Tomer Corymbosa Posted December 25, 2005 Share Posted December 25, 2005 so i have to know - how do i grow this plant from seeds - i'm gonna have fresh seeds from pods - about 40...i'm gonna do my last growin experience on this plant - and i'm gonna do it right (after i've failed 4 times...)please' i need a detailed instructions.Thank you very much! Quote Link to comment Share on other sites More sharing options...
apothecary Posted December 26, 2005 Share Posted December 26, 2005 I hear it isn't easy to grow them from seed, so if you do get a repeatable technique going, post it please! <___base_url___>/uploads/emoticons/default_smile.png Quote Link to comment Share on other sites More sharing options...
AndyAmine. Posted December 26, 2005 Share Posted December 26, 2005 I think Teo had some luck wiht them, you may like to ask him? Quote Link to comment Share on other sites More sharing options...
Tomer Corymbosa Posted December 26, 2005 Author Share Posted December 26, 2005 i need all the info you can give me.(if u know about it..)and thanks i'll pm teo anyway. Quote Link to comment Share on other sites More sharing options...
planthelper Posted December 26, 2005 Share Posted December 26, 2005 i think to remeber that lorax grew heaps of them by seed, aswell as gom.so wait for what they have to say.i would, fill pots with searls seedraising mix, than compact the surface, now water a bit, than place seeds, than sprinkle a tiny ammount of additional soil evenly and compact again. now water again using a sprayer, so to make sure you don't wash the seeds out of the mixture.finaly cover the pots with sheets of glass or plastic. Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted December 27, 2005 Share Posted December 27, 2005 i used normal potting mix, kept humid, seeds sown on surface, wait months, they look like weeds when they first germinate. Quote Link to comment Share on other sites More sharing options...
planthelper Posted December 28, 2005 Share Posted December 28, 2005 so we could guess they need light to germinate, that could explain why many people had trouble getting them up. Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted December 29, 2005 Share Posted December 29, 2005 yeah i think a number of factors light, heat, and freshness of seed. plus low germination rate. has anyone with plants from me had them flower?? Quote Link to comment Share on other sites More sharing options...
Bongchitis Posted December 29, 2005 Share Posted December 29, 2005 40cm tall and in good nick..........no flowers yet. Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted December 29, 2005 Share Posted December 29, 2005 the seed from them might be better if two can cross pollinate. some of the ones i sent off had flowers when i sent them. Quote Link to comment Share on other sites More sharing options...
Stonehenge Posted December 31, 2005 Share Posted December 31, 2005 My plants are in flower, I suppose I should gather the seed and try to grow some. I'll try surface sowing and see how that does. Quote Link to comment Share on other sites More sharing options...
planthelper Posted December 31, 2005 Share Posted December 31, 2005 there are two distinctive types around.one (teo's, gom's {mine hasn't flowered yet}) which has a bit broader, chubby leaves, another prominet feature with this one is that sometimes the new growth flush, has an orange color.the other one, has less chubby leaves and it's new growth flushes never turn orange.i think to remeber a post wher somebody said that only the new flush, orange colored leave type is strong, but i don't support this view, but maybe the "golden shine" variety is more potent.i intend to x-pollinate the two. Quote Link to comment Share on other sites More sharing options...
