we who inhabit a mysterious, musky and mellifluous world. Through pharmacogenetic study of human idiosyncrasy [Ott 1997] with respect to genes for our pheromonereceptors, it is theoretically possible to develop individually customized "cocktails" of pheromones, personalized philtreprescriptions. Such a paramount philtre would in principle be capable of transforming virtually any compatible individual into that "most concupiscible object" (to paraphrase Laurence Sterne) more desirable than which "neither could your heart desire, nor your concupiscence covet." • References Birchler, U.B,. 1975. "Die Rolle der Frau bei der Liebeskrankheit und den Liebestränken," Sudhoffs Archiv 59(3): 311-320. Budavari, S. et al. [Eds.] 1996. The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals. Merck & Co., Inc. Chamakura, R.P. 1994. "Bufotenine --- a hallucinogen [sic] in ancient snuff powders of South America and a drug of abuse on the streets of New York City," Forensic Science Review 6: 1-18. Clark, J.T. et al. 1984. "Enhancement of sexual motivation in male rats by yohimbine," Science 225: 847-849. Conrad III, B. 1988. Absinthe: History in a Bottle. Chronicle Books. Díaz del Castillo, B. 1976. Historia verdadera de la conquista de la Nueva España. Editorial Porrúa, México. [original edition in 1632] di Tomaso, E. et al. 1996. "Brain cannabinoids in chocolate," Nature 382: 677-678. Dorries, K.M. 1997. "Olfactory 'consciousness'?," Science 278: 1550. [letter to ed.] Fabing, H.D. & J.R. Hawkins 1956. "Intravenous bufotenine injection in the human being," Science 123: 886-887. Gómez Fernández, J.R. 1999. Las plantas en la brujeria medieval (propiedades y creencias). Celeste Ediciones. Grinspoon, L. & J.B. Bakalar 1979. Psychedelic Drugs Reconsidered. Basic Books, Inc. Hansen, H.A. 1978. The Witch's Garden. Unity Press. Danish original 1976. Heksens Urtegård. Laurens Bogtrykkeri. Hines, P.J. 1997. "Unconscious odors," Science 278: 79. Holden, C. 1999. "Whiff of good cheer, just for women," Science 285: 1845. Holy, T.E. et al. 2000. "Responses of vomeronasal neurons to natural stimuli," Science 289: 1569-1572. Ishay, J.S. & V.A. Paniry 1979. "Effects of caffeine and various xanthines on hornets and bees," Psychopharmacology 65: 299-309. Kennedy, J.G. 1987. The Flower of Paradise: The Institutionalized Use of the Drug Qat in North Yemen. D. Reidel. Keverne, E.B. 1999. "The vomeronasal organ," Science 286: 716-720. Leary, T. 1966. "Playboy interview: Timothy Leary," Playboy 13(9): 93 et seq. Maugh II, T.H. 1982. "The scent makes sense," Science 215: 1224. Michael, R.P. et al. 1974. "Human vaginal secretions: Volatile fatty-acid content," Science 186: 1217-1219. Morgan, A., 1995. Toads and Toadstools: The Natural History, Folklore, and Cultural Oddities of a Strange Association. Celestial Arts. Mortimer, W.G. 1901. Peru. History of Coca: "The Divine Plant" of the Incas. J.H. Vail & Co. Reprint, 1974. And/Or Press. Müller-Ebeling, C. & C. Rätsch 1986. Isoldens Liebestrank: Aphrodisiaka in Geschichte und Gegenwart. Kindler Verlag. Müller-Ebeling, C. et al . 