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H Gilles

Publications and source records attributed to H Gilles.

7 recordsLinked to original sources

The chemotherapy of onchocerciasis. XIV. Studies with mebendazole citrate.

Twenty patients from an area of vector control in the savannah region of northern Ghana with moderate to heavy infection with Onchocerca volvulus were randomised to receive two priming doses of levamisole 150 mg on two occasions followed either by mebendazole-citrate (500 mg) given daily or twice daily for 14 days. The two dose levels produced a similar effect on skin microfilariae (80-88% reduction) with a very mild systemic clinical reaction: low levels were maintained over 42 weeks. Both regimes were embryotoxic for O. volvulus; an effect which was transient in the single dose group but persisted for more than three months in the twice daily dose group. Mebendazole-citrate appeared to be absorbed more predictably than has been observed previously for mebendazole. The degree of systemic exposure as determined by measurement of AUC (0-24 h) was 2.5 times greater for the twice daily dose as compared to the single dose and this fact was reflected in the efficacy of the two dose regimes against the adult female worms at three months.

Adult

Uroporphyrinogen III, an intermediate in the biosynthesis of the nickel-containing factor F430 in Methanobacterium thermoautotrophicum.

Factor F430 is a nickel-containing porphinoid present in methanogenic bacteria. The synthesis of this nickel tetrapyrrole from 5-aminolevulinic acid was studied in Methanobacterium thermoautotrophicum. This anaerobic archaebacterium was found to accumulate [14C]uroporphyrinogen III (1.8 mumol/g) when growing on nickel-free medium (less than 50 nmol/l) supplemented with 2 mM 5-amino-[14C]levulinic acid. The accumulated urophorphyrinogen III was quantitatively converted to factor F430 when the cells were incubated in aminolevulinate-free medium with 5 microM NiCl2. The newly synthesized factor had the same specific radioactivity as the precursor uroporphyrinogen III. These findings indicate that the nickelporphinoid is biosynthetically derived from uroporphyrinogen III. The presence and some properties of the enzymes catalyzing the synthesis of uroporphyrinogen III from 5-aminolevulinic acid in M. thermoautotrophicum are also described.

Aminolevulinic Acid

Malaria.

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Brain Diseases