woof woof woof Posted December 31, 2005 Share Posted December 31, 2005 Okay Okay,...... why the heck isn't there any info on the chemistry of CZ? Or by which mechanisms it works?He he ,.. in the good ol days, I used to drink CZ :saufen2: - and my gawd, what a nasty taste. With no noticed effects from. ( to me it is the most nastiest tasting plant I have tried. )I gave up on it. I am not drinking it till i find out more about it! Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted January 4, 2006 Share Posted January 4, 2006 growing from seed gave me a wide variety of plants, some that even tasted nice but i dont know the activity of them. there was a paper out that discussed the effects but i dont think it pinned down a specific compound. calea for me was always hit and miss, somtimes i got the effects others i got nothing, for me it was a great deep sleep which was full of dreams and i woke up feeling great. the key i found was big doses and i hadta fall asleep within a few minutes of taking it otherwise it didnt work, which is harder then it sounds.i found calea to be very synergistic with psychedelics. i used it in a smoking mix ontop of which i would smoke spice, the mix consisted of roughly 1 part calea, heimia, damiana and sometimes some normal sally leaf, the damiana was for taste as calea and sally always tasted horrible.my initial interest in ethnobotany was aroused by castaneda and poisenous plants, i wanted to take peyote and datura, when i stumbled across erowid i was amazed and took interest in many of the legal highs which had non psychedelic effects, i wasnt interested in psychedelics. things change though <___base_url___>/uploads/emoticons/default_smile.pngcalea for me is part of a large list of plants which we dont quite know the full potential of, heimia is another in the long list which many people look over in the rush for the easier to understand plants with more definite and striking effects. for me these plants would be great to study but with so many plants and so little time its hard to choose. a dream of mine is a ethnobotanical institute where not only the pharmacology and chemistry are studied but the growing harvesting and even genetics of the plants can be studied. hehe good dream but maybe someday if i win lotto or become rich <___base_url___>/uploads/emoticons/default_smile.png Quote Link to comment Share on other sites More sharing options...
t st tantra Posted January 18, 2006 Share Posted January 18, 2006 inspired by teos success i decided ,last autumn[?] to have another go at these.and i seem to have 10 to 20 little plants,some have their 3rd set of true leaves and have springy stems.dont know when i should transplant them?i used coco peat on top of potting mix and placed fresh seed straight from plant to soil top.then watered in ,hoping the water would wash some in a little.the pot sat in a saucer of water in a warm to hot spot with a little direct light.i use calea ,smoke a few leaves,to clear the senses,a traditional use and add it to smoking mixes to increase visual content. t s t . Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted January 19, 2006 Share Posted January 19, 2006 they are so hardy you can transplant them when ever. yeah i used it to increase visuals in smoking mixtures, works really well. Quote Link to comment Share on other sites More sharing options...
Rev Posted January 19, 2006 Share Posted January 19, 2006 i have an affection for calea plants tooits form ,it texture, colours and effectsits my version of cannabis cos i cant take the real thingwhen coming down its a great smoke before bed - especially with tablespoon or 3 of strong alcoholic calea tincture.unlike some other minor ethnobotanicals i am convinced of the efficacy of this herb when its growj right and picked and treated righti mean if someone gave you some seedy hemp mad into a cup of tea under the guise that that was cannabis then youd have the wrong impression wouldnt you...i think to remeber a post wher somebody said that only the new flush, orange colored leave type is strongid like to source this and any other distinctive forms.i have my own experiences with producing high quality Calea and with the strain i have i know how to do thatyou have to observe the plant closely and test it and youll see when its bestThere is info on Calea if you dig for itdig this...:D;)Journal of Ethnopharmacology 18 (1986) 229-243 Eleavier ScientificPublishers Ireland LtdPSYCHOPHARMACOLOGIC ANALYSIS OF AN ALLEGEDONEIROGENIC PLANT: CALEA ZACATECHICHILILIAN MAYAGOITIA. Jose-Luis Diaz and Carlos M. CONTRERASDepartamenta de Psicobiologia y Cunducto, Instituto Mexicano de Psiquiatria,Antiguo Camino a Xochimilco 101, San Lorenzo Huipulco Tlalpan 14370 andDepartamento de Fisiologia. Instituto de Investigaciones Biomedicas,Universidad Nacional Autonoma de Mexico, Apartado Postal 70228. CiudadUniversitaria, Coyoacan 04510 (Mexico, D.F.)