1998. Hexenmedizin: die Wiederentdeckung einer verbotenen Heilkunst--schamanische Traditionen in Europa. AT Verlag. Newland, C.A. 1962. My Self and I. Coward-McCann, Inc. Ott, J. 1985. The Cacahuatl Eater: Ruminations of an Unabashed Chocolate Addict. Natural Products Co. Ott, J. 1995. The Age of Entheogens & The Angels' Dictionary. Natural Products Co. Ott, J. 1996. Pharmacotheon: Entheogenic Drugs, Their Plant Sources and History. Natural Products Co. [second edition densified; original 1993] Ott, J. 1997. Pharmacophilia or The Natural Paradises. Natural Products Co. Castillian translation 1998. Phantastica. Ott, J. 2001a. Shamanic Snuffs or Entheogenic Errhines. Entheobotanica. German translation 2001. Nachschatten Verlag. Ott, J. 2001b. "Pharmañopo-psychonautics: Human intranasal, sublingual, intrarectal, oral and pulmonary pharmacology of bufotenine," Journal of Psychoactive Drugs 33(3): 273- 282. Pané, R. 1974. Relacion acerca de las antigüedades de los indios. Siglo Veintiuno Editores, México. [original manuscript of 1496] Pezzella, S. 1978. Magia delle Erbe: De un Testo Anonimo del '500. Edizioni Mediterranee. Pittler, M.H. 1998. "Yohimbine in the treatment of erectile dysfunction," Fortschritte der Medizin 116(1-2): 32-33. Pope, H.G. 1967. "Tabernanthe iboga: An African narcotic [sic] drug of social importance," Economic Botany 23(2): 174-184. Raghavan, V. & H.K. Baruah 1958. "Arecanut: India's popular masticatory -- History, chemistry and utilization," Economic Botany 12(4): 315-345. Rätsch, C. 1997. Plants of Love: The History of Aphrodisiacs and a Guide to their Identification. Ten Speed Press. Rätsch, C. 1996. Urbock: Bier Jenseits von Hopfen und Malz. AT Verlag. Rudgley, R. 1998. The Encyclopædia of Psychoactive Substances. Abacus. Shulgin, A.T. and A. Shulgin 1991. PIHKAL: A Chemical Love Story. Transform Press. Shulgin, A.T. and A. Shulgin 1997. TIHKAL: The Continuation. Transform Press. Sitaram, S. et al. 1978. "Human serial learning: Enhancement with arecholine [sic] and impairment with scopolamine," Science 201: 274-276. Sterne, L. 1935. The Life & Opinions of Tristram Shandy Gentleman. The Heritage Press. [original of 1759-1767] Torres, C.M. 1998. "The role of cohoba in Taíno shamanism," Eleusis n.s. 1: 38-50. Turner, W.J. & S. Merlis 1959. "Effect of some indolealkylamines on man," Archives of Neurology and Psychiatry 81: 121-129. Wasson, R.G. 1957. "Seeking the magic mushroom," Life, 13 May issue, 42(19): 100 et seq. Wasson, V.P. 1957. "I ate the sacred mushroom," This Week (Sunday newspaper supplement), 19 May issue, pp. 8 et seq. Wasson, V.P. & R.G. Wasson 1957. Mushrooms Russia and History. Pantheon Books.

