Condition and fate of larvae from insecticide-treated female tsetse flies Glossina palpalis

Many larvae from wild-caught female Glossina palpalis palpalis R.-D. treated topically with dieldrin or sumicidin or sumithrin or permethrin failed to pupariate and many larvae from mothers treated with sumicidin or sumithrin or neopynamin formed small or malformed puparia which failed to eclode. Puparia produced soon after maternal handling often did not emerge and many produced by flies starved more than 3 days also did not emerge. Very many puparia from dieldrin-treated mothers failed to emerge and non-emergence was common for puparia from flies treated with endosulfan or sumithrin or deltamethrin. Non-emerging puparia were produced soon after pyrethroid-treatment, probably due to effects on larval integumentand muscles, but were produced later after organochlorine-treatment, due to ingestion of insecticide by larvae while in utero.

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Résumé Les expériences ont porté sur des femelles sauvages de Glossina palpalis palpalis R.D. capturées dans la nature. Les comparaisons ont porté sur l'état et les performances de lots de pupes provenant de mouches non-traitées et de larves mûres traitées localement avec de l'acétone (témoin) ou avec 14 insecticides différents.Toutes les larves témoin se sont nymphosées, mais le taux d'échec augmentait avec la diéldrine, la sumicidine, la sumithrine et la permethrine. Les pupes anormales (petites ou déformées) étaient plus nombreuses dans le lot témoin que dans le lot non-traité, et les fréquences étaient plus élevées que chez le témoin avec la sumidicine, la sumithrine et la néopynamine.Seulement 3 mouches sont issues de 107 pupes anormales; il n'y a eu aucune éclosion pour 28% des pupes du lot témoin contre 15% pour le lot non-traité. Pour le témoin le taux d'émergence était faible dans les pupes formées le premier jour (jour du traitement), par suite de la manipulation maternelle; il n'a pas augmenté jours 2 et 3, mais a diminué par la suite à cause du jeûne in utero. Les doses élevées de tous les insecticides réduisent plus les émergences que les doses faibles. Les organophosphates et le propoxur ne limitent pas les émergences, mais elles sont réduites par l'endosulfane, la sumithrine et la deltaméthrine, et très fortement par la diéldrine. Les pupes stériles ont été surtout formées dès le traitement aux pyréthroïdes (jour 1); et surtout plus tard (jours 2 et 3) lors des traitements aux organochlorés. L'ingestion par la larve in utero de grandes quantités d'insecticides pendant les 3 jours précédant la parturition était la principale cause de mortalité, et aussi de la forte tolérance aux organochlorés des femelles prégnantes. Les effets de pyréthroïdes sur l'activité musculaire réduisent aussi les émergences.Aucune mouche ne s'est alimentée après les traitements.

     

Chromosome analysis in chorionic villi samples from the first trimester elective terminations

Chorionic villi sampling (CVS) has become a first trimester alternative to amniocentesis for prenatal diagnosis. The cytogenetic findings in 150 experimental samples are presented. The ages of the mothers ranged from 12 to 35 years, but the majority of them were 18 and 19 years of age. Various parameters of culturing and processing the samples in order to improve the method, were investigated. Short term incubation for 48 h was the method routinely employed in processing the biopsies for cytogenetic analysis. In the first series of 100 cases one mosaic case (46,XX/45,X), one Robertsonian translocation (13;14), one marker chromosome and one fragment were found. The foetal tissues were not analysed for chromosomes. In the second series of 50 samples, one case of mosaicism was found in the chorionic villi (46,XX/47,XX, 18q-), but this abnormality was absent in the foetal tissue. One variant inv(9) was observed in the foetal tissue as well as in the chorionic villi. In all other cases the karyotypes from the chorionic villi samples matched those of the corresponding foetal samples. There was no maternal contamination in this series of 50 samples. The discrepancies in the cytogenetic results from other investigators are discussed.     