(Accepted October 8. 1986)SummaryCalea zacatechichi is a plant used by the Chontal Indians of Mexico to obtaindivinatory messages during dreaming. At human doses, organic extracts of theplant produce the EEG and behavioral signs of somnolence and induce lightsleep in cats. Large doses elicit salivation, ataxia. Retching and occasionalvomiting. The effects of the plant upon cingulum discharge frequency weresignificantly different from hallucinogenic-dissociative drugs (ketamine,quipazine, phencyclidine and SKF-10017). In human healthy volunteers, lowdoses of the extracts administered in a double-blind design against placeboincreased reaction time end time-lapse estimation. A controlled nap sleepstudy in the same volunteers showed that Calea extracts increased thesuperficial stages of sleep and the number of spontaneous awakenings. Thesubjective reports of dreams were significantly higher than both placebo anddiazepam, indicating an increase in hypnagogic imagery occurring duringsuperficial sleep stages.IntroductionDreams are important in mesoamerican cultures. They are believed to occur ina realm of suprasensory reality and, therefore, are capable of conveyingmessages (Lopez-Auatin. 1980). The use of plant preparations in order toproduce or to enhance dreams of a divinatory nature constitutes an ethno-pharmacological category that can be called "oneiromancy" and which justifiesrigorous neuropharmacological research. There are several plants used inIndian communities of Mexico to obtain divinatory messages from dreams.Several puffball mushrooms (Lycoperdon spp.), wrongly reported ashallucinogens (Ott et al., 1975), are eaten fresh by Mixtec Indians beforegoing to bed in order to dream (Diaz, 1975. 1979). Nahuatl Indians from theSierra de Puebla use an as yet unidentified species of Salvia, known by thename of Xiwit, for the same purpose (Tim Knab, pers. commun.). The plantknown as Bakana to the Tarahumara Indians, which has been reported to be ananalgesic, antipsychotic and divinatory agent (Bye. 1979), was later found tobe employed for dreaming during night sleep (William Merrill, pers. commun.).Finally, Calea zacatechichi Schl. (Compositae) is used in the same context bythe Chontal Indians of Oaxaca. C. zacatechichi is a plant of extensivepopular medicinal use in Mexico (Diaz. 1976). An infusion of the plant(roots, leaves and stem) is employed against gastrointestinal disorders, asan appetizer. cholagogue, cathartic, antidysentry remedy, and has also beenreported to be an effective febrifuge. With other aromatic Compositae, dryC. zacatechichi is used as insecticide (Diet, 1975). There is also someinformation concerning psychotropic properties of this plant that requirefurther clarification (Schultes and Hofmann, 1973).The pioneer study on the appetizer properties of zacatechichi, conducted atthe Institute Medico Nacional of Mexico, mentioned some psychoactive effects(Sandoval, 1882). MacDougall (1968) reported that a Chontal informant knewthat the leaves of the plant were to be either smoked or drunk as an infusionto obtain divinatory messages. Subsequent interviews with MacDougall'sinformant and active participation in ceremonial ingestion revealed that theplant is used for divination during dreaming (Diaz, 1975). Whenever it isdesired to know the cause of an illness or the location of a distant or lostperson, dry leaves of the plant are smoked, drunk and put under the pillowbefore going to sleep. Reportedly, the answer to the question comes in adream. A collection of interviews and written reports concerning thepsychotropic effects of these preparations on 12 volunteers has beenpublished (Diaz. 1975, 1979). Free, reports and direct questioning discloseda discrete enhancement of all sensorial perceptions, an increase in imagery,mild thought discontinuity, rapid flux of ideas. and difficulties inretrieval. These effects were followed by somnolence and a short sleep duringwhich lively dreams were reported by the majority of the volunteers. Thesepreliminary observations suggested that the psychotropic effects of the plantwere similar to those interesting from ethnobotanical. psychological andneuropharmacological of the "cognodysleptic" drugs, whose prototype ismarihuana (Cannabis sativa)(Diaz, 1979). The possible effects upon dreamingare the most perspectives.C. zacatechichi is a shrub measuring 1-1.5 m in height. The plant has manybranches with oviform and opposite leaves (3-5 cm long and 2-4 cm wide). Theleaves show serrated borders, acute endings and a short petiole. They arerugose and pubescent. The inflorescence is small and dense (comprising around12 flowers each) with the pedicels shorter than the heads (Martinet, 1939).The plant grows from Mexico to Costs Rice in dry savannas and canyons(Schultes and Hoffmann, 1973). The name of the species comes from Nahuatl"zacatechichi" which means "bitter grass' and is the common name of the plantall over Mexico. It is also known with the Spanish names of "zacate de perro"(dog's grass), "hoja madre" (mother's leaf) "hoja de dies" (Cod's leaf), andthle-pela-kano in Chontal Diaz, 1975).Several sesquiterpene lactones had been isolated from the plant. Calaxin andciliarin were identified by Ortega et al. (1970), and the germacranolides,1B-acetoxy zacatechinolide and l-oxo zacatechinolide, by Bohlmann and Zdero(1977). Quijano at al. (1977. 