Male G Spot

[youtube http://www.youtube.com/watch?v=1oJ_lvkBa5s&w=420&h=315]

Tetrahydrocannabinol

Tetrahydrocannabinol, also known as THC, Δ9-THC, Δ9-tetrahydrocannabinol (delta-9-tetrahydrocannabinol), Δ¹-tetrahydrocannabinol (using an older numbering scheme), or dronabinol, is the main psychoactive substance found in a variety of plants; most abundantly so in the Cannabis plant. It was isolated by Raphael Mechoulam and Yechiel Gaoni from the Weizmann Institute in Rehovot, Israel in 1964. In pure form it is a glassy solid when cold and becomes viscous and sticky if warmed. THC has a very low solubility in water, but a good solubility in most organic solvents such as ethanol or hexane. As in the case of nicotine and caffeine, THC's most likely function in Cannabis is to protect the plant from herbivores or pathogens [1]. THC also possesses high UV-B (280-315 nm) absorption properties, protecting the plant from harmful radiation. Pharmacology Its pharmacological actions are the result of its binding to the cannabinoid receptor CB1, located in the brain. The presence of these specialized receptors in the brain implied to researchers that endogenous cannabinoids were manufactured by the body, so the search began for a substance normally manufactured in the brain that binds to these receptors, the so-called natural ligand or agonist, leading to the eventual discovery of anandamide, 2 arachidonyl glyceride (2-AG) and other related compounds. This story resembles the discovery of the endogenous opiates (endorphins, enkephalins, and dynorphin), after the realization that morphine and other opiates bound to specific receptors in the brain. THC has analgesic effects that, even at low doses, causes a "high", and medical cannabis can be used to treat pain. Other effects include: relaxation; euphoria; altered space-time perception; alteration of visual, auditory, and olfactory senses; disorientation; fatigue; and appetite stimulation. It also has anti-emetic properties, and also may reduce aggression in certain subjects. Toxicity According to the Merck Index, 12th edition, THC has a LD50 value of 1270 mg/kg (male rats) and 730 mg/kg (female rats) administered orally dissolved in sesame oil. If this were scaled up to an adult human, the LD50 would be between approximately 50 and 86 g for a 68 kg (150 lb) female or male person respectively. This would be equivalent to 1-1.8 kg of cannabis with a 5% THC content (roughly average) taken orally. The LD50 value for rats by inhalation of THC is 42 mg/kg of body weight. It is important to note, however, that toxicity studies in animal models do not necessarily correlate to human toxicity. THC receptor distribution in the rat CNS is different from that of humans, meaning that there is the significant possibility that toxicity in humans varies from the published animal LD50 studies. There has never been a documented fatality from marijuana or THC overdose. Absorption is limited by serum lipids which can become saturated with THC, thus the inherent solubility may mitigate toxicity. Studies of the distribution of the cannabinoid receptors in the brain explain why THC's toxicity is so low (i.e., the LD50 of the compound is so large): parts of the brain that control vital functions such as respiration do not have many receptors, so they are relatively unaffected even by doses larger than could ever be ingested under any normal conditions. Research A number of studies indicate that THC may provide medical benefits for cancer and AIDS patients by increasing appetite and decreasing nausea. It has been shown to assist some glaucoma patients by reducing pressure within the eye, and is used in the form of cannabis by a number of multiple sclerosis patients to relieve the spasms associated with their condition. Studies also indicate a variety of negative effects associated with constant, long-term use, including short-term memory loss. However, other studies have refuted this, claiming the MRIs of long term users show little or no difference to MRIs of the non-using control group. Although using positron emission tomography (PET), at least one study indicates altered memory-related brain function in marijuana users . The long-term effects of THC on humans have been disputed because its status as an illegal drug makes research difficult. Preliminary research on synthetic THC has been conducted on patients with Tourette syndrome, with results suggesting that it may help in reducing nervous tics and urges by a significant degree. Animal studies suggested that Marinol and nicotine could be used as an effective adjunct to neuroleptic drugs in treating TS. Research on twelve patients showed that Marinol reduced tics with no significant adverse effects. A six-week controlled study on 24 patients