PubMed Health⌕ Search

Biomedical subjects

C Goto

Publications and source records attributed to C Goto.

27 records · Page 2Linked to original sources

Lethal efficacy of extract from Zingiber officinale (traditional Chinese medicine) or [6]-shogaol and [6]-gingerol in Anisakis larvae in vitro.

The authors previously reported that an extract from Zingiber officinale, traditionally eaten along with raw fish and used in traditional Chinese medicine, effectively destroyed Anisakis larvae in vitro. In this study, we analyzed the effective components of ginger rhizomes. Methanol extracts were fractionated after first being treated with HCl at pH 3, then with NaHCO3 at pH 10, and, finally, with NaOH at pH 13 (fraction 1). In general, this fraction is rich in neutral substances. [6]-Shogaol and [6]-gingerol, known neutral components of ginger rhizomes, were detected using gas chromatography and were found to be the most prevalent components in the fraction, occurring in quantities that resulted in a dose-dependent killing efficacy. Authentic [6]-shogaol and [6]-gingerol could kill Anisakis larvae at a minimal effective dose of 62.5 and 250 micrograms/ml, respectively. However, the concentration of [6]-gingerol in fraction 1 was greater than 20 times that of [6]-shogaol, making the former the most active component in the fraction. Furthermore, synergistic effects between [6]-gingerol and a small amount of [6]-shogaol were observed. Pyrantel pamoate, an available antinematodal drug, had no lethal effect, even at a concentration of 1 mg/ml. In saline solution containing [6]-shogaol (62.5 micrograms/ml), greater than 90% of larvae lost spontaneous movement within 4 h and were destroyed completely within 16 h. Microscopical examinations showed destruction of the digestive tract and disturbances of culticulae.

Animals↗

[Mutagenesis of amino and/or methyl analogs of acridine in Salmonella and yeast: a comparison between the spot-test and the pre-incubation methods].

The relationship between mutagenic activities and chemical structure of acridine derivatives was examined by using Salmonella typhimurium strains TA 1537 and TA 1977 and yeast Saccharomyces cerevisiae. Most analogs with amino and/or methyl group(s) caused frameshift-type mutation in Salmonella without mammalian microsomal enzyme activation. The 9-amino analogs were strong mutagens and mutagenicity was also increased when 10-position was methylated in 1-amino and 2-amino compounds. However, 9-amino derivatives did not cause mitochondrial mutation in yeast, where 3,6-diamino and/or 10-methyl groups were structural requisites for significant mutagenic activity. In comparison with the pre-incubation method, the spot-test method was shown to be less sensitive. The mutagenicity of some compounds could not be detected by the spot-test method. Mutagenic activities of these drugs were revealed and increased markedly with an increase in pre-incubation period up to 20 min, suggesting that the pre-incubation of tester bacteria with a compound prior to a mutagenicity assay is necessary for the detection of mutagenesis of these compounds.

Acridines↗