1978) identified caleocromenes A and B andcaleins A and B. while Ramos (1979) found caleicins I and II. Herz and Kumar(1980) isolated acacetin, o-methyl acacetin, zexbrevin and an analogue, aswell as several analogues of budlein A and neurolenin B, including calein A.C. zacatechichi samples show differences in chemical composition, which hasled Bohlmann et al. (1981) to suggest that chemical taxonomy may help toreclassify the genus. Further taxonomic work is required since our Chontalinformant distinguishes between "good" and "bad" varieties according to theirpsychotropic properties.In the present paper we report some properties of zacatechichi extracts uponcat behavior and EEG, human reaction time, nap EEG, and subjectiveexperiences.Materials and methodsPlant collection and extract preparations "Good" samples of C. zacatechichiwere collected under the guidance of the Chontal informant near Tehuantepec,Oaxaca during November, 1978. Specimens of this collection were identified byDr. Miguel Angel Martinet Alfaro at the National Herbarium of Mexico as C.zacatechichi despite the Fact that there were minor morphological differencesrelative to previously collected material. The samples were identical withcollections made in the area of the isthmus of Tehuantepec.One kilogram of the dried plant (stem and leaves) was mashed and extractedwith hexane until exhaustion in a Soxhlet apparatus. This fraction was driedand 308 of an solvent-free hexane extract were obtained. The remainingmaterial was thoroughly extracted with methanol and the organic fractionevaporated. This procedure resulted in 86 g of a solvent-free gummy residuecalled the methanol extract. Both extracts were separated in fractions andpacked in gelatin capsules for pharmacological experiments. The dose wasestimated in the following manner: the human dose for divinatory purposesreported by the Chontal informant is "a handful" of the dried plant. Sincethe mean weight of many handfuls taken by several people was 60g we decidedthat the average human dose (HD-1) is around 1 g/kg of dried-mashed material.Therefore, the HD-1 for the hexane extract was 30 mg/kg, and 86 mg/kg for themethanol extract. In the experiments with cats. doses of HD-2. -4. -6 and -10of both extracts were used. The EEG; effects of C. zacatechichi extracts werecompared with those elicited by phencyclidine (Bio-ceutic Laboratories),quipazine (Miles Research Products). ketamine (Parke Davis) and SKF-10047(Smith Kline B French), and industrial solvent toluene. which can produce theappearance of 6 cps spike and wave activity in the cingulum of cats. Duringthe appearance of this electrographic activity animals show "hallucinatory"behavior (Conteras et al.. 1979, 1984).Behavioral toxicology in catsThis first experiment was performed in order to assess the possible toxicbehavioral effects of C. zacatechichi extracts. For this purpose three malecats (3 kg each) were used. Observations were done from 1300 to 1500 h in asound-attenuated recording chamber (109 x 76 x 74 cm) with a triple-glasswall. Each animal was placed in the cage and its behavior was recorded for1 h prior to oral administration of a gelatin capsule (25 x 8 mm) containinga zacatechichi extract and 2 h thereafter. Each capsule was placed inside themouth and swallowing was forced by giving 2-3 ml of saline solution. Theextracts (methanol or hexane) and doses (HD-1, HD-2. HD-4. HD-10) wererandomly assigned and tested only once. Two cats were observed three timesand the third animal twice. Between tests each animal was allowed to rest for6 days. Sampling ad libitum (Altmann. 1974) was used to evaluate the cats'response. Attention was given to abnormal behaviors such as ataxia, bizarrepostures and movements directed to non-existing objects (Fischer. 