showed the patients taking Marinol had a significant reduction in tic severity without serious adverse effects. Seven patients dropped out or had to be excluded from the study, one due to adverse side-effects. More significant reduction in tic severity was reported with longer treatment. No detrimental effects on cognitive functioning and a trend towards improvement in cognitive functioning were reported during and after treatment. Marinol's usefulness as a treatment for TS cannot be determined until/unless longer controlled studies on larger samples are undertaken. Recent research has shown that many adverse side effects, generally known as the "stoner" stereotype, fail to hold up to the scientific method. Recent studies with synthetic cannabinoids show that activation of CB1 receptors can facilitate neurogeneration, as well as neuroprotection, and can even help prevent natural neural degradation from neurodegenerative diseases such as MS, Parkinson's, and Alzheimer's. This, along with research into the CB2 receptor (throughout the immune system), has given the case for medical marijuana more support. In in-vitro experiments THC at extremely high concentrations, which could not be reached with commonly consumed doses, caused inhibition of plaque formation, the cause of Alzheimer's disease, better than currently approved drugs.[8] THC may also be an effective anti-cancer treatment, with studies showing tumor reduction in mice, conducted in 1975.[9] Chemical name (−)-(6aR,10aR)-6,6,9-trimethyl- 3-pentyl-6a,7,8,10a-tetrahydro- 6H-benzo[c]chromen-1-ol Chemical formula C21H30O2 Molecular mass 314.46 g/mol Glass transition 9.3 °C Boiling point 155-157 °C (vacuum, 0.07 mbar) Solubility (water) 2.8 mg/L (23 °C) Solubility (saline) 0.77 mg/L (NaCl, 0.15 M) pKa 10.6 log P 3.78 (water @ pH 7 / octanol) CAS number 1972-08-3

Eric Shevin, Attorney at Law

MEDICAL MARIJUANA EXPERTISE Mr. Shevin represents clients exclusively in the area of State and Federal criminal law with a focus on marijuana and drug cases. Mr. Shevin’s practice also represents clients in matters dealing with medical marijuana business formation and corporate representation. Presently, Mr. Shevin teaches a course on Medical Marijuana Laws to the Los Angeles County Judiciary, provides continuing legal education on Medical Marijuana Laws for the National Business Institute and teaches at the NACDL Advanced Criminal Law Seminar in Aspen, Colorado. Mr. Shevin represents individuals nationally and has won significant victories for his clients in Hawaii, Louisiana, North Carolina, Utah, Arkansas, Missouri, Ohio, New York, Nevada, Texas and Tennessee. Mr. Shevin has been featured and/or quoted in more than 25 articles and news stories including the following media outlets: Los Angeles Times, Los Angeles Daily Journal, ABC News, CBS News, MSNBC, Newshour with Jim Lehrer, Huffington Post, National Public Radio, Hartford Courant, Orange County Register, The 420 Times, West Coast Leaf, Marijuana Anti Prohibition Project, Press Enterprise, Metropolitan News Enterprise, Hemp Evolution, The Compassion Club, Cannabis News, The Medical Marijuana Magazine, The Marijuana News, OC Weekly and High Times Freedom Fighter of the month. Boy did I find all kinds of interesting case work while googling Mr. Shevin. He seems to have seen it all and then some. I hope we become friends and only friends.

The PMS/Pot Proclamation

By "Dr Kate" - Monday, August 31 1998 Eat some chocolate, run a hot bath and bask in the remedy that is straight from mother earth! Feel better, Ladies! Sourced from Cannabis Culture Mag Hundreds of testimonials show that marijuana can alleviate PMS! In the 1800's cannabis was commonly used by women to ease menstrual cramps and labour pains. Yet by 1920, women were influenced into thinking that the symptoms they had around their period were due to innate physical problems, and their reproductive organs were often removed as a cure. Nowadays, women are often told that their very real physical symptoms are psychological, and handed a script for a prescription for antidepressants or tranquilizers. These harsh drugs take weeks to build up in the system enough to produce a noticeable effect. It seems like overkill to take something that can throw many of the body's systems out of balance and cut down sex-drive, every day of the month, to try to cut symptoms that typically last 3-5 days, before and during a woman's period. Often, all that's needed to relax the tense, stimulate the sluggish, and soothe the crampy, is a couple of puffs of RCMP ? Royal Canadian Marijuana Products. We can now proclaim to the world that for many women PMS is hugely alleviated by cannabis resin. The proof lies in my collection of testimonial letters submitted by women from around the globe