Trophic effects of essential fatty acids on pig skin

The daily oral administration of 3 ml of two oils (So-5407 and So-1129) containing essential fatty acids (EFAs) for 16 weeks resulted in a transient increase in cell proliferative activity in the skin of female Large White pigs. The So-5407 oil contained 7% gamma-linolenic acid (GLA) whereas So-1129 was an oil of similar composition, but with no GLA. Hyperplasia of the epidermis was observed after the administration of both oils, and this was characterized by an increase in the size of the rete pegs. The maximum effect occurred at 4 weeks after the start of oil administration, at which time the number of viable cell layers had increased by a factor of approximately 1.5, and mean epidermal thickness (excluding the stratum corneum) was approximately 40% greater than that of the epidermis prior to oil administration. There was a marked increase in the labelling index (LI) of the basal cell layer of the epidermis in pigs receiving So-5407. Maximum LIs were quantified at 4 weeks after the start of administration and were 18.8 ± 1.3% and 13.1 ± 1.7% for pigs receiving So-5407 and So-1129, respectively. After this time the LI declined prgressively and had returned to values within normal limits (P>0.1) by 8 weeks after the start of administration of both oils. A similar pattern of change in the LI was seen in the follicular epithelium, although the peak values at 4 weeks after the start of oil administration of 12.2 ± 1.8% and 10.8 ± 0.9 for the groups receiving So-5407 and So-1129, respectively, were lower than in the epidermis. Labelled cells were also counted in the papillary dermis and maximum values were again seen at 4 weeks after the start of oil administration. Of the two oils, So-1129 had the greatest effect, with the number of labelled cells in the papillary dermis being a factor of three to four-fold higher than in skin prior to oil administration, between 2 and 12 weeks after the start of administration.     

Similar effects of platelet-derived growth factor and epidermal growth factor on the phosphorylation of tyrosine in cellular proteins

Platelet-derived growth factor (PDGF) stimulates the phosphorylation of proteins at tyrosine when added to quiescent 3T3 cells, as evidenced by the increase in the amount of phosphotyrosine, relative to phosphoserine and phosphothreonine, in cellular proteins. The increase was detected within 1 min of adding PDGF and was maximal by 5 min. This effect showed the same dependence on PDGF concentration as did association of 125I-PDGF with the cells. In different 3T3 cell lines the magnitude of the increase was approximately proportional to the number of PDGF receptors per cell. A number of proteins phosphorylated at tyrosine in response to PDGF have been detected by two-dimensional gel electrophoresis. They include a pair of related 45 kilodalton phosphoproteins, a pair of related 43 kilodalton phosphoproteins and a 42 kilodalton phosphoprotein. Similar changes were noted when quiescent 3T3 cells were incubated with epidermal growth factor. Possibly, these phosphoproteins are primary substrates of the tyrosine protein kinases activated by the receptors for PDGF and epidermal growth factor, and are involved in physiological effects common to the two growth factors.     

Oscillations and efficiency in glycolysis

We suggest that temporal oscillations of concentrations of intermediates in biochemical reaction systems may enhance the efficiency of free energy conversion (reduce dissipation) in those reactions. Experiments on glycolysis are used to estimate the Gibbs free energy changes along the glycolysis mechanism, and to postulate a construct for the glycolysis "machine" which involves: the PFK reaction as the primary oscillophor; the GAPDH reaction as a phase-shifting device; and the PK reaction with the property of intrinsic oscillatory response at resonance with the driving frequency. Analysis of a simple reaction mechanism with these postulated properties shows that the conversion of free energy from reactants to products is more efficient in an oscillatory than a steady state operation. The efficiency of free energy conversion in glycolysis from glucose + ADP to products + ATP is estimated to be increased by 5--10% due to oscillations. This may have been relevant for the evolutionary development of oscillations such as in glycolysis, especially in anaerobic cells.     

