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Yoshihito Ohmae

3 papers in the library · 167 citations · publishing 2002-2003

Papers

Morphological and chemical analysis of magic mushrooms in Japan.

Forensic science international December 17, 2003 Kenji Tsujikawa, Tatsuyuki Kanamori, Yuko Iwata et al. 79 citations

Hallucinogenic mushrooms circulating in Japan were analyzed using scanning electron microscopy and high-performance liquid chromatography. Psilocybe cubensis contained psilocin (0.14–0.42%) and psilocybin (0.37–1.30%) in the whole mushroom, with higher concentrations in the cap than the stem. Copelandia species contained psilocin (0.43–0.76%) and psilocybin (0.08–0.22%) in the whole mushroom, again with more alkaloid in the cap. Psilocybe cubensis is psilocybin-rich, while Copelandia is psilocin-rich. The combination of SEM and optical microscopy was effective for observing characteristic fungal tissues such as basidiomycetes, spores, cystidia, and basidia.

In vivo metabolism of 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in the rat: identification of urinary metabolites.

Journal of analytical toxicology March 1, 2002 Tatsuyuki Kanamori, Hiroyuki Inoue, Yuko Iwata et al. 61 citations

In rats, the psychoactive compound 2C-B is broken down into at least six distinct breakdown products through two main metabolic pathways. One pathway converts 2C-B into an aldehyde, which is then further processed into an alcohol and a carboxylic acid. The other pathway produces metabolites where a methyl group is removed from either the 2- or 5-position of the molecule, followed by acetylation of the amino group. These findings indicate that the body metabolizes 2C-B through multiple chemical changes, resulting in a variety of metabolites that are excreted in urine.

Excretory Profile of 4-Bromo-2,5-dimethoxy-phenethylamine (2C-B) in Rat

JOURNAL OF HEALTH SCIENCE April 1, 2003 T. Kanamori, K. Tsujikawa, Yoshihito Ohmae et al. 27 citations

After oral administration of 10 mg/kg of the psychoactive substance 2C-B to male Wistar rats, the main metabolite found in urine was 5-O-desmethyl-N-acetyl-2C-B, accounting for 13.2% of the dose. Other urinary metabolites included 2-O-desmethyl-N-acetyl-2C-B (5.8%), 2-O-desmethyl-2C-B (3.5%), a carboxylic acid compound (1.9%), 5-O-desmethyl-2C-B (1.2%), and an alcoholic compound (0.8%). Only 0.2% of the original 2C-B was excreted unchanged in urine. In faeces, only two acetylated metabolites were detected. Most hydroxyl-containing urinary metabolites were recovered as conjugates.