via the internet and regular post. These personal experiences prove that women should be insisting on access to this good herb if they are victims of this disorder, which can be disabling and even marriage-threatening in extreme cases. Almost 200 letters, stories, and submissions are powerfully convincing, many poignant to the point of inspiring tears in the eye of the reader, some too private to ever print. What follows are just a few typical examples: Hi Dr Kate. I have used marijuana cigarettes for my premenstrual rages and grumpiness for the last 15 years. Works like a charm. My family is glad. What else would you like to know? A husband writes: My wife has used marijuana to control nausea and lessen cramps. It seems to work very well, even in low doses. A Canadian lady writes: About your medical marijuana and menstrual discomforts, etc. I have used it for many years for pre-menstrual cramps and bitchiness? PMS! It helps me to mellow out and to tolerate the intense lower pains that I get once a month for about 3 days. From a man in the US: My live-in girlfriend suffered from severe cramps and depression for 2 to 3 days a month during her period. She did not smoke pot until I suggested it might help out with this, since watching her suffer was agonizing for me too. The results were even better than expected, and she continues to smoke pot for this condition. She did do some rare occasional recreational smoking, but every cycle the pot would make her life considerably easier. She has since moved to a state where anti-pot laws are severe, so she often does without for this reason. And finally, from a teenager: Dear Dr Kate, I have smoked up since I was 14. Now I'm 17. My mom found out and so I had to stop, but when it's that time of the month, I sneak over to my friend's house if she has some, because it really helps the cramps and headache. Herbal remedy experts In my studies of herbal remedies and natural healing methods I have found only a small handful of herbal expert writers courageous and honest enough to include cannabis in their repertoires. One of these is the late,great Dr John R Christopher, author of School of Natural Healing, the greatest herbal and natural healing instructive text. He and other early herbalists call cannabis by the name Indian Hemp, but there is no doubt they are referring to the medicinal herb. Dr Christopher lists cannabis in 11 different categories of usefulness, including Hypnotic, Antispasmodic, Analgesic, and Emmenagogue, which is described as follows: Herbs that are female correctives to the reproductive organs, which stimulate and promote a normal menstrual function, flow and discharge. Susun Weed is the only prominent herbalist of our time who is brave enough to speak up in defense of the much-slandered herb. She also explains that cannabis as an important emmenagogue, and describes the benefit of a couple of puffs of nice, warm bronchial-dilating smoke as "good exercise for the lungs." I quote her "Wise Woman" philosophies often, because they are full of common-sense insights and down-to-earth wisdom. She has knowledge only experience can bring. Susun is revered among midwives and natural women of all ages who want to take responsibility for their own bodies. Dr Kate can be reached by email at: galbraithe@upanet.uleth.ca. Home Remedies and Natural Cures for Menstrual Cramps Treatment From HomeRemedies.com Menstrual Cramps Home Remedy Using Heating Pads Many women have found that a heating pad placed on your lower back or abdomen helps to ease the pain and discomfort of menstrual cramps. If you don't have a heating pad, one can be easily made by filling a sock with flaxseeds or uncooked rice and heating it in the microwave for 1 to 2 minutes. Menstrual Cramps Home Remedy Using Chamomile Chamomile is widely used to treat gynecologic complaints such as menstrual cramps and discomfort related to premenstrual syndrome (PMS). Add 2 teaspoons of dried Chamomile flowers to a cup of boiling water and let it steep for at least 5 minutes. If you are using a package of Chamomile tea bags, then follow the directions as stated on the box. Honey or sugar can be added for taste. A good preventive measure is to start drinking Chamomile tea a couple of days before you are expecting your period, and then drink at least 2 cups everyday during your period. It also feels great if you use your hot mug as a hot compress for your lower abdomen while you are drinking it. Vitamins and Minerals for Treating Menstrual Cramps Foods and supplements that are rich in B-vitamins, calcium, magnesium, and zinc have been found to reduce the pain, bloating and other symptoms of menstrual cramps. In particular, calcium is known to help maintain muscle tone as well as prevent cramps and pain. For most women, a