Search PubMed⌕ Search

Biomedical subjects

G M Alder

Publications and source records attributed to G M Alder.

21 records · Page 2Linked to original sources

Common action of certain viruses, toxins, and activated complement: pore formation and its prevention by extracellular Ca2+.

Haemolysis by Sendai virus, alpha-toxin, and activated complement is inhibited by high concentrations of divalent cations. In Daudi cells, sublytic amounts of these agents induce the following changes: collapse of surface membrane potential, uptake of Na+ and loss of K+ from cells, and leakage of phosphorylated metabolites from cells. The changes induced by Sendai virus and complement are sensitive to physiological concentrations of extracellular Ca2+. It is concluded that fluctuations in plasma Ca2+ concentration may affect the damaging action of certain pore-forming agents on susceptible cells.

Bacterial Toxins↗

The effect of Ca2+ on virus-cell fusion and permeability changes.

Sendai virus-mediated permeability changes in Lettre cells or red blood cells are affected by extracellular Ca2+ in the following way: the lag period to onset of permeability changes is lengthened and the subsequent extent of leakage is reduced. Ca2+ neither stimulates nor inhibits fusion of the viral envelope to the plasma membrane of Lettre cells or red blood cells. It is concluded that Ca2+ protects cells against virally-induced permeability changes in a manner not involving membrane fusion.

Calcium↗

The effect of air resistance on the jumping performance of insects.

A spring gun was constructed to propel objects at known velocities of between 1 and 4.5 m.s-1. This was used to project insects and various models in a vertical trajectory. By comparing the height attained in air by the insects or models with the height theoretically possible in vacuo, the energy lost against air resistance was observed. Small insects have a higher frontal area to mass ratio than larger ones so have relatively more aerodynamic drag and attain lower heights. The observed effect may be expressed in terms of the drag coefficient, CD. Fleas and locusts have CD of about 1. Winged flies have CD of about 1.5 which falls to about 1 when the wings are amputated and to about 0.8 when the legs are amputated. Aptery is advantageous in jumping insects. From experiments with models, it appears that the optimal condition for small jumping insects is that the body should be as compact as possible to reduce the frontal area to mass ratio. Thus dense spherical bodies are favoured. Some species of jumping insect have densities of about 1 mg.mm-3 while some flying beetles and flies have densities between 0.3 and 0.8 mg.mm-3. The Reynolds number at which the experiments were performed was from 65-205 for fleas up to 740-2340 for locusts. The models operated in similar ranges. At a velocity which would propel a larger animal to a height of 1 m, fleas weighing 0.4 mg only reach about 0.4 m. At lower initial velocities, proportionately less energy is wasted against air resistance so the jump efficiency is higher. Most fleas jump to a height of about 0.1 m with an efficiency of 0.8 while locusts jump to a height of 0.35 m with an efficiency of over 0.9. Air resistance is thus an important scale effect in jumping insects and provides its own design constraints.

Air↗