1969).EEG activity in catsSeveral common EEG effects to a series of hallucinogenic compound have beenreported by Winters et al. (1972). A dissociative action in multi-unitaryactivity between the reticular formation and basolateral amygdala and ahypersynchronic rhythm (2-3 cpa) in cortical recording are the two mostcharacteristic features. Tracheal administration of neurotoxic industrialsolvents produce limbic discharges while cats display "hallucinatorybehavior" (Contreras et al., 1979). The following experiment was designed toascertain whether C. zacatechichi extracts share these neurophysiologicalactions.Six adult male cats were stereotaxically implanted with stainless steelconcentric bipolar electrodes in the basolateral amygdala. the septum andcingulum according to the atlas of Snider and Niemer (1961). Epiduralelectrodes were placed on the cortex at the marginal circumvolution. Aftersurgery the animals were allowed a & 1 week recovery period. Each cat wasused as its own control and the effects of oral administration ofzacatechichi extracts (HD-6) were compared to those of phencyclidine (400ug/kg i.m.), quipazine (10 mg/kg i.p.), ketamine (6 mg/kg i.m.) and SKF-10047(3 mg/kg i.m.). These drugs are dissociative psychodysleptics and produce 6cps wave-and-spike activity in cingulum recording in addition to thecharacteristic hypersynchronic rhythm (Contreras at al., 1984). In eachexperiment, control recordings were taken in addition to at 60 min and + 120min after drug administration.Reaction Time and Time-lapse estimation in humansMeasurement of reaction time to a light flash and the ability to calculatefixed lapse times in humans allows the identification of hypnotic compounds(Fernandez-Guardiola et al., 1972). Objective evaluations of time perceptionmodification by marihuana have been achieved with the same technique(Fernandez-Cuardiola et al., 1974). From the experiments performed in cats itappeared that zacatechichi had hypnotic properties. Therefore, we chose thisexperimental paradigm to evaluate human effects. The study was performed in5 healthy volunteers (3 women and 2 men. ages 23-34) according to theprocedure described by Fernandez-Guardiola et al. (1972, 1974). The subjectswere informed about the experiment and the known effects of the plant and awritten consent was obtained. Capsules containing either a Calea extract(HD-1) or placebo were administered 1 H before the task in a double-blindrandomized design, where neither the volunteers nor the evaluator knew whichsubstance had been ingested. The first session did not involve theadministration of any substance in order to habituate the subjects to theexperimental manipulations. Physiological responses recorded included EEG,electromyogram, electrocardiogram, and galvanic akin response. All sessionswere done at the same time period (1700-1820 h). A complete session consistedof alternated 10-min periods for reaction-time evaluation and 10-min periodsfor time-lapse estimation. In the reaction-time periods the subjects wereinstructed to press a button with their dominant hand as soon as possibleafter a light wee dashed. Intervals between consecutive dashes were of 10-sduration. In the following 10 min, alternating with the reaction-time periods,the subjects were asked to estimate the dash intervals by pressing the buttoneach time they thought the light should have been dashed. The entire testlasted 80 min. Analysis of variance was used to assess results between andwithin individuals, the protected "t" and Least Significant Difference testswere used in paired comparisons.Sleep recordings in humansThe conventional procedure for EEG recording of sleep (Rechtschaffen andhales. 1968) was used in a similar double-blind randomized design which inthis case, included a low dose of an active hypnotic drug (diazepam, 2.5mgorally). In order to standardize the nap session, all volunteers were askedto reduce their normal sleep time by 2 h the night before testing. Theextract, diazepam or placebo capsule was ingested 1 H prior to the recordingsession (1700-1900 h). The physiological variables recorded includedrespiratory and heart rates, number of nap episodes, total time spent inwakefulness (W). in slow wave sleep stages (SWS stages I to IV) and in rapid-eye-movement sleep (REM) (Rechtschaffen and Kales, 1968). The respiratoryrate was recorded by means of a thermistor located in the nostril andconnected to a polygraph amplifier measuring the air temperature in eachinhalation-exhalation cycle. This is an indirect method which provides thefrequency and amplitude of respiratory rate. Data analyses were done by meansof factorial analysis of variance (ANOVA). For paired comparisons, theStudent Newman-Keuls test was used.Dream reportsThe psychological effects of Calea extracts were evaluated by the applicationof directed questionnaires and analysis of free reports of the subjectivesensations and dreams in all human volunteers after the reaction-time, napsessions and the following night. Neither the subjects, the interviewer northe evaluator knew whether the individual