daily intake of 800 mg of calcium is recommended, which can be found in 3 cups of milk. Increasing magnesium is also recommended, since it helps the body absorb calcium. Good sources of magnesium include beans, whole wheat, tofu, salmon, shrimp, nuts, and vegetables. Regular Exercise as a Natural Cure for Menstrual Cramps Exercise is considered to be a natural way to reduce muscle tension and elevate one's mood. Therefore, maintaining a regular exercise program, including something as simple as walking for 20 minutes each day, can help reduce the severity of menstrual cramps. Ginger Root Tea to Relieve Menstrual Cramps Ginger root has been found to help relieve the pain associated with menstrual cramps. Therefore, a simple soothing herbal tea can made from Ginger as follows: Slice a handful of ginger root Let the pieces simmer in boiling water for 15 minutes Using a strainer, pour the tea into a drinking cup or mug Add some honey as a natural sweetener if desired

ORGASM BENEFITS

Aug 11, 2011 | By Ken Chisholm An Orgasm is Good For You! According to JAMA (the Journal of the American Medical Association), 43 percent of American women suffer from some form of "Female Sexual Dysfunction"--often placing the blame on themselves for their inability to reach orgasm. Stop blaming yourself. If you are alone, masturbation will help you find what feels right for you. If you have a partner, talk to him. Often, the clitoris is under-stimulated during sexual intercourse--which is what prevents many women from having an orgasm. If you have orgasms due to your cervix being stimulated, tell your partner this (or whatever else does it for you). Orgasms relieve tension! The faster heartbeat, the increased blood flow and the muscular tautness associated with sexual pleasure all come to a relaxing conclusion with an orgasm, and in the process relieve tensions pent up in your nervous system. Orgasms help you sleep better. While an orgasm is followed in the male by a quick drop in blood pressure and sudden relaxation, the effect on women is more progressive, but no less important. Orgasms act as a natural tranquilizer. That wonderful release of endorphins is very calming. Orgasms calm your cravings for junk food, and sometimes for cigarettes. Sexual stimulation activates the production of phenetylamine, a kind of natural amphetamine that regulates your appetite. So before you pig out, maybe you should go to your room. :) Orgasms burn calories. Orgasms can work as natural pain management. If you have ever noticed yourself forgetting about a headache or menstrual cramps while masturbating or having sex, it is not simply a psychological phenomenon. Endorphins (natural compounds that are close to morphine) are released by your body during sex, and can increase your tolerance of pain by as much as 70 percent during orgasm. This will vary from person to person. (If you are in the hospital, forget trying this, due to the lack of privacy.) What's The Difference Between Clitoral and Vaginal Orgasms? The difference between a "clitoral" and a "vaginal" orgasm lies in where you are being stimulated to achieve orgasm, not where you feel the orgasm. This may clear up some of the confusion around this common question. The clitoris has a central role in elevating feelings of sexual tension. During sexual excitement, the clitoris swells and changes position. The blood vessels throughout the entire pelvic area also swell, causing engorgement and creating a feeling a fullness and sexual sensitivity. Your inner vaginal lips swell and change shape. Your vagina balloons upward and your uterus shifts position in your pelvis. For some women, the outer third of their vagina and the cervix are also very sensitive, or even more sensitive than the clitoris. When these areas are stimulated during intercourse or other vaginal penetration, these women can have intense orgasms. This would be what is referred to as a vaginal orgasm without clitoral stimulation. Sigmund Freud made a pronouncement that the "mature" woman has orgasms only when her vagina, but not her clitoris, is stimulated. This, of course, made the man's penis central to a woman's sexual satisfaction. Many sexual-health experts still disagree about any actual female ejaculation, although you will find plenty of websites that want to teach you how to bring this about for a fee; here, you can check it out for free. For more on the often misunderstood G-spot, see that page. In reality, orgasms are a very individual experience, and there is no one correct pattern of sexual response. Whatever feels wonderful to you, makes you feel alive and happy and connected with your partner is what matters. Last updated on: Aug 11, 2011 Read more: http://www.livestrong.com/article/13903-orgasm-benefits/#ixzz1fYFxNWeD