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Yukihiro Goda

16 papers in the library · 401 citations · publishing 2003-2015

Papers

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MAM-2201, a synthetic cannabinoid drug of abuse, suppresses the synaptic input to cerebellar Purkinje cells via activation of presynaptic CB1 receptors.

Neuropharmacology August 2015 Tomohiko Irie, Ruri Kikura-Hanajiri, Makoto Usami et al.

Herbal products containing synthetic cannabinoids-initially sold as legal alternatives to marijuana-have become major drugs of abuse. Among the synthetic cannabinoids, [1-(5-fluoropentyl)-1H-indol-3-yl](4-methyl-1-naphthalenyl)-methanone (MAM-2201) has been recently detected in herbal products and has psychoactive and intoxicating effects in humans, suggesting that MAM-2201 alters brain...

DOI: 10.1016/j.neuropharm.2015.02.025 (opens in new tab) Full text (opens in new tab) Cerebellum Mam-2201 Neurotransmitter release Purkinje cell +1

Methylone and Monoamine Transporters: Correlation with Toxicity

Current Neuropharmacology March 1, 2011 Chiharu Sogawa, Norio Sogawa, Kazumi Ohyama et al. 50 citations

Methylone (2-methylamino-1-[3,4-methylenedioxyphenyl]propane-1-one) is a synthetic hallucinogenic amphetamine analog, like MDMA (3,4-methylenedioxy- methamphetamine), considered to act on monoaminergic systems. However, the psychopharmacological profile of its cytotoxicity as a consequence of monoaminergic deficits remains unclear. We examined here the effects of methylone on the transporters...

Enzyme‐assisted synthesis of the glucuronide conjugate of psilocin, an hallucinogenic component of magic mushrooms

Drug Testing and Analysis February 2, 2011 Takuji Shoda, Kiyoshi Fukuhara, Yukihiro Goda et al. 8 citations

An enzyme‐assisted synthesis of psilocin glucuronide (PCG), a metabolite excreted in the urine of magic mushroom (MM) users, is described. In the presence of Aroclor 1254 pretreated rat liver microsomes, psilocin and the cofactor UDPGA were incubated for 20 h. Purification by HPLC gave PCG in 19% yield (3.6 mg). The compound structure was characterized by MS and NMR. The milligram amounts of...

DOI: 10.1002/dta.244 (opens in new tab) Glucuronide Metabolite Chromatography Urine +4

Analysis of Newly Distributed Designer Drugs Detected in the Products Purchased in Fiscal Year 2008

Yakugaku Zasshi February 1, 2010 Nahoko Uchiyama, Norimasa Miyazawa, Maiko Kawamura et al. 16 citations

Thirty-two psychotropic substances were listed as designated substances (Shitei-Yakubutsu, 31 compounds and 1 plant) in Japan by the Pharmaceutical Affairs Law in April 2007 for preventing the abuse of these substances. Subsequently, other psychoactive compounds were also added to this category, 40 substances (classified as 12 tryptamines, 17 phenethylamines, 3 piperazines, 6 alkyl nitrites, 1...

DOI: 10.1248/yakushi.130.263 (opens in new tab) Designer drug Phenethylamines Tryptamines Amine gas treating +3

Effects ofPsilocybe argentipeson Marble-Burying Behavior in Mice

Bioscience Biotechnology and Biochemistry August 23, 2009 Yoshihiro Matsushima, Osamu Shirota, Ruri Kikura-Hanajiri et al. 77 citations

Psilocybe argentipes is a hallucinogenic mushroom. The present study examined the effects of P. argentipes on marble-burying behavior, which is considered an animal model of obsessive-compulsive disorder. P. argentipes significantly inhibited marble-burying behavior without affecting locomotor activity as compared with the same dose of authentic psilocybin. These findings suggest that P....

