Alterations of 3,4-dihydroxyphenylethylamine and its metabolite 3,4-dihydroxyphenylacetic produced in rat brain tissues after systemic administration of saxitoxin

We have measured the dopamine levels in some discrete rat brain regions after acute intraperitoneal administration of saxitoxin (STX). STX is one of the several toxins that causes paralytic shellfish poisoning (PSP). PSP is a serious public health concern through the world. Certain dinoflagellates are able of producing STX, a powerful neurotoxic compound, which blocks the voltage sensitive sodium channels, entailing to the appearance of the main symptoms of poisoning by PSP: muscular paralysis and respiratory depression. The goal in this study was to analyze the effect of STX on dopamine levels in discrete rat brain regions after its acute intraperitoneal administration. Different experimental periods were analyzed for STX doses (5 and 10 μg kg⁻¹ body weight). With low dose, experimental periods were: 30, 60 and 120 min. With high dose, experimental period was just 30 min. At the end of each experimental period, animals were sacrificed by cervical dislocation. Brains were removed and dissected in: hypothalamus, striatum, midbrain, brain stem, right and left hemispheres. This is to our knowledge, the first report in which a sublethal dose of STX administered intraperitoneally results in an acute alteration of dopamine (DA) production and its metabolite 3,4-dihydroxyphenylacetic acid (DOPAC).     

Enzymic sulphation of p-nitrophenol and steroids by larval gut tissues of the southern armyworm (Prodenia eridania Cramer)

1. An enzyme system that catalyses the sulphation of p-nitrophenol, cholesterol, alpha-ecdysone, beta-sitosterol, dehydroepiandrosterone, oestrone and four other steroids of plant and insect origin was obtained from the soluble fraction of southern-armyworm gut tissues. 2. The enzyme system required ATP and inorganic sulphate, and activity was slightly enhanced in the presence of GSH. 3. The properties of this enzyme system with respect to pH, temperature, substrate and protein concentrations and various cofactors and reagents were studied. At -23 degrees C the enzyme preparation could be stored for 2 weeks without drastic loss of activity. At the end of storage for 1 month the loss of activity was approx. 21%. 4. The possible involvement of this enzyme system in insect endocrine control is discussed.     

Antioxidant effects of dopamine and related compounds.

The antioxidant and free radical scavenging effects of dopamine, noradrenaline, tyramine, and tyrosine were investigated and compared with alpha-tocopherol. The antioxidant effect of dopamine and its related compounds on peroxidation of linoleic acid were in the order of dopamine > alpha-tocopherol = tyramine > tyrosine > noradrenaline as measured by the thiocyanate method. These amine compounds had reducing power, and a scavenging effect on reactive oxygen species, i.e., superoxide anion and hydroxyl radical. The results for reducing power and scavenging effect of these amine compounds had a similar trend as their inhibition of linoleic acid peroxidation. The antioxidant activity of these amine compounds in soybean oil was also evaluated by the Rancimat method. The induction time to reach 100 meq/kg peroxide value (POV) of soybean oil for dopamine, alpha-tocopherol, tyramine, tyrosine, noradrenaline, and control were 9.0, 8.2, 8.0, 6.4, 4.6, and 4.3 h, respectively. The antioxidant efficacy of amine compounds seems to be correlated with the numbers of hydroxy groups and their position on the phenolic ring.     

Microdetermination of norepinephrine, 3,4-dihydroxyphenylethylamine, and 5-hydroxyyptamine from single extracts of specific rat brain areas

The conditions reported by Toru and Aprison (4) for extracting ACh in specific brain areas were tested to determine whether 5-HT, NE, and dopamine were also extracted quantitatively. It was found that the extraction solution used in brain ACh determinations, 15% 1N formic acid plus 85% acetone ($\text{v}\text{v}$), was also excellent for extraction of NE, 5-HT, and dopamine from different brain areas. Experimental conditions are given for the microdetermination of all three biogenic amines in such a single extract of a specific rat brain area. The methods are based on previously published fluorometric methods; these have been scaled down or modified slightly to permit analyses of small aliquots. The concentration of 5-HT, NE, and dopamine in the telencephalon, diencephalon plus mesencephalon, pons plus medulla oblongata, and cerebellum of the rat are also reported using the described micromethods after extraction with 15% 1 N formic acid plus 85% acetone ($\text{v}\text{v}$).     

Studies of the inhibition of dopamine beta hydroxylase by thiono-sulfur containing compounds.

The inhibitory effect of several thione and thioether compounds on dopamine β hydroxylase has been examined. Carbon disulfide and propylthioracil inhibited the enzyme competitively and showed a Ki of 1.1 × 10⁻⁴ and 1.0 × 10⁻⁴M, respectively. Dialysis reversed the inhibition but N-ethylmaleimide did not. The thioethers methionine, benzylmethyl sulfide, thiazole and 2-amino-thiazole had no inhibotory effect on enzymatic activity. No evidence of oxidative metabolism of the thione inhibitors by dopamine β hydroxylase could be detected.     

Extensive conjugation of dopamine (3,4-dihydroxyphenethylamine) metabolites in cultured human skin fibroblasts and rat hepatoma cells.

[G-3H]Dopamine (3,4-dihydroxyphenethylamine) metabolism in human skin fibroblasts and rat hepatoma cells in culture was determined by high-pressure liquid-chromatographic analysis of both cell extract and uptake medium. Conjugated metabolites were selectively hydrolysed by incubation with arylsulphatase or beta-glucuronidase before analysis. The principal metabolites of dopamine in fibroblast cells are 3-methoxytyramine 4-O-sulphate and 3-methoxytyramine. No significant differences, either in the amounts of these metabolites or in the amount of dopamine metabolism, were observed in fibroblasts from both normal and homocystinuric individuals. In rat hepatoma cells, the major metabolite of dopamine was 3-methoxytyramine 4- or 3-O-glucuronide; lower concentrations of dopamine 4- or 3-O-glucuronide, 4-hydroxy-3-methoxyphenylacetic acid, 3,4-dihydroxyphenylacetic acid and two unidentified glucuronide conjugates were also observed. Significant differences in the relative concentrations of these metabolites in cell and uptake medium were observed in both cell systems.     