had taken a plant extract,diazepam, or placebo. The results were compared by the binomial test.Results and discussionBehavioral toxicology in catsSome minor behavioral changes were observed with low doses of both extracts(HD-1 and HD-2). The cats stared for long periods of time and 30 min afterthe administration of the zacatechichi extracts somnolence and sleep werefrequently observed. The HD-4 and HD-1O doses of the hexane extract producedataxia, bilateral contractions of nasal and maxillar muscles, and stereotypedpendulum head movements. The HD-10 dose also induced salivation with vomitingoccurring about 90 min after administration. The methanol extract producedataxia (HD-4) and compulsive grooming (HD-2). A common toxic effect of bothextracts (doses HD4 and HD-10) was retching and thick salivation.It was not clear if these effects were elicited by direct central nervoussystem stimulation or in response to local gastric irritation caused by somebitter principle of the plant. This activity was noted by Giral and Ladabaum(1959) and may be responsible for the appetizer properties of C. zacatechichi.Stare and pendular head movements can be elicited by several psychoactivedrugs such as toluene (Alcaraz et al., 1977; Contreras et al., 1977),quipazine (Sales et al.. 1966, 1968) and dopamine agonists (Ernst.1967).These effects are. therefore, not specific for any one of the several classesof psychoactive compounds. Moreover, staring and pendular head movements maymerely be indications of somnolence. In order to analyze more precisely theneural effects, electrophysiological recordings were taken in free-movingcats.EEG activity in catsBoth plant extracts produced similar EEG changes which were very differentfrom the other drugs used. The hexane extract induced 3 cps largevoltage rhythms in the cortex, cingulum and septum while the methanol extractprovoked 8 slowing of the EEG rhythm more predominant in subcorticalstructures. Somnolence was observed during the appearance of these changes.A quantitative analysis of frequency of discharge in the cingulum wasperformed for all drugs tested. The hexane extract produced only minorchanges while the methanol extract clearly decreased the frequency. Thisresponse is in contrast to the known psychodysleptic compounds which producedecreases of 6-7 cps (Contreras et al., 1984).The results of these experiments show that zacatechichi does not share theneurophysiological effects of the dissociative psychodysleptics and onlyinduces the behavioral and EEG signs of somnolence and sleep. The apparentlow toxicity of the plant in these experiments and its history of ethno-botanical use allowed us to ascertain the hypnotic potency, dream-inducingeffects and other psychotropic properties in human beings. Reaction time andtime-lapse estimation in humans. No differences among the three treatmentswere found for human rate, galvanic skin response and EEG recordings. Withthe methanol extract, short periods of sleep (stage I) usually appearedbetween flash intervals, and the subjects were awakened by the light. Bothextracts produced a statistically significant slowness of reaction-time:250 ms with placebo, 280 ms with hexane extract and 290 ms with methanolextract (P zacatechichi extracts. The methanol extract increased estimation by 3 s onaverage (P change was not significantly different from controls.The characteristic EEG slowness and the increased reaction times of subjectstreated with both extracts suggested that zacatechichi may contain hypnoticcompounds. Moreover, a larger effect was elicited by the methanol extractsuggesting that the active compounds might be found in the polar fractions.An increase in time-lapse estimation and a weak respiratory analeptic effectshave been reported after marihuana administration (Fernandez-Guardiola etal., 1974).Sleep recordings in humansSince the experiment just discussed did not allow an analysis of sleepstages, the possibility of sleep and dream modifications by zacatechichi wastested in a nap study conducted in the same human volunteers. Heart rate,total time and frequency of each stage of sleep did not change with anytreatment in comparison to placebo (Fig. 5). However, it was found that thefrequency of W and SWS-IV stages were significantly modified by treatments(W F(3,32)= 5.28, P comparisons showed that, upon onset of sleep, the methanol extract anddiazepam increased significantly the frequency of W stages (P compared to placebo. In contrast, methanol extract and diazepam decreasedsignificantly (P sleep were not significantly modified by treatments, SWS-I and SWS-II showeda alight increase in comparison to placebo and, in contrast, SWS-III and REMstages decreased slightly. Respiratory rate was significantly modified bytreatments (F(3,400)=79.92, P