DOI: 10.1271/bbb.90095 (opens in new tab) Full text (opens in new tab) Psilocybin Obsessive compulsive Animal model Hallucinogen +1

[Chemical and DNA analyses for the products of a psychoactive plant, Voacanga africana].

Yakugaku Zasshi August 1, 2009 Ruri Kikura-Hanajiri, Takuro Maruyama, Akinori Miyashita et al. 15 citations

Voacanga africana (Apocynaceae) is a small tropical African tree. The root bark and seeds of this tree contain a number of alkaloids, including ibogaine (a hallucinogenic/aphrodisiac compound in bark), tabersonine (a major constituteent of seeds) and other voacanga alkaloids, traditionally used in Africa for religious purposes. Recently, some kinds of products containing this plant (root bark...

DOI: 10.1248/yakushi.129.975 (opens in new tab) Full text (opens in new tab) Ibogaine *voacanga africana* research Ethnobotany Phytochemistry +25

Simple and Rapid Screening for Psychotropic Natural Products Using Direct Analysis in Real Time (DART)-TOFMS

Yakugaku Zasshi June 1, 2009 Maiko Kawamura, Yukihiro Goda, Ruri Kikura-Hanajiri 19 citations

Direct Analysis in Real Time (DART) is a novel ionization technique that provides for the rapid ionization of small molecules under ambient conditions. To investigate the trend of non-controlled psychotropic plants of abuse in Japan, a rapid screening method, without sample preparation, was developed using DART-time of flight mass spectrometer (TOFMS) for plant products. The major psychotropic...

DOI: 10.1248/yakushi.129.719 (opens in new tab) Dart ion source Mass spectrometry Noscapine Chromatography +2

Analysis of Designer Drugs Detected in the Products Purchased in Fiscal Year 2006

Yakugaku Zasshi October 1, 2008 Nahoko Uchiyama, Ruri Kikura-Hanajiri, Nobuo Kawahara et al. 46 citations

Many psychotropic substances are easily available in Japan via the Internet, thus the spread of drug abuse is becoming more serious problem. To avoid drug abuse, 32 substances have been controlled in Japan since April in 2007 by the Pharmaceutical Affairs Law as designated substances (Shitei-Yakubutsu, classified as 11 tryptamines, 11 phenethylamines, 2 piperazines, 6 alkyl nitrites, 1...

Analytical Data of Designated Substances (Shitei-Yakubutsu) Controlled by the Pharmaceutical Affairs Law in Japan, Part II: Color Test and TLC

Yakugaku Zasshi June 1, 2008 Nahoko Uchiyama, Maiko Kawamura, Hiroyuki Kamakura et al. 17 citations

Many psychotropic substances are readily available in Japan via the Internet. To avoid the spread of drug abuse, some drugs have been controlled as designated substances (Shitei-Yakubutsu) in Japan since 2007 by the Pharmaceutical Affairs Law. Twenty-nine designated substances (classified as tryptamine, phenethylamine and piperazine types) were analyzed using color tests and TLC. The color...

[Authentication and ultra performance liquid chromatography (UPLC)/MS analysis of magic mint, Salvia divinorum and its related plants].

Yakugaku Zasshi 2008 Takuro Maruyama, Hiroyuki Kamakura, Ruri Kikura-Hanajiri et al. 14 citations

Ultra performance liquid chromatography (UPLC)/mass spectrometry (MS) analysis was performed to investigate whether commercial Salvia cultivars available in the Japanese market contain salvinorin A (1), which is an hallucinogen present in magic mint (Salvia divinorum) prior to the regulation of S. divinorum by the Japanese Pharmaceutical Affairs Law. In addition, a previously reported method to...

Phylogenetic relationship of psychoactive fungi based on rRNA gene for a large subunit and their identification using the TaqMan assay (II).

Forensic Science International November 10, 2006 Takuro Maruyama, Nobuo Kawahara, Kazumasa Yokoyama et al.

