Lack of Gastric Inhibitory Polypepetide (GIP) response to vagal stimulation in the rat

The effect of sham feeding on the plasma concentration of gastric inhibitory polypeptide (GIP) was studied in unrestrained rats bearing chronic gastric fistulas and jugular catheters. While no increase of plasma GIP concentration could be detected during sham feeding (fistula open), during normal feeding (fistula closed), plasma GIP concentrations rose rapidly. In contrast to GIP, plasma insulin concentrations showed a rapid and phasic response during sham feeding in the absence of changes of glycemia. In anesthetized rats electrical stimulation of the vagus nerve was without any effect on plasma GIP concentration, while plasma insulin increased rapidly by as much as 150 percent. It is concluded that under the conditions used, the full gastric and/or intestinal phases of food ingestion are necessary to trigger GIP release, and that vagal activation alone is unable to stimulate GIP release in the rat.     

Breath ethane generation during clinical total body irradiation as a marker of oxygen-free-radical-mediated lipid peroxidation: A case study

Total body irradiation (TBI) is used therapeutically for treatment of leukemias and other malignancies of the hemopoietic system. Ionizing radiation produces oxygen free radicals that contribute to cytotoxicity. Breath collected from one patient undergoing therapeutic TBI showed measurable changes in levels of ethane during treatment. Breath ethane is a marker of lipid peroxidation of n-3 fatty acids. The TBI treatment involved 4 days of irradiation. The largest changes in breath ethane occured on Day 2. The increased levels of breath ethane on Day 2 were correlated to clinical manifestations of toxicity. The correlation of the onset of gastrointestinal side effects with higher levels of breath ethane suggests that breath ethane may be a clinically useful measure of the toxicity of various TBI fractionation treatment protocols currently in use at different medical centers. The levels of breath ehtane on the other days of treatment were lower, suggesting that the oxidative-antioxidative balance of the patient may be important in protection against free radical mediated injury. These results for a single patient suggest that breath ethane may be a promising approach to elucidate the role of antioxidants in clinical TBI and should be extended for verification to a larger volunteer patient population.     

A re-investigation of the kinetics of alkaline degradation of phenyl β-d-glucopyranoside and some other glycosides

Previous investigators of mechanisms of alkaline degradation of glycosides in which the 2-hydroxyl group is trans to the aglycon concluded that the major reaction-pathway occurs via an SnicB substitution by the C-2 oxyanion at C-1. Recent reports also suggested that, for the phenyl d-glucopyranosides, direct Sn2 substitution by hydroxyl ion at C-1 competes isgnificantly with the SnicB pathway. We now conclude that the latter hypothesis was in error, because of failure to allow for variation in activity values for hydroxyl ion and water. For the nitrophenyl glycosides, however, we confirm that Sn2AR reactions compete with the SnicB pathway.     

The primary structure of porcine glicentin (proglucagon)

The primary structure of porcine glicentin has been established. The molecule consists of 69 amino acid residues and has a molecular weight of 8128. The sequence of glicentin 1–30 represents the glicentin-related pancreatic peptide (GRPP) previously isolated from porcine pancreas. The sequence 33–61 represents the full sequence of glucagon and the sequence 64–69 is a C-terminal hexapeptide. These three sequences, GRPP, glucagon and the hexapeptide are linked by two Lys-Arg pairs which probably represent the sites for post-synthetic enzymatic cleavages. Glicentin thus fulfils the structural requirements for being proglucagon.     

Jejunal factor stimulating insulin release in the isolated perfused canine pancreas and jejunum.

In the present study using an isolated perfused preparation of canine jejunum and pancreas, an insulin-releasing factor was found in the venous effluent of the jejunum. Insulin secretion by the pancreas rose twofold after 10% glucose was infused in the lumen of the jejunum and remained at a high level even after the stimulus was discontinued. No modification of the exocrine pancreatic secretion occurred during the insulin release, and therefore it seems unlikely that gastrin, secretin or cholecystokinin-pancreozymin were released by the jejunal mucosa. In control experiments the values of hyperglycaemia observed previously and intraluminal hyperosmolarity were tested: at these levels, they did not affect insulin secretion. The nature of this intestinal insulin-releasing factor remains unknown however, but may be identifiable when intestinal hormones in blood can be assayed reliably.     