methanol extract increased (P Although this small increase may lack physiological relevance, it doessuggest a pharmacological effect upon respiratory rate. These results supportthe idea that zacatechichi extracts, particularly the methanol fraction,contain compounds with activity equivalent to sub-hypnotic diazepam doses.Ingestion of the plant produces a light hypnotic state with a decrease ofboth deep slow-wave sleep and REM periods. The question of the ethnobotanicaluse and open trial reports of dream enhancement was studied in the followingsection by the evaluation of subjective reports during the sleep study.Dream reportsThe quantitative results concerning hypnagogic imagery and dreams aresummarized in Table 1. Data from the reaction-time and the nap sessions endthe following night were pooled. Significantly more dreams (P comparison to placebo) were reported after the methanol extract. Similarly,the number of dreams reported during naps was significantly higher followingthe administration of the plant extracts than with diazepam (P can be appreciated that, although not significant, the number of dreamsreported was greater after the ingestion of Calea extracts than placebo. Amore detailed analysis of dream content is shown in Table 2. The number ofsubjects that did not remember dreaming was always greater after placebo anddiazepam administration and. conversely, the individuals that reported morethan one dream per session were always the ones treated with zacatechichiextracts. The dreams reported by subjects ingesting Calea extracts, were of ashorter content (measured by the number of lines written in the report).Spontaneous reports of emotions and nightmares were not different among thefour treatments. Nevertheless, with the methanol extract more colors duringdreaming were mentioned. These results show that zacatechichi administrationappears to enhance the number and/or recollection of dreams during sleepingperiods. The data are in agreement with the oneirogenic reputation of theplant among the Chontal Indians but stand in apparent contradiction to theEEG sleep-study results. It is well known that dreaming activity iscorrelated to the REM or paradoxical phase of sleep (Aserinsky and Kleitman,1953) and it could be expected that a compound that increases dream wouldalso increase REM stage frequency or duration, as it has been shown to occurwith physostigmine (Sitaram et al., 1978). In contrast, zacatechichiincreases the stages of slow wave sleep and apparently decreases REM sleep.This also occurs with low doses 12-10 mg) of diazepam (Harvey, 1982). Despitethis similarity in EEG effects, diazepam decreases dreaming reports (Firth,1974) while zacatechichi extracts enhances them. Such discrepancy may beexplained by the fact that dreaming and imagery are not restricted to the REMepisodes but also occur during slow wave sleep (SWS I and II) as livelyhypnagogic images (Roffwarg et al., 1962). Such images are reported as briefdreams and are known to be enhanced by marihuana (Hollister, 1971). All thissuggests that Calea zacatechichi induces episodes of lively hypnagogicimagery during SWS stage I of sleep, a psychophysiological effect that wouldbe the basis of the ethnobotanical use of the plant as an oneirogenic andoneiromantic agent.AcknowledgmentsThe authors wish to express their gratitude to Dr. Alfredo Ortega for advicein the preparation of the plant extracts.References(removed, completely illegible)-----------------------------------------------------------------------------Downloaded from: TAC Ethnobotanicalshttp://www.madlex.com/tac/ethno.htm----------------------------------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
t st tantra Posted January 25, 2006 Share Posted January 25, 2006 sorry please disregard the above post ,they turned out to be something else.i'll try crossing the 2 varieties next time.i've tried 2 forms now and concider both active.the one which i know and love,the same as torstens ext and gomaos's plants seems more stimulant and much less visual,but active at a slightly lower dose,a few leaves in a smoke.this form clears my senses.this reddish tinged form from teo seems heavily visual,fantasically so,the colour tones,contrasts,control of variable perspective.....blah blah ....colours never seen before.....i could see anything,go anywhere[with vilca and cyprus]. but the dose would be closer to 6 leaves,as rev says its fine by itself.dosnt seem to clear my head though.i always got a blue visual tone with the old calea,this new one has sort of all colours and silver static . t s t . Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted January 25, 2006 Share Posted January 25, 2006 shit i wish i had kept a plant lol Quote Link to comment Share on other sites More sharing options...