Inhibition of aromatase activity in the rat by aminoglutethimide and related compounds

Two compounds possessing aromatase inhibitory activity have been evaluated for their effects on oestradiol (E2) biosynthesis in the rat. These compounds, structurally related to aminoglutethimide (1), were administered intra-peritoneally at two dose levels to 10 week old female rats previously treated with pregnant mares' serum gonadotrophin (PMSG, 100 i.u. subcutaneously every other day for 9 days). Three hours after dosing, blood was collected and plasma oestradiol levels determined by RIA. Aminoglutethimide, 3-(4'-aminophenyl-3-ethylpyrrolidine-2,5-dione (2) and N-methyl-3-(4'-aminophenyl)-3-ethylpyrrolidine-2,5-dione (3) decreased E2 blood levels by 98, 97 and 82% of control levels respectively (n = 6) at a dose of 50 mg/kg. Similarly effective inhibition was also observed at a dose of 25 mg/kg (n = 4). Ovarian aromatase activity, assessed by incubating the homogenised ovaries of treated rats with tritium-labelled androstenedione (0.2 microM) or testosterone (1 microM), indicated that residual enzyme activity was reduced compared with controls. Aminoglutethimide, and the new pyrrolidinedione aromatase inhibitors 2 and 3, are therefore effective inhibitors of E2 biosynthesis in the rat with functioning ovarian activity.     

Inhibition of retinoic acid metabolising enzymes by 2-(4-aminophenylmethyl)-6-hydroxy-3,4-dihydronaphthalen-1(2H)-one and related compounds

In a search for inhibitors of all-trans retinoic acid (RA)-metabolising enzymes as potential agents for the treatment of skin conditions and cancer we have examined 2-(4-aminophenylmethyl)-6-hydroxy-3,4-dihydronaphthalen-1(2H)-one (5). Compound (5) is a moderate inhibitor of RA-metabolising enzymes in mammalian cadaverous tissue microsomes and homogenates as well as RA-induced enzymes in cultured human genital fibroblasts and HaCat cells. Overall (5) was more potent than or equipotent with ketoconazole, a standard inhibitor, in the cadaverous systems but less active towards the RA-induced cell culture systems. Examination of the data suggests that RA-induction generates metabolising enzymes not present in the cadaverous systems, which are more susceptible to inhibition by ketoconazole than (5).     

C-(polyacetoxy)alkyloxadiazolines and related compounds

The (phenylacetyl)hydrazones of d-galactose, d-glucose, d-mannose, d-arabinose, l-arabinose, d-xylose, and l-sorbose were prepared. The d-galactose and d-arabinose derivatives were converted into their per-O-acetylated derivatives (8 and 9, respectively). The acyclic structure of 8 was proved from its direct preparation by the condensation of(phenylacetyl)hydrazine with penta-O-acetyl-aldehydo-d-galactose. Cyclization of 2,3,4,5,6-penta-O-acetyl-aldehydo-d-galactose (phenylacetyl)hydrazone with boiling acetic anhydride yielded a mixture of two products that could be separated by fractional recrystallization, to give 3-acetyl-5-benzyl-2-(polyacetoxy)alkyl-1,3,4-oxadiazolines; a mechanism for the reaction was proposed. The n.m.r. and mass spectra of some of these derivatives were discussed.     

Studies on plant growth-regulating substances: The metabolism of indole-3-acetonitrile and related compounds in wheat and pea tissues

The plant growth-regulating activity of a number of new indole derivatives is reported. It is shown that indole-3-acetonitrile (IAN) is converted to indole-3-carboxylic acid by metabolism within wheat and pea tissues, and the mechanism of this a-oxidation reaction has been studied. The relevant indole compounds were synthesized and their metabolism investigated by T.L.C. techniques. N -Methylindole-3-acetonitrile was also shown to be degraded by a-oxidation in wheat and pea tissues and this was separately investigated. While no definite conclusions can be drawn, the evidence indicates that conversion of indole- and Af-methylindole-3-acetonitriles to the corresponding indole-3-aldehyde-cyanohydrins can occur. These compounds then become metabolized to the aldehydes and then to the respective indole-3-carboxylic acids. Indole- and A⁷-methylindole-3-glyoxylic acids do not appear to be involved in the a-oxidation reaction to any significant extent. Relevant studies on the metabolism of indole-3-acetaldehyde-cyanohydrin are also described.     

Studies with 3,5-diiodo-4-hydroxybenzonitrile (ioxynil) and related compounds in soils and plants

The inactivation of the herbicide ioxynil by contact with soil has been investigated. Shaking solutions of the sodium salt with acid soils led to a precipitation of the herbicide. With alkaline soils, a small amount of ioxynil became adsorbed on the soil particles. With unsterilized soils, hydrolysis to 3,5-diiodo-4-hydroxybenzoic acid occurred, with 3,5-diiodo-4-hydroxy-benzamide as an intermediate product. Liberation of iodide ion in this system was also demonstrated. The phytotoxicity of ioxynil is enhanced by exposure of treated plants to light. The reduction in chlorophyll level of bean leaf tissue treated with ioxynil and other dihalogenohydroxybenzonitriles when exposed to light has been determined. Evidence is presented showing that although ioxynil is poorly translocated in the dwarf bean plant, its degradation products appear in the shoots of these plants after the herbicide has been supplied through the roots.