"Magic mushroom (MM)" is the name most commonly given to psychoactive fungi containing the hallucinogenic components: psilocin (1) and psilocybin (2). We investigated the rRNA gene (internal transcribed spacer (ITS) and large subunit (LSU)) of two Panaeolus species and four Psilocybe species fungi (of these, two are non-psilocybin species). On the basis of sequence alignment, we improved the...

[DNA and chemical analyses of commercial fly agaric-related products].

Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan April 1, 2005 Takuro Maruyama, Nobuo Kawahara, Toshimitsu Fukiharu et al.

Since June 6, 2002, psilocin and psilocybin-containing fungi (commonly called "magic mushrooms") have been regulated by the Narcotics and Psychotropics Control Law in Japan. However, various fly agaric-related products are now entering the Japanese market via the internet. In this study, fly agaric-related products available in this way were investigated for raw materials by DNA analysis and...

Determination of psilocybin in hallucinogenic mushrooms by reversed-phase liquid chromatography with fluorescence detection

Talanta January 7, 2005 Kimie Saito, Toshimasa Toyo’oka, Masaru Kato et al. 35 citations

The determination of psilocybin was carried out by reversed-phase liquid chromatography (HPLC) with fluorescence (FL) detection. Psilocybin was labeled with 5-dimethylaminonaphthalene-1-[N-(2-aminoethyl)]sulfonamide (DNS-ED) at 60 degrees C for 4h in the presence of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) as the activation reagent. The resulting derivative was separated on a...

DOI: 10.1016/j.talanta.2004.11.031 (opens in new tab) Psilocybin Hallucinogen Reversed-phase chromatography Fluorescence spectroscopy +1

Phylogenetic relationship of psychoactive fungi based on the rRNA gene for a large subunit and their identification using the TaqMan assay.

Chemical & pharmaceutical bulletin June 1, 2003 Takuro Maruyama, Kazumasa Yokoyama, Yukiko Makino et al.

"Magic mushrooms" (MMs) are psychoactive fungi containing the and Psychotropics Control Law in Japan. Because there are many kinds of MMs and they are often sold even as dry powders in local markets, it is very difficult to identify the original species of the MMs by morphological observation. Therefore, we investigated the rRNA gene for a large subunit (LSU) of several MMs to classify them by...

DOI: 10.1248/cpb.51.710 (opens in new tab) Full text (opens in new tab) Agaricales Rna, fungal Hallucinogens Phylogeny +5

Concise Large-Scale Synthesis of Psilocin and Psilocybin, Principal Hallucinogenic Constituents of “Magic Mushroom”

Journal of Natural Products May 30, 2003 Osamu Shirota, Wataru Hakamata, Yukihiro Goda 90 citations

The concise large-scale syntheses of psilocin (1) and psilocybin (2), the principal hallucinogenic constituents of "magic mushroom", were achieved without chromatographic purification. The key step in the synthesis of 2 was the isolation of the dibenzyl-protected intermediate (7) as a zwitterionic derivative (8), which was completely identified by means of 2D NMR analyses.

DOI: 10.1021/np030059u (opens in new tab) Psilocybin Hallucinogen Mushroom Stereochemistry

Discrimination of Psychoactive Fungi (Commonly Called "Magic Mushrooms") Based on the DNA Sequence of the Internal Transcribed Spacer Region.

Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi) 2003 Takuro Maruyama, Osamu Shirota, Nobuo Kawahara et al. 14 citations

'Magic mushrooms' (MMs) are psychoactive fungi containing the hallucinogenic compounds, psilocin (1) and psilocybin (2). Since June 6, 2002, these fungi have been regulated by the Narcotics and Psychotropics Control Law in Japan. Because there are many kinds of MMs and they are sold even as dry powders in local markets, it is very difficult to identify the original species of the MMs by...

DOI: 10.3358/shokueishi.44.44 (opens in new tab) Internal transcribed spacer Sequence biology Genetics