Competitive interactions and the availability of sleeping sites for a diurnal coral reef fish

A field study was made to test whether the population size of a diurnal reef fish, the wrasse Thalassoma bifasciatum (Bloch), was limited by inter- or intraspecific competition for sleeping shelter. T. bifasciatum is often attacked at dusk by two small territorial damselfishes, Eupomacentrus dorsopunicans (Poey) and E. planifrons (Cuvier). Although these three species sleep in the same general habitats, there are qualitative differences in the types of holes they use and how they use them. Wrasse holes are usually in these damselfishes' territories, but damselfish attacks do not prevent wrasses entering holes. Wrasses infrequently defend their holes intraspecifically. They regularly change their holes, with little intra- or interspecific aggressive interaction. When its hole is removed, a wrasse is late in retiring but finds a hole near its old one with little aggressive interaction, and does not have a higher mortality rate. Empty wrasse holes are rarely refilled, and then only by conspecifics. Wrasses added to reefs find unoccupied holes and do not usurp other fishes' holes. Damselfish defend their eggs and food against the wrasse, but not their sleeping shelter, nor living space per se. Sleeping sites are not limiting the wrasse, but are present in a surplus. Intraspecific hole defense by a wrasse prevents a delay in its retiring that would increase the risk of crepuscular predation on it.     

Territorial Behavior and Ecology of the Anemonefish Amphiprion melanopus on Guam1)

Field observations and experiments on the Indo-Pacific anemonefish Amphiprion melanopus at Guam show that it colonizes the aggregating sea anemone Physobrachia douglasi extensively and nearly exclusively. There are an average of four fish per colony. The total standard length of anemonefish at each aggregation is highly correlated with the total area covered by resident anemones, suggesting both a carrying capacity and some form of social control of growth of anemonefish²). Inter-colony migration of juveniles, as well as larval recruitment, may contribute to maintenance of the optimum colony size. Adults do not migrate. Both juveniles and adults defend territory. Juvenile territories are mutually exclusive areas within the confines of the anemone aggregation, while adult territories are considerably larger than the area covered by the anemone aggregation. Though territories of mated ♀♀ and ♂♂ overlap completely, female emphasis is peripheral relative to the ♂. Adult conspecific intruders are attacked more heavily and at greater distances than are juveniles. Intraspecific territoriality in juveniles probably reflects the limited availability of critical habitat. In adults it may function to protect the pair bond. Interspecific aggression is less intense and appears to protect both the spawn and host anemones from various predators.     

On the Stability of Messenger RNA and Ribosomal RNA in the Brains of Control Human Subjects and Patients with Alzheimer''s Disease

The levels of the mRNAs encoding the G protein subunits GS alpha, G beta 1, and G beta 2 were measured by northern blotting in the frontal cortex and hippocampus of control subjects and of patients with a clinical and histopathological diagnosis of dementia of the Alzheimer type (DAT). There was no significant difference, in either brain region, between the control and DAT groups for any of the G protein mRNAs measured. The degree of intersubject variability was very high, e.g., GS alpha mRNA in the frontal cortex (mean optical density +/- SD) was 405 +/- 342 in the control group versus 305 +/- 207 in the DAT group. The extent of generalised RNA degradation was assessed by detecting the breakdown products of 28S rRNA. RNA degradation was present in tissue samples from every human subject studied. The extent of 28S rRNA degradation in each subject was found to be related to the levels of G protein mRNA detected. The degree of RNA degradation in human subjects was found to be very variable and unaffected by the presence of DAT. RNA degradation correlated poorly with postmortem interval and this was confirmed by a controlled study of postmortem degradation in rat tissue. The possibility that the relative hypoxia and ischaemia in patients immediately before death could influence RNA degradation is discussed. The variable extent of RNA degradation means that great care must be taken to ensure the validity of RNA analyses undertaken in human postmortem brain, particularly when techniques are employed (such as in situ hybridisation) that themselves give no indication of RNA integrity.