[Mass spectrometric structure analysis of fatty acid mixtures from biological material after gas capillary chromatographical separation].

The identification of mixtures of fatty acids from biological materials is possible by electron impact ionization mass spectra of methyl esters after their capillary gas chromatographic separation. Mass spectra of pyrrolidine derivatives are used for the determination of double bond positions in unsaturated fatty acids. 97 different fatty acids (saturated, unsaturated, branched, cyclic, hydroxy, oxo, epoxy and methoxy) and other compounds (alkanes, halogens, phthalates, ketones, aldehydes) were identified in yeast and bacterial biomasses, lipid-containing animal tissues and human sera as well as fish and plant oils (77 preparations).

[Toxicological effect of a fatty acid mixture in rats].

The effects of a fatty acids mixture containing nearly 50% odd numbered fatty acids (PC-Säure) were studied in a subchronic toxicity test in male and female rats. The animals received PC-Säure in their diet at levels of 0, 1.25, 2.

Investigation of selected toxicological parameters of gamma-pentachlorocyclohexene (gamma-PCCH).

The toxic effects of the gamma-hexachlorocyclohexane metabolite gamma-pentachlorocyclohexene (gamma-PCCH) were studied by acute and subacute (6 weeks) experiments. The investigations included cerebral convulsibility with chemoshock (Tetrazolium), reactivity with hot plate method, the learning ability with learning tests, and peripheral nervous activity (EMG). Nociceptive reaction time was not influenced, the learning process (6 weeks) was inhibited by gamma-PCCH.

[The subacute toxicity of glucosylthiazolidine-4-carbonic acid in rats].

Glucosylthiazolidine-4-carbonic acid, an intermediate of the Maillard reaction between D-glucose and L-cysteine, was given in doses of 0, 25, 50 or 100 mg/kg b.w. by oral intubation to male and female rats for 21 days.

[Distribution and metabolism of azoxybenzene in the rat].

No sex differences could been shown after absorption and distribution of azoxybenzen in the rat. The highest level occur in the thyroid gland, the adrenals and in the fat tissues. The maximum level was reached 30 min.