Characteristics of an inhibitor of the Na+/K+ pump in human cerebrospinal fluid

Human cerebrospinal fluid (CSF) inhibits the Na+/K+ pump in human red cells and the activity of purified Na+/K+-ATPase (Halperin, J. A., Shaeffer, R., Galvez, L., and Malavé, S. (1985) Proc. Natl. Acad. Sci. U.S. A. 80, 6102-6104, 1983; Halperin, J. A., Martin, A. M., and Malavé, S. (1985) Life Sci. 37, 561-566. We describe here some properties of the CSF inhibitor of the Na+/K+ pump. Active material was extracted from human CSF with 50% methanol and then concentrated and desalted by ultrafiltration. This extract inhibited, in a dose-dependent manner, the ouabain-sensitive influx of K+ into human red cells and the activity of purified Na+/K+-ATPase. Partial separation of the inhibitory activity was achieved by gel filtration and reverse-phase high performance liquid chromatography. Inhibition of both pump and enzyme was specific in that other red cell membrane transport systems or enzymes examined were not influenced by CSF extracts. Dialysis and ultrafiltration experiments indicate that the molecular weight of the inhibitor is approximately equal to 600. The inhibitory activity is sensitive to proteolytic enzymes indicating that the inhibitor might be a small peptide. In the presence of CSF extract the K0.5 for external K+ to stimulate the Na+/K+ pump increased from 1.4 to 3.1 mM, suggesting that the CSF inhibitor competes with external K+ for stimulation of the pump. We estimate that the concentration of the inhibitor in CSF might be approximately equal to 50 pg/ml, a value close to the concentration of other active peptides found in human CSF.     

Angiogenic activity of human tumor plasma membrane components

Plasma membranes from the human colon adenocarcinoma cell line HT-29 have been isolated and examined for the presence of angiogenic activity. Membrane-associated macromolecules extracted with Triton X-100 were fractionated on immobilized wheat germ agglutinin. The fraction which bound specifically (about 200 ng of protein/mL packed cells) was highly angiogenic when assayed on the chick embryo chorioallantoic membrane. As little as 0.2 ng of this human tumor derived material consistently induced neovascularization. Similarly, 1-2 ng of this material implanted into the rabbit cornea induced new vessel growth (5-8 mm) within 10 days. The plasma membranes of eight other human tumor lines were examined for angiogenic activity. For each, the wheat germ agglutinin bound material induced neovascularization at the low nanogram level. In contrast, the wheat germ agglutinin bound material derived from purified plasma membranes of two normal human diploid fibroblast cell lines failed to induce an angiogenic response on the chick chorioallantoic membrane, even at microgram levels.     

Fine-structural alterations in Leishmania tropica within human macrophages exposed to antileishmanial drugs in vitro

The mechanism of action of antileishmanial compounds is poorly understood. Ultrastructural changes in Leishmania tropica within human macrophages exposed in vitro to Pentostam, pentamidine, amphotericin B, WR 6026, ketoconazole, and Formycin B were examined in these experiments. In Pentostam-treated cultures, some organisms exhibited diminished definition of mitochondrial and other membranes, while other organisms had completely disintegrated. Pentostam-exposed macrophages demonstrated loss of membrane definition in the absence of further alterations; it is therefore hypothesized that impaired macrophage membrane function may contribute towards the effect of this drug against macrophage-contained organisms. Leishmania parasites in pentamidine-treated cultures initially demonstrated swollen kinetoplasts and fragmentation of the kinetoplast DNA core. The initial observed effect of the other four drugs on the parasites was cytoplasmic condensation. These ultrastructural studies suggest that all five non-antimonial drugs may have different mechanisms of action than antimony (Pentostam) against Leishmania.     

The role of nickel in acetyl-CoA synthesis by the bifunctional enzyme CO dehydrogenase/acetyl-CoA synthase: enzymology and model chemistry

 CO dehydrogenase/acetyl-CoA synthase (CODH/ACS) is one of the four known nickel enzymes. It is a bifunctional protein that catalyzes the oxidation of CO to CO₂ at a nickel iron-sulfur cluster (Cluster C) and a remarkable condensation reaction between a methyl group (donated from a methylated corrinoid iron-sulfur protein), carbon monoxide, and coenzyme A to form acetyl-CoA at a separate nickel iron-sulfur cluster (Cluster A). This review focuses on the current understanding of the structure and function of Cluster A and on related model chemistry. It describes studies that uncovered the first example of a biological organometallic reaction sequence. The mechanism of acetyl-CoA synthesis includes enzymebound methylnickel, iron-carbonyl, and acylmetal intermediates. Discovery of the methylnickel species constituted the first example of an alkylnickel species in biology and unveiled a new biological role for nickel. Received: 10 April 1996 / Accepted: 4 July 1996