Zyxin-VASP interactions alter actin regulatory activity in zyxin-VASP complexes

Cell-cell and cell-substrate adhesions are sites of dramatic actin rearrangements and where actin-membrane connections are tightly regulated. Zyxin-VASP complexes localize to sites of cell-cell and cell-substrate adhesion and function to regulate actin dynamics and actin-membrane connections at these sites. To accomplish these functions, zyxin recruits VASP to cellular sites via proline-rich binding sites near zyxin’s amino terminus. While the prevailing thought has been that zyxin simply acts as a scaffold protein for VASP binding, the identification of a LIM domain-VASP interaction could complicate this view. Here we assess how zyxin-VASP binding through both the proline rich motifs and the LIM domains alters specific VASP functions. We find that neither individual interaction alters VASP’s actin regulatory activities. In contrast, however, we find that full-length zyxin dramatically reduces VASPmediated actin bundling and actin assembly. Taken together, these results suggest a model where zyxin-VASP complexes occur in complex organizations with suppressed actin regulatory activity.     

New discoveries of vertebrates from a near-shore marine fauna from the Early Miocene of northwestern Venezuela

New discoveries from a recently described nearshore marine fauna from northwestern Venezuela of presumed early Miocene age are reported. The fossils consist of a cranial portion of a crocodile assigned to the Tbmistominae, confirming the presence of this group in South America, and the scapula of a cetacean with affinities to the Platanistoidea. The stratigraphic section of the fossil locality ‘Cerro La Cruz’ consists of ca. 87 m of clayey marls interbedded with thin hardground units, with the upper strata being gypsiferous. The fossils were found in sandstones stratigraphically above this sequence.      

The population dynamics of eyeflukes Diplostomum spathaceum and Tylodelphys clavata (Digenea: Diplostomatidae) in rainbow and brown trout in Rutland Water: 1974–1978

The development of populations of eyeflukes Diplostomum spathaceum and Tylodelphys clavata in trout introduced into Rutland Water is related to the availability of infected Limnaea pereger, the first intermediate host, and the differential resistance to eyeflukes in Salmo gairdneri and S. trutta. The numbers of snail and fish intermediate hosts were monitored from impoundment of the Gwash in 1974 to completion of the reservoir in 1978. High infection rates in coarse fish in the feeder streams in 1974 are related to high infection rates in Limnaea pereger. Large eyefluke populations in introduced rainbow trout but not in brown trout confirm their differential resistance. Differences in levels of infection in seine-netted and rod-caught rainbow trout suggest that heavily infected fish could not respond to the fishermens' lures. Reduced numbers of eyeflukes in rainbow trout from 1979 onwards are related to the vast increase in volume of the reservoir in 1977 and decrease in abundance of Limnaea pereger.     

Why Lyme disease is common in the northern US,but rare in the south: The roles of host choice,host-seeking behavior,and tick density

Lyme disease is common in the northeastern United States, but rare in the southeast, even though the tick vector is found in both regions. Infection prevalence of Lyme spirochetes in host-seeking ticks, an important component to the risk of Lyme disease, is also high in the northeast and northern midwest, but declines sharply in the south. As ticks must acquire Lyme spirochetes from infected vertebrate hosts, the role of wildlife species composition on Lyme disease risk has been a topic of lively academic discussion. We compared tick–vertebrate host interactions using standardized sampling methods among 8 sites scattered throughout the eastern US. Geographical trends in diversity of tick hosts are gradual and do not match the sharp decline in prevalence at southern sites, but tick–host associations show a clear shift from mammals in the north to reptiles in the south. Tick infection prevalence declines north to south largely because of high tick infestation of efficient spirochete reservoir hosts (rodents and shrews) in the north but not in the south. Minimal infestation of small mammals in the south results from strong selective attachment to lizards such as skinks (which are inefficient reservoirs for Lyme spirochetes) in the southern states. Selective host choice, along with latitudinal differences in tick host-seeking behavior and variations in tick densities, explains the geographic pattern of Lyme disease in the eastern US.

Lyme disease is common in the northeastern United States, but rare in the southeast, even though the tick vector is found in both regions. This study shows that this is largely because the tick vectors attach abundantly to rodents (which are good hosts for the Lyme bacteria) in the north, and to lizards (which are relatively poor hosts for Lyme bacteria) in the south.