mescalito Posted January 25, 2006 Share Posted January 25, 2006 I've been playing with oneirogenics on and off for a few years now and Calea is one of the best imho. Others worth considering are mugwort,blue lotus and definitely L.inebrians. I only ever tried the leaves from the one Calea plant/strain from Andrew and always had effects consistent with those described in that paper Rev kindly pasted(thanks Rev!). He had/has the variety where the leaves would turn orangey red and they smelled very strongly of turpines as did the smoke. Normally I'd smoke 3 large cones through a bamboo pipe but a bong works fine just before going to bed and that would bring on the most visual meaningful and brightly coloured dreams every time...but alas the bag of leaf Andrew kindly gave me ran out a fair while back (wink wink nudge nudge ^_^ ) From the last 5g of that batch left I made a ghetto style 5x using cheap white spirits which was markedly more potent so I'd agree the above paper is spot on with alcohol extn being the best way to catch the actives. I hope Andrew doesn't mind me saying but I reckon he has quite a potent variety worth cloning if Calea is easy enough to clone that is?? Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted January 25, 2006 Share Posted January 25, 2006 calea is very easy to propagate Quote Link to comment Share on other sites More sharing options...
apothecary Posted January 25, 2006 Share Posted January 25, 2006 I just got a cutting of goms variety from smogs a few days ago (along with about 45g of fresh leaf which is drying now), if anyone has one of the other varieties and is willing to spare a cutting please pm me for a trade? :DI think Calea extract, Lotus extract and powderised mandrake root all together would make a fine dream smoking mix. Quote Link to comment Share on other sites More sharing options...
t st tantra Posted January 26, 2006 Share Posted January 26, 2006 shit i wish i had kept a plant lolumm,what does this mean?by the way ,what was the source of the seed you grew from?i had thought the effects of calea accumulative but got little from last nights effort,maybe a weak variant.number 20 may be the one i was most impressed with ,still picking bits and peices of not quite mature plants that are not in full sun yet.so things should develop more.like the bitter medicinal flavour of the smoke.a salvia dream herb, xiwit ?bakana? t s t . Quote Link to comment Share on other sites More sharing options...
teonanacatl Posted January 27, 2006 Share Posted January 27, 2006 lol i got rid of all plants that seeded easily, calea, heimia, mg. cos i was seeing little ones growing where i haddent planted them. so i sold all my plants with numbers which i hope everyone kept on the plant. my seed was from my own plant from gomaos. Quote Link to comment Share on other sites More sharing options...
Tomer Corymbosa Posted March 18, 2006 Author Share Posted March 18, 2006 ok ok guys! listen to this!i have G E R M I N A T I O N of Calea ! ! ! few days ago i recieved seed pods of Calea zacatechichi from Shamans' Palace (lot of seeds!!!).i took out the seeds from the pods .took little pot with moist regular soil,i sprinkled the seeds and spray water on the seeds .i didnt cover the seeds!! not even tiny layer.i bulid mini greenhouse and put the pot in.today as normal i looked to see if something changed and 2 seedlings came up!so now we know! Calea needs LIGHT for germination.of course i got fresh seeds so we must consider this...but another great thing is they have germinated in few days and from other people's reports it took months to seeds comin up....so maybe i have luck and maybe not...i should wait to see.now i'm affraid from the bad white fungi will kill the seedlings....if they will survive the week i'll take pics...till than Quote Link to comment